Gut microbiome and symptoms in females with irritable bowel syndrome: a cross-sectional analysis.


Journal

Beneficial microbes
ISSN: 1876-2891
Titre abrégé: Benef Microbes
Pays: Netherlands
ID NLM: 101507616

Informations de publication

Date de publication:
28 May 2024
Historique:
received: 24 07 2023
accepted: 01 05 2024
medline: 1 6 2024
pubmed: 1 6 2024
entrez: 31 5 2024
Statut: epublish

Résumé

Irritable bowel syndrome (IBS), a disorder of gut-brain interaction, is associated with abdominal pain and stool frequency/character alterations that are linked to changes in microbiome composition. We tested whether taxa differentially abundant between females with IBS vs healthy control females (HC) are associated with daily gastrointestinal and psychological symptom severity. Participants (age 18-50 year) completed a 3-day food record and collected a stool sample during the follicular phase. They also completed a 28-day diary rating symptom intensity; analysis focused on the three days after the stool sample collection. 16S rRNA gene sequencing was used for bacterial identification. Taxon abundance was compared between IBS and HC using zero-inflated quantile analysis (ZINQ). We found that females with IBS (n = 67) had greater Bacteroides abundance (q = 0.003) and lower odds of Bifidobacterium presence (q = 0.036) compared to HC (n = 46) after adjusting for age, race, body mass index, fibre intake, and hormonal contraception use. Intestimonas, Oscillibacter, and Phascolarctobacterium were more often present and Christensenellaceae R-7 group, Collinsella, Coprococcus 2, Moryella, Prevotella 9, Ruminococcaceae UCG-002, Ruminococcaceae UCG-005, and Ruminococcaceae UCG-014 were less commonly present in IBS compared to HC. Despite multiple taxon differences in IBS vs HC, we found no significant associations between taxon presence or abundance and average daily symptom severity within the IBS group. This may indicate the need to account for interactions between microbiome, dietary intake, metabolites, and host factors.

Identifiants

pubmed: 38821492
doi: 10.1163/18762891-bja00015
doi:

Substances chimiques

RNA, Ribosomal, 16S 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

259-273

Auteurs

K J Kamp (KJ)

16181University of Washington, School of Nursing, P.O. Box 357266, Seattle, WA 98195, USA.

A M Plantinga (AM)

Williams College, Williamstown, MA, USA.

K C Cain (KC)

16181University of Washington, School of Nursing, P.O. Box 357266, Seattle, WA 98195, USA.

R L Burr (RL)

16181University of Washington, School of Nursing, P.O. Box 357266, Seattle, WA 98195, USA.

C-S Tsai (CS)

16181University of Washington, School of Nursing, P.O. Box 357266, Seattle, WA 98195, USA.

Q Wu (Q)

Baylor College of Medicine and Texas Children's Hospital, Houston, TX, USA.

S Y So (SY)

Baylor College of Medicine and Texas Children's Hospital, Houston, TX, USA.

S Badu (S)

Baylor College of Medicine and Texas Children's Hospital, Houston, TX, USA.

T Savidge (T)

Baylor College of Medicine and Texas Children's Hospital, Houston, TX, USA.

R J Shulman (RJ)

Baylor College of Medicine and Texas Children's Hospital, Houston, TX, USA.

M M Heitkemper (MM)

16181University of Washington, School of Nursing, P.O. Box 357266, Seattle, WA 98195, USA.

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Classifications MeSH