Evidence map›Paper›PMID 42872427›Full record

ReviewBMJ medicine2026

Pathogenesis, screening, and diagnosis of hypertrophic cardiomyopathy.

Kendra M Gilreath, Darrell B Newman, Steve R Ommen, Jeffrey B Geske

Abstract readReview
In one paragraph

Review in BMJ medicine, 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

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

4 authors.

Kendra M GilreathMayo Clinic Alix School of Medicine, Mayo Clinic, Rochester, MN, USA.
Darrell B NewmanDepartment of Cardiovascular Disease, Mayo Clinic, Rochester, MN, USA.
Steve R OmmenDepartment of Cardiovascular Disease, Mayo Clinic, Rochester, MN, USA.
Jeffrey B GeskeDepartment of Cardiovascular Disease, Mayo Clinic, Rochester, MN, USA Geske.Jeffrey@mayo.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypertrophic cardiomyopathy is a common heritable heart disease. The disease is genetically, anatomically, and clinically heterogeneous. Hypertrophic cardiomyopathy is inherited in an autosomal dominant pattern but has allelic heterogeneity, incomplete penetrance, and variable expressivity. Beyond family screening, clinical evaluation for hypertrophic cardiomyopathy is often prompted by identification of symptoms or detection of a heart murmur, additionally, abnormal electrocardiogram or imaging results performed for another reason can provide evidence. Evaluation should include obtaining a patient's history, a physical examination, cardiac imaging, and, often, genetic testing. Prognosis is variable; major causes of morbidity and mortality are caused by sudden cardiac death, heart failure, and atrial fibrillation with associated stroke risk. An understanding of the pathogenesis at the genetic, cellular, and individual levels helps clinicians to implement appropriate screening, recognise clinical manifestations, and improve the treatment of patients with hypertrophic cardiomyopathy. The understanding of this condition is evolving, with recent advances and insights into its pathogenesis, refinement of risk stratification, and use of artificial intelligence in screening, diagnosis, and prognostication.

Indexed as

Cardiomyopathy, HypertrophicDeath, Sudden, CardiacElectrocardiographyGenetic TestingHumansPrognosisCardiologyCardiomyopathiesPathology

Identifiers

PMID42872427
PMCPMC13663709

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.