Semaglutide, marketed under brand
names like Wegovy, Mounjaro and Ozempic, is a GLP-1 receptor agonist originally
approved for treating type 2 diabetes and more recently for obesity. The global
semaglutide market is $27 billion in 2024. The broader market for GLP-1
receptor agonists, which includes semaglutide, is expected to experience
significant growth. Analysts project that this market could reach between $150
billion and $200 billion by the early 2030s.
Semaglutide is a dream for
pharmaceutical companies. The overweight can forget about diets and exercise;
they just need a weekly self-administered dose and wait to lose 20% of their
bodyweight in the first year. If they stop taking the drug all the weight will
just come straight back, so the patient needs to take the drug for life.
Semaglutide is expensive, but nothing
like the price hoped for by those developing elusive autism drugs.
Some obese people save so much money
on food it covers the cost of their semaglutide.
Obesity is so damaging that
semaglutide should have a transformative impact on healthcare.
On the other hand, the idea that
society might increasingly rely on pharmaceutical solutions instead of
encouraging lifestyle changes feels rather Orwellian, with a shift away from
personal responsibility, fostering dependency on external control. In a society
where health problems like obesity are "fixed" by a drug, self-regulation
through lifestyle choices will be de-emphasized, giving the impression that
human behavior is best managed through a weekly shot.
In the novel Brave New World by Aldous
Huxley, published in 1932, people in a highly controlled society all take a
drug called soma to feel good, maintain emotional stability, and suppress
negative feelings.
No Wegovy/Mounjaro moment likely for autism
For people who get their information from social media it appears that such an effortless Wegovy/Mounjaro moment exists for autism. You just send a reply to Facebook post and get a message back telling you where to buy the miracle cure to autism.
Looking at the world of
pharmaceuticals many parents hoped that Suramin would be the cure to autism.
Recently I saw yet another rather
misleading headline:
Lithium restores brain function and behavior
in Autism
Really, what it should say is:
Lithium may restore brain function and
behavior in Autism caused by Dyrk1a mutation if given while a baby.
Here is the article.
Lithium Restores Brain Function and
Behavior in Autism
Lithium, a drug widely used for bipolar disorder, may also treat autism spectrum disorder (ASD), according to new research. The study found that lithium restored brain function and reduced behavioral symptoms in mice with Dyrk1a gene mutations, a known ASD risk factor.
Administered
during the juvenile period, lithium normalized brain size, improved neural
connectivity, and eased anxiety and social deficits, with benefits persisting
into adulthood.
This
breakthrough highlights lithium’s potential to address core ASD mechanisms
through its action on Kalirin-7, a molecule critical for synaptic function. The
findings underscore the importance of early intervention and targeted
treatments for ASD.
The
team discovered that lithium’s therapeutic effects are partly mediated through
its action on Kalirin-7, a molecule essential for synaptic structure and
function.
By
targeting this molecule, lithium helped to restore balance in the brain’s
signaling networks, addressing one of the core mechanisms of ASD.
“This
is an exciting breakthrough,” said Dr. Roh Junyeop, a senior researcher and
co-first author of the study.
“Dyrk1a
mutations disrupt neural connectivity, much like a traffic jam or roadblocks in
a city. Lithium helps to clear the congestion, restoring smooth communication
between neurons.”
Director
Kim Eunjoon emphasized the potential impact of these findings, stating, “Our
research shows that lithium, a widely used drug for bipolar disorder, could also
serve as a treatment for ASD. The fact that its effects persist long after
treatment ends underscores the importance of early intervention during critical
developmental windows.”
This
study, published in the journal Molecular Psychiatry on December 5, not only
paves the way for new therapeutic approaches for ASD but also underscores the
critical importance of early diagnosis and intervention.
It
offers hope to families and individuals affected by ASD, suggesting that
targeted treatments may one day reduce the burden of this complex disorder.
Too little Dyrk1a leads to small
brains, autism and low IQ. In Down syndrome there is too much Dyrk1a expression
and this is a contributing factor to low IQ. You need just the right amount of
Dyrk1a for optimal brain development and then a higher IQ. Too much Dyrk1a also
leads to Alzheimer’s which is why there can be early onset in those with Down
syndrome.
Don’t give lithium to someone with Down
syndrome.
GSK-3β and Dyrk1a
In previous posts we did look at
something called GSK-3β, which plays a role in autism.
GSK-3β and DYRK1A
are two enzymes that play significant roles in regulating cell signaling,
neurodevelopment, and brain function. They also interact with each other. Both
play a role in the Wnt signaling pathway, which is disturbed in much autism and
some cancer.
Lithium in Autism
Lithium carbonate is a prescription
drug used to treat bipolar.
Lithium orotate is an OTC product that
some people do use to treat autism. The dosages are usually very low compared
to what is used in bipolar.
It is not uncommon to be diagnosed
with bipolar and autism.
Is Lithium a game changer for Autism?
While some people may well benefit,
the usage to date shows that lithium is not a game changer for most autism.
Mebendazole for some Autism and indeed Down
syndrome
I did propose years ago that Mebendazole/Vermox,
the cheap drug used to treat pinworms in children, might have potential to
treat some autism. Mebendazole is a Wnt inhibitor (the opposite of Lithium). I
did receive a message recently that Mebendazole was beneficial in one reader’s
son. Not much Mebendazole is absorbed into the bloodstream but you can maximize
it by taking it with a fatty meal. It does cross the blood brain barrier.
Mebendazole has been shown to inhibit
DYRK1A in laboratory settings, which could potentially address the effects of
DYRK1A overexpression seen in conditions like Down syndrome. Since Down syndrome
is diagnosed very early, treatment could start very early, which is critical to
optimize the developing brain.
Mebendazole - Wnt Inhibition and other effects
Mebendazole is known to inhibit
components of the Wnt signaling pathway. Inhibition of Wnt could potentially
normalize overactive or dysregulated pathways, leading to more balanced
dendritic spine dynamics in individuals with autism. In autism, there is often
an imbalance in dendritic spine formation and pruning, leading to either
excessive or insufficient connectivity. Modulating Wnt signaling could potentially
restore this balance, improving synaptic function and related behaviors.
Mebendazole has been shown to have
anti-inflammatory properties. Since neuroinflammation is often elevated in
autism, this could indirectly improve symptoms.
Mebendazole also stabilizes
microtubules, which are critical for intracellular transport and synaptic
function. This might indirectly benefit neuronal communication in autism.
Conclusion
Autism is far more complicated and
heterogeneous than obesity so sadly there can never be a simple Wegovy/Mounjaro
moment. Best not to listen to Autism
Moms telling you otherwise on Facebook.
On the plus side there are numerous partially effective therapies, sitting on the shelf in the pharmacy that do benefit specific types of autism. You just have to find what works in your very specific case.
I was recently asked a German mother if I have a spreadsheet listing all the possible therapies, what the benefits are, and in what order to try them. It is a very rational request, but there is so much variation that this would not be a simple task.