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Thursday 29 November 2018

What, When and Where of Autism – Critical Periods and Sensitive Periods



When time is of the essence

All kinds of dysfunctions may appear in autistic brains, which in itself make it a highly complex condition. There is also the when and where aspects of these dysfunctions, which often gets overlooked, or lost in oversimplification.
This then has to fit into the concept of critical periods, that I introduced in an earlier post. 

Critical periods are times during the brain’s development when it is particularly vulnerable to any disturbance, for example an excitatory/inhibitory imbalance.
This then leads to another related concept which is that of sensitive periods; these are periods when the person should be responsive to particular therapy.
Sensitive periods are very important to be understood by those planning clinical trials, because a therapy may indeed be effective only when given within a specific time window. During this time the person is sensitive to the therapy, but they will not be a responder after the time window has passed.
I am pleased to say that more research is beginning to consider the when aspect and not just the what aspect of biological dysfunction in autism.
The where aspect reflects the fact that in one part of the brain there might be, say, NMDA hypofunction, while in another part the opposite is present, NMDA hyperfunction.  Since most therapies come as pills you swallow, you cannot treat one part of the brain for one problem and another part of the brain for the opposite problem. There is currently no way around this issue, you just have to do what is best for the brain overall. In practical terms it means you may make one problem better, but create a new one. 


New research in a mouse model suggests that the drug rapamycin can reverse autism-like social deficits -- but only if given early. The study is the first to shed light on the crucial timing of therapy to improve social impairments in a condition associated with autism spectrum disorder. Its findings could help inform future clinical trials in children with tuberous sclerosis complex. 

Full Paper:

  

Mefenamic Acid
I have mentioned mefenamic acid (Ponstan) in several posts. It is the only human autism therapy currently in development that has a treatment window.  It is suggested that the sensitive period to take this drug is the second year of life, to avoid severe non-verbal autism. 

Conclusion
The good news is that we have seen time and again that it is never too late to treat autism. Clearly the earlier you do start, the more extensive the long term benefit should be. So once you realize that intervention is possible, best not to delay.
When autism  is of a single gene origin, there really should eventually be scope to make some kind of permanent fix, if you can intervene very early and so still during that intervention’s sensitive period.  This might involve something very clever like gene editing, which you cannot do at home, or it might be just some drug therapy, like Rapamycin in TSC1 as in the above study.





10 comments:

  1. Hi Peter,to help with my son dismotility Iam giving him mosapride, a 5HT4 receptor agonist. It has gastroprokinetic effect facilitating acetylcholine release in the gut.It has safe cardiac profile.Do you now if combining it with a PDE4 inhibitor the effect would be enhanced? It also would help with sensory processing?
    Valentina

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    Replies
    1. Valentina, the common PDE4 inhibitor in most countries is Roflumilast (Daxas), it does have the common side effect of making people vomit. This effect often wears off, but if you already have some GI problems I would be cautious.

      I think the Japanese drug Ibudilast is very likely a much safer PDE4 inhibiting drug and it is being developed in the Western world to treat multiple sclerosis.

      Delete
    2. Peter, what do you think about diazepan as true PDE4 inhibitor? I could use it in a ver low dose with mosapride.I can not get Ibudilast.
      Valentina

      Delete
    3. Valentina, there are different types of PDE4. By inhibiting PDE4D you get the emetic effects (vomiting) so ideally you want a very selective drug.

      For depression you would inhibit PDE4A, for schizophrenia and bipolar you would inhibit PDE4B. Such selective drugs do not exist.

      Diazepam is a positive allosteric modulator of GABAa receptors and in people who respond to bumetanide it likely will make them anxious rather than calmer. Diazepam is also a PDE4 inhibitor.

      I think diazepam would have a negative effect on your son.

      It is a pity Ibudilast is not approved outside of Japan.

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    4. Peter, it had a negative effect, but I think it could have been a matter of When.Regarding bumetanide I stopped because I was concerned about his chronic constipation and a possible loss of potassium. Nothing happened.Yesterday he got 12 with congratulations in his last history exam, the best note here, was the only one in his class!.I think Zarontin is making a difference
      Valentina

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  2. Valentina, I have neither read or experienced any effect of PDE4 inhibition on gut motility (guess vomiting by high doses of Rolipram doesn't count). Also, I havent seen any obvious synergies or negative interactions with 5HT receptor agonists/antagonists with PDE4i, though I haven't used anything acting on the 5HT4r specifically.

    /Ling

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    Replies
    1. Thanks Ling,there is a study in PubMed about the synergistic effect between the two.It seems that the effect is only at GI level, that was my doubt, what happens at brain level.
      Valentina

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  3. Hi everyone,

    I just found a couple of interesting papers and wanted to share them with the community:

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6258166/

    Brain hyperserotonemia causes autism-relevant social deficits in mice

    "Results
    Social deficits were observed in both heterozygous knockout mice (HZ) and homozygous knockout mice (KO), but increases in general anxiety were only observed in KO mice. Two weeks of dietary restriction of the serotonin precursor tryptophan ameliorated both brain hyperserotonemia and ASD-relevant social deficits in Sert HZ and KO mice. The expression of rather distinct sets of genes was altered in Sert HZ and KO mice, and a substantial portion of these genes was also affected by tryptophan depletion. Tryptophan depletion in Sert HZ and KO mice was associated with alterations in the expression of genes involved in signal transduction pathways initiated by changes in extracellular serotonin or melatonin, a derivative of serotonin. Only expression of the AU015836 gene was altered in both Sert HZ and KO mice. AU015836 expression and ASD-relevant social deficits normalized after dietary tryptophan restriction.

    Conclusions
    These findings reveal a Sert gene dose-dependent effect on brain hyperserotonemia and related behavioral sequelae in ASD and a possible therapeutic target to normalize brain hyperserotonemia and ASD-relevant social deficits."

    -------------------------

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6258310/

    A pilot dose finding study of pioglitazone in autistic children

    "Results
    Maximum tolerated dose: there were no serious adverse events (SAEs) and as such the maximum tolerated dose within the range tested was 0.75 mg/Kg once daily.
    Safety: overall, pioglitazone was well tolerated. Two participants discontinued intervention due to perceived non-efficacy and one due to the inability to tolerate interim blood work. Three participants experienced mild neutropenia.
    Early evidence of efficacy: statistically significant improvement was observed in social withdrawal, repetitive behaviors, and externalizing behaviors as measured by the Aberrant Behavior Checklist (ABC), Child Yale-Brown Obsessive Compulsive Scale (CY-BOCS), and Repetitive Behavior Scale–Revised (RBS-R). Forty-six percent of those enrolled were deemed to be global responders.

    Conclusions and relevance
    Pioglitazone is well-tolerated and shows a potential signal in measures of social withdrawal, repetitive, and externalizing behaviors. Randomized controlled trials using the confirmed dose are warranted."


    Have a great night everyone!

    AJ

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  4. Hi Peter,

    Hope all is well. Have you ever thought about switching Monty over to Rapamycin? Since most of your drugs in your poly pill modify the immune response why not stop the T-Cell sensescents? The decrease of TFN-Alpha, IFN-y-, and Mig with Bumetanide creates the high responders. Just food for thought.

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7217787/

    https://journals.lww.com/americantherapeutics/Fulltext/2021/10000/Rapamycin_Sirolimus_Improves_the_Behavior_of_an.21.aspx#:~:text=TO%20THE%20EDITOR-,Rapamycin/Sirolimus%20Improves%20the%20Behavior%20of%20an%208%2DYear%2DOld%20Boy%20With%20Nonsyndromic%20Autism%20Spectrum%20Disorder,-Hu%2C%20Lin%2DYan

    -Stephen

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    Replies
    1. Stephen, Everolimus is used in people with TSC type autism. It is very expensive.

      My polypill drugs are very cheap.

      Delete

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