Published July 20, 2024 | Version v1
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Restoring Microbiome-Immune Function in Autism Spectrum Disorder using VDR-BIF Method

Description

Autism Spectrum Disorder (ASD) is a multifaceted neurodevelopmental condition with complex etiologies involving microbiome, genetic, environmental, and immunological factors. Recent advancements have underscored the pivotal role of the gut microbiome in influencing neurological and immune functions. Dysbiosis, characterized by microbial imbalance, is consistently observed in microbiome testing of ASD patients, revealing the presence of Small Intestinal Bacterial Overgrowth (SIBO), Small Intestinal Fungal Overgrowth (SIFO), and biofilm formations. This form of testing has significantly contributed to our understanding of the microbiome's role in ASD. The connection between single nucleotide polymorphisms (SNPs) and microbiome composition highlights the microbiome's impact on neurotransmission and immune system regulation.

 

Additionally, the increased intestinal permeability, commonly known as "leaky gut," is implicated in systemic inflammation and the compromise of the blood-brain barrier, leading to "leaky brain" and exacerbating neurological symptoms in ASD. This study elucidates how Vitamin D Receptors (VDRs) are downregulated by the influx of lipopolysaccharides (LPSs), mycotoxins, and other potential toxins via the NF-κB pathway. Our research demonstrates that dietary improvements, vitamin D supplementation with cofactors, and other gut-supportive supplements can reduce intestinal hyperpermeability, thereby allowing the immune system to upregulate VDRs. Enhanced VDR function enables vitamin D metabolites to bind effectively to their respective receptors. Furthermore, dietary interventions that reduce leaky gut improve the mucin layer barrier and enhance tight junction function. Calcitriol, a form of vitamin D, plays a crucial role in tightening these junctions, which helps reduce leaky gut. This process subsequently mitigates neuroinflammation by restoring the integrity of the blood-brain barrier. Using the VDR-BIF (Vitamin D Receptor - Blood Immunofluorescence) Method implemented by Beltran et al, we have been able to non-invasively measure VDR expression, providing a significant advancement over procedural biopsies.

 

This method allows healthcare providers to study VDR dynamics in patients with autism or autoimmune conditions, making the research more accessible and less invasive. These findings provide a promising avenue for therapeutic interventions aimed at improving the quality of life for individuals with ASD, highlighting the potential of the VDR-BIF Method in clinical practice.

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