I just watched this interview by Dr John Campbell, and I'm glad I did.
It runs into something that was discussed in the MTHFR mutation community several decades ago - that of (synthetic) folic acid build up in the blood, and it's blocking mechanism to (natural) folate. I didn't think this was a big deal at the time - other than perhaps contributing to fatigue and DNA methylation not working so well. However it seems the research by these two (and others) has is questioning this.
So a quick FYI before digging into this topic.
Folic acid is a synthetic chemical, and not a vitamin. It can have a small percentage converted into folate in the body.
Folate is what the body needs, and is an actual vitamin/naturally occurring product.
Many Dr's, websites, and research papers confuse folic acid (synthetic) for folate (natural) and vice versa.
The 'fortification of food' with things like folic acid since the 80's is potentially causing a great deal of health problems. Most off the shelf vitamins are folic acid. I should also mention that most off the shelf vitamins also contain a form of B12 that is really not good for you (cyanocobalamin - cobalamin combined with cyanide).
The reason given for this public health intervention, was because it could prevent neural tube defects in babies. A better option would be mothers who may be prone to this (i.e. have a MTHFR type mutation), should be getting natural folate from foods - and/or a proper folate supplement (methylated folate).
Please note I am not a doctor and this isn't medical advice - if you are pregnant or attempting to get pregnant, please do your own research.
Here are the links from under the video:
From the video (if I understand this correctly) they said that folic acid tends to bind to the folate receptors more tightly than folate would - meaning they can block the folate transport receptors for some time. This means cellular folate deficiency, as none is getting through - even though blood levels would read high due to folic acid.
It takes a long time for the body to rid itself of folic acid because of this. It can (see the paper above) also trigger an immune reaction to folate receptors - presumably because that's how the body get's the folic acid out of the receptors. These immune flare ups tend to go away once the body has cleared itself of folic acid.
Many other diseases/problems are associated with the immune system attacking folate receptor-α (or treated by stimulating folate receptor-α, which may be blocked by folic acid) - including a bunch of cancers (ovarian, breast, prostate, epithelial etc), kidney disease, fertility problems (and possibly PCOS), lung and ear infections - to name a few.
It runs into something that was discussed in the MTHFR mutation community several decades ago - that of (synthetic) folic acid build up in the blood, and it's blocking mechanism to (natural) folate. I didn't think this was a big deal at the time - other than perhaps contributing to fatigue and DNA methylation not working so well. However it seems the research by these two (and others) has is questioning this.
So a quick FYI before digging into this topic.
Folic acid is a synthetic chemical, and not a vitamin. It can have a small percentage converted into folate in the body.
Folate is what the body needs, and is an actual vitamin/naturally occurring product.
Many Dr's, websites, and research papers confuse folic acid (synthetic) for folate (natural) and vice versa.
The 'fortification of food' with things like folic acid since the 80's is potentially causing a great deal of health problems. Most off the shelf vitamins are folic acid. I should also mention that most off the shelf vitamins also contain a form of B12 that is really not good for you (cyanocobalamin - cobalamin combined with cyanide).
The reason given for this public health intervention, was because it could prevent neural tube defects in babies. A better option would be mothers who may be prone to this (i.e. have a MTHFR type mutation), should be getting natural folate from foods - and/or a proper folate supplement (methylated folate).
Please note I am not a doctor and this isn't medical advice - if you are pregnant or attempting to get pregnant, please do your own research.
The paper under the video:Direct link to the paper, https://www.researchgate.net/public...ning_title_Cerebral_folate_disruption_and_ASDhttps://www.youtube.com/redirect?event=video_description&redir_token=QUFFLUhqbDhBUGcyYjBKLUIwRWx3V1BSdGpCclFoaU13d3xBQ3Jtc0trWkxhaHJVWURGTUhwNEZTWjFZQmxvUHYwSDQxWjVpTGtUSF95VjJwR1RxODdzM1hxLWlBSWpyU3BhYlJReFFkektxRmxtNGRnbjdOX3piSTI1VFp0S1lkMnJkdHBfSkQ5N0U2YWdMZm53eVl5V0xtNA&q=https://www.researchgate.net/publication/396231370_Disruption_of_Cerebral_Folate_Metabolism_as_a_Unifying_Framework_for_Autism_Spectrum_Disorder_Risk_and_Causation_Running_title_Cerebral_folate_disruption_and_ASD&v=4cIIN5-vn5E
Disruption of Cerebral Folate Metabolism as a Unifying Framework for Autism Spectrum Disorder Risk and Causation Running title: Cerebral folate disruption and ASD
Dr Tim Kelly, https://x.com/DrTimothyKelly
Dr Clare Craig, https://x.com/ClareCraigPath
Friend or Faux, https://x.com/fauxlate
Fauxlate: The drug in our food, https://x.com/fauxlate
Disruption of Cerebral Folate Metabolism as a Unifying Framework for Autism Spectrum Disorder Risk and Causation Running title: Cerebral folate disruption and ASD
- October 2025
Autism spectrum disorder (ASD) arises from diverse influences that rarely align into a single explanatory model. Here, we propose a unifying framework centred on disrupted cerebral folate metabolism acting across sensitive developmental windows. Reduced folates are essential for nucleotide synthesis and methylation and their transfer to the developing brain relies on high-affinity folate receptor-α (FRα) transport at the placenta and choroid plexus. Disruption of this pathway, through genetic variants, synthetic folic acid (sFA) producing unmetabolised folic acid (UMFA), or folate receptor autoantibodies (FRAAs), can impair neurodevelopment during critical stages from gestation to infancy and beyond. Using a Capacity-Load-Trigger (CLT) framework, we integrate evidence across genetics, pharmacology, immunology and epidemiology. Capacity reflects intrinsic susceptibility (e.g. folate-pathway polymorphisms) [for example MTHFR]; Load arises from exogenous pressures such as sFA exposure, drugs that deplete one-carbon intermediates, or FRAA-mediated blockade; and Triggers include infection, fever, or metabolic stress that break immune tolerance in predisposed hosts. Regional vulnerability is predicted to follow CSF diffusion distance and metabolic demand, with fronto-parietal association cortex, basal ganglia, long white-matter tracts and cerebellar hemispheres most affected when CSF folate is low in utero. This framework reconciles paradoxical findings, where both folate deficiency and excess sFA/UMFA exposure increase risk and clarifies how timing and 1 location of disruption shape phenotype. It identifies a mechanistically defined, potentially treatable subgroup and generates testable predictions for biomarkers, exposure timing and neuroanatomical patterns.
From the video (if I understand this correctly) they said that folic acid tends to bind to the folate receptors more tightly than folate would - meaning they can block the folate transport receptors for some time. This means cellular folate deficiency, as none is getting through - even though blood levels would read high due to folic acid.
It takes a long time for the body to rid itself of folic acid because of this. It can (see the paper above) also trigger an immune reaction to folate receptors - presumably because that's how the body get's the folic acid out of the receptors. These immune flare ups tend to go away once the body has cleared itself of folic acid.
Many other diseases/problems are associated with the immune system attacking folate receptor-α (or treated by stimulating folate receptor-α, which may be blocked by folic acid) - including a bunch of cancers (ovarian, breast, prostate, epithelial etc), kidney disease, fertility problems (and possibly PCOS), lung and ear infections - to name a few.