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Polyphenol-Related Gut Metabotype Signatures Linked to Quality of Life in Postmenopausal Women: A Randomized, Placebo-Controlled Crossover Trial

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dc.contributor.author Jarrin-Orozco, María-P
dc.contributor.author Romo-Vaquero, María
dc.contributor.author Carrascosa, Concepción
dc.contributor.author Pertegal-Ruiz, Miriam
dc.contributor.author Berna, José
dc.contributor.author Puigcerver, Julio
dc.contributor.author Saura-Sanmartin, Adrián
dc.contributor.author Espinosa-Salinas, Isabel
dc.contributor.author García-Nicolás, María
dc.contributor.author Ávila-Galvez, María-A
dc.contributor.author Espín, Juan-C
dc.date.accessioned 2026-03-09T08:43:59Z
dc.date.available 2026-03-09T08:43:59Z
dc.date.issued 2025-11-15
dc.identifier.citation Jarrín-Orozco MP, Romo-Vaquero M, Carrascosa C, Pertegal M, Berná J, Puigcerver J, et al. Polyphenol-Related Gut Metabotype Signatures Linked to Quality of Life in Postmenopausal Women: A Randomized, Placebo-Controlled Crossover Trial. Nutrients. 15 de noviembre de 2025;17(22):3572. doi:10.3390/nu17223572
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/25147
dc.description.abstract Background/Objectives: Interindividual variability in polyphenol metabolism may help explain the inconsistent effects of polyphenol intake on health outcomes. This study compared, for the first time, (i) polyphenol-related gut microbiota metabotypes (urolithins: UM0, UMA, UMB; equol: EP, ENP; lunularin: LP, LNP) and their clusters (MCs) in non-medicated premenopausal (Pre-M) and postmenopausal (Post-M) women and (ii) the impact of an 8-week intake of a polyphenol-rich plant extract mixture (PPs) on the quality of life (QoL) of Post-M. Methods: Polyphenol metabotypes were determined in urine via UPLC-QTOF-MS after a 3-day intake of PPs containing resveratrol, pomegranate (ellagitannins and ellagic acid), and red clover (isoflavones) in Pre-M (n = 120) and Post-M (n = 90) women. QoL was assessed with the short-form Cervantes Scale in a randomized, placebo-controlled crossover trial (8-week PPs vs. placebo), completed by 78 Post-M participants. Results: At baseline, Pre-M and Post-M women showed only minor differences in metabotype and MC distributions linked to menopausal status. MC3 (UMA+EP+LP) predominated in Pre-M, while MC7 (UMA+EP+LNP) was most frequent in Post-M. PPs intake in Post-M women led to modest shifts in metabotype and MC distributions toward Pre-M patterns. Quantitative metabolite production was comparable between groups, except for equol, which showed a median 2.8-fold increase after PPs intake in EP Post-M women. Clinically meaningful improvements (score reduction ? 6.7 points) in QoL were observed in the Psychic domain in EP women (28%, p = 0.039) and in the Menopause and Health domain, specifically in EP (24.1%, p = 0.004), MC3 (22.5%, p = 0.043), and MC4 (UMB+EP+LP; 41.3%, p = 0.022), were mainly driven by a reduction in hot flashes (p = 0.001). Conclusions: These findings support metabotyping as a tool to guide targeted dietary strategies and enhance QoL through precision health in Post-M women.
dc.language.iso eng
dc.publisher MDPI
dc.rights Atribución/Reconocimiento 4.0 Internacional
dc.rights.uri https://creativecommons.org/licenses/by/4.0/deed.es
dc.subject.mesh Humans
dc.subject.mesh Female
dc.subject.mesh Quality of Life
dc.subject.mesh Polyphenols/urine/metabolism/administration & dosage
dc.subject.mesh Postmenopause/metabolism
dc.subject.mesh Middle Aged
dc.subject.mesh Cross-Over Studies
dc.subject.mesh Gastrointestinal Microbiome/drug effects
dc.subject.mesh Plant Extracts/administration & dosage
dc.subject.mesh Adult
dc.subject.mesh Aged
dc.subject.mesh Premenopause
dc.title Polyphenol-Related Gut Metabotype Signatures Linked to Quality of Life in Postmenopausal Women: A Randomized, Placebo-Controlled Crossover Trial
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 41305622
dc.relation.publisherversion https://www.mdpi.com/2072-6643/17/22/3572
dc.type.version info:eu-repo/semantics/publishedVersion
dc.identifier.doi 10.3390/nu17223572
dc.journal.title Nutrients
dc.identifier.essn 2072-6643


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