Evidence map›Paper›PMID 42210082›Full record

Observational studyBMC cardiovascular disorders2026

Cardiovascular disease risk factors in women with O-desmethylangolensin producing and non-producing gut microbial metabotypes: an observational study.

Holly Childs, Cara L Frankenfeld, Allyson Dailey, Robin Couch, Margaret Slavin

Abstract readObservational StudyMulticenter StudyComparative Study
In one paragraph

Observational study in BMC cardiovascular disorders, 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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2 · The registry

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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

5 authors.

Holly ChildsDepartment of Nutrition and Food Science, University of Maryland, College Park, MD, USA.
Cara L FrankenfeldMaineHealth Institute for Research, Center for Interdisciplinary & Population Health Research, Westbrook, ME, USA.
Allyson DaileyInstitute of Advanced Biomedical Research, George Mason University, Fairfax, VA, USA.
Robin CouchInstitute of Advanced Biomedical Research, George Mason University, Fairfax, VA, USA.
Margaret SlavinDepartment of Nutrition and Food Science, University of Maryland, College Park, MD, USA. mms@umd.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDaidzein, an isoflavone in soy, is metabolized to O-desmethylangolensin (ODMA) by select gut bacteria. Not all individuals have gut microbiomes capable of producing ODMA, resulting in ODMA producer and non-producer metabotypes. A limited body of research suggests that ODMA producers have lower systolic blood pressure, percent body fat and total cholesterol, compared to non-producers. More work is needed to confirm this relationship in other populations.

methodsData from the Study of Women's Health Across the Nation (SWAN), a study of women in their middle years, was used. A subset of women who reported consumption of isoflavones in diet or supplements was included for this analysis. Urinary ODMA and daidzein of 148 participants were measured via HPLC-MS-MS to classify metabotypes: ODMA (nmol/L)/daidzein (nmol/L) = 0, non-producers (n = 23); ODMA (nmol/L)/daidzein (nmol/L) > 0 but less than 0.5, low-producers (n = 90); and ODMA (nmol/L)/daidzein (nmol/L) > 0.5, high-producers (n = 35). Multivariable linear regression models were used to compare cardiovascular disease (CVD) risk markers among groups. Models were adjusted for age, race, self-reported health, blood pressure medication, smoking, menopausal status and anthropometry.

resultsODMA non-producers had higher systolic blood pressure (adj. mean difference = 7.6 mmHg, 95% CI: 1.1, 14.1, p = 0.02) compared to high producers. Another trend but not statistically significant difference observed included higher fasting serum glucose (adj. mean difference = 6.1 mg/dl, CI: -0.9, 13.2, p = 0.09) in ODMA non-producers when compared to ODMA producers.

conclusionsIn this diverse sample of U.S. women, this study observed higher blood pressure in ODMA non-producers than ODMA producers. This aligns with prior work associating ODMA producers with a more favorable CVD risk profile compared to non-producers, and provides additional evidence that this gut microbial metabotype may be related to cardiovascular health.

Indexed as

BacteriaCardiovascular DiseasesGastrointestinal MicrobiomeIsoflavonesMetabolomicsAdultAgedBiomarkersDietary SupplementsFemaleHeart Disease Risk FactorsHumansMiddle AgedPhenotypeRisk AssessmentUnited StatesBiomarkersdaidzeinIsoflavonesO-desmethylangolensinCardiovascular diseaseDaidzeinIsoflavoneMetabotypeMicrobiomeO-desmethylangolensinODMA

Identifiers

PMID42210082
PMCPMC13419030

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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.