Exploring the Role of Vitamin D and the Gut Microbiome: A Cross-Sectional Study of Individuals with Irritable Bowel Syndrome and Healthy Controls.


Journal

Biological research for nursing
ISSN: 1552-4175
Titre abrégé: Biol Res Nurs
Pays: United States
ID NLM: 9815758

Informations de publication

Date de publication:
07 2023
Historique:
pmc-release: 01 07 2024
medline: 9 6 2023
pubmed: 11 1 2023
entrez: 10 1 2023
Statut: ppublish

Résumé

Irritable bowel syndrome (IBS) is a common disorder of gut-brain interaction with multifaceted pathophysiology. Prior studies have demonstrated higher rates of vitamin D deficiency in individuals with IBS compared to healthy controls (HC), as well as associations of vitamin D concentration with IBS symptoms. A systematic review of 10 mouse and 14 human studies reported a positive association between vitamin D (serum levels and supplementation) and beta diversity of gut microbiome in a variety of conditions. The present retrospective case-control study aimed to compare vitamin D (25(OH)D) plasma concentrations and gut microbiome composition in adult women with IBS (n=99) and HC (n=62). Plasma concentrations of 25(OH)D were assessed using the Endocrine Society Guidelines definition of vitamin D deficiency (25(OH)D <20 ng/ml) and insufficiency (25(OH)D >20-<30 ng/ml). 16S rRNA microbiome gene sequencing data was available for 39 HC and 62 participants with IBS. Genus-level Bifidobacterium and Lactobacillus and phylum-level Firmicutes and Bacteroidetes relative abundances were extracted from microbiome profiles. Results showed vitamin D deficiency in 40.3% (n=25) vs. 41.4% (n=41), and insufficiency 33.9% (n=21) vs. 34.3% (n=34) in the HCs vs. IBS groups, respectively. The odds of IBS did not differ depending on 25(OH)D status (p=0.75 for deficient, p=0.78 for insufficient), and the average plasma vitamin D concentration did not differ between IBS (mean 24.8 ng/ml) and HCs (mean 25.1 ng/ml; p=0.57). We did not find evidence of an association between plasma 25(OH)D concentration and richness, Shannon index, Simpson index or specific bacterial abundances in either HCs or the IBS group.

Identifiants

pubmed: 36624571
doi: 10.1177/10998004221150395
pmc: PMC10404909
doi:

Substances chimiques

Vitamin D 1406-16-2
RNA, Ribosomal, 16S 0

Types de publication

Systematic Review Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

436-443

Subventions

Organisme : NINR NIH HHS
ID : K23 NR020044
Pays : United States
Organisme : NINR NIH HHS
ID : R01 NR013497
Pays : United States
Organisme : NINR NIH HHS
ID : R01 NR014479
Pays : United States
Organisme : NINR NIH HHS
ID : R01 NR001094
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK056338
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK130517
Pays : United States

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Auteurs

Sarah W Matthews (SW)

School of Nursing, University of Washington, Seattle, WA, USA.

Anna Plantinga (A)

Williams College, Williamstown, MA, USA.

Robert Burr (R)

School of Nursing, University of Washington, Seattle, WA, USA.

Kevin C Cain (KC)

Department of Biostatistics and Office for Nursing Research, School of Nursing, University of Washington, Seattle, WA, USA.

Tor Savidge (T)

Department of Pathology and Immunology, Baylor College of Medicine, Houston, TX, USA.
Department of Pathology, Texas Children's Microbiome Center, Texas Children's Hospital, Houston, TX, USA.

Kendra Kamp (K)

School of Nursing, University of Washington, Seattle, WA, USA.

Margaret M Heitkemper (MM)

School of Nursing, University of Washington, Seattle, WA, USA.

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Classifications MeSH