Evidence map›Paper›PMID 42289650›Full record

ArticleBMC microbiology2026

Gut microbiota composition and functional pathways associated with metabolic syndrome in Mexican adult women: cross-sectional analysis.

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

Abstract read
In one paragraph

Article in BMC microbiology, 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Berenice Rivera-Paredez *Centro de Investigación en Políticas, Población y Salud (CIPPS), Facultad de Medicina, Universidad Nacional Autónoma de México (UNAM), Mexico City, 04510, Mexico.
Adriana Becerra-Cervera *Laboratorio de Genómica del Metabolismo Óseo, Instituto Nacional de Medicina Genómica (INMEGEN), Mexico City, 14610, Mexico.
Diana I Aparicio-BautistaLaboratorio 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.
Tania V López-PérezLaboratorio de Genómica del Metabolismo Óseo, Instituto Nacional de Medicina Genómica (INMEGEN), Mexico City, 14610, Mexico.
Alberto Hidalgo-BravoServicio de Medicina Genómica, Instituto Nacional de Rehabilitación Luis Guillermo Ibarra Ibarra (INRLGII), Mexico City, 14389, Mexico.
Tania G Sánchez-PimientaSecretaría de Ciencia, Humanidades, Tecnología e Innovación (SECIHTI), Mexico City, 03940, Mexico.
Berenice Palacios-GonzálezLaboratorio de Genómica del Envejecimiento del Instituto Nacional de Medicina Genómica (INMEGEN), en el Centro de Investigación sobre Envejecimiento (CIE-CINVESTAV Sur), Mexico City, 14610, Mexico.
Samuel Canizales-QuinterosDepartamento de Biología, Facultad de Química, Unidad de Genómica de Poblaciones Aplicada a la Salud, Universidad Nacional Autónoma de México (UNAM)/Instituto Nacional de Medicina Genómica, Mexico City, 14210, Mexico.
Jorge SalmerónCentro de Investigación en Políticas, Población y Salud (CIPPS), 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.ORCID 0000-0003-4515-0777

Funding

Consejo Nacional de Ciencia y Tecnología 7876Consejo Nacional de Ciencia y Tecnología CF-2019- 102962
6 · The paper itself

Abstract

backgroundThe gut microbiota (GM) plays a key role in maintaining metabolic homeostasis by regulating energy balance, inflammatory pathways, and hormone metabolism. Its role in metabolic syndrome (MetS) is particularly relevant in postmenopausal women, who experience profound metabolic and endocrine changes that increase their vulnerability to cardiometabolic diseases. In Mexico, MetS affects nearly half of postmenopausal women, yet the mechanisms linking hormonal decline, metabolic alterations, and the GM remain poorly understood. This study evaluated the association between GM composition, functional potential, and MetS severity in Mexican women.

resultsIn postmenopausal women, GM diversity decreases progressively as the number of MetS components increases. Women with MetS showed enrichment of Lactobacillus, Roseburia, and Escherichia/Shigella, and depletion of Akkermansia and Christensenellaceae R-7 group. Functional prediction revealed alterations in amino acid, lipid, and carbohydrate metabolism. Pathways related to Branched-Chain Amino Acids (BCAA) degradation, D-alanine, and histidine metabolism were disrupted. Women with five MetS components exhibited the most pronounced functional shifts, including altered sphingolipid and glutathione metabolism. Serum alanine (ALA) concentrations were higher in women with MetS and increased with MetS severity, suggesting metabolic stress or impaired fatty acid processing.

conclusionThe presence and severity of MetS are associated with GM composition in Mexican postmenopausal women. Findings support the potential of microbiota-based biomarkers and interventions to reduce metabolic risk in this population.

Indexed as

BacteriaGastrointestinal MicrobiomeMetabolic SyndromeAdultCross-Sectional StudiesFecesFemaleHumansMexicoMiddle AgedPostmenopauseRNA, Ribosomal, 16SRNA, Ribosomal, 16SGut microbiotaMenopauseMetabolic syndrome

Identifiers

PMID42289650
PMCPMC13491776

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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.