Related Experiment Video
Updated: Feb 14, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Clinical Outcomes in Patients With Nonobstructive, Labile, and Obstructive Hypertrophic Cardiomyopathy
Dai-Yin Lu1,2,3, Iraklis Pozios1, Bereketeab Haileselassie1,4
1Johns Hopkins Hypertrophic Cardiomyopathy Center of Excellence, Baltimore, MD.
Insights
Hypertrophic cardiomyopathy (HCM) patients with obstructive or nonobstructive forms face higher risks of adverse cardiovascular events. Nonobstructive HCM shows increased arrhythmia risk, while labile HCM has a benign course, guiding risk stratification and management.
Area of Science:
- Cardiology
- Genetics
- Internal Medicine
Background:
- Hypertrophic cardiomyopathy (HCM) is a prevalent inherited cardiac condition.
- HCM is characterized by variable left ventricular outflow tract obstruction.
- Understanding hemodynamic variations is crucial for patient outcomes.
Purpose of the Study:
- To compare cardiovascular outcomes across three hemodynamic groups in a large hypertrophic cardiomyopathy cohort.
- To identify specific risks associated with obstructive, nonobstructive, and labile HCM.
- To inform risk stratification and management strategies for different HCM phenotypes.
Main Methods:
- Prospective enrollment of 705 HCM patients from January 2005 to June 2015.
- Phenotypic characterization using echocardiography to assess left ventricular outflow tract pressure gradients.
- Composite cardiovascular end point including atrial fibrillation, ventricular arrhythmias, heart failure, and death, with a mean follow-up of 3.4 years.
Main Results:
- Obstructive HCM patients were older with higher BMI and NYHA class.
- Nonobstructive HCM patients had higher rates of sustained ventricular tachycardia/ventricular fibrillation and ICD implantation.
- Obstructive and nonobstructive HCM were significantly associated with more adverse events compared to labile HCM.
Conclusions:
- Nonobstructive HCM is linked to significant morbidity and higher arrhythmic risk.
- Labile HCM demonstrates a relatively benign clinical course.
- Tailored risk stratification for nonobstructive HCM and less aggressive management for labile HCM are suggested.
Background:
Hypertrophic cardiomyopathy (HCM) is a common inherited cardiac disease characterized by varying degrees of left ventricular outflow tract obstruction. In a large cohort, we compare the outcomes among 3 different hemodynamic groups.
Methods And Results:
We prospectively enrolled patients fulfilling standard diagnostic criteria for HCM from January 2005 to June 2015. Detailed phenotypic characterization, including peak left ventricular outflow tract pressure gradients at rest and after provocation, was measured by echocardiography. The primary outcome was a composite cardiovascular end point, which included new-onset atrial fibrillation, new sustained ventricular tachycardia/ventricular fibrillation, new or worsening heart failure, and death. The mean follow-up was 3.4±2.8 years. Among the 705 patients with HCM (mean age, 52±15 years; 62% men), 230 with obstructive HCM were older and had a higher body mass index and New York Heart Association class. The 214 patients with nonobstructive HCM were more likely to have a history of sustained ventricular tachycardia/ventricular fibrillation and implantable cardioverter defibrillator implantation. During follow-up, 121 patients experienced a composite cardiovascular end point. Atrial fibrillation occurred most frequently in the obstructive group. Patients with nonobstructive HCM had more frequent sustained ventricular tachycardia/ventricular fibrillation events. In multivariate analysis, obstructive (hazard ratio, 2.80; 95% confidence interval, 1.64-4.80) and nonobstructive (hazard ratio, 1.94; 95% confidence interval, 1.09-3.45) HCM were associated with more adverse events compared with labile HCM.
Conclusions:
Nonobstructive HCM carries notable morbidity, including a higher arrhythmic risk than the other HCM groups. Patients with labile HCM have a relatively benign clinical course. Our data suggest detailed sudden cardiac death risk stratification in nonobstructive HCM and monitoring with less aggressive management in labile HCM.
More Related Videos
09:16Isolation and Characterization of Cardiac Mesenchymal Stromal Cells from Endomyocardial Bioptic Samples of Arrhythmogenic Cardiomyopathy Patients
Published on: February 28, 2018
05:34A Mouse Model to Evaluate the Long-Term Structural and Functional Outcomes after the Reversal of Prolonged Unilateral Ureteric Obstruction
Published on: July 18, 2025
Related Concept Videos
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Cardiomyopathy II: Dilated Cardiomyopathy
Cardiomyopathy IV: Restrictive Cardiomyopathy
Cardiomyopathy V: Interprofessional Care
Cardiomyopathy I: Introduction and Classification
Cardiomyopathy VI: Nursing Management