Comparison of Long-Term Outcome between Apical and Asymmetric Septal Hypertrophic Cardiomyopathy
Shuoyan An1, Chaomei Fan, Lirong Yan
1Key Laboratory of Clinical Trial Research in Cardiovascular Drugs, Ministry of Health, Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Insights
Asymmetric septal hypertrophic cardiomyopathy (ASHCM) carries a worse prognosis than apical hypertrophic cardiomyopathy (ApHCM), with higher cardiovascular mortality and morbidity. Late gadolinium enhancement (LGE) is a key predictor of cardiovascular death in these patients.
Area of Science:
- Cardiology
- Cardiovascular Disease Research
- Hypertrophic Cardiomyopathy
Background:
- Prognosis in hypertrophic cardiomyopathy (HCM) is influenced by age, gender, and outflow tract obstruction.
- Apical hypertrophic cardiomyopathy (ApHCM) and asymmetric septal hypertrophic cardiomyopathy (ASHCM) are distinct HCM phenotypes.
- Comparative long-term outcome data between ApHCM and ASHCM, adjusted for key prognostic factors, are limited.
Purpose of the Study:
- To compare the long-term prognosis of ApHCM versus ASHCM.
- To evaluate outcomes after controlling for diagnostic age, gender, and outflow tract obstruction.
- To identify independent predictors of cardiovascular mortality in HCM patients.
Main Methods:
- Retrospective analysis of 540 patients (270 ApHCM, 270 ASHCM) from a single-center cohort.
- Matching of ApHCM and ASHCM groups by age, gender, and outflow tract obstruction.
- Comparison of clinical characteristics and long-term cardiovascular outcomes.
Main Results:
- ASHCM patients experienced significantly higher cardiovascular mortality (6.3% vs. 0.7%) and morbidity (39.9% vs. 18.5%) compared to ApHCM patients.
- Mean follow-up was 6.6 years for ASHCM and 7.6 years for ApHCM.
- Late gadolinium enhancement (LGE) and unexplained syncope were independent predictors of cardiovascular mortality.
Conclusions:
- ASHCM is associated with a worse long-term prognosis than ApHCM, independent of age, gender, and outflow tract obstruction.
- LGE is a significant predictor of cardiovascular death in HCM.
- Unexplained syncope independently predicts increased risk for sudden cardiac death.
Objectives:
As reported, diagnostic age, gender and presence of outflow tract obstruction have an impact on prognosis in patients with hypertrophic cardiomyopathy. The aim of this study was to compare the long-term outcome between apical hypertrophic cardiomyopathy (ApHCM) and asymmetric septal hypertrophic cardiomyopathy (ASHCM) after the exclusion of these factors.
Methods:
A total of 540 patients (270 with ApHCM and 270 with ASHCM) identified in a consecutive single-center cohort were retrospectively studied. The two groups were matched by diagnostic age, gender and the presence of outflow tract obstruction. Clinical characteristics and long-term outcomes were compared.
Results:
The mean follow-up duration in ASHCM and ApHCM were 6.6 ± 5.5 and 7.6 ± 4.1 years, respectively. During follow-up, 16 patients experienced cardiovascular death in the ASHCM group, while 2 patients experienced cardiovascular death in the ApHCM group (6.3 vs. 0.7%, p < 0.01). Cardiovascular morbidity in the ASHCM and ApHCM groups were 39.9 and 18.5% (p < 0.01). In the multivariate Cox regression analysis late gadolinium enhancement (LGE; HR 4.81, 95% CI 1.28-78.0, p = 0.03) and unexplained syncope (HR 9.68, 95% CI 1.9-17.2, p < 0.01) were independent predictors for cardiovascular mortality. Unexplained syncope was independently associated with a higher risk for sudden cardiac death (HR 4.3, 95% CI 1.2-15.3, p = 0.02).
Conclusions:
After eliminating the interference of diagnostic age, gender and outflow tract obstruction, ASHCM represented a worse prognosis with a higher incidence of cardiovascular mortality and morbidity than ApHCM. LGE was a strong predictor for cardiovascular death.
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