Related Experiment Video
Updated: Sep 12, 2025

Scanning Electron Microscopy of Macerated Tissue to Visualize the Extracellular Matrix
Published on: June 14, 2016
Systematic Review and Meta-Analysis Comparing Long-Term Outcomes in Apical Versus Nonapical Hypertrophic
Jonathan V Lee1, Mirela Emmanuela1, Andrew Patricio2
1Faculty of Medicine, Universitas Pelita Harapan, Tangerang, Indonesia.
Insights
Apical hypertrophic cardiomyopathy (ApHCM) patients generally have better outcomes than non-ApHCM patients, with lower risks of major adverse cardiovascular events and mortality. However, apical aneurysms are more common in ApHCM.
Area of Science:
- Cardiology
- Genetics
- Internal Medicine
Background:
- Hypertrophic Cardiomyopathy (HCM) is a leading inherited cause of Sudden Cardiac Death (SCD).
- Apical HCM (ApHCM) is a distinct phenotype, traditionally considered more benign.
- Emerging data suggest an increasing rate of adverse outcomes in ApHCM.
Purpose of the Study:
- To compare the long-term clinical outcomes of ApHCM versus non-ApHCM patients.
- To evaluate differences in adverse events, including mortality, arrhythmias, and heart failure.
Main Methods:
- Systematic review and meta-analysis of cohort studies comparing ApHCM and non-ApHCM.
- Data extracted from PubMed, ScienceDirect, and Cochrane Library.
- Outcomes assessed included major adverse cardiovascular events (MACE), mortality, SCD, VT, and heart failure endpoints.
Main Results:
- ApHCM patients had significantly lower risks of MACE (OR=0.48) and all-cause mortality (OR=0.44) compared to non-ApHCM.
- No significant difference was observed in the risk of SCD or sustained monomorphic VT.
- Apical aneurysms were more prevalent in the ApHCM group.
Conclusions:
- Apical HCM demonstrates a more favorable long-term prognosis compared to other HCM phenotypes.
- Phenotypic classification is crucial for accurate prognostication and personalized management of HCM patients.
- Further research may clarify the specific mechanisms driving outcomes in ApHCM.
Abstract:
Hypertrophic Cardiomyopathy (HCM) is the most common inherited cardiomyopathy that causes Sudden Cardiac Death (SCD). Apical HCM (ApHCM) tends to be more benign than other phenotypes of HCM. However, recent data showed the rate of adverse outcomes of ApHCM is increasing. We aim to compare the long-term outcome of ApHCM with non-ApHCM patients. We extracted data from PubMed, ScienceDirect and Cochrane Library using the keywords "apical hypertrophic cardiomyopathy", "nonapical hypertrophic cardiomyopathy", and "septal hypertrophic cardiomyopathy". Inclusion criteria include cohort studies comparing ApHCM with non-ApHCM. The endpoints were clinical, arrhythmia-related, and heart failure-related outcomes. Study quality assessed by Newcastle-Ottawa Scale (NOS). We present data as Odds Ratio (OR) for dichotomous and Mean Differences (MD) for continuous data. From 6 included cohort studies (8,179 patients), the risk of MACE was lower in ApHCM compared to the non-ApHCM group (OR = 0.48, 95% CI = 0.40-0.59, p <0.00001). The risk of all-cause mortality was also lower in the ApHCM group (OR = 0.44, 95% CI = 0.30-0.63, p <0.0001). We found no difference in the risk of SCD and sustained monomorphic VT. A similar result was also found in heart-failure endpoints. However, apical aneurysm is more common in ApHCM. All included studies were considered good quality by NOS. In conclusion, our study suggests a more benign clinical course of ApHCM compared to non-ApHCM patients. The phenotypic identification of each HCM patient is essential to stratify the prognosis and lead to better management strategies.
More Related Videos
12:45Benefits of Cardiac Resynchronization Therapy in an Asynchronous Heart Failure Model Induced by Left Bundle Branch Ablation and Rapid Pacing
Published on: December 11, 2017
14:35Post-Myocardial Infarction Heart Failure in Closed-chest Coronary Occlusion/Reperfusion Model in Göttingen Minipigs and Landrace Pigs
Published on: April 17, 2021
Related Concept Videos
Cardiomyopathy III: Hypertrophic Cardiomyopathy
Cardiomyopathy V: Interprofessional Care
Cardiomyopathy II: Dilated Cardiomyopathy
Cardiomyopathy I: Introduction and Classification
Cardiomyopathy IV: Restrictive Cardiomyopathy
Heart Failure II: Pathophysiology