Evidence map›Paper›PMID 42676332›Full record

ArticleFrontiers in physiology2026

Gastrointestinal metabolites: a potential bridge connecting gut microbiota and myocardial metabolic reprogramming in acute myocardial infarction.

Jingxin Zhang, Xiang Xiao, Xuefei Gao, Jiazhen Li, Haoyue Shi, Jing-Yan Han, Yin Li, Lin Li

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Article in Frontiers in physiology, 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

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

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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

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No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Jingxin Zhang *Department of Integration of Chinese and Western Medicine, School of Basic Medical Sciences, Peking University, Beijing, China.
Xiang Xiao *Tasly Microcirculation Research Center, Peking University Health Science Center, Beijing, China.
Xuefei GaoGraduate School, Beijing University of Chinese Medicine, Beijing, China.
Jiazhen LiGraduate School, Beijing University of Chinese Medicine, Beijing, China.
Haoyue ShiBeijing Hospital of Traditional Chinese Medicine, Capital Medical University, Beijing, China.
Jing-Yan HanDepartment of Integration of Chinese and Western Medicine, School of Basic Medical Sciences, Peking University, Beijing, China.
Yin LiDepartment of Integration of Chinese and Western Medicine, School of Basic Medical Sciences, Peking University, Beijing, China.
Lin LiDepartment of Integrative Cardiology, China-Japan Friendship Hospital, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Gut microbiota plays a significant role in the occurrence and progression of multisystem disease. Previous studies have indicated that the intestinal microenvironment is closely linked to metabolic and cardiovascular diseases, yet its underlying mechanism remains unclear. We aimed to explore the association between the gut microbiota-metabolite network and cardiovascular function with the transcriptomic changes in the myocardium of acute myocardial infarction (AMI) mice. Methods: Eight-week-old C57BL/6J mice were adaptively fed for 7 days and then divided into the AMI model group and Sham group. After surgery, multiple approaches were used to assess the physiological and pathological changes in mice. At 7 days post-surgery, cardiac sections were analyzed using H&E staining and Masson staining. The gastrointestinal contents collected from the AMI and Sham group mice were analyzed by 16S rRNA sequencing and untargeted metabolomics and apical myocardial tissues were harvested for transcriptomic detection. followed by multi-omics association analysis between the differential gut microbiota and metabolites. Taking metabolites as the bridge, an integrated multi-omics correlation analysis was conducted. Results: Compared with the Sham group, mice in the AMI group exhibited obvious myocardial pathological damage and significant depletion of gut microbiota such as Conclusions: Myocardial injury in AMI may show a link between the remodeling of gut microbial structure. Correlative correlations indicate that altered gastrointestinal metabolites, as products of gut microbiota, are closely associated with myocardial metabolic reprogramming after AMI, whereas causal effects remain to be verified by further functional experiments.

Indexed as

acute myocardial infarctionbiomarkergastrointestinal metabolitesgut microbiotamyocardial metabolic reprogrammingnon-invasive diagnosis and treatment

Identifiers

PMID42676332
PMCPMC13526554

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