Albert Einstein – perhaps an Aspie, but not a TBCB autistic
Today’s post was prompted by a very matter of fact approach proposed to deal with autism caused when both mother and father carry a single mutation in the TBCB gene. The unaffected parents produce a child with a 25% chance of having autism and a very specific movement disorder because the child has mutations in both of its copies of the gene.
The TBCB gene helps make something
called tubulin, which is one of the three main components of the cytoskeleton.
The cytoskeleton plays a role in many
well-known neurodegenerative disorders such as Parkinson's disease, Alzheimer's
disease, Huntington's disease, and amyotrophic lateral sclerosis (ALS).
Disruptions in tubulin's normal function can impair cellular processes, including those involved in neuronal signaling and motor control, contributing to movement disorders. So we should not be surprised that one feature of TBCB autism is a difficulty in learning how to walk
Israeli researchers discover gene mutation in Ashkenazi Jews that can cause autism
In non-Jewish populations, the occurrence of the mutation in TBCB is 5 in 100,000.
In Ashkenazi Jews, the rate is 1 in 80.
The Israeli Health Ministry incorporated a screening test for the TBCB gene mutation as part of the national healthcare basket in November, making it accessible to all couples planning for pregnancy.
As reported in the Times of Israel, the parents’ options proposed are:
“They can choose to have an abortion, she said, or to have in-vitro fertilization with genetic screening, in which only embryos without two abnormal copies of the TBCB gene are put into the uterus.
The third option is to keep the pregnancy, she said.
A year after the child is born, she said, parents will be able to see if their child has difficulty with motor development.
In that case, “they can give the child physiotherapy at an early age and help them develop,” Bratman-Morag said.
The illness “causes them difficulties with walking, but they can learn to live with that,” she said.
I don’t think you could be quite so blunt in other countries. The autism self-advocates would go bananas. Their worst dreams have actually materialized – "eugenics" has arrived and in Israel of all places.
The IVF therapy suggested is a very pragmatic approach. I am really surprised they propose it.
The arguments are similar to those that surround Down syndrome. In the world’s most advanced countries, like Denmark and Iceland, almost all DS fetuses are aborted. In the US the number of live births actually went up, according to the chart below.
The difference with TBCB is that you can test the parents before conception and not just the fetus.
Source https://downsyndroom.nl/wp-content/uploads/2022/09/down-syndrome-population-usa-factsheet.pdf
The downside of Endogamy
Many genes are tagged as being associated with higher IQ, or higher educational attainment and some of these are also linked to autism.
Like it or not, some groups of people are cleverer than others, Albert Einstein might have been at the extreme for Ashkenazi Jews, but he comes from a clever genetic group. These discrete genetic groups are created by what is politely referred to as endogamy (marrying within the community), biologically it is interbreeding.
Unfortunately, there are also downsides caused by centuries of interbreeding particularly within a group that started out relatively small. European royal families famously suffered from it; in their quest for political alliances they created very unhealthy bloodlines. The Habsburg dynasty took marrying their cousins to an extreme in their quest to keep territory and wealth in the family. This led to infertility, intellectual disability, physical disability, reduced lifespan and the famous Habsburg pronounced lower jaw. For American readers, this family were the royalty in Austria-Hungary, Spain, Holy Roman Empire (Germany etc), Belgium, Luxembourg, Netherlands etc. Very briefly a Habsburg, Maximilian I, was Emperor of Mexico - he was executed by firing squad in 1867.
Ashkenazi Jews are descended from communities that lived in Central and Eastern Europe in the middle ages. The majority now live in the United States. Of 11 million people, 6 million live in the United States. In the world there are another 5 million non-Ashkenazi Jews. In Israel there are 7 million Jewish people and the largest group is Mizrahi, who are descended from the Middle East and North Africa.
For Ashkenazi Jews the following medical conditions are known to be over represented:
- Bloom syndrome
- Canavan disease
- Cystic fibrosis
- Dihydrolipoamide dehydrogenase deficiency
- Familial dysautonomia
- Familial hyperinsulinism
- Fanconi anemia type C
- Gaucher disease
- Glycogen storage disease type 1A
- Joubert syndrome
- Maple syrup urine disease
- Mucolipidosis type IV
- Nemaline myopathy
- Niemann-Pick disease type A
- Spinal muscular atrophy
- Tay-Sachs disease
- Usher syndrome type 1F
- Usher syndrome type III
- Walker-Warburg syndrome
Four cancer genes are known to cause problems
- BRCA1 and BRCA2, linked to
- Breast cancer and ovarian cancer in women
- Breast cancer and prostate cancer in men
- Melanoma
- Pancreatic cancer
- About one in every 40 Ashkenazim has a BRCA mutation; in the general population, the rate is about one in every 400 people.
- GREM1, linked to colon cancer
- APC, linked to colon cancer
This is a wealthy group of people living in a country that looks after the health of rich people very well. That must be the reason why the group has been so well studied. I was a little surprised.
The recent research in Israel has identified the TBCB gene to be an autism gene and that mutations are substantially more come in Ashkenazi Jews.
The mutation is not more common in the other Jewish ethic groups (Sephardi, Mizrahi, Ethiopian, Yemenite, Bukharan, Indian, Kavkazi, Karaite, Cochin, Kaifeng).
Conclusion
I was a little surprised to learn recently from a chat with a kindergarten teacher who worked in Qatar that many of the kids already knew who they were going to marry. “He’s my cousin and I am going to marry him when I grow up,” said the little girl. This kind of arranged marriage is still common there. Well the Habsburgs also did it, so a European can hardly judge them.
Consanguineous marriage (cousin marriage) is alive and well.
Mixing up the gene pool looks to me like the best way to go.
In ancient times forced mixing was common. The Vikings used to abduct young women on the raiding trips across Europe, this continued until the Christianization of Scandinavia between the 9th and 12th centuries. In the wilder parts of the Balkans there was a practise called otmitza up until the 1800s, which can be best described as bride kidnapping, where the bride would be brought from a distant community over the mountains. In parts of Central Asia the practise of ala kachuu (to take and flee) continues to this day. In Kyrgyzstan 14% percent of married women say they were kidnapped. The UNDP have a special program to try and stop it.
When it comes to reducing neurodevelopmental disorders mixing up the gene pool looks the best option. Modern technology risks taking society in the opposite direction with online dating apps matching Aspie girl with Aspie boy to then potentially produce a more severe kind of autism, but then their bloodlines end. Mother Nature can indeed be harsh.
I wonder what will be the next genetic test for autism to join Israel’s “national healthcare basket.” Some people will like the idea and others will not, but it looks like the future is already here.
Thank you for all your research and posting them. Its was an interesting informative read both me n my husband enjoyed this read. You have another new reader.
ReplyDeleteHi Peter, this could be big news related to cause & possible future therapy for idiopathic autism. Scientists have discovered alternations of the neuronal protein CPEB4 are likely the cause of idiopathic autism or the other 80% not known gene related.(see attached link)
ReplyDeletehttps://www.news-medical.net/news/20241204/Scientists-identify-molecular-mechanism-behind-idiopathic-autism.aspx
It would be great if a single gene/protein was behind 80% of autism. Then you could have a single silver bullet to treat most people's autism.
DeleteI think the reality is very much more complex. Hopefully I am wrong.
Delete
A small comment from
ReplyDeletesomeone interested in prehistory: recently, with new tech, we were able to analyze several prehistoric cemeteries in europe to give us answers on the lives of women: were they married in their community or elsewhere or at what age?
We did find the expected, that women were married into other communities than where they were born. But the surprising thing was their age. At that historical time, women would start kenstruatin at 12-14, similar ti girls today. But they would be married off at 16-18. This we know because the young women who died in their own communities aka were not married off yet to elsewhere, were of that age.
So, even thousands of years ago, people thought that a barely menstruating child was not fit for marriage or childbirth.
Interesting Autism casestudy about Antabuse and Autism.
ReplyDeletehttps://pmc.ncbi.nlm.nih.gov/articles/PMC10473095/
-Stephen
Peter, did Monty have dysgraphia? Did bumetanide help with this? Thanks!
ReplyDeleteStephen
Kids with autism often have very poor hand writing. Monty did a lot of work practising how to write and ended up with very neat handwriting.
DeleteBumetanide helped greatly with cognition and knowing how to learn. I think the hours spent doing practise worksheets is what really mattered. This was all done at home, not part of school work.
Thank you!
DeletePeter, would you happen to remember a blog that you linked to long ago, written by a woman with autism who had a PANS-like regression as an adult and she wrote a book about it? I remember that her website was no longer in service and I had to use the wayback machine. She had some interesting posts that I want to revisit.
ReplyDeleteThat one I do not recall. The were cases of adults with NMDAR encephalitis which appears as acute and onset schizophrenia. There was a book and a film.
DeletePeter! I mistook your blog for a different autism blog. It was linked to on thinkingautism.Org.UK and the woman's website was called athinking patient.com
DeletePeter, do you still use cinnamon for Monty? What specific improvements did you notice? MH
ReplyDeleteMH, it is not easy to give a teaspoon of Ceylon cinnamon a day. I used to put it in two large gelatin capsules. I thought it did give an incremental boost to cognition, which is important if you are following the mainstream school curriculum.
DeleteCinnamon has broad health benefits just like cocoa flavonols, beetroot juice and many other foods. If you are limited to foods and OTC supplements then cinnamon should be on your list to trial. Pharmaceuticals tend to give a much greater benefit.
Hi Peter and all ,
ReplyDeleteMerry Christmas and happy holidays to you all and your family.
Gabbana, thanks for the greeting. Best wishes to you and your family.
DeletePeter, what's the current theory why excitation/inhibition equilibrium is impaired?
ReplyDeleteAlso, Merry Christmas and happy new year.
-Stephen
Stephen, an excitatory-inhibitory imbalance is thought to exist in most severe autism. It can exist for a wide range of reasons, one or more of which may exist in those affected.
DeleteThis imbalance refers to a disruption in the balance between excitatory (glutamate-mediated) and inhibitory (GABA-mediated) signaling in the brain.
1. Genetic Mutations
Mutations in genes regulating synaptic function, such as SHANK, NRXN, and NLGN, can disrupt synaptic communication and shift the E/I balance.
Abnormalities in genes regulating ion channels, like SCN2A and CACNA1C, affect neuronal excitability.
2. Altered GABAergic Function
Reduced GABA synthesis or signaling leading to insufficient inhibitory control.
Decreased expression of GABAergic receptors and transporters has been noted in some cases.
3. Excessive Excitatory Signaling
Increased glutamatergic activity or excessive synaptic connectivity can lead to hyperexcitability.
Dysregulated glutamate transporters or receptor expression may result in excitotoxicity and impaired signal modulation.
4. Neuroinflammation
Chronic neuroinflammation and altered microglial activity can affect synaptic pruning and neurotransmitter regulation, contributing to the E/I imbalance.
5. Developmental Synaptic Changes
During normal brain development, there is a shift from excitatory to inhibitory dominance. Disruption in this developmental process can cause a persistent E/I imbalance in ASD.
In effect GABA is working in reverse due to elevated intracellular chloride.
6. Impaired Neuronal Connectivity
Abnormalities in brain connectivity, such as hyperconnectivity in local circuits and hypoconnectivity in long-range circuits, can result in a functional E/I imbalance.
7. Metabolic and Environmental Factors
Oxidative stress and mitochondrial dysfunction in neurons can impair the production and regulation of neurotransmitters.
Prenatal exposure to toxins, infections, or stress can also disrupt the E/I balance.
8. Epigenetic and Regulatory Mechanisms
Dysregulation of transcription factors and epigenetic modifications (e.g., DNA methylation, histone acetylation) can alter the expression of genes involved in excitatory and inhibitory signaling.
Thank you. I've been reading a handful of studies from this French researcher Dr. Davidovic and her p-cresol experiments. It appears p-cresol lowers dopamine in the brain significantly.
DeleteTHE MICROBIOTA-DERIVED METABOLITE P-CRESOL INDUCES SOCIAL INTERACTION DEFICITS IN MICE BY A POTENTIAL DEREGULATION OF CATECHOLAMINES BIOSYNTHESIS
https://www.ibroneuroreports.org/article/S2667-2421(23)00098-2/fulltext
This is from Dr. Ben-Ari research
These results lead the researchers to conclude that high levels of chloride – causing constant GABA activity in CGINs – contribute to the motor problems produced by dopamine depletion. And this contribution can be reduced by lowering the levels of chloride in the cells via the treatment of the NKCC1 chloride importer, bumetanide.
https://www.nature.com/articles/s41467-018-03802-y
https://cureparkinsons.org.uk/2021/10/bumetanide-2/.
Maybe bumetanide works because it negates the effects of low dopamine in the brain? Also, sodium benzoate also increase dopamine in the brain.
Stimulation of Dopamine Production by Sodium Benzoate, a Metabolite of Cinnamon and a Food Additive
https://pmc.ncbi.nlm.nih.gov/articles/PMC8150256/
-Stephen
if the TBCB gene predicts autism-related movement disorder, how accurately does it predict autism itself (with or without movement disorders)
ReplyDeleteIf the TCBC gene test predicts autism-related movement disorder, does it also accurate predict autism itself (or the severity of autism) with or without the movement disorder, which not all autistic kids have
ReplyDeleteI think if both parents have the mutation the child will have the syndrome that features both autism and the movement disorder. Nearly all syndromes are a spectrum so the severity will likely vary from person to person.
Delete