tisdag 28 november 2023

Causes of dry eyes and dry mucous membranes - Anticholinergic medication

 

Acetylcholine - Function and Role in the Body. How certain medication affects Muscarinic receptors and causes dry eyes, dry mucous membranes, and other anticholinergic side effects

To understand what acetylcholine is, one must first comprehend what a Synapse is: A Synapse is a connection between two neurons or between a neuron and a target cell. However, the connection is not electrical; instead, it occurs chemically through neurotransmitters. The signaling process unfolds as an electrical signal reaches the presynaptic nerve cell. Various types of neurotransmitters are then released from it, which are received by receptors on the postsynaptic nerve cell. From here, the chemical signals are once again converted into electrical ones, leading to an electrical nerve impulse being sent to the relevant part of the body. One such crucial neurotransmitter is acetylcholine.c

Acetylcholine is a neurotransmitter released from postganglionic nerves. This neurotransmitter is found, among other places, in the synapses between nerves and muscles, and the body utilizes this neurotransmitter to chemically transmit nerve signals to other cells such as neurons, muscle cells, and glandular cells.

When it comes to muscles, it's acetylcholine that is responsible for ensuring that the nerve impulse reaches its destination so that the muscle can contract. An enzyme called acetylcholinesterase then rapidly breaks down the remaining acetylcholine in the synapse, allowing for a new signal to be sent to the muscle for further movement. Therefore, acetylcholine is essential for various functions, including our ability to move.

Acetylcholine is also present in the brain's cortex, where it helps maintain normal electrical activity and, consequently, wakefulness. Additionally, acetylcholine is the neurotransmitter responsible for allowing electrical signals to reach glands in the body, triggering the production of secretions. Examples of such glands include salivary glands and tear glands. Acetylcholine also influences the secretion of digestive enzymes. For instance, acetylcholine is the neurotransmitter that prompts the pancreas to produce bile, which is crucial for breaking down fats in food.

In short, it can be said that acetylcholine regulates all types of secretion in the body. This ranges from saliva, tears, nasal mucin, to secretions and enzymes in the intestines. Additionally, acetylcholine functions to contract the muscles in the intestinal wall, aiding in the breakdown of the food we eat and its gradual movement downward through the intestines. From the aforementioned points, one can thus conclude that acetylcholine plays an extensive and highly important role in the human body. Medications that affect the production of this neurotransmitter can therefore have significant impacts on the body.

Medications and their effects on the neurotransmitter acetylcholine.

Systems in the body where signals are transmitted by acetylcholine are referred to as cholinergic. This is important to know because there are various types of medications that have so-called anti-cholinergic effects. Anti-cholinergic effects mean that the medication blocks the function of acetylcholine. When this effect is blocked, nerve signals do not reach the body parts that normally receive signaling via the neurotransmitter. In concrete terms, this means that tear glands, sweat glands, and salivary glands, for example, do not receive the signal to produce secretions. The switch for these body parts is effectively turned off. However, the impact doesn't only extend to the mentioned organs. All bodily functions that involve larger or smaller glands are affected. This includes the lungs, intestinal lining, reproductive organs, nasal lining, throat, mouth, and so on.

Deepening the understanding of the function of the neurotransmitter acetylcholine:

To delve a bit deeper into how acetylcholine functions, it's worth mentioning that acetylcholine activates muscarinic and nicotinic receptors in the body. Concerning muscarinic receptors, there are five types: M1, M2, M3, M4, and M5. Below is a general explanation of where these different types of receptors are located and how they impact the body. The information below is primarily sourced from the study titled "Muscarinic receptors: their distribution and function in body systems, and the implications for treating overactive bladder."

You can access the study at the following link: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1751864/

Muscarinic acetylcholine receptor M1:

This receptor is commonly found in the central nervous system and in exocrine glands. Exocrine glands are those that secrete substances through channels to the body's mucous membranes. Examples of such glands include sweat glands, tear glands, salivary glands, the prostate gland, mucous glands in the respiratory tract, the exocrine part of the pancreas, mammary glands, glands in the ear canal, sebaceous glands (found in the skin), and more.

Speaking of sebaceous glands, these are found in various parts of the body in slightly different forms and with different functions. In English, they're referred to as "Sebaceous glands." The Meibomian glands in the eyelids are one type of sebaceous gland. Other examples of similar sebaceous glands in the body are located in the nose, specifically in the outer part of the nasal cavity, on the male genitalia (particularly on the glans penis), in the female genitalia (such as the labia minora and nipples), and more.

Muscarinic M1 receptors are also present in the brain, specifically in the hippocampus, cerebral cortex, and peripheral ganglia. Muscarinic M1 receptors also influence involuntary bodily functions, memory, and learning.

Muscarinic acetylcholine receptor M2:

These receptors are located in the heart and lungs, where they are responsible for slowing down the heart rate. Inhibiting the M2 receptor with anticholinergic medications like Atropine increases heart rate. The receptor is also found in the smooth muscle throughout the body, which covers many of the body's tubular cavities such as blood vessels, internal organs, intestines, esophagus, trachea, and the sphincter muscles. M2 receptors are also present in the dermis, close to hair follicles.

Muscarinic acetylcholine receptor M3:

The M3 receptor is found in various locations in the body, including the smooth muscles (as described above). Activation of this receptor typically leads to an increase in intracellular calcium and consequently a cholinergically-induced contraction in smooth muscle. This receptor is involved in processes such as intestinal motility (intestinal movement), where the smooth muscles around the intestines contract to facilitate digestion, cleansing, and emptying of the bowels. It's also involved in the contraction of the bladder during urination and the constriction of bronchi in the lungs.

Muscarinic acetylcholine receptor M4:

The M4 receptor is also present in the lungs and the central nervous system. Activation of the M4 receptor inhibits the release of acetylcholine in the striatum. The striatum is a region in the brain present in both hemispheres, affecting our cognition. It controls reward perception, future reward anticipation, decision-making, action planning, reinforcement, and motivation. The dorsal (upper) striatum controls impulsivity and inhibition of such impulses. In humans, the striatum activates in response to rewards or unexpected/intense stimuli. Dysfunction in the striatum can lead to conditions like depression and obsessive-compulsive disorder. Due to its involvement in reward perception, the striatum is also related to addiction. It's known to contribute to the reinforcing effects of stimulants, such as alcohol, through dopaminergic stimulation.

Muscarinic acetylcholine receptor M5:

The M5 receptor is present in many organs, but comprehensive explanations and research are lacking. Some known aspects include the fact that acetylcholine binding to the M5 receptor triggers several cellular responses, such as adenylate cyclase inhibition, phosphoinositide breakdown, and potassium channel modulation.

Muscarinic receptors in the body, localization, and function:

Muscarinic receptors are found throughout the body. Below are therefore just a few examples of where to find the receptors and what functions they have in the various tissues.

Bladder: All 5 Muscarinic receptors are found here, but M2 and M3 have been shown to be dominant. Both receptors have the function of contracting the bladder during urination.

Salivary glands: M1 and M3 receptors. Activation of both receptors leads to secretion of saliva.

Intestines: In studies of guinea pigs, M1-M5 have been found in the smooth muscle of the intestine. As far as humans are concerned, M2 and M3 are considered to be the receptors with the most functionality. However, M2 receptors are the receptors of which there are the most in number. In studies on dogs, it has been shown that the M3 receptor is the one most responsible for bowel movements through the activation of smooth muscle.

The brain: All 5 receptors are found here. Muscarinic receptors in the brain activate a variety of signaling pathways important for modulation of neuronal excitability, synaptic plasticity and feedback regulation by Acetylcholine.

The eyes: M1-M5 are found here, i.e. all Muscarinic receptors. The percentage distribution of each receptor type is as follows: M3 60-75%, M2 5-10%, M4-10%, M1 7%. In the Iris Sphincter (pupil muscle) 5%.

In studies on mice, it has been found that the M3 receptor contracts a smooth muscle in the eye called the "Iris Sphincter muscle" in English. This musculature is part of the Iris (I.E. the colored area that surrounds the pupil). The muscle's function is to contract the pupil to regulate the amount of light entering the eye.

In studies on rabbits, it has also been found that the M5 receptor works by contracting the so-called "Ciliary muscle" of the eye. DVS in the ring-shaped muscle of the eye which is responsible for accommodation. A process that occurs when the eye focuses on an object. (During accommodation, the lens either flattens or becomes concave). Further studies have also established that further influence on the pupil's ability to contract or dilate occurs through influence on the M2 receptor.

As for the M1 receptor, this is present in the Iris, Sclera (the white area around the iris) and in the epithelial cells that lie in front of the lens, i.e. between the lens capsule and the lens fibers. These epithelial cells are responsible for homeostasis of the lens. Homeostasis means that the body arranges the perfect conditions for optimal functioning of the organ. For example, the right fluid balance, the right temperature, the right PH, the right concentrations of blood sugar, mineral balance, etc.

Animal studies have also established that M1, M2 and M3 receptors can activate goblet cells (cells that produce secretions) on the conjunctiva (the conjunctiva of the eye). That is, the epithelial membrane that covers the inside of the eyelids and the membrane that covers the white part of the eye. The goblet cells on this membrane produce the secretion that is a significant part of the tear film.

Anticholinergics thus have many negative effects on the eye and from the text above you can now understand why a direct effect of Anticholinergics is light sensitivity and difficulty focusing the gaze as well as problems with dryness and blurred vision. From earlier in the text, we have also established that anticholinergics also shut down sebum production in the skin's sebaceous glands. The meibomian glands in the eyelids that produce fat for a stable tear film are to be considered a specialized sebaceous gland. Therefore, Anticholinergics also negatively affect this part of the tear film.

The Lacrimal Gland: At the time of writing, I have not been able to find any documents showing which Muscarinic receptors are found in the Lacrimal Gland. However, it has been found that the secretion of tears has increased if the Muscarinic receptor (M3) has been stimulated via the intake of a Muscarinic Agonist.

Source: Muscarinic receptor agonists and antagonists: effects on ocular

The heart: Muscarinic receptors M1, M3, M5 have been identified in the human heart. In animal studies, activation of certain Muscarinic receptors has been found to affect heart rate.

The nose: Muscarinic receptors are also found in the mucous membrane of the nose. These receptors play an important role in regulating vasoconstriction and vasodilation of the blood vessels in the nose (the ability of the blood vessels to increase or decrease in diameter). They thus control the function by allowing the turbinates (nasal breathing organs) to swell or contract as needed. In a research study (1.2) carried out on rabbits, it has been established that the secretion of Acetylcholine leads to vasodilatation, i.e. the diameter of the blood vessels increases and the mucous membrane of the nose swells, whereby the passage of air decreases.

Research study (1.2): M1 and M3 muscarinic receptors mediate relaxation and contraction in canine nasal veins: https://pubmed.ncbi.nlm.nih.gov/21679501/

In addition, the Muscarinic receptors also control the secretion-producing goblet cells in the mucosa. An activation of the Muscarinic receptors in the mucous membrane takes place through the signaling substance Acetylcholine and the consequence of this leads to a Parasympathetic reaction in the nervous system where goblet cells (small glands) in the mucous membrane are triggered to secrete secretions.

In study (1.1) "Muscarinic receptor subtypes in human nasal mucosa: characterization, autoradiographic localization, and function in vitro" they looked at the function of Muscarinic receptors M1, M2 and M3 in the nasal mucosa. Here it was concluded that receptor M1 and M2 coexisted in submucous glands (small glands inside the mucous membrane). It was also concluded that M1 receptors can control glandular secretion, while M3 receptors can regulate both secretion from glands and the control of blood vessel diameter in the nasal mucosa.

Research study (1.1): https://pubmed.ncbi.nlm.nih.gov/8427708/

Below you can see an in-depth lecture on Muscarinic receptors.

Antagonist and Agonist explanation

To understand which medications affect the effect of Acetylcholine and subsequently the Muscarinic receptors, you need to know what an Antagonist and an Agonist are.

An Agonist is a substance or medicine that binds to a receptor in a Synapse and stimulates activity in the Synapse. As an example, the following can be mentioned: An Agonist that attaches to a receptor that leads to a muscle thus causes the muscle to contract. An Agonist thus promotes bodily function.

An Antagonist, on the other hand, is a substance or drug that binds to the receptor in a Synapse and which then counteracts the action of the Synapse. That is, an antagonist can reduce or block the signal that would normally have been sent out from the Synapse. When the receptor is blocked, it can no longer perform its function. Body function is inhibited or completely shut down. Below you can see an in-depth film about antagonism and Agonism.

Muscarinic antagonist and anti cholinergic effect

A Muscarinic antagonist is thus a substance or medicine that binds to the Muscarinic receptor but counteracts these natural functions. The nerve signaling out of the synapse is thus weakened or blocked completely and thus the body's natural effect of Acetylcholine is blocked or reduced. The body function that would normally take place if nerve impulses were sent out from the Synapse will thus be affected by being completely absent or by being weakened. Medicines that are muscarinic antagonists are also referred to as anti cholinergic. Such a medicine has what is called an anti-cholinergic effect. That is, the medicine affects the Cholinergic system in the body negatively. Signaling is inhibited or blocked completely.

Anticholinergics a summary

So if you take medicines with an anti-cholinergic effect, all the functions that the Muscarinic receptors M1-M5 normally activate are affected. If you have read the text above, you now realize that there is an extensive negative impact on the body where many body signals are stopped or hindered that would normally be sent to various glands, tissues and organs. One of the most extensive effects this type of medicine has is that it affects all the body's glands. That is, the anticholinergic effect blocks the effect of Acetylcholine. The substance prevents the Muscarinic receptor from sending nerve impulses to the body's glands to produce secretions. This causes mucous membranes to dry out. If you take such a medication for a long time, the consequences can be great and many times irreversible. There are many who have had permanent problems with dry eyes after taking, for example, Antihistamines that have a strong anti-cholinergic effect for longer periods.

Now that you know this, you need to check if the medication you are taking has an anti-cholinergic effect. To do so, you may need to know what to search for. Here are some common names:

Anti cholinergic medication / Cholinergic blockers / Cholinergic antagonists / Muscarinic antagonists / Medications that have cholinergic effects / Medications that affect the cholinergic system / Parasympatholytics

Side effects of Anticholinergics - A list

NOTE: Below is not a complete list of side effects of Anticholinergics

Skin: Drier skin as the production of sebum in the sebaceous glands is inhibited. Reduced sweating with possible heatstroke as a result

Lungs: Impaired secretion in the bronchial mucosa, i.e. in the lungs. Increases risk of throat lung infection caused by breeze on antimicrobial effect of saliva and secretions

Eyes: When taking Anticholinergics - Accommodation difficulties (difficulty focusing the gaze). When taking Anticholinergics - Impaired vision caused by inhibitory effect on the tear film

When taking Anticholinergics - Increased pressure in the eye. This occurs because the muscle that releases the pressure in the eye is deactivated when acetylcholine is blocked. High pressure in the eye can over time cause Keratoconus and Glaucoma. Two conditions that impair vision. PS: High pressure in the eye is treated with the drug Pilocarpine, which is a Cholinergic Agonist and thus activates this muscle.

The three layers of the tear film are inhibited, ie less amount of Tears, Mucin and lipids. Long lasting Blepharitis and dysfunction of the meibomian glands in the eyelids. Finally, cell death of the meibomian glands with chronic dry eyes as a result. In the long run, erosions on the cornea (ulcers) that cause permanent poor vision (Astigmatism).

This is caused by chronic dryness where the cornea is damaged. NOTE This type of vision defect may be impossible or very difficult to correct with glasses. People who have suffered from dry eyes for years are also seen to a greater extent than other individuals to have developed Keratoconus. A conical shape change of the eye that causes impaired vision and increased dryness.

In the long run, inhibiting and lasting negative effect on all glands of the eye = Chronic dry eyes.

In the long run, the Meibomian glands in the eyelids can form back or have impaired function. The same thing can happen with the lacrimal gland and or with all the small goblet cells that sit on the eye and in the mucous membrane around the eye.

Dilation of the pupils (Mydriasis) with consequences see below:

Light sensitivity, Eye pain, blurred vision, headache. Glaucoma in predisposed patients

If you want to read about drugs that cause "dry eye disease" (chronic dry eyes), I would like to refer you to a good page here: 5 Worst Drugs that Cause Dry Eye Disease

Below you can also listen to a good lecture about the cause of dry eyes beyond Drug causes.


Mouth:
Dry mouth with bad breath
Dry mouth with difficulty swallowing due to lack of saliva
Long-term tooth decay as a result of dry mouth

Cognitive ability
Cognitive impairment (drowsiness, brain fog, lack of energy)
Impaired ability to concentrate
Mild confusion (especially in the elderly)
Hallucinations (visual or auditory)

Bladder
Urine retention (difficulty emptying the bladder), this when smooth muscle in the walls of the bladder is negatively affected
Incontinence (difficulty holding in urine)

Intestine and Stomach
Decreased intestinal peristalsis (bowel movements)
Constipation or change in stool consistency
Changes in stool consistency

In the long term, the gut is negatively affected in several different ways. The first way anticholinergics affect is that it inhibits the activity of smooth muscle. Such musculature is found in several different places in the body, the intestinal wall being one such place. This inhibits the intestine's ability to move food back and forth to break it down (break it down). A possible consequence of this is nutritional deficiency. Another consequence is constipation. The intestine must clean itself between meals and push the food on to the large intestine. This allows the gut to rest and recover. If this function is inhibited or blocked, it can lead to an overgrowth of pathogenic (bad) bacteria that irritates and irritates the mucous membrane. In addition, anticholinergics work in the same way in the gut as they do in the body's other glands. It lowers the production of secretions. A secretion that partly contains enzymes but also has an important function of creating a protective membrane in the intestine. 

If you take anticholinergics for a long time, you get less secretions in the intestine. This together with a possible overgrowth of pathogenic bacteria affects the intestinal mucosa negatively with irritation and possibly low-grade inflammation. If, on top of this, you already have an intestinal disease such as Ulcerative Colitis and or Crohn's disease, this can contribute to triggering a relapse. In addition, anticholinergics can worsen or give rise to increased intestinal permeability in the long term. This is because the protective layer of secretions is missing at the same time as there are pathogenic bacteria that irritate the mucous membrane. A continuous increase in intestinal permeability over a long period of time is very negative for health and leads to the development of food intolerances. It also leads to an excessive activation of the immune system which is largely localized to the inside of the intestine. To read more about this refer to searching yourself on: Intestinal permeability or leaky gut.

Inhibition of muscle contraction in smooth muscle
Smooth muscle is muscle tissue that is controlled by the autonomic nervous system (the involuntary nervous system). This muscle tissue sits in the walls of the body's many tubular cavities. Some examples are in: Intestines, bladder, blood vessels, esophagus, trachea and sphincter. Another place that also has smooth muscle is the area closest to the body's hair follicles. When you take anticholinergics, you completely inhibit or block nerve signals to smooth muscle. Since we have so many organs that contain this, it can have negative consequences for each individual organ. To take an example, it can be mentioned that Anticholinergics cause problems with urination if the signal to be sent to the smooth muscle of the bladder is inhibited or blocked. The bladder then has difficulty contracting and emptying may be difficult or impossible to complete fully.

source: The problems of anticholinergic adverse effects in older patients

NOTE: In 2011-2012 I worked at an HVB home for addicts. Here we had a younger guy between 23-26 years old. The person in question had stopped taking drugs but was now taking Atarax at a high dose (sedating and sleep-inducing medication with a strong anti-cholinergic effect). As previously described, a common anticholinergic effect is that nerve signals to smooth muscle in the bladder are inhibited. Despite his young age, he had to use a catheter to empty his bladder. Thus anti cholinergic medicine can have such a strong effect even on younger individuals.

Generally
Dryness problems from all the body's mucous membranes
Dryness problems in the vagina in both men and women
Dry nose and increased risk of infection due to lack of protective secretions

So now we have a relatively good picture of how anticholinergic medicine affects the body. But why do we need to know this? Yes, my experience is that few pharmaceutical companies write out all the side effects that are related to Anti Cholinergic influence. Hence, we ourselves need to have background knowledge to be able to determine whether a medicine we take or intend to take will have an anti-cholinergic effect. Many problems today such as dry eyes, dry mouth and generally dry mucous membranes are today considered to be age-related. The question is, however, is this really the whole truth? Or could it be that older people are given medications that have an anti-cholinergic effect and at the same time are more sensitive to this than younger people? Yes, in any case, they like to hide a complete list of side effects in FASS on all the anti-cholinergic effects a medicine could have. In the best case, it might be written that the medication has an anti-cholinergic effect, but most laymen lack the knowledge to understand what this means. In addition, my own experience is that many doctors lack knowledge about anticholinergic effects and which medications have such effects. Personally, I have applied to the Eye clinic at the local hospital somewhere 7-10 times. On each occasion I have asked if the medication I am taking could be the cause of my dry eyes? Never once have I received an answer that this is the case. This is believed to be that current medicine (antihistamine) and Zolpidem have strong anticholinergic effects.

What are anticholinergics used for?

Here are some examples:

(1) Overactive bladder, i.e. if you have to urinate frequently. Here, the drug works by blocking the nerve signal to the bladder.

(2) In diarrhoea, here too the signal to smooth muscle is blocked, in this case the muscle that pushes the food forward in the intestine. Such a blocked signal leads to a slower intestinal passage and should thus be able to counteract diarrhea as the colon gets more time to reabsorb the liquid.

(3) In Parkinson's. In this disease, you have, among other things, involuntary muscle movements, and as you probably remember, acetylcholine is the signal substance that causes the muscles to contract. With the help of an anticholinergic drug, this signal can thus be blocked.

(4) Excessive sweating, here the signaling to sweat glands is blocked.

(5) In Asthma. In this condition, you get an excessive contraction of smooth muscle in the Bronchi (in the lungs). Anticholinergics thus also block the signal to the muscle here. The result is that the muscle relaxes and the person in question then gets better oxygenation and breathing.

(6) Sleep problems. In many cases, sleep problems are due to a brain that cannot stop thinking. Such a brain has a high level of nerve signaling between the different areas of the brain and the person in question does not descend into dominance by the Para sympathetic nervous system. Because Acetylcholine is a neurotransmitter that allows Neurons to send nerve signals, the neurotransmitter acts activatingly in the brain. If you then use anticholinergic sleep medication such as Atarax, Propavan, Zolpidem, Lergigan, Oxascand, etc., the effect of Acetylcholine in the brain is blocked. The signaling thus goes down, the thoughts slow down and the person in question becomes tired.

(7) Worry and anxiety. The reason that anticholinergics are used for these conditions is, as described above for sleep disorders, that it reduces nerve signaling in the brain. This calms the flow of thought and gives rise to a more relaxed state.

(8) Allergies. In case of allergy to, for example, grass and pollen etc., the immune system overreacts against substances that are actually harmless. During this reaction, Histamine is secreted, a substance that leads to swelling and increased secretion from mucous membranes. This can mean, for example, that the nose and eyes run. By giving antihistamine, you block histamine receptors and thus turn off nerve signals to mucous membranes to produce more secretions. Here you also need to know that Histamine and Acetylcholine are two bioactive substances that are similar. In amino acid sequencing of the Histamine 1 receptor, it has been found that this is more than 30% similar to the Muscarinic Acetylcholine receptor. Therefore, antihistamines also have an anticholinergic effect.

Study: Editorial Anticholinergic activity of antihistamines

Quote from study: “Histamine and acetylcholine are similar bioactive substances. In fact, the synergic action of histaminergic neurons and acetyl-choline neurons elevates alertness levels and promotes cognitive function (Blandina et al., 2004). The amino acid sequence (primary structure) of H1 receptors shows greatest similarity to that of a muscarinic acetylcholine receptor, and the two show a homology of 30% or more. Therefore, classical first-generation antihistamines, such as promethazine, have an anticholinergic activity. This anticholinergic activity induces symptoms such as drymouth, visual disturbances (mydriasis, photophobia, and diplo-pia), tachycardia, urinary retention, constipation, agitation, and confusion (high-dose administration).

(9) Motion sickness is a condition that is also treated with anticholinergics. Effect occurs when nerve signals to the balance center are inhibited.

Final words to the paragraph: When it comes to the medical use of anticholinergic drugs, it can also be good to know that certain conditions are treated directly by the anticholinergic effect of the medication. For example, certain anticholinergic medication is used against excessive urination to block the nerve signal to the bladder. In other cases, you use medications that have a different goal and a different effect on the body, but where you instead get a cholinergic effect as a side effect. This of course means that you cannot Google your way to the medicine that has an anticholinergic effect by searching for "What are anticholinergics used for".

Drug list Anticholinergics

Unfortunately, I have not managed to find a complete list of all drugs with anticholinergic effects. The list below, presented in English, is thus far from comprehensive. The Anticholinergic group is considerably larger than this list shows. Therefore, I instead urge you to seek more information about the particular medicine you are wondering about. For example, you can google: "anticholinergic effects of antihistamines" or, for example, "anticholinergic effects of Propiomazine" and so on.

In general, it can be said that most drugs that in one way or another have a dampening effect on the Autonomic Nervous System have an anti-cholinergic effect. That is, sleeping pills, sedatives, antipsychotics and antidepressants. Some other common groups are also Incontinence medicines and Antihistamines. Note that Antihistamines are a group of drugs that are used both for allergies, sleep problems and anxiety. They have an anticholinergic effect and in addition they also have another mode of action which means that they affect the Histamine receptors in the body. This makes them EXTREMELY drying and is therefore one of the most drying preparations available today. There are many people who have had their eyes chronically dry after a period of using these types of medications. In fact, many antihistamines are used precisely to inhibit mucus formation in various conditions. Hence, the medicine is purely designed to dry out mucous membranes.

Also note that long-term use of, for example, antihistamines can cause permanent functional impairment in mucous membranes even after the medication has been stopped. There are therefore good reasons to stay away from these types of medications and from other medications with anticholinergic effects.

NOTE The list below may be the name of the medication or in some cases the name of the active substance in the medication. Also note that the names are the English ones, the Swedish names may differ partially or completely.


You can also check the Okloka list. This is a list of medicines that should not be given to the elderly as they have a high risk of side effects. This often means that older people are even more negatively affected by medications with a large anticholinergic effect than younger people are. Hence, many of the medicines found on this list are anticholinergic medicines. Before we continue with my own compiled list of anticholinergics, it should also be mentioned that there are drugs that are a Muscarinic Agonist. That is, drugs that, unlike Muscarinic Antagonists, strengthen the signaling to the body's cholinergic system. These agents can thus strengthen the body's ability to, for example, produce secretions from the body's glands, so they have the opposite effect to Anticholinergics.

Here are examples of medicines with Muscarinic Agonism

TYRVAYA: (also known by the name: OC-01). This is an FDA approved Medicine in the form of a nasal spray that will be launched in November 2021. Oyster Point Pharma is the company behind this medicine. The drug requires a prescription and at the time of writing is not available in Europe.

"TYRVAYA, formerly known as OC-01, is believed to bind to cholinergic receptors in the nose to help activate the parasympathetic nervous system, thus increasing basal tear production to improve the signs and symptoms of dry eye disease. This medication provides a new and convenient way to administer dry eye treatment without further irritating the ocular surface"

Bethanechol: A muscarinic agonist used to treat postoperative and postpartum nonobstructive functional urinary retention and neurogenic atony of the bladder with retention.

Cevimeline: A muscarinic agonist with parasympathomimetic activities that is used for the symptomatic treatment of dry mouth in patients with Sjögren's Syndrome.

Pilocarpine: A muscarinic cholinergic agonist used on the eye to treat elevated intraocular pressure, various types of glaucoma, and to induce miosis. Also available orally to treat symptoms of dry mouth associated with Sjogren's syndrome and radiotherapy.

NGX267: Investigated for use/treatment in alzheimer's disease and schizophrenia and schizoaffective disorders.

Methacholine: A parasympathomimetic bronchoconstrictor used to diagnose bronchial hyperreactivity in subjects who do not have clinically apparent asthma.

Dietary supplement to increase the production of Acetylcholine

There are no dietary supplements that directly add Acetylcholine to the body. However, there are Choline supplements which are a precursor to Acetylcholine that the body itself can use to produce Acetylcholine. However, whether the body really makes more Acetylcholine just because you take supplements is questionable. If you still want to try Choline as a supplement in order to e.g. increase secretion production in mucous membranes, the recommended daily intake is 550 mg per day for men and 425 mg for women. Normally, you get this through your diet. If you want to test a higher dose, you should be aware that the upper limit of Choline supplementation is set at 3500 mg per day. Below is a list of preparations that could improve dry eye problems.

Huperzine A (acetylcholine reuptake inhibitor)
Alpha GPC (recommended dose: 250-300 mg/day)
CDP-choline / Citicoline (Cytidine 5'-diphosphocholine)
Choline bit rate
Ginko biloba
Bacopa monnieri
Acetyl-L-carnitine
Choline

Test of dietary supplements above: I myself have tested some preparations above to relieve dry eyes, here is the evaluation: Choline Bitartrate (Kolin) from the company Bulk, tested for about 2 months and it is not possible to notice any difference that the eyes would be less dry. Have taken 300-500 mg per day with a single intake in the morning.

Addendum Nov 2021: Medical machines to relieve dry eyes

Truetear is an electrical device that you insert into your nose. This gives sends an electrical signal into the nasal mucosa which causes the eyes to water. Follow the link above to read more.

Kinetic Oscilliatorisk Stimulans (KOS): At the time of writing, Källmark's clinic in Stockholm has an ongoing study that is planned to be completed in March 2022. The study tests whether the KOS method, which is normally used for stuffy noses, can also provide benefits for people who suffer from dry eyes . The KOS method involves placing a vibrating balloon inside the nose. The vibrations from this then activate nerves in the nose that send signals to the brain. Here, the signal is considered to be able to contribute to a release of stem cells that can help with dry eyes.
 
Below, I have made a half-hearted attempt to collect some medications with anticholinergic effects in different groups. As I previously mentioned. This is not a complete list. Some names may refer to the name of the medicine itself and some may refer to the name of the active substance. The names can be both in Swedish or English. Often the English names are similar to the Swedish ones.

List of Anticholinergic Medications

Opioids
Oxycontin
Oxynorm
Dolcontin
Durogesic (patch)
Norspan (patch)

Parkinson's Medications
Pargitan
Akineton

Antidepressants
Tryptizol
Anafranil
Sensaval
Parexetine
Ludiomil
Maprotiline
Saroten
Clomipramine

Antipsychotics
Levomepromazine
Clozapine Actavis
Clozapine Sandoz
Leponex
Nozinan
Hibernal
Clozapine
Olanzapine
Seroquel
Trilafon
Truxal

Antihistamine Medications
English names:
Azelastine (Optivar)
Carbinoxamine (palgic)
Cyproheptadine
Desloratadine (Clarinex)
Emedastine eye drops (Emadine)
Hydroxyzine (Atarax, Vistaril)
Levocetirizine oral (Xyzal)
Brompheniramine (Dimetane)
Cetirizine (Zyrtec)
Chlorpheniramine (Chlor-Trimeton)
Clemastine (Tavist)
Diphenhydramine (Benadryl)
Fexofenadine (Allegra)
Loratadine (Alavert, Claritin)

Swedish names:
Nozian
Propavan
Atarax
Theralen
Lergigan
Periactin

Strong Anticholinergic Effect
Atropine
Akineton
Pargitan
Hyoscyamine
Butylscopolamine
Methylscopolamine
Scopolamine
Dicyclomine
Oxybutynin
Tolterodine
Solifenacin
Darifenacin
Fesoterodine
Morphine
Trihexyphenidyl
Biperiden
Levomepromazine
Chlorprothixene
Chlorpheniramine
Hydroxyzine
Clomipramine
Amitriptyline
Nortriptyline
Maprotiline
Dimenhydrinate
Dexchlorpheniramine
Alimemazine
Promethazine
Thiethylperazine
Cyproheptadine

Allergy Medications
Desentol
Lergigan
Theralen

Sleep Aid Medications
Atarax
Atyxine
Ambien
Flunitrazepam
Hydroxyzine Alternova
Hydroxyzine EQL
Theralen
Lergigan
Propavan
Promethazine
Propiomazine
Oxytocin
Benzodiazepines (group)
Zolpidem
Zopiclone

Mixed Group
Atropine
Atarax
Akineton
Biperiden
Dispal
Ercotina
Egazil
Hyoscyamine
Carbamazepine
Lergigan
Orphenadrine
Theralen
TCA
Diazepam
Stesolid
Scopolamine
Scopolamine
Propavan

söndag 1 oktober 2023

Bota Autoimmun sjukdom genom en kost låg på stärkelse - Lär dig kopplingen mellan Klebsiella och HLA-B27 genen

Har du en autoimmun sjukdom? Har stärkelserika livsmedel en tendens att förvärra dina symtom? Forskning tyder på att individer som har autoimmunitet relaterade till en viss uppsättning gener som kallas HLA-B27 kan ha nytta av att minska sitt stärkelseintag. Läs vidare för att undersöka om en diet med låg stärkelse är rätt för dig.

Många miljöfaktorer har varit inblandade i utvecklingen av autoimmun sjukdom, inklusive användning av antibiotika, födelse genom kejsarsnitt, kemisk exponering, dålig kost och sömnbrist, bland annat. Även om man allmänt tror att sjukdomsdebut kräver en miljötrigger har de flesta autoimmuna tillstånd också en genetisk komponenter. En särskild grupp av gener som har starkt associerats med olika autoimmuna sjukdomar är HLA-B27. I den här artikeln kommer jag att diskutera HLA-B27 och rollen som en tarm-mikrob har som kallas för Klebsiella, och varför en diet med låg stärkelse kan vara effektiv för dem som har en HLA-B27-associerad autoimmun sjukdom.

Vad är det här med HLA?

HLA är en förkortning för humant leukocytantigen. ”Leukocyter” är de vita blodkropparna som ansvarar för att skydda din kropp från infektion och främmande ämnen. Antigen avser i detta fall cellytproteiner. Sammanfattat kan man säga att HLA i huvudsak är en grupp av gener som bestämmer vilka proteiner som finns på ytan av dina immunceller.

Människor har totalt 23 par kromosomer varav ett par kommer från varje förälder. Du ärver därför en uppsättning HLA-gener från din mamma och en från din far i moder- och faderversionerna av kromosom 6. HLA är en mycket polymorf gen, vilket innebär att det finns många olika möjliga genuppsättningsvarianter, eller "haplotyper" som du kan ha.

Det stora antalet olika haplotyper utvecklades sannolikt för att möjliggöra en finjustering av immunsystemet. Nackdelen är dock att vissa haplotyper också predisponerar en individ för en viss sjukdom i immunsystemet. Du kanske har läst min tidigare artikel där jag nämnde HLA-haplotypernas roll i känsligheten för mögelsjukdom. HLA-DQ-haplotyper har också associerats med celiaki, medan HLA-DRB1 har associerats med reumatoid artrit. För resten av denna artikel kommer jag att fokusera på HLA-B27 och dess koppling till autoimmun sjukdom.

HLA-B27 är associerad med olika autoimmuna sjukdomar

Förekomsten av HLA-B27 varierar mellan etniska grupper och befolkningar över hela världen men är i allmänhet inte så vanlig haplotyp. Endast 8 procent av kaukasierna, 4 procent av nordafrikaner, 2 till 9 procent av kineserna och 0,1 till 0,5 procent av japanerna har HLA-B27.

Den närmast associerade autoimmuna sjukdomen med HLA-B27 är ankyloserande spondylit (AS), en inflammatorisk sjukdom där en del av ryggkotorna smälter samman och hämmar rörligheten. Uppskattningsvis är 88 procent av personer med AS är HLA-B27-positiva, dock kommer endast en bråkdel av HLA-B27-positiva människor att utveckla AS. Andra autoimmuna sjukdomar som är associerade med en HLA-B27 inkluderar Crohns sjukdom, ulcerös kolit, psoriasis, reaktiv artrit & uveit

HLA-B27 är som tidigare nämnt polymorf vilket innebär att det finns flera olika undertyper, idag känner vi till mer än 100 sådana. Många av de vanligaste undertyperna av HLA-B27 så som exempelvis B2704 och B2705 är associerade med ökad risk för AS. Detta samtidigt som andra undertyper som HLA B2706 och B2709 verkar skyddande mot sjukdomen. 

Kopplingen till Klebsiella

Redan på 1980 talet identifierades forskare att AS-patienter hade förhöjda nivåer av serum IgA, vilket tyder på en onormal rörelse av mikrober från tarmen till blodomloppet. Mer nyligen identifierades via mikrobiom-analys en större förekomst av en gramnegativ bakterie som heter Klebsiella i avföringsprover från patienter med AS. I enlighet med deras hypotes om bakterietillströmning i blodomloppet fann forskare att dessa patienter också hade förhöjda nivåer av anti-Klebsiella-antikroppar i blodet.

Biokemiska studier har visat att Klebsiella har två molekyler som bär sekvenser som liknar HLA-B27. Forskare har antagit att denna "molekylära efterlikning" möjliggör korsreaktivitet mot kroppens egen vävnad. Med andra ord producerar immunsystemet antikroppar mot Klebsiella i ett försök att ta bort bakterien från blodomloppet. Dessa antikroppar kan också ”av misstag” binda till HLA-B27 genen. Denna idé om antikroppar som binder till kroppsegen vävnad är karakteristisk för autoimmunitet.

Även om Klebsiella är en av de mest studerade mikroorganismerna i förhållande till HLA-B27 och autoimmun sjukdom så finns det andra mikrober som också har visat sig kunna orsaka korsreaktioner. Exempelvis har Proteus-bakterier föreslagits vara involverade i utvecklingen av Reumatoid artrit via samma molekylära efterlikningsmekanism som Klebsiella. 

Varför kan en diet med låg stärkelse hjälpa?

Biokemiska studier av Klebsiella har visat att denna bakterie växer till mest i antal om personen i fråga äter komplexa kolhydrater, det vill säga stärkelse. Den växer däremot inte i antal på protein, fett eller på cellulosa från växter. Detta gör att vi kan styra mängden av klebsiella i tarmen beroende på vad vi äter. De flesta enkla sockerarter som glukos absorberas i den övre delen av tunntarmen och tar sig därför inte så långt ner som till som tjocktarmen där majoriteten av mikroberna finns, inklusive Kelebsiella-mikroben. Enkla sockerarter från kosten är därför inte tillgängliga för Klebsiella.

Stärkelse däremot är inte så lätt att smälta eller absorbera och en del av stärkelsen förblir intakt när födan når tjocktarmen varvid Klebsiella kan använda denna till sin egen fördel. Klebsiella har visat sig tillverka pullulanas, ett enzym som gör det möjligt för dem att bryta ner stärkelse till enkla sockerarter för energi och tillväxt. Flera studier har tillämpat denna kännedom på människor. En randomiserad kontrollstudie delade in människor i två grupper enligt följande: 

En diet med högt kolhydratinnehåll, en med lågt proteininnehåll samt en med lågt kolhydratinnehåll. 

De jämförde sedan överflödet av Klebsiella i fekala prover. Det genomsnittliga antalet Klebsiella var 30 000 / gram i gruppen med hög andel kolhydrater jämfört med 700 / gram i gruppen med låg mängd kolhydrater. En annan studie visade att en diet med låg andel stärkelse minskade totalt serum IgA hos AS-patienter. Majoriteten av dessa patienter rapporterade också en minskning av symtomens svårighetsgrad och i vissa fall till och med en fullständig Remission av sjukdommen.

Tre steg mot Remission

Nu när du bättre förstår vetenskapen bakom HLA-B27-associerad autoimmun sjukdom följer här är tre saker du kan göra för att vidta åtgärder för att minska inflammation och värk.

Ta reda på din Haplotype: Det bästa och mest exakta sättet att bestämma din haplotyp är att begära ett blodprov från din läkare som använder en riktad DNA-sekvenseringsmetod för att identifiera vilka alleler du bär. 

Experimentera med ditt stärkelse / kolhydratintag: Om du inte har tillgång till genetisk testning eller om du är HLA-B27 negativ kan du fortfarande göra ett självexperiment för att se hur du personligen tolererar stärkelse. Jag är en stor förespråkare av experiment för att hitta den diet som är rätt för dig. Eileen Laird från Phoenix Helix har skrivit ett utmärkt inlägg där hon delar resultaten av sina egna och flera andra Paleo autoimmuna bloggares stärkelseexperiment. Många fann att de tål vissa former av stärkelse men inte andra. Att känna till detta är verkligen värdefullt eftersom vi vet att en diet som saknar fermenterbar fiber som stärkelse kan vara skadlig för tarmmikrobiotans långvariga hälsa.

Läk din tarm: En frisk tarm är helt helt avgörande för att uppnå och bibehålla optimal hälsa. En läckande tarm tillåter bakterier och dietproteiner att ta sig in i blodomloppet vilket framkallar en kraftig reaktion från immunförsvaret. Oavsett din HLA-haplotyp och oavsett om du är positiv eller negativ för HLA-B27 genen så är det av högsta vikt att stärka tarmbarriärens integritet för att minska på inflammationen i kroppen. Att verkar för en mångsidig, hälsosam tarmflora kan också hjälpa till att hålla Klebsiella och andra potentiellt problematiska mikrober borta.

PS: Personligen är jag negativ för HLA-B27 men har under 10 års tid av aktiv ulcerös kolit ändå utvecklat ledvärk som är relaterad till Klebsiella och andra bakterier som ger samma typ av korsreaktion till kroppsegen vävnad. Genom att vara extremt strikt och hålla mig borta från stärkelserik mat så kan jag i viss mån kontrollera inflammationen i lederna.

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torsdag 3 augusti 2023

Damage from nose surgery and why it´s underdiagnosed

One of the most common surgery’s that are done is nose surgeries, today they are so common that people often forget about how much nasal injure and complications they can cause. If looking into the nasal post-surgery groups at Facebook it is also obvious that many surgeons completely neglect to inform the patients about how the nose function and what possible complications of surgery there might be. Sure, many may mention bleeding and infection, but that’s just short-term complications. The long term complications with Atrophic Rhinitis and Empty nose syndrome, nerve pain and severe dryness is just something that many surgeons will never mention. Many stories also shows that people asked for one type of surgery but ended up having one or several other surgeries they never signed up for. I have read several story’s where people all over the world signed up just for a septum surgery but came out the other end with a total amputation of the inferior turbinate’s, causing then lifelong dryness, infections and suffocation.

In this blogpost I will go thru why complications from nose surgeries is underdiagnosed and hidden away from patients interested in having a nasal surgery. I hope you get a good read and learn something that can save your own life or someone else’s. And sorry English is not my first language so you will have to live with some misspelling etc.

Before you continue to read I recommend you to look at theese videos to thoroughly understand what nasal surgery can cause.

 
This is is why damage from nose surgery is underdiagnosed
Based on my own experience and other patients I have been talking to there is no follow up on turbinate and septum surgery. In my case I only got 2 documents in the year following the surgery where only 1 question was asked. Do you still have nasal congestion? And this is in Western Europe – Sweden, witch is considered to have good documentation and healthcare. If no follow up on complications was done here, how much follow-up would can we assume that they do in developing countries? When no follow-up is done it’s impossible to get good and true data on how many patients who get complications from nose surgeries!

2 in many cases Empty nose syndrome (ENS) or secondary Atrophic Rhinitis takes years to develop after surgery. Why is this? Because it’s not only about what’s taken out but what’s left behind. When you first do the surgery you start up with a healthy mucosa membrane and it takes a while for the cells to go into metaplasia/Cellular adaption. When aggressive turbinate surgery is done the following happens:

- The nose gets to open and that dries out the whole mucosa, every time the nose gets really dry there will be some damage to the epithelial cells.

- When aggressive turbinate surgery is done the nasal cycle will cease to function, this could be due to nerve damage but most likely to the over opened nose. Even if the nasal cycle still remains the heavily resected turbinate’s can no longer swell much enough to obstruct each nostril vice versa. When this never happens, none of the nostrils will ever get a chance to moist and repair itself like the nasal cycle is designed for. In the long run this to will to damage the mucosa.

- Since cells that secrete immune modulating substances are damaged or removed by the surgery, the remaining part of the nasal mucosa is perfectly set up for bacterial adhesion and following inflammation that further can damage the mucosa. Furthermore when cells are damaged by surgery or literally cut out, the individual also loses a great number of the mucus producing goblet cells with will lead to dryness. When this happens during prolonged periods the remaining mucus producing goblet cells will also get damaged where their ability to produce mucus will be reduced. The Atrophic process then continues by itself in a negative spiral where the more and more function of the nose is lost every year... Also it’s important to understand that it’s the anterior part of the turbinate, the turbinate head, that is most active, this part of the nose has the highest number of mucus producing goblet cells per square centimeter. If this part is lost during surgery its extra seriously. And just for let you know, it’s often surgeons remove this part of the turbinate’s completely.
This things mentioned above is an explanation to why Empty nose syndrome and Secondary atrophic rhinitis is often is delayed several years after the surgery. After prolonged exposure to dryness and to infections the mucosa finally gets into a metaplasia stage where the ciliated cells and the goblet cells change from one type of cell to another. The new cells that develops loses their old function and is replaced by cells that have more in common with skin cells than with epithelial mucosa membrane cells. This is when the Secondary atrophic rhinitis is developed and that can take years, especially for those who live in a humid forgiving climate.

Metaplasia or adaptive cell response is something the body is forced into when it feels that it’s under too much cellular stress. For example this is observed in smokers. The ciliated cells in the throat can no longer handle the excessive volume of smoke and as a survival method they is forced to change from one cell type to another. This will make the cells to survive, and that’s good. But but it doesn’t comes for free since the original function of the cells is lost with discomfort and problems for the individual.

3 Further more, patients is not informed about what the turbinate’s are and what they do. Patients will not get the information that most land living mammals have developed turbinate’s for millions of years to help them with acclimatization of breathing in both -20 c and + 40 c. Also people who go for a septoplasty (correction of a deviated septum) will not get the info that a part of their turbinate (or all) will get resected so that the surgeon easily and comfortably can operate at the septum. The problem with this is:

First the patient don’t actually know what has been done in the nose, they don’t realize that an organ or a part of an important organ has been removed that has important function for the mucosa. If dryness coms along how could a patient connect this with the surgery when they actually don’t know what has been done in the nose?

Personally I went to fix a deviated septum and after some moths I developed light dryness that slowly increased every following year. In my case I just thought I had done a septum surgery and could not understand why I was so dry in the nose. First 4 years later I went to do another x-ray and then I discovered that 50% of the original length of the inferior turbinate’s was gone. The first anterior part of the turbinate did not exist at all any more, both tissue and bone was resected. Suddenly it was obvious why I had suffered with nose pain, dryness and breathing discomfort for years. 

My point is: When people start to get strong symptoms of Empty nose syndrome or Secondary Atrophic rhinitis first years after their surgeries, how in the world should they do the connection between symptoms and the nose surgery? Many patients will never even realize this connection, and all those cases of bad outcomes of surgeries will not be documented. Also, if they go to the healthcare system the knowledge about Empty nose syndrome is almost nonexistence. Especially in other countries than the US. This will also make complications from the surgery not documented.       

Plus, if the patients doesn’t even know that a part of their turbinate’s has been resected, how should they ever do the connection between surgery and symptoms themselves?

4 Personally I went back to the same surgeon that did the surgery to tell about my complications when I first discovered at my second x-ray that my inferior turbinate’s was resected, but that was 4 years after the surgery. When people discovers this so long after the surgery the surgeon don’t even remains at the same clinic any more in many cases. This cause that the surgeon will never know about the complications. Also from taking to many Empty nose syndrome patients I discovered that many are so stressed out and are so angry at their surgeon that they will never ever want to see him again. This too will cause many complications of surgeries not to be mentioned to the documented.

5 Many doctors and surgeons say that they don’t believe in Empty nose syndrome and actually there is no diagnose code for it and because of this complications from nose surgeries will never ever get documented.

6 Personally I went back to talk to the surgeon that did the surgery at me and strangely he actually confessed that it was his surgery that caused my Secondary atrophic rhinitis / Empty nose syndrome. But even when he confessed this for me he never wrote any code or diagnose of anything.

7 most surgeons don’t want to admit failure and complications because it’s not something that it’s considered good for their carriers. Most likely many of the surgeons who did a bad surgery don’t want to document anything about it because it’s not in their interests.

8 There is many developing countries that don’t have a functional system for reporting and documenting mal practice or bad surgery outcome. Patient who underwent nose surgery in all those countries will never get their complications documented anywhere.

9 Even if the complication from nose surgeries was perfectly documented, who would gather the information? Who would ever have something to gain from this? Most studies that are done in the world is performed by multinational drug companies with the goal of creating a product to earn money on. What kind of money can be earnt by making the conclusion that many people get complications from nose surgeries? None! Would the healthcare systems in each country really care about this? Doctors/surgeons are educating themselves for many years taking up big loans to support those years of study. It’s highly unlikely that any of those persons would admit that this specific surgery that they are educated on is causing harm to the patients. If that is confessed how can the surgeon continue making money then? My point is, No one has anything to gain from condemning nose surgeries and therefor such a study or gathering of info will never be done. Therefore more people will continue to get their lives sabotaged by the healthcare system.

10 Doctors say that there is just a few thousand people in the Empty nose syndrome awareness group and point out as an evidence that not so many patients are affected negatively from nose surgeries because there is just so few members. Well first of all, I google complications of nose surgery in Sweden and I found nothing at all about this. Even when info can be obtained in US when googling, this is not the case in many other countries. This causes that a lot of people never ever get to hear about Empty nose syndrome and therefore never ever gets the opportunity to be a member of the group. Besides, how many people in the world speak English good enough to be a member of the Empty nose syndrome awareness group? Also not all people in the world have Facebook! And finally, I have been a member of this group for 9 months now and during those months a saw many leaving the group because it gets too negative for them. And for those that actually manage to get some healing, they also leave the group to go one with their lives.

11 To distinguish how many people who get complications from nose surgery one can not only look at those patients that have a full blown Empty nose syndrome. You need to look at al symptoms, everything from light dryness to Atrophic Rhinitis, post nasal drip, recurrent nose infections etc.

Finally, the evolution has developed turbinate’s in most of the land living mammals to moisten and heat the air for optimal oxygen uptake in the lungs, reduce water loss during exhalation, to defend the body for pathogens and to be able to handle different kind of environmental conditions without discomfort. The animals with turbinate’s should be able to live in desert climates, subtopic climates, artic climates and humid tropic climates without causing discomfort when breathing. The evolution has developed this organs over hundred thousands of years and in the last 50-100 years some surgeons just decided that the evolution is wrong – “this organs is unimportant and can be removed without any consequences. This is just a naïve and an uneducated thought. Or it’s probably not about education at all because surgeons and doctors must know how important the turbinate’s are. It’s probably more about protecting their own future income stream and profession.

When ones decides to be a surgeon there must be a conviction that some parts of the body is unnecessary and can be removed without any complications but that’s not how the body and evolution works. If a specific body part would had been unnecessary the body and the evolution would have liquidated that by itself a long time ago.

Lastly I would like to say, there is records of 20% of people with a total Turbinectomy develops fully blown Empty nose syndrome (ENS) but it does not say anything about other symptoms from turbinate and septum surgeries.

If a large part of an important organ is removed it’s obvious that this will cause future problems. Maybe there will be no fully blown ENS but other symptoms like nerve pain and severe dryness and burning when inhaling is just serious enough to tell people the truth about this.

People deserves to know about possible consequences about the surgeries and people also deserves to get the truth told about what the turbinate’s are and what functions they have. Because I know, surgeons are not stupid, they passed the education and must have the intelligence to understand that turbinate surgeries will damage the nasal function in many cases, especially if it’s done aggressively.

We and future patients deserve to know the truth because it’s not only about our lives is about all the people we have around us that we love, they will be as affected by this as we do. Empty nose syndrome is a serious condition and people’s life’s get absolutely ruined by this, people loses their jobs, partners and joy in life and quite a few ending up committing suicide.

It’s a great cost not only for the individual but also for society and it’s not too much to ask that surgeons can tell the truth before surgery. We and future patients deserve to know what the turbinate’s are and how surgery at them or the septum can affect our future life’s.

And mostly important, the surgeons really need explain to to us what procedure that will be done. I have been reading so many stories about people who went for a septum plastic or a nose beauty surgery that ended up losing the whole inferior/middle turbinate’s, or a big part of it. That’s just criminal to do to an individual.

The surgeons have to consider: Many people come to you quite uneducated because we trust you. We believe that you know what you are doing after so many years education and therefore it’s important that you proper inform about everything, and also not doing things during surgery that wasn’t mentioned before.

Some surgeons and doctor says that they don’t want to inform about complications because it such a low risk but please consider this:

If you, your wife or your kids was about to board an airplane where there was a 5 % risk of catastrophic failure with death or life long consequences for health. Would you really board then? If that plane went down and your kid was on it, wouldn’t you think that you should had been told about the risk before? Isn’t that your right to know even when it’s only a 5% risk? Especially when there is such a serious consequences. Because that’s what it is for patients, its serious consequences and in many cases even suicides.

How come aggressive turbinate surgery is done in a modern world with all the knowledge there is? Particulary without informing the patients about the risks?

Well, to become a surgeon/doctor, just to enter the education you need pretty good grades from school. Also I guess you have to be pretty smart to succeed with the education. So by this we can point out that it cannot be about unintelligence. It has to be from something else!

So, could it be lack of education? I would say yes, and no. I don’t know exactly how many years it take to become a surgeon but I know it’s many, and during those years for sure all students will learn what the turbinate’s are, how they function and they must also understand how important they are. But at the same time I don’t know if the education looks enough into possible complications from surgeries. Why is this?

Because, first there is no long-term follow up on those who had nose surgery so even if the students would like to look into this th ere is almost no studies at all about this. Secondly imagen yourself, you have become interested in surgery and decided to educate yourself. Then first of all you have convinced yourself about surgery is a good thing that can help people, after that you join a big group and an organization that already has this this conviction to, even stronger than yourself. How could you ever question this? Because if you do so you will also question yourself? And up of that, having another opinion than you fellow students or colleagues will make you a criticized outcast excluded from the community. Are anyone really up to this just to claim what’s right or not? No, most people are not up to it, they can’t stand to be constant questioned. This is why nothing will ever change about this, people chose to go the easy way and adopt to everybody else. This is why more people will continue to be damaged from aggressive nose surgeries.

Also one important thing is that doctors and students get so convinced that they truly think they know better than hundred thousand years of evolution, they really believe that an organ can be removed without complications. Students and doctors letting themselves being brainwashed by their own and the organizations convictions that certain organs are unnecessary. 

So why do I mention this, because it’s extremely important to know for patients. If you ask your surgeon about possible consequences from surgery X or Y, this is like going to the hairdresser asking if she thinks you need a haircut? Of course the hairdresser will say yes, so will the surgeon because of his conviction that organs can be removed without problems.

And one important thing is also, the surgeon just sees the surgery and the short time afterwards, the conclusion they make from this is: I removed body part X or Y but the tissue around have now healed anyway. They don’t see the patients 3, 4, 5 or 10 years later. They don’t have a clue about long term complications for the patients.

But most important is the following, Imagen yourself in this situation. You have spent years of your life education yourself to become a surgeon, you are now in heavily debt to the bank but finally you started to make some GOOD money ether by employment or by your own business. You know one, two or maybe three types of surgeries and suddenly someone comes and tell you that you have to stop doing 1-2 of those because they actually damage people. Would you do that really? When all other surgeons are doing the same procedure and when you was told by school that this kind of surgeries can be done without complications? Would you risk your employment or your business because some patient claim that they have bend damaged by their surgery? No I don’t believe so! 99 % will definitely continue anyway, especially when the system is designed that way so that you could never be able to sue a surgeon for causing you damage.

Take a look at the surgeon Palo Macchiarini in sweden, he did untested experimental surgeries where he implanted a plastic trachea in patients and many of them actually died. But still, he is a free man and don’t need to take any responsibility of those deaths. This is important to remember for us patients, because when the system is built like this it’s easy to understand that doctors and surgeons don’t feel like they have to inform us about complication. They know, if something goes wrong, they are safe any way.

Also, don´t know how it works in the rest of the world, but in Sweden you don’t want to see people upset, worried stressed or afraid. If you tell the truth about possible complications from a surgery then the surgeons and the doctors see how the patient gets worried and this is hard to deal with. It’s just easier to work with people who don’t know about the risks because they are calm and ask less questions. Imagen yourself everyday dealing with people who is worried, a much easier work day would be to just to handle happy relaxed people.

So finally I just want to say, I’m not against surgeries or surgeons when such an intervention is necessary, for example when someone had an accident or it someone having cancer that cannot be treated in another way. But I’m very much against al surgeries when the process and the possible complications is not thoroughly described for the patient. And also I’m very much against it when body parts is removed that could had been treated without surgery. For example when it’s about septum and turbinate surgery.

The doctors don’t tell you that it’s absolutely normal to have a more or less deviated septum, few persons have a perfect 100% straight septum and that’s not anything that should be corrected with surgery. Why is this? Because the turbinate’s will adapt for this during life, they get smaller at one side of the nose and bigger at the other side. And most important, nasal congestion has to do with an over reactive immune system caused by food intolerances, allergies and bad food that irritates and inflames the body and the immune system. And how do I know this? Because I did an IGG food intolerance test and discovered many foods I didn’t tolerate. After that I removed those foods and changed to the Specific Carbohydrate Diet, a few month later I was cured from what the doctors say (an incurable chronic gut disease). So no it has gone 2,5 years and the Ulcerative colitis has totally vanished. I’m not even taking medicines for it anymore. It’s just sadly that I made this discovery to late, not a single person in the Swedish “fantastic” healthcare system ever told me about that food intolerance and inflammatory foods could be the cause of everything from nasal congestion to a chronic autoimmune disease. Instead I was recommended to have a totally unnecessary nose surgery at the septum and the turbinate’s with now has caused Empty nose syndrome and an extremely daily suffering.

One have to understand that doing a turbinate surgery is not treating the underlying cause of nasal congestion. It is like cutting the hand of because you have joint pain!

Turbinate’s are organs, developed in most of the land living mammals during hundred thousand years of evolution. It cannot just be removed to get rid of congestion without any complications, it’s obvious when you think about it.


And yes if the entire turbinate’s is removed there is nothing to block the nose but the patient will get much worse conditions than nasal congestion from this. This kind of surgeries have to stop and my goal is spread the knowledge to the world so that patients can make informed decisions about nose surgery. If I could get just one person to stop themselves from going true this surgery that will mean that my now sabotaged and miserable life would not be in vein.

So if you are a surgeon who reads this, please inform your patients about everything you plan to do in the nose, thoroughly explain what the turbinate’s are and how the nose function. Please don’t do anything you never mentioned to do in the nose and finally spend a good amount of time informing you patients about long term complications, do not only tell about short term risk of bleeding and infection. Please also make sure that the patient been investigated for IGE, AGA IGG food intolerances and other things that can irritate the immune system. And if you are a patient, make sure you really understand how different foods can affect inflammation in the body. If not an accident has happened that crocked the nose, most, if not all persons can get rid of nasal congestion only by removing foods and environmental factors, stress and other conditions that will irritate the immune system. If you have immune disorders the first thing that will be affected is the mucous membranes in the body, that’s just how it works. If that immune condition can be controlled the swollen and irritated mucus membrane will ease of to.

And please do consider, ones an organ is removed, it’s gone forever. It cannot ever come back. Witch also means the function of it is gone forever. Many doctor says that other organs do take over and you will not get problems but that just not true. This is just something they say to calm dawn worried patients. If the turbinate’s is removed or a large part of it is removed, no other cells can compensate for that. You will develop dryness and other problem, it’s just a matter of how long time it take for the healthy remaining cells to degenerate.

Finally consider: If you have a septal deviation/ crocked septum the normal procedure is that the turbinate’s is also reduced and the patient will never know about it. In my case if took 4 years before I discovered that 50% of my turbinate’s was removed by scissors. For 4 years I had been walking around not understanding why in the world I was just getting dryer and dryer in the nose for every month. The healthcare system just don’t think that something important to say to the patients and that’s really sick. It’s sick because they don’t tell you about it, but it even sicker because they do 2 interventions at the same time. Why would anyone would like to do this? Isn’t it much better to do as little intervention as possible, just fixing the deviated septum and then just wait and see if that’s enough. No they do all this at ones because they want to be able to show good data of how many patients that now breaths perfectly after surgery. When this is done at the same time they obvious don’t care at all about possible complications for the patient later on in life.

Anders Arbrandt Specialist i öron- näs- och halssjukdomar

There are surgeons al over the world doing this kind of surgeries, Sweden is not an exception. The surgeon who damaged me works at Sahlgrenska university hospital and has gotten no objection by the medical board. He still continues doing his job damaging more people with the same method of surgery every week. In Sweden there is also a none-fault insurance system where the surgeons themselves never can be financial liable for the damage they do to people. The clinic is forced to have an insurance and if the surgeons do something that damaging the patient it’s the insurance company that will have to pay for it. (LÖF). Unfortunately it’s very difficult to get a compensation from this insurance. When it’s about nose surgeries is most of the time impossible. Even if it should be possible it’s not going to affect the clinic any way. A clinic pays the same fee to the insurance company even if it has 1 damaged patient every year or 100. If the patient is not happy with the decision from the insure company he or she can take it to court. But this is an expensive and complicated process extremely hard to win against the medical profession. A profession that will try to do everything they possible can not to be convicted in court. Only a very few cases ever reach the court and most of them will end in a loss for the patient. Both emotionally, financially and legally.

Even if the patient would win the process it’s not the surgeon himself that will have to compensate the patient but instead the employer. So the surgeon goes free anyway. It’s only in a very few cases that the surgeon has ever been sentenced and in those cases the surgeon pretty much have deliberately tried to harm the patient. So once a person has admitted to surgery there is no chance for justice after a potential damage.

Finally it also has to be mentioned that the Swedish law (Patientskadelagen) don’t care about if the surgeon or the clinic has warned the patients about damage and complications from the surgery. At the same time this law doesn’t care about if the patient has given his consent to surgery or not. After knowing this is easy to understand whey clinics to aggressive nose surgeries and don´t warn about the complications.