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Nutrigenomics framework identifies vitamin B3 as potential therapy for NAXD deficiency disorder

By

Isha H. Jain1,2,10,16 Send email to [email protected]

3d ago· 64 min readenNews

Summary

This article presents a nutrigenomics framework that systematically identifies monogenic diseases that can be treated with vitamin supplementation. Using genome-wide CRISPR screens under varying vitamin B2 and B3 levels, researchers discovered that NAXD (NAD(P)HX dehydratase) is the top hit in the vitamin B3 screen. NAXD repairs an aberrant hydrated form of NADH. The study demonstrates that vitamin B3 therapy rescues NAD(P)(H) metabolism, prevents brain pathology, and extends lifespan by more than 40-fold in a Naxd knockout mouse model, offering a potential therapy for NAXD deficiency—a lethal neurodevelopmental disorder.

Key quotes

· 3 pulled
We developed a nutritional genomics framework to systematically identify monogenic diseases responsive to micronutrient modulation.
In the vitamin B3 screen, NAD(P)HX dehydratase (NAXD) was the top hit; this enzyme repairs an aberrant, hydrated form of NADH.
In this Naxd KO mouse model, vitamin B3 rescues NAD(P)(H) metabolism, prevents brain pathology, and extends lifespan by more than 40-fold.
Snippet from the RSS feed
A nutrigenomics framework identifies genetic diseases amenable to vitamin B2 and B3 therapies. This approach nominates vitamin B3 as a therapy for NAXD deficiency, a lethal neurodevelopmental disorder. In this Naxd KO mouse model, vitamin B3 rescues NAD(P

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