Evidence map›Paper›PMID 41583618›Full record

ReviewArchives of medical sciences. Atherosclerotic diseases2025

Efficacy and safety of myosin inhibitors for symptomatic hypertrophic cardiomyopathy: systematic review and meta-analysis.

Mohammad Hazique, Sameer Lohana, Sunam Kafle, Jasgit Bhinder, Kunal N Patel, Jawad Basit, Abdul Rasheed Bahar, Jared Kvapil, M Chadi Alraies

Abstract readReview
In one paragraph

Review in Archives of medical sciences. Atherosclerotic diseases, 2025. 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

9 authors.

Mohammad HaziqueNuvance Health/Vassar Brothers Medical Center, Poughkeepsie, NY, USA.
Sameer LohanaNuvance Health/Vassar Brothers Medical Center, Poughkeepsie, NY, USA.
Sunam KafleNuvance Health/Vassar Brothers Medical Center, Poughkeepsie, NY, USA.
Jasgit BhinderNuvance Health/Vassar Brothers Medical Center, Poughkeepsie, NY, USA.
Kunal N PatelDepartment of Cardiology, University of Kansas Medical Center, Kansas City, USA.
Jawad BasitDepartment of Medicine, Rawalpindi Medical University, Rawalpindi, Pakistan.
Abdul Rasheed BaharDepartment of Internal Medicine, Detroit Medical Center/Wayne State University, Detroit, MI, USA.
Jared KvapilDepartment of Cardiology, University of Kansas Medical Center, Kansas City, USA.
M Chadi AlraiesDepartment of Cardiology, Wayne State University, MI, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Hypertrophic cardiomyopathy (HCM) is a common genetic cardiac disorder associated with significant morbidity and mortality. Cardiac myosin inhibitors (MIs), including mavacamten and aficamten, offer a novel therapeutic approach for HCM. Methods: An online database search was performed from inception to September 2024. We selected randomized controlled trials (RCTs) that compared mavacamten with placebo/guideline medical treatment for HCM. Results: Six RCTs involving 1,081 participants were analyzed. Cardiac myosin inhibitors significantly reduced left ventricular outflow tract (LVOT) gradients at rest (-70.22 mm Hg, 95% CI: -85.42 to -55.03) and during the Valsalva maneuver (-61.44 mm Hg, 95% CI: -71.10 to -51.78). Patients experienced improved functional status, with a pooled risk ratio (RR) of 2.21 (95% CI: 1.75 to 2.80, Conclusions: MIs significantly improve symptomatic, functional, and biomarker outcomes in symptomatic HCM while maintaining an acceptable safety profile, highlighting their potential as a transformative treatment option. Further studies are warranted to evaluate long-term efficacy and safety.

Indexed as

aficamtenhypertrophic cardiomyopathyleft ventricular outflow tract gradientmavacamtenmeta-analysismyosin inhibitorsNT-proBNPNYHA classsystematic review

Identifiers

PMID41583618
PMCPMC12828646

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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.