Related Experiment Video
Updated: Mar 27, 2026

An Approach to Study Shape-Dependent Transcriptomics at a Single Cell Level
Published on: November 2, 2020
Evolution and Transformation of Hypertrophic Cardiomyopathy From a High Risk to a Treatable Low Mortality Disease
Barry J Maron1, Steven R Ommen2, Rick A Nishimura2
1HCM Center, Lahey Hospital and Medical Center Burlington MA USA.
Insights
Hypertrophic cardiomyopathy (HCM) treatment has dramatically improved, with mortality rates now comparable to the general population. Advances in personalized therapies offer patients a better prognosis and increased longevity.
Area of Science:
- Cardiology
- Genetics
- Internal Medicine
Background:
- Hypertrophic cardiomyopathy (HCM) was historically considered rare, untreatable, and associated with a poor prognosis.
- Significant advancements over six decades have transformed HCM into a manageable global condition.
Purpose of the Study:
- To review the evolution of hypertrophic cardiomyopathy (HCM) management.
- To highlight contemporary treatment strategies and their impact on patient outcomes and longevity.
Main Methods:
- Review of clinical inflection points and breakthroughs in HCM research.
- Analysis of data from dedicated HCM programs and observational studies.
- Evaluation of pharmacologic and interventional treatment options.
Main Results:
- HCM-related mortality has decreased to ≤0.5%/year in optimally treated patients.
- Implantable defibrillators, surgical myectomy, and anticoagulation have improved survival and reduced complications.
- Novel pharmacologic agents, such as cardiac myosin inhibitors, are emerging as effective treatments.
Conclusions:
- Modern management strategies have significantly improved the prognosis for hypertrophic cardiomyopathy (HCM) patients.
- Personalized treatment approaches offer the potential for normal longevity, a stark contrast to previous outcomes.
- Continued patient-centered research is crucial for optimizing care across the HCM clinical spectrum.
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.
More Related Videos
Related Concept Videos
Cardiomyopathy V: Interprofessional Care
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Cardiomyopathy II: Dilated Cardiomyopathy
Heart Failure V: Medical Management
Cardiomyopathy I: Introduction and Classification
Heart Failure IV: Classification and Diagnostic Evaluation

