Evidence map›Paper›PMID 41427705›Full record

ArticleMicrobiology spectrum2026

Progressive and concordant alterations in transcriptional and gut microbiota across aortic valve calcification severity.

Jue Wang, Ruihang Qu, Wenhao Huang, Yue Chen, Yun Li, Qingqing Lin, Ziji Wu, Hangfei Yan, Tingting Yu, Chiyin Wang and 3 more

Abstract read
In one paragraph

Article in Microbiology spectrum, 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

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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

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

13 authors.

Jue Wang *Department of Cardiac Surgery, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Ruihang Qu *Key Laboratory of Laboratory Medicine, Ministry of Education, Institute of Genomic Medicine, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Wenhao HuangDepartment of Cardiac Surgery, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Yue ChenKey Laboratory of Laboratory Medicine, Ministry of Education, Institute of Genomic Medicine, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Yun LiKey Laboratory of Laboratory Medicine, Ministry of Education, Institute of Genomic Medicine, Wenzhou Medical University, Wenzhou, Zhejiang, China.
Qingqing LinDepartment of Rheumatology and Immunology, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Ziji WuDepartment of Rheumatology and Immunology, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Hangfei YanDepartment of Rheumatology and Immunology, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Tingting YuDepartment of Rheumatology and Immunology, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Chiyin WangDepartment of Rheumatology and Immunology, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Xinlei RenDepartment of Cardiac Surgery, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Xiaobing WangDepartment of Rheumatology and Immunology, Changzheng Hospital, Naval Medical University, Shanghai, China.ORCID 0000-0002-4302-2213
Jinyu WuKey Laboratory of Laboratory Medicine, Ministry of Education, Institute of Genomic Medicine, Wenzhou Medical University, Wenzhou, Zhejiang, China.ORCID 0000-0001-5476-301X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Calcific aortic valve disease (CAVD) is a common disorder associated with substantial morbidity and mortality. Although the gut microbiome has complex associations with cardiovascular disease, its variation across the calcification spectrum in CAVD remains poorly defined. We profiled aortic-valve transcriptomes from 31 patients spanning graded calcification and paired these with matched stool microbiome profiles. We identified subtle yet widespread transcriptional changes in mild CAVD (m-CAVD), consistent with a progressive relationship between calcification burden and gene-expression remodeling. At the community level, the gut microbiome in m-CAVD exhibited an intermediate configuration between non- and higher-calcification profiles, suggesting an early shift in the gut ecosystem along the disease continuum. At the genus level, we identified 11 taxa associated with stage; notably, IMPORTANCE: Calcific aortic valve disease is a common valvular heart disease. Due to the difficulty in sampling arterial calcified tissues, research on the interaction between their gene expression and the gut has been limited. In this study, by analyzing the transcriptional profiles of calcified aortic valve tissues from patients with different levels of calcification and the characteristics of their corresponding gut microbiota, we identified consistent features between lesion gene expression and gut microbiota variation. This provides important evidence for the association between the gut microbiota and disease development stages, offering a new perspective for understanding disease progression and early intervention.

Indexed as

Aortic ValveAortic Valve StenosisBacteriaCalcinosisGastrointestinal MicrobiomeAgedFecesFemaleHumansMaleMiddle AgedTranscriptomeaortic valve calcificationfunctional analysisgut microbiotatranscriptional profiles

Identifiers

PMID41427705
PMCPMC12889152

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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.