Evidence map›Paper›PMID 40351396›Full record

ArticleJournal of geriatric cardiology : JGC2025

Association between blood pressure traits, hypertension, antihypertensive drugs and calcific aortic valve stenosis: a mendelian randomization study.

Wen-Hua Lei, Jia-Liang Zhang, Yan-Biao Liao, Yan Wang, Fei Xu, Yao-Yu Zhang, Yanjiani Xu, Jing Zhou, Fang-Yang Huang, Mao Chen

Abstract read
In one paragraph

Article in Journal of geriatric cardiology : JGC, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

10 authors.

Wen-Hua LeiDepartment of Cardiology, West China Hospital, Sichuan University, No.37 Guoxue Street, Chengdu 610041, China.
Jia-Liang ZhangDepartment of Cardiology, West China Hospital, Sichuan University, No.37 Guoxue Street, Chengdu 610041, China.
Yan-Biao LiaoDepartment of Cardiology, West China Hospital, Sichuan University, No.37 Guoxue Street, Chengdu 610041, China.
Yan WangDepartment of Cardiology, West China Hospital, Sichuan University, No.37 Guoxue Street, Chengdu 610041, China.
Fei XuDepartment of Cardiology, West China Hospital, Sichuan University, No.37 Guoxue Street, Chengdu 610041, China.
Yao-Yu ZhangDepartment of Cardiology, West China Hospital, Sichuan University, No.37 Guoxue Street, Chengdu 610041, China.
Yanjiani XuDepartment of Cardiology, West China Hospital, Sichuan University, No.37 Guoxue Street, Chengdu 610041, China.
Jing ZhouDepartment of Cardiology, West China Hospital, Sichuan University, No.37 Guoxue Street, Chengdu 610041, China.
Fang-Yang HuangDepartment of Cardiology, West China Hospital, Sichuan University, No.37 Guoxue Street, Chengdu 610041, China.
Mao ChenDepartment of Cardiology, West China Hospital, Sichuan University, No.37 Guoxue Street, Chengdu 610041, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Hypertension is associated with an increased risk of calcific aortic valve stenosis (CAVS). However, the directionality of causation between blood pressure traits and aortic stenosis is unclear, as is the benefit of antihypertensive drugs for CAVS. Methods: Using genome-wide association studies (GWAS) summary statistics, we performed bidirectional two-sample univariable mendelian randomization (UVMR) to assess the causal associations of systolic blood pressure (SBP), diastolic blood pressure (DBP), and pulse pressure (PP) with CAVS. Multivariable mendelian randomization (MVMR) was conducted to evaluate the direct effect of hypertension on CAVS, adjusting for confounders. Drug target mendelian randomization (MR) and summary-level MR (SMR) were used to estimate the effects of 12 classes of antihypertensive drugs and their target genes on CAVS risk. Inverse variance weighting was the primary MR method, with sensitivity analyses to validate results. Results: UVMR showed SBP, DBP, and PP have causal effects on CAVS, with no significant reverse causality. MVMR confirmed the causality between hypertension and CAVS after adjusting for confounders. Drug-target MR analyses indicated that calcium channel blockers (CCBs), loop diuretics, and thiazide diuretics via SBP lowering exerted protective effects on CAVS risk. SMR analysis showed that the CCBs target gene Conclusions: Hypertension has a causal relationship with CAVS. Managing SBP in hypertensive patients with CCBs may prevent CAVS. ARBs might exert protective effects on CAVS independent of blood pressure reduction. The relationship between diuretics and CAVS is complex, with opposite effects through different mechanisms.

Identifiers

PMID40351396
PMCPMC12059563

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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.