Evidence map›Paper›PMID 42050441›Full record

ArticleBMC cardiovascular disorders2026

End-stage valvular heart disease requiring heart transplantation: risk profile, surgical modifiers, and myocardial pathology.

Yifan Wang, Yiqi Zhao, Weiteng Wang, Hao Jia, Xiao Chen, Han Mo, Zhe Sun, Xiaohu Wang, Songren Shu, Hongjie Shi and 4 more

Abstract read
In one paragraph

Article 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.

0numbers the graph read from it
0cells of the map it votes in
0citing papers 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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3 · Its place in the literature

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0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

14 authors.

Yifan Wang *Beijing Key Laboratory of Xenotransplantation, Fuwai Hospital, National Centre for Cardiovascular Disease, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100037, China.
Yiqi Zhao *Beijing Key Laboratory of Xenotransplantation, Fuwai Hospital, National Centre for Cardiovascular Disease, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100037, China.
Weiteng Wang *Department of Cardiac Surgery, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing, 100037, China.
Hao JiaBeijing Key Laboratory of Xenotransplantation, Fuwai Hospital, National Centre for Cardiovascular Disease, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100037, China.
Xiao ChenBeijing Key Laboratory of Xenotransplantation, Fuwai Hospital, National Centre for Cardiovascular Disease, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100037, China.
Han MoShenzhen Key Laboratory of Cardiovascular Disease, Fuwai Hospital, Chinese Academy of Medical Sciences, Shenzhen, 518000, China.
Zhe SunShenzhen Key Laboratory of Cardiovascular Disease, Fuwai Hospital, Chinese Academy of Medical Sciences, Shenzhen, 518000, China.
Xiaohu WangBeijing Key Laboratory of Xenotransplantation, Fuwai Hospital, National Centre for Cardiovascular Disease, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100037, China.
Songren ShuBeijing Key Laboratory of Xenotransplantation, Fuwai Hospital, National Centre for Cardiovascular Disease, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100037, China.
Hongjie ShiDepartment of Cardiovascular Surgery, Zhongnan Hospital of Wuhan University, 169 Donghu Road, Wuhan, 430071, China.
Zhiling LuoDepartment of Cardiac Surgery, Fuwai Yunnan Hospital, Chinese Academy of Medical Sciences, Affiliated Cardiovascular Hospital of Kunming Medical University, Kunming, China.
Xiumeng HuaBeijing Key Laboratory of Xenotransplantation, Fuwai Hospital, National Centre for Cardiovascular Disease, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100037, China.
Hao CuiBeijing Key Laboratory of Xenotransplantation, Fuwai Hospital, National Centre for Cardiovascular Disease, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100037, China.
Jiangping SongBeijing Key Laboratory of Xenotransplantation, Fuwai Hospital, National Centre for Cardiovascular Disease, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100037, China. fwsongjiangping@126.com.

Funding

Beijing Natural Science Foundation Z240015Fuwai Yunnan Hospital Strategic Project No.2025YFKT-ZL-04National Natural Science Foundation of Basic Research Program for Young Students 823B2007National Natural Science Fund for Distinguished Young Scholars of China 82125004Research Project of Fuwai Yunnan Hospital, Chinese Academy of Medical Sciences 2025YFKT-PT-01Shenzhen Medical Research Special Fund B2502042Shenzhen Science and Technology Innovation Commission JCYJ20220818103414030
6 · The paper itself

Abstract

backgroundEnd-stage valvular heart disease (VHD) constitutes a small but high-risk subset of heart transplant (HTx) recipients, and data describing their natural history and determinants of progression to HTx are limited. We aimed to characterize the clinical, genetic, surgical, and pathological substrates of patients undergoing HTx for end-stage VHD and to assess whether timely cardiac valvular surgery (CVS) mitigates progression to end-stage heart failure.

methodsWe retrospectively screened 961 consecutive recipients who underwent HTx for end-stage heart failure between January 2012 and December 2023. Patients with non-ischemic end-stage VHD due to a primary aortic valve lesion were identified by echocardiography and further adjudicated using cardiac magnetic resonance and explant pathology. After excluding ischemic and non-valvular cardiomyopathies and other predefined conditions, 45 patients constituted the final cohort.

resultsOf the 45 recipients, 78% had undergone prior CVS. CVS performed before heart failure or malignant ventricular arrhythmia was associated with a longer interval from symptom onset to HTx. In contrast, genetic variants were associated with earlier disease onset but did not significantly shorten the progression interval to HTx. Among 27 patients with prosthetic valves, 22 (77%) had structurally and hemodynamically preserved prostheses at the time of HTx, indicating that terminal HF predominantly reflected advanced myocardial disease rather than prosthetic failure. Explanted hearts consistently demonstrated extensive replacement fibrosis, and patients with malignant ventricular arrhythmias exhibited more prominent adipose replacement.

conclusionsAmong patients transplanted for end-stage VHD, valve intervention performed prior to major clinical decompensation was associated with longer time intervals to HTx within this transplanted cohort. Most prosthetic valves showed preserved function at the time of HTx, supporting the concept that terminal heart failure in this setting often reflects advanced myocardial remodeling rather than prosthetic valve failure.

Indexed as

Heart FailureHeart TransplantationHeart Valve DiseasesHeart Valve Prosthesis ImplantationMyocardiumAdultAgedDisease ProgressionFemaleGenetic Predisposition to DiseaseHumansMaleMiddle AgedRetrospective StudiesRisk AssessmentRisk FactorsClinical phenotypesGenetic mutationsHeart transplantationValvular heart diseaseValvular surgery

Identifiers

PMID42050441
PMCPMC13267388

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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.