Evidence map›Paper›PMID 42943571›Full record

ReviewMicroorganisms2026

Gut and Intraplaque Microbiota in Atherosclerosis: Mechanistic Insights and Emerging Therapeutic Targets.

Qijian Zhao, Zhichao Lai, Yuyao Feng, Jiang Shao, Kang Li, Shi Huang, Bao Liu

Abstract readReview
In one paragraph

Review in Microorganisms, 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

7 authors.

Qijian ZhaoDepartment of Vascular Surgery, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100730, China.
Zhichao LaiDepartment of Vascular Surgery, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100730, China.
Yuyao FengDepartment of Vascular Surgery, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100730, China.ORCID 0000-0002-4374-4478
Jiang ShaoDepartment of Vascular Surgery, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100730, China.
Kang LiDepartment of Vascular Surgery, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100730, China.
Shi HuangFaculty of Dentistry, University of Hong Kong, Hong Kong SAR, China.
Bao LiuDepartment of Vascular Surgery, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100730, China.

Funding

Beijing Municipal Natural Science Foundation L248071Beijing Physician Scientist Training Project BJPSTP-2026-18Capital's Funds for Health Improvement and Research grant no. 2026-2-4013National High Level Hospital Clinical Research Funding 2025-PUMCH-A-179National Key Research and Development Program of China 2023YFC2415100National Natural Science Foundation of China 82470516the National Natural Science Foundation of China 62503501the National Natural Science Foundation of China 825B2013
6 · The paper itself

Abstract

Atherosclerosis remains a major cause of cardiovascular morbidity and mortality. Growing evidence suggests that microbiota-host interactions contribute to atherosclerosis through systemic and local mechanisms. This review summarizes current evidence on gut microbiota, microbial metabolites, and plaque-associated microbial signals, and discusses their potential therapeutic implications. Gut dysbiosis may contribute to atherosclerosis through multiple metabolite-dependent, immune, vascular, and metabolic pathways. Recent multi-omics and experimental studies further indicate that microbiota influence vascular biology beyond compositional changes alone. In parallel, plaque-associated microbial signals, potentially originating from the oral cavity or gut, may contribute to local inflammation, oxidative stress, necrotic core expansion, and plaque vulnerability. We further discuss a putative gut-oral-intraplaque axis, a potential local microbial metabolite microenvironment within plaques, and possible cross-kingdom interactions between gut fungi and bacteria. Together, these findings support an integrated framework in which microbiota may shape atherosclerosis through interconnected systemic and local pathways, with potential implications for biomarker development and microbiota-targeted therapies.

Indexed as

atherosclerosiscardiovascular diseasegut microbiotaintraplaque microbiotametabolitestherapeutic strategies

Identifiers

PMID42943571
PMCPMC13707795

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

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.