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Monday 25 July 2022

Autism in Norway: The 7-fold increase in Autism linked to Maternal Migration

 

The Olso to Bergen line is one of Europe’s most beautiful railways

 

I did have another sense of déjà vu, when I read about the big spike in autism in one city in Norway.  Norway is a very expensive country, but well worth a visit.  We enjoyed it.  One of Monty’s former 1:1 assistants emigrated to Norway to work in their excellently funded special needs therapy system.  

A decade ago, there was a peak in media interest in Somali autism clusters in Sweden, Minneapolis and San Diego. Refugees had been taken to live in far away lands, with very different environmental conditions.  They soon started to produce children with a very high incidence of autism. This was a surprise to all the academics and a shock to the parents.   The Somali-Swedes even started calling it the Swedish disease, because they had never encountered such children before in Somalia.

 

Swedish study dissects autism risk in immigrants

Swedish migration: Only specific groups of immigrants — those from low-income countries and those who migrated near or during pregnancy — have an increased risk of autism, suggests a new study.

 

The Swedish Disease (Link to the old blog post)

 

A few hundred posts later after my one on the “Swedish disease”, it really is absolutely no surprise that the Norwegians have experienced the same phenomenon. 

 

Risk of autism seven times higher in Norwegian children with immigrant mothers


A study was conducted after health professionals started noticing a concerning pattern.

Researchers concluded in a recent Norwegian study that children of foreign-born mothers have a far higher risk of being diagnosed with autism. The study included 142 children aged 2-6 years old with an autism diagnosis in Sør-Trøndelag in mid-Norway.

The risk of autism in these children was just over seven times higher if the children were born of immigrant mothers.

The over-representation of this population indicates that the mothers' immigrant backgrounds may impact the development of autism, the researchers behind the study write in an article in Tidsskriftet, the journal of the Norwegian Medical Association. 

 

The actual research paper:

 

Autism spectrum disorder in preschool children in Sør-Trøndelag 2016–19

BACKGROUND

Autism spectrum disorder (ASD) is an umbrella term covering a range of conditions characterised by challenges with social interaction, restricted interests and repetitive behaviours. The prevalence of ASD has increased significantly in recent years, and there is a clinical impression of a preponderance of cases among young children whose mothers were not born in Norway.

MATERIAL AND METHOD

The study included 142 children aged 2 to 6 years who were diagnosed with autism in the county of Sør-Trøndelag, Norway in the period 2016–2019. The following information was collected: age at onset of symptoms and diagnosis, primary diagnosis, ADOS-2 (Autism Diagnostic Observation Schedule) scores, whether the child was born in Norway and the mother's country of birth.

RESULTS

Children of mothers born outside of Norway had a 7.7 times higher risk of being diagnosed with autism than children of Norwegian-born mothers, with an annual incidence of 0.74 % and 0.10 % respectively. These children were diagnosed earlier, at an average age (standard deviation) of 41.9 (11.8) and 51.8 (18.1) months respectively (95 % CI 4.7 to 15.2); a p-value of <0.001 for the difference. They also had a higher ADOS score, with an average (standard deviation) of 19.0 (6.2) and 15.3 (7.1) respectively.

INTERPRETATION

The preponderance of autism diagnoses may be an indication that the mothers' country of origin has an impact on the development of the condition. This has implications for adaptions to the assessment and follow-up of this patient group.

MAIN FINDINGS


The incidence of autism spectrum disorder was higher among children of migrant mothers than children of Norwegian-born mothers.

Children of migrant mothers were younger at the time of diagnosis and had more severe symptoms than children of Norwegian-born mothers. 

Clinical impressions suggest an overrepresentation of autism spectrum disorder (ASD) among young children of migrant mothers and that the severity of ASD is greater in this group. This impression is supported by an official Norwegian report from 2020, where data from the Norwegian Patient Registry suggests an increased risk of autism in young children with a minority background (1).

 

 


Age at symptoms onset in preschool children with autism spectrum disorder in Sør-Trøndelag 2016–19 divided into six-month intervals (n = 133). The difference in reported symptom onset between the two groups is not statistically significant.

 


Country of origin for mothers of preschool children diagnosed with ASD in Sør-Trøndelag 2016–19 (N = 142).

  

The study included 142 children in Sør-Trøndelag diagnosed with ASD in the period 2016–19 (Table 1). Parents of 80 of the children (56 %) reported their first concern about symptoms between 12–24 months of age (Figure 1). The difference in age at symptom onset between children of migrant mothers and children of Norwegian-born mothers was not statistically significant.

 Our findings suggest that the mother's migration background is associated with an increased risk of ASD in preschool children, as well as more severe symptoms and a younger age at diagnosis. The findings suggest that the mother's migration background may influence the development of ASD.

Previous studies support our findings of an increased risk for ASD in children of migrant mothers (9–11, 22).

We found a higher mean ADOS score in children of migrant mothers compared with children of Norwegian-born mothers. This group was also younger at the time of diagnosis. A plausible explanation could be that these children were identified and examined at an earlier age because they had more severe symptoms. An Australian study (12) found that children of mothers who migrated from low-income countries were younger at the time of diagnosis and had an increased risk of intellectual disability. Our findings may indicate greater severity of the disorder in children of migrant mothers. The association between higher ADOS scores and early age of diagnosis was shown in both groups. This indicates that young children with clear signs of developmental disorder are identified and evaluated early, regardless of the mother's country of origin. 

A Swedish study (10) found that the mother's migration background increased the risk for ASD independent of the migration background of the father. A Finnish study (11) found no increased risk of ASD among children where only the father had a migrant background.

CONCLUSION AND IMPLICATIONS

This study supports the clinical impression that ASD is overrepresented among children of migrant mothers. The incidence of ASD was 7.7 times higher in children of migrant mothers than children of Norwegian-born mothers. Our findings also suggest that children with ASD of migrant mothers are younger at the time of diagnosis and have more severe symptoms.

   

It’s the Immune system, forget Vitamin D

One explanation for those Somali autism clusters a decade ago was vitamin D; researchers thought that the pregnant mothers in Sweden were short of sunshine.   But what about the big Somali autism cluster in very sunny San Diego? 

The immune system adapts very slowly to its environment and gets used to living along side a wide family of bacteria from the environment.

Adults will struggle to adapt to changes in their bacterial environment.  Consider a Western backpacker travelling around India on the cheap, he is going to get sick, or just lose a lot of weight.  I chose the latter when I did this.  If you want to lose weight, take a budget trip to India.  Visit Scandinavia and you will not get sick, but it will lighten your wallet. 

For the fetus created in Somalia, it is the lack of exposure to the expected bacteria in Sweden or Norway that upsets the immune system. It ends up over-reacting and damaging itself.  

  

Conclusion 

Migration from very poor countries to very rich ones, while pregnant, risks seriously disrupting development of the immune system of the fetus and its vital calibration process.  The result may be autism or other neurological conditions.  In Norway a 7-fold increase in autism has been found; they did not measure the impact on related, but less troubling disorders like ADHD and dyslexia.

Not only is there 7x more autism, but it is more severe autism, with a higher score on the ADOS scale.

Clearly many people do not get advance knowledge of when they might become a refugee.  Very poor countries have very high birth rates and so young females are quite likely to be pregnant at any given time.

We know that any kind of severe stress also increases the incidence of autism.  Examples in the research include extreme weather events like hurricanes. Wars, fleeing from home, journeying overland in harsh conditions will be very stressful.

We can use this data to further the wider understanding of how the immune system is a factor in the increase in autism prevalence worldwide. We can then consider modifying the immune system to protect the future fetus from autism and indeed pure auto-immune conditions (asthma, eczema, IBS etc).  The simple way to do this is to add back exposure to bacteria that your grand parents and great grand parents would have been exposed to.  In particular, this means exposure to domesticated animals, even just cats and dogs.

We were recently in Pelion, Greece and over there you cannot avoid contact with animals.  Cats and dogs are roaming freely in cafes and restaurants, mainly outside but not exclusively.  Several times a day you will brush up against some four-legged new friend.  Are auto-immune diseases less prevalent in Greece?  What do you think?

Ideally you would be exposed to cows, horses, sheep, goats etc.  Take a hike through the countryside or visit a farm.  Don’t try and sterilize your shoes afterwards.

This kind of animal contact is nowadays uncomfortable to many people, but over tens of thousands of years your immune system has been trained to expect it.

Another take home message is that nobody is reading all this autism research and putting the pieces together; you have to do it for yourself.






 

30 comments:

  1. Peter,

    This is unfortunate but not unexpected for people like me. In my very close circle of about 15 Indian families who emigrated to the US around child bearing ages, four of the families including mine have an autistic child. Many of these kids (but not their NT siblings) show a history of eczema or long spells of cold through out their first 2-3 years of life before they are even diagnosed with autism. This is also reflected in the allergy tests done on blood serum or skin prick tests. When I dug further, I found out that the grandmothers in 3 out of 4 cases have a history of asthma/arthritis. This is too much to be a coincidence.

    The question is whether the damage is complete for these kids or whether some sort of immunotherapy would help my 5 year old son or my friend's 2.5 year old daughter. One option we were given was to have these allergy shots over a long period of time. I tried to put it off since it involves a lot of injections for a small child, but I am wondering if that is worth it in the long run.

    Anvesh

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    1. Anvesh, I was contacted a few years ago by a British Indian. His son with severe autism improves significantly when he goes back to India on family visits. Clearly there is an ongoing environmental influence in his case.

      Have you ever taken your son to India. If you did, was there any change in the severity of his autism symptoms?

      You would think that it is too late to undo any damage done by an aberrant immune system. It seems that while you cannot undo the effects of the first 5 years of years of brain development, you may be able to fine-tune current functioning and future brain development. The brain does not fully mature until synaptic pruning is completed in you mid 20s. At 5 years of age the brain is near adult size, but it is still plastic and so you can still mould its development.

      Delete
    2. Peter,

      As a matter of fact, we are in India now and have been here since March of this year. Soon after coming here, we started Leucovorin .. first 5mg and then eventually 10mg. In about a week I noticed a marked improvement in his speech- his spoken words more or less doubled and I did not really notice any hyperactivity. Since we started the medication so close to the move, I am not sure if its the environment or the meds (Leucovorin + Zyrtec + L-Carnitine), but he has shown a much higher rate of improvement since we came here. He stays outdoors most of the time and seems to enjoy it. Also, we live in an apartment complex in Bangalore with a common play area, so there are lots of opportunities for play. He does struggle and quickly exits any sort of communicative play, but he likes to hang around with the kids and race or climb with them. The school also has been surprisingly patient and optimistic with him. The therapy options are however limited and the doctors laugh me out of the room when I bring up things like FMT. But we have decided to move back to India for good with the hope that the social environment will make up for the other drawbacks.

      Interestingly my neighbor mentioned that her daughter develops summer rashes when in the US but not in India.

      Anvesh

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  2. Hi Peter, I know you have thoughtfully considered the idea that excessive or poorly timed infant immunization is a factor in autism and decided it is not, but having experienced our son regressing after his 21 month shots I wonder if these immigrant babies or mothers are getting a lot of vaccines at one time in order to migrate into the western countries?
    If a baby or toddler gets a lot of shots in one day it can certainly induce aluminum toxicity in some of them. Just a thought.
    Thanks for all your work

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    1. In this study they were looking mainly at children who were born in the highly developed country (Norway in this case), so they would have had the same vaccine schedule as the local kids.

      Of note is that fact that in US there are far more vaccinations given to babies and young children. Even a flu vaccine is given from the age of 6 months; in Europe it is only old or at-risk people who get it. In Europe you are left to catch chickenpox, in the US they vaccinate against it.

      Your immune system does need to get some challenges.

      Giving too many vaccines in rapid succession was shown by Dr Jon Poling, supported by his friends from Johns Hopkins, to be the cause of his daughter's severe autism. He received millions of dollars for her care from U.S. Vaccine Injury Compensation Program.

      Parents of a child at risk of mitochondrial disease need to take precautions when taking vaccinations.

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  3. I've just finished reading An Epidemic of Absence by science journalist Moises Velasquez-Manoff. He makes a very good case for your explanation, very well researched (the book is from 2012).

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    1. It's about the old friends hypothesis, btw. Best, Leen (forgot to sign a few days ago)

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  4. Hi Peter, I have been following your site for sometime now. Great information. Thanks for the blog.

    My 4.5 year old son (35lbs) has been diagnosed with moderate ASD. We found both types of FRalpha antibodies in his blood. He is now on Leucovorin (20 mg/day) and he seems to be getting better at his speech.

    Based on your blog, I decided to try PharmaNAC for him. I gave him half tablet (450mg) in the morning and within an hour we have seen regressive behavior in terms of OCD, playing with one electronic toy for the whole day and lots of crying for something simple.

    I wanted to get your opinion on this. Does this mean he has no oxidative stress or should I try it for few days. Do you know of any other medications for people where NAC reacts quite the opposite way?
    We were also thinking of trying carnitine since he had low levels last year when he fell sick and he has a bit of hypotonia.

    Thanks,
    Rajesh

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    1. Rajesh, you are not the first person to contact this blog who found a negative reaction to the use of NAC.

      There are 2 possibilities, your son might be one of the rare people with autism who do not have oxidative stress. The opposite state called reductive stress does exist. It is when there are more antioxidants than oxidants. Reductive stress is a feature of some disease and it is in the peer reviewed literature.

      Your son might just have a negative reaction to NAC, or another ingredient in PharmaNAC. NAC contains sulfur/sulphur and some people have an allergy to this. A sulfonamide allergy is one well known specific allergy and these people cannot tolerate Bumetanide.

      If ParmaNAC is not tolerated, try a different antioxidant like carnosine, vitamin E, vitamin C or an exotic one like Astaxanthin.

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    2. Thank you Peter. I tried acai berry extract before this and I saw similar negative behavior. Then I had attributed to some other ingredients present in the extract. But now that NAC also shows similar results may indicate that anti-oxidants are causing the undesired behavior (?). I noticed before that when we give him acai berry juice, he is in a much better mood and is more present. This was the reason why I tried acai berry extract. Now, I am not really sure what helped him when I gave him acai berry juice.

      I am also planning to give him L-carnitine because he had low carnitine levels in his blood when he was sick last year. I am not sure if he has low levels now but I thought of trying it next since he has a bit of hypotonia and he always has a tendency to lean on others for no reason. Is carnosine same as L-carnitine? Is L-carnitine an anti-oxidant?

      If my son really has reductive stress, can I confirm it with another test or any other medication that I can try which may possibly help him? Do you know what other medications can be eliminated because of the fact that NAC shows negative reaction?

      Thank you! - Rajesh

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    3. Ramesh, it is premature to draw conclusions.

      Try carnitine, many people with autism and some mitochondrial dysfunction respond well. It is not really an antioxidant, but is very important.

      Carnosine is already present in your body and it functions as an antioxidant. It is a common autism supplement. Give it a try.

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    4. Thank you. I am planning on giving him 50 mg/kg/day of carnitine in two doses. Start with half this dose first and then go to full dose in a week. Does that sound okay? I will try to get Carnosine as well soon.

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    5. Hi Peter,

      I want to update you on carnitine doses. We gave him 250 mg (15mg/kg/day) and immediately we saw that he became quieter and a bit lost. He used to make lots of nonverbal sounds and was hyperactive before. Now he is slightly weak and does not make sounds. I feel he is a bit lost as well. We have been giving him Leucovorin for two months and saw significant increase in speech but with carnitine, it seems that speech has gone down slightly (or may be it is my bias). I am not sure what to make of this. I am planning to reduce the dose to 100 mg and see how it effects him.

      Can you tell me what are the adverse effects of carnitine that people have seen before. Given that NAC showed adverse effects, does it make sense to continue carnitine or not?

      Also, we got MitoSwab buccal test results, he has complex 1 deficiency. So in theory carnitine should help him right?

      Thanks,
      Rajesh
      (Ps: I am posting in my previous thread for continuity)

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    6. Rajesh, at your dosage you would not expect there to be any negative effects, in an otherwise healthy person. At much higher doses there can be GI problems.

      Some people are very sensitive to the colors and bulking agents added to pills. This might be the problem.

      I wonder how accurate the buccal test is. It is not an approved test, it is experimental.

      Other readers have been told, based on this test, that they have Complex 1 deficiency but the mito cocktail shows no effect.

      If your carnitine has no benefit, I would stop using it. You could try the very popular Spectrum Needs mito cocktail and see if that helps.

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  5. I agree with this too.In the Nigerian community in the Uk too we have a lot of children with Autism and in most special schools there are a lot of ethnic minority children too.I read the Finland paper too some months ago.I grew up in a university town in the south western part of Nigeria and we all lived in the university quarters and mostly attended the primary, secondary and university .We all knew each other and this was like a village.My mum taught in the university school and she only saw one case of autism in her 30 years of working in the university school.There were other cases of children with downs syndrome but just one case of autism.
    Now in the UK 3 of my friends that we moved from Nigeria and had children the same year all have children with autism though mine is the most severe and some others that we grew up together also have a child with autism and I do not believe it is genetic as we have no history of people with disabilities in our families.
    Now there are cases of children with autism in Nigeria but nowhere near the number of children here so it is definitely environmental.
    Apinke

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    1. Apinke, my mother was a family doctor seeing all the young children in a large medical clinic, because all the other doctors were male. Until the MMR vaccine story appeared she said nobody spoke about autism and she had almost never seen it. Just one child came to her mind, who eventually was institutionalized because the parents could not cope. That was it, pretty much like with your Mum in Nigeria.

      Nowadays everyone is talking about being on the spectrum, but it is not the same autism as 50 years ago, which was exclusively severe autism.

      What we really need to know is the incidence of severe autism, like you are dealing with. The way the data is collected makes it impossible to say with certainty. Everyone has their own opinion,

      Delete
    2. I agree with you data needs to be collected on the severe ones as everyone says they are on the spectrum but I doubt if that will happen.If autism was being treated the way cancer is taken serious, then there would have been some headway but we are being left to get on with it which is a shame.
      Please what medication can be used for a very aggressive 11 year old boy with challenging behaviour.He's a friends son and almost beat up mum today .He attacked and slapped her and is minimally verbal.Hes currently on sertraline and mum says its anxiety.
      Thank you
      Apinke

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    3. Interesting about your mums observations too.When I tell people this they say its not possible and that the children were probably hidden away and not diagnosed which I know is not true as we all knew each other.So it means something is wrong somewhere.Hopefully there will be research in the nearest future as the statistics at the moment are alarming.
      Apinke

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    4. Apinke, There are very many reasons why an 11 year old boy might become very aggressive.

      If he goes to a psychiatrist a likely outcome would be a prescription for an anti-psychotic drug like Risperidone or Aripiprazole (Abilify). This may, or may not be effective, but is linked to very troubling side effects that may not get mentioned: tardive dyskinesia (tics that may become permanent) obesity and high prolactin levels causing males to grow breasts etc.

      Normally there is an underlying problem, medical or emotional that drives the aggression.

      In some people it is a GI dysfunction, that when cured solves the problem. There are many causes of GI dysfunction. In some people just adding a good bacteria as a probiotic (eg Biogaia Gastrus) solves the problem. Note that in some people this same bacteria actually triggers raging and aggression.

      In some people it can be a sign of minor seizures, called sub-epileptiform activity, this would show up on an EEG. It is like
      the step before epilepsy.

      It can even be a problem with his teeth, or pain somewhere else in his body.

      In our case is was allergy related, usually just a pollen allergy, but we have had rare episodes due to food allergy. The solution was Verapamil plus antihistamines and mast cell stabilizers.

      The Mum needs to look at all of the cormorbid health issues her son has to narrow down the underlying cause of the aggression. This is not easy, but in the end she will figure out the cause. She should keep a diary of what he eats, any GI or other problems, his daily activities and how much aggression there is. Then she might spot connections.

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    5. Thank you so much Peter he’s on1mg of apripazole.I will share this with his mum .It is very helpful

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  6. Hi Peter,
    I would like to share my child's story with you. I as a parent had to travel to Canada to complete my postgraduate education. I came from middle eastern country, and my child was 9 months old when we arrived at Canada. He was very normal from all aspects at that time. I stayed for 1 year there, where I noticed him changing in behavior and regress in speech. His first medical appointment was because of skin rash that was explained as allergy, then he was easily getting ear infections, may be 3 times before we get the official diagnosis in my original country. My child is now 5 years old and still moderate to severe autism, minimally verbal with some cognitive delay. This article really brought my attention, to an important undiscovered risk factor for autism.
    Giving that my child left his original environment in an early age, then appeared to have autism in a western country, would that be considered as supporting this article's idea. What do you think are the candidate risk factors?
    I would like to hear from you Peter.
    Thank you

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    1. Much autism is polygenic and multifactorial where many individual risk factors happen to come together to trigger the condition, it requires multiple hits, like some cancers.

      If your child had been born in Canada that would have been a much bigger potential risk, than arriving at the age of 9 months. By nine months much of the initial brain development has been completed, but issues like mitochondrial dysfunction triggering regressive autism are still a threat till the age of about 5.

      You will never now for sure if your time in Canada contributed to your child’s autism.

      Delete
  7. I have now used Varga peptide nasal
    spray for about 4 weeks and it has brought on very noticeable effects in speech and communication - she has gone from barely being able to dialogue to being able to keep a line of 5-10 exchanges spontaneusly and fast. She never asked to telephone anyone, now she does 3-5 times a week and she has learned her fathers phone number by heart (I make her use a landline phone for older people with big buttons so she can learn the idea of phone numbers before just pressing a name in her phone book). she will explain things she feels and they are more nuanced things - like missing someone. I could go on and on - a lot of great changes.
    Also an interesting development but for the worse: last year, with our second dose, we lost overnight the behaviour of self soothing through masturbation. We do know its natural at her age to discover masturbation (she was 8) and we did not even consider it in any way as pathological. Turns out it was - it went away overnight with the 2nd ivig dose. It has not happened once since then - however, ragweed season has started and so has this behaviour again.
    My idea is that she is trying to self soothe and produce some kind of neurotransmitter thingy in her brain which is affected by inflammation.
    Any ideas? Would it affect Gaba or dopamine or what?

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    1. One key autism gene seems to be Shank3 and in people with Phelan–McDermid syndrome (PMS) also known as 22q13 deletion syndrome, its thought that the main issue is with lack of Shank3.

      Intranasal insulin was trialed on kids with this syndrome, with some benefit.

      I have also written posts about other conditions like Alzheimer’s, where Intranasal insulin has showed promise in the research.

      “Intranasal insulin was studied in six PMS patients and resulted in marked short-term improvements in gross and fine motor activities, cognitive functions and educational level. Similarly, long-term positive effects were found for gross and fine motor activities, nonverbal communication, cognitive functions, and autonomy. However, one patient showed changes in balance, extreme sensitivity to touch and general loss of interest, and one patient complained of intermittent nasal bleeding [43]. No adverse effects on glucose levels or HbA1c levels were found [12]. To validate this effect, a randomized, double-blind, placebo-controlled clinical trial was conducted in 25 patients aged 1 to 16 years with a molecularly confirmed 22q13.3 deletion involving the SHANK3 gene. A significant effect was found for cognition and social skills for children older than 3 years, who generally show a decrease in development. Intranasal insulin did not cause serious adverse events. However, clinical trials in larger study populations are required to test the therapeutic effect and safety in PMS [39].”

      Gábor Varga, a Hungarian parent of a child with this syndrome has developed what he believes is superior to insulin, he uses Proinsulin C-peptide spray, which he also sells. He sells a wide range of other supplements.

      I was surprised he can legally sell his intranasal Proinsulin C-peptide spray for skin care.

      He has now been banned from advertising them, he was claiming it can treat very many diseases.

      https://www.gvh.hu/en/press_room/press_releases/press-releases-2020/the-hungarian-competition-authority-has-banned-the-advertising-of-c-peptide-products

      But he still sells them.

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  8. An acquaintance adopted a baby from an African country. The US required that the baby take antibiotics for 3 months as a part of the requirements! The child now has severe autism. I wonder if these mothers from African countries are being required to take antibiotics as part of immigration. If major amounts bacteria in the body are killed off by a broad-spectrum anti-biotic, that could leave room for yeasts to flourish, and upon stopping the antibiotics, opportunistic pathogenic bacteria, could take over.

    Also, I’m sure vaccines are a requirement for these pregnant/nearly pregnant mothers to immigrate. A battery of vaccines can spike a person’s immune system reaction very high. But I’m still more curious about whether antibiotics are required as it was for the adoption I referenced.

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  9. How are you peter it is my first comment here I always want to make comment on your articles but I did not may be cause of my bad English , I have twins 3.2 years old diagnosed with autism at 3 years but I start early at 2 years cause I was suspecting they are on spectrum , I started with nemeteck protocol (inulin+olive+omega 3) and (coq 10+ pqq + nac+ glutathione) and PEA I got very good result like riding bicycle and doing puzzle also shot football follow some simple instruction but after this I did not see any more improvement only slightly improvement in eye contact and they are still non verbal using only one word (mama ) and a lot of bubbling but never used any word else , I went doctors in my country (Egypt) and she start with (cerebrolysin injection +peractam + memantine+ b12 injection +folinic acid +probiotic + digestive enzyme ) and some other medicines but all I see more hyperactivity and sensory issue (putting hand and stuff in mouth ) so I stopped and went to other doctor who using (bumetanide +b complex + L glutamine +zinc +gaba ) and I saw best improvement ever one my kids in eye contact and follow instruction then add rifaximin for 10 days and I saw good improvement in social like waving bye bye and drag me from hand to watch him while he sliding but still now words and now I don’t know what I have to add cause I believe bumetanide make huge different in my kids but speech still I want your suggestions I know you are not a doctor but for me you are better knowledge than 90% of doctors in autism field. Thanks for your blog which guide me to search for doctor who prescribe bumetanide .

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  10. We moved from the UK (with my wife originally from Hungary) to Katy, Texas, just weld of Houston. Within 3 years we had our first child Eddie, how has autism. I do note that Katy has a very large demographic of foreigners, and also has a very large amount of autistic children. Our second child, born a couple or years later is NT. I have always thought there was some link to us moving to the US and our Eddie's condition. I wonder if it is something to do with gut bacteria that is severely put out of whack by moving continent. Who knows.

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    1. I was contacted by another UK expat near Houston, working in the oil industry. She said there are many kids with autism over there, and not just mild autism. I think there are multiple factors, the different level/type of bacterial exposure looks like one factor. Other factors may include high IQ parents and alpha females, as in the tech sector in California.

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    2. I'll take that as a compliment (also on behalf of my wife)!

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