Evidence map›Paper›PMID 42157060›Full record

ArticleGenes & nutrition2026

Common genetic variants in vitamin D metabolism-related genes affect gut microbiota diversity in postmenopausal women.

Adriana Becerra-Cervera, Rogelio F Jiménez-Ortega, Diana I Aparicio-Bautista, Tania V López-Pérez, Edgar Denova-Gutiérrez, Berenice Palacios-González, Alberto Hidalgo-Bravo, Samuel Canizales-Quinteros, Jorge Salmerón, Berenice Rivera-Paredez and 1 more

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Article in Genes & nutrition, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Adriana Becerra-CerveraLaboratorio de Genómica del Metabolismo Óseo, Instituto Nacional de Medicina Genómica (INMEGEN), Mexico City, 14610, Mexico.
Rogelio F Jiménez-OrtegaServicio de Medicina Genómica, Instituto Nacional de Rehabilitación Luis Guillermo Ibarra Ibarra (INRLGII), Mexico City, 14389, Mexico.
Diana I Aparicio-BautistaLaboratorio de Genómica del Metabolismo Óseo, Instituto Nacional de Medicina Genómica (INMEGEN), Mexico City, 14610, Mexico.
Tania V López-PérezLaboratorio de Genómica del Metabolismo Óseo, Instituto Nacional de Medicina Genómica (INMEGEN), Mexico City, 14610, Mexico.
Edgar Denova-GutiérrezDepartamento de Nutrición, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, 14080, Mexico.
Berenice Palacios-GonzálezLaboratorio de Genómica del Envejecimiento, Instituto Nacional de Medicina Genómica (INMEGEN), en el Centro de Investigación sobre Envejecimiento (CIE-CINVESTAV Sur), Mexico City, 14610, Mexico.
Alberto Hidalgo-BravoServicio de Medicina Genómica, Instituto Nacional de Rehabilitación Luis Guillermo Ibarra Ibarra (INRLGII), Mexico City, 14389, Mexico.
Samuel Canizales-QuinterosUnidad de Genómica de Poblaciones Aplicada a la Salud, Departamento de Biología, Facultad de Química-UNAM/Instituto Nacional de Medicina Genómica, Mexico City, 14210, Mexico.
Jorge SalmerónCentro de Investigación en Políticas, Población y Salud (CIPPS) de la Facultad de Medicina, Universidad Nacional Autónoma de México (UNAM), Mexico City, 04510, Mexico.
Berenice Rivera-ParedezCentro de Investigación en Políticas, Población y Salud (CIPPS) de la Facultad de Medicina, Universidad Nacional Autónoma de México (UNAM), Mexico City, 04510, Mexico.
Rafael Velázquez-CruzLaboratorio de Genómica del Metabolismo Óseo, Instituto Nacional de Medicina Genómica (INMEGEN), Mexico City, 14610, Mexico. rvelazquez@inmegen.gob.mx.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecent studies have demonstrated that vitamin D (VD) influences gut microbiota (GM) by regulating epithelial barrier function and immune responses, thereby affecting microbial composition and diversity. Additionally, host genetic factors, particularly single-nucleotide variants (SNVs) in genes related to VD metabolism, may influence GM composition. Postmenopausal women are a particularly relevant population to assess the impact of these SNVs, as this group experiences reduced hormonal variability and a higher burden of vitamin D deficiency (VDD), enabling clearer evaluation of the association between vitamin D-related genetic variants and gut microbiota composition.

objectiveTo explore the relationship between SNVs in genes involved in VD metabolism and their impact on GM.

methodsWe genotyped nine variants: rs10741657 (CYP2R1), rs6013897 (CYP24A1), rs10877012 (CYP27B1), rs10783219 and rs4516035 (VDR), rs4588 and rs7041 (GC), rs4944957 and rs3794060 (NADSYN1). GM was characterized by sequencing the V4 hypervariable region of the 16S rRNA gene. We compared taxon abundance at the genus level across host genotypes using the dominant model. Quantile regression was used to analyze non-mean diversity responses, and PICRUSt2 identified functional pathways. We also calculated the genetic risk score (GRS) using rs4516035, rs3794060, and rs4944957, which were associated with lower alpha diversity.

resultsAlpha microbial diversity differed significantly for the VDR (rs4516035) and NADSYN1 (rs3794060, rs4944957) variants, both for risk alleles and genotypes. Differential abundance analysis identified taxonomic disparities, notably in the genera DTU014, Fusobacterium, Negativibacillus, Pseudomonas, Peptococcus, and [Clostridium]_innocuum_group. PICRUSt2-predicted functional pathways for the rs4516035- C allele revealed significant glutamine-glutamate, folate, galactose, and fatty acid metabolism. A GRS was associated with lower alpha diversity indices and differences in the insulin signaling pathway and oxidative phosphorylation.

conclusionsThese findings highlight the role of SNVs in GM modulation and suggest potential implications for VD metabolism and host health.

Indexed as

Genetic variantsGut microbiotaPostmenopausal womenVitamin D

Identifiers

PMID42157060
PMCPMC13361054

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LicenceCC BY-NC-ND
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.