Evidence map›Paper›PMID 41878858›Full record

ReviewJournal of the American Heart Association2026

Evolution and Transformation of Hypertrophic Cardiomyopathy From a High Risk to a Treatable Low Mortality Disease With Contemporary Clinical Research Strategies.

Barry J Maron, Steven R Ommen, Rick A Nishimura, William J McKenna, Harry Rakowski, Mark V Sherrid, Iacopo Olivotto, Eugene Braunwald, Martin S Maron

Abstract readReview
In one paragraph

Review in Journal of the American Heart Association, 2026. 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

9 authors.

Barry J MaronHCM Center, Lahey Hospital and Medical Center Burlington MA USA.ORCID 0000-0002-1710-8670
Steven R OmmenMayo Clinic, Cardiovascular Medicine Rochester MN USA.ORCID 0000-0002-9410-0920
Rick A NishimuraMayo Clinic, Cardiovascular Medicine Rochester MN USA.ORCID 0000-0003-4651-9740
William J McKennaInstitute of Cardiovascular Science University College London UK.ORCID 0000-0001-7994-2460
Harry RakowskiDivision of Cardiology, Peter Munk Cardiac Centre Toronto General Hospital Toronto Ontario Canada.ORCID 0000-0001-5494-366X
Mark V SherridLangone Hypertrophic Cardiomyopathy Program, Leon Charney Division of Cardiology NYU Langone Health New York NY USA.ORCID 0000-0003-4972-7780
Iacopo OlivottoCardiovascular Medicine University of Florence Florence Italy.ORCID 0000-0003-1751-9266
Eugene BraunwaldDivision of Cardiovascular Medicine Brigham and Women's Hospital and Department of Medicine Harvard Medical School Boston MA USA.
Martin S MaronHCM Center, Lahey Hospital and Medical Center Burlington MA USA.ORCID 0000-0002-9923-3853

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Once considered rare and essentially untreatable with a grim prognosis and reduced life expectancy, hypertrophic cardiomyopathy (HCM) has evolved substantially over 6 decades. Ultimately, HCM has become a contemporary global disease with pharmacologic and interventional options offering effective personalized treatment for all adverse disease pathways. Striking reduction in HCM-related mortality to ≤0.5%/year in optimally treated cohorts is now comparable to that expected in the US general population, lower than most other disease risks to living, and 10-fold less than the earliest estimates. The few deaths directly related to HCM are now largely attributable to advanced (end-stage) heart failure in patients with nonobstructive HCM. Determinants of this transformation to a lower risk disease are evident in hallmark clinical inflection points and breakthroughs, including dedicated HCM programs assembling large clinical databases in which focused (and unfunded) physician-investigators have derived data directly from patients in clinical practice. Evidence-based observational studies report emergence of contemporary treatment strategies enhancing survival: implantable defibrillators prevent arrhythmic sudden death globally with 95% sensitive patient selection using an American Heart Association/American College Cardiology risk stratification algorithm; low-risk, high-benefit surgical myectomy reverses outflow obstruction and heart failure in >90% with a long-term survival benefit; and aggressive anticoagulation has reduced embolic strokes. Recent novel pharmacologic alternatives (cardiac myosin inhibitors) are proving effective in relieving obstruction/symptom burden and changing disease management. These principles and time-tested patient-centered research strategies uniquely tailored to the heterogeneous HCM clinical spectrum are pivotal in providing practice insights, offering a vulnerable population more optimistic prognosis including opportunity to achieve normal longevity not available to prior generations of patients.

Indexed as

Cardiomyopathy, HypertrophicDeath, Sudden, CardiacDefibrillators, ImplantableHeart FailureHumansPrognosisRisk AssessmentRisk FactorsTreatment Outcomeatrial fibrillationdefibrillatorsheart failuremortalitymyectomysudden death

Identifiers

PMID41878858
PMCPMC13323182

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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.