Evidence map›Paper›PMID 41877018›Full record

SynthesisBMC cardiovascular disorders2026

Mavacamten and atrial fibrillation: assessing the risk through FAERS and meta-analysis.

Lingqing Ding, Xinhang Liao, Yongkuan Yang, Congqin Chen, Jie Xiao

Abstract readMeta-AnalysisObservational Study
In one paragraph

Synthesis 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.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Lingqing Ding *Department of Pharmacy, Xiamen Cardiovascular Hospital of Xiamen University, School of Medicine, Fujian Branch of National Clinical Research Center for Cardiovascular Diseases, Xiamen, China.
Xinhang Liao *Department of Pharmacy, Xiamen Chang Gung Hospital Hua Qiao University, Xiamen, Fujian, China.
Yongkuan Yang *School of Electrical Engineering and Automation, Xiamen University of Technology, Xiamen, China.
Congqin ChenDepartment of Pharmacy, Xiamen Cardiovascular Hospital of Xiamen University, School of Medicine, Fujian Branch of National Clinical Research Center for Cardiovascular Diseases, Xiamen, China.
Jie XiaoDepartment of Pharmacy, Xiamen Cardiovascular Hospital of Xiamen University, School of Medicine, Fujian Branch of National Clinical Research Center for Cardiovascular Diseases, Xiamen, China. xmheart@126.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMavacamten is a novel selective cardiac myosin inhibitor indicated for patients with obstructive hypertrophic cardiomyopathy (oHCM). Given its negative inotropic properties, which theoretically reduce myocardial contractility and affect left atrial systolic function, concerns have arisen about its potential association with an increased incidence of atrial fibrillation (AF). The study aims to assess this potential association.

methodsWe employed a dual approach combining real-world data analysis and evidence synthesis. First, disproportionality and time-to-onset analyses were performed using the FDA Adverse Event Reporting System (FAERS) across two models: the general population (Model 1) and an HCM-specific cohort (Model 2). Independent risk factors for AF were identified using logistic regression. Second, a meta-analysis of placebo-controlled trials was conducted to evaluate the safety profile of mavacamten, with pooled risk ratios (RRs) and 95% confidence intervals (CIs) .

resultsIn the disproportionality analysis, Model 1 revealed a signal for AF with mavacamten (adjusted ROR 18.54, 95% CI 11.53–29.80, P < 0.05; EB05 11.55). In contrast, no significant disproportionality signal was observed in Model 2 (aROR 4.28, 95% CI 1.30–14.07, P = 0.017; EB05 0.74). The time-to-onset analysis indicated a random failure type for AF occurrence in mavacamten-treated patients. The meta-analysis included five RCTs and one retrospective cohort study. Compared with placebo, mavacamten was not associated with an increased risk of AF (RR = 0.92, 95% CI 0.80–1.06, P = 0.12).

conclusionOur findings did not identify a significant association between mavacamten and AF in patients with HCM. These results should be interpreted with caution due to the limited number of studies and small sample sizes.

Indexed as

Adverse Drug Reaction Reporting SystemsAtrial FibrillationCardiomyopathy, HypertrophicCardiovascular AgentsAdultAgedBenzylaminesCardiac MyosinsFemaleHumansIncidenceMaleMiddle AgedOdds RatioPharmacovigilanceRisk AssessmentBenzylaminesCardiac MyosinsCardiovascular AgentsMYK-461Uracilatrial fibrillationhypertrophic cardiomyopathymavacamtenmeta-analysispharmacovigilance study

Identifiers

PMID41877018
PMCPMC13134309

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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.