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Role of Myocardial Fibrosis in Hypertrophic Cardiomyopathy: A Systematic Review and Updated Meta-Analysis of Risk
Marcelo Imbroinise Bittencourt1, Samária Ali Cader1, Denizar Vianna Araújo1
1Hospital Universitário Pedro Ernesto da Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ - Brazil.
Insights
Myocardial fibrosis is a key predictor of sudden death in hypertrophic cardiomyopathy (HCM). This meta-analysis confirms fibrosis and other risk markers (RMs) predict severe arrhythmic outcomes, highlighting the need for improved risk prediction models.
Area of Science:
- Cardiology
- Genetics
- Pathology
Background:
- Hypertrophic cardiomyopathy (HCM) is a significant cause of sudden death (SD).
- Myocardial fibrosis is increasingly recognized as a potential correlate of SD in HCM patients.
Purpose of the Study:
- To conduct a systematic review and meta-analysis of risk markers (RMs) for severe arrhythmic outcomes in HCM.
- To specifically emphasize the role of myocardial fibrosis as a predictor of SD in HCM.
Main Methods:
- Systematic review and meta-analysis of studies from MEDLINE, LILACS, and SciELO databases.
- Inclusion of studies addressing severe arrhythmic outcomes and specific RMs in HCM.
- Utilized relative risks (RRs) with random models, setting significance at p < 0.05.
Main Results:
- Twenty-one studies involving 14,901 patients were analyzed.
- Myocardial fibrosis emerged as the strongest RM for severe arrhythmic outcomes (RR, 3.43).
- Other significant RMs included family history of SD, severe ventricular hypertrophy, syncope, non-sustained ventricular tachycardia (NSVT), and abnormal blood pressure response to exercise (ABPRE). Left ventricular outflow tract obstruction (LVOTO) was not a significant predictor in this analysis.
Conclusions:
- Myocardial fibrosis and other identified RMs are confirmed predictors of severe arrhythmic outcomes in HCM.
- The findings underscore the necessity for developing novel prediction models for managing HCM patients at risk of sudden death.
Background:
Hypertrophic cardiomyopathy (HCM) is associated with sudden death (SD). Myocardial fibrosis is reportedly correlated with SD.
Objective:
We performed a systematic review with meta-analysis, updating the risk markers (RMs) in HCM emphasizing myocardial fibrosis.
Methods:
We reviewed HCM studies that addressed severe arrhythmic outcomes and the certain RMs: SD family history, severe ventricular hypertrophy, unexplained syncope, non-sustained ventricular tachycardia (NSVT) on 24-hour Holter monitoring, abnormal blood pressure response to exercise (ABPRE), myocardial fibrosis and left ventricular outflow tract obstruction (LVOTO) in the MEDLINE, LILACS, and SciELO databases. We used relative risks (RRs) as an effect measure and random models for the analysis. The level of significance was set at p < 0.05.
Results:
Twenty-one studies were selected (14,901 patients aged 45 ± 16 years; men, 62.8%). Myocardial fibrosis was the major RISK MARKER (RR, 3.43; 95% CI, 1.95-6.03). The other RMs, except for LVOTO, were also predictors: SD family history (RR, 1.75; 95% CI, 1.39-2.20), severe ventricular hypertrophy (RR, 1.86; 95% CI, 1.26-2.74), unexplained syncope (RR, 2.27; 95% CI, 1.69-3.07), NSVT (RR, 2.79; 95% CI, 2.29-3.41), and ABPRE (RR, 1.53; 95% CI, 1.12-2.08).
Conclusions:
We confirmed the association of myocardial fibrosis and other RMs with severe arrhythmic outcomes in HCM and emphasize the need for new prediction models in managing these patients.
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