Evidence map›Paper›PMID 42577841›Full record

ArticleFrontiers in microbiology2026

Gut microbiome dynamics and cardiometabolic disease progression: evidence from a secondary data analysis of pooled clinical datasets.

Scott D Wrigley, Sarah A Johnson, Christopher L Gentile, Tiffany L Weir

Abstract read
In one paragraph

Article in Frontiers in 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.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

4 authors.

Scott D WrigleyIntestinal Health Lab, Department of Food Science and Human Nutrition, Colorado State University, Fort Collins, CO, United States.
Sarah A JohnsonDepartment of Health, Nutrition, and Food Sciences, Florida State University, Tallahassee, FL, United States.
Christopher L GentileIntegrative Cardiovascular Physiology Lab, Department of Food Science and Human Nutrition, Colorado State University, Fort Collins, CO, United States.
Tiffany L WeirIntestinal Health Lab, Department of Food Science and Human Nutrition, Colorado State University, Fort Collins, CO, United States.

Funding

The Obese Microbiota as a Novel Regulator of Vascular Function: A Translational ApproachR01HL144611 · NHLBI · COLORADO STATE UNIVERSITY · PI GENTILE, CHRISTOPHER L, WEIR, TIFFANY L · 2019 to 2022
$1.4M
NHLBI NIH HHS R01 HL144611
6 · The paper itself

Abstract

Purpose: Individuals with cardiometabolic disease (CMD) often exhibit decreased microbial alpha diversity and/or differences in beta diversity indices than those without CMD. However, it is unclear if these compositional changes in the gut microbiome are a cause or a consequence of CMD. Research suggests individual bacterial species act as drivers of disease, inducing shifts in microbial community and host metabolism. During this process, large-scale compositional changes can develop secondarily, obscuring the original microbial drivers. This study aimed to characterize the gut microbiota of healthy individuals compared to those with early risk factors for CMD to determine whether specific microbial taxa and community associations exist with early stages of hypertension, vascular dysfunction, dyslipidemia, and overweight/obesity. Procedure: Baseline anthropometric, physiological, and gut microbiome data from three clinical studies previously conducted by our research groups were compiled and re-analyzed. Results: No differences in alpha and/or beta diversity were observed across CMD parameters. Through a consensus-based differential abundance analysis, we observed that several health-related taxa decreased as CMD levels increased, including Implications: The loss of health-associated gut microbiota, along with decreased network connectivity and increased network fragmentation, may play a role in the progression of CMD.

Indexed as

cardiovascular diseasedyslipidemiaendothelial functiongut microbiomehypertensionmicrobial networks

Identifiers

PMID42577841
PMCPMC13455506

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Registered trials

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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.