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Published on: August 8, 2022
Gender-related differences in the clinical presentation and outcome of hypertrophic cardiomyopathy
Iacopo Olivotto1, Martin S Maron, A Selcuk Adabag
1Regional Referral Center for Myocardial Diseases, Azienda Ospedaliera Universitaria Careggi, Florence, Italy. olivottoi@ao-careggi.toscana.it
Insights
Women with hypertrophic cardiomyopathy (HCM) are diagnosed later, more symptomatic, and face a higher risk of advanced heart failure. Early detection in women is crucial for timely treatment and improved outcomes.
Area of Science:
- Cardiology
- Genetics
- Endocrinology
Background:
- The impact of gender on hypertrophic cardiomyopathy (HCM) clinical presentation and progression is not well understood.
- HCM is a complex condition with varied clinical trajectories.
Purpose of the Study:
- To investigate gender-specific differences in a multicenter cohort of patients with hypertrophic cardiomyopathy (HCM).
Main Methods:
- A study involving 969 consecutive patients diagnosed with HCM across Italy and the U.S.
- Patient data were collected and followed for an average of 6.2 years.
Main Results:
- Female patients were older at diagnosis, more symptomatic (NYHA class), and more likely to have left ventricular outflow obstruction.
- Women were less frequently diagnosed incidentally, with female gender independently associated with a higher risk of symptom progression to advanced heart failure.
- Mortality rates and sudden cardiac death risk were comparable between genders.
Conclusions:
- Women with HCM present differently, often with more severe symptoms and outflow obstruction, and have an increased risk of disease progression.
- These disparities may stem from social, endocrine, or genetic factors, highlighting the need for increased clinical suspicion in women.
- Prompt diagnosis and intervention, including obstruction relief, are vital for managing HCM in women and preventing adverse events like sudden death or stroke.
Objectives:
The goal of this study was to assess gender-related differences in a multicenter population with hypertrophic cardiomyopathy (HCM).
Background:
Little is known regarding the impact of gender on the heterogeneous clinical profile and clinical course of HCM.
Methods:
We studied 969 consecutive HCM patients from Italy and the U.S. followed over 6.2 +/- 6.1 years.
Results:
Male patients had a 3:2 predominance (59%), similar in Italy and the U.S. (p = 0.24). At initial evaluation, female patients were older and more symptomatic than male patients (47 +/- 23 years vs. 38 +/- 18 years; p < 0.001; mean New York Heart Association [NYHA] functional class 1.8 +/- 0.8 vs. 1.4 +/- 0.6; p < 0.001), and more frequently showed left ventricular outflow obstruction (37% vs. 23%; p < 0.001). Moreover, female patients were less often diagnosed fortuitously by routine medical examination (23% vs. 41% in male patients, p < 0.001). Female gender was independently associated with the risk of symptom progression to NYHA functional classes III/IV or death from heart failure or stroke compared with male gender (independent relative hazard 1.5; p < 0.001), particularly patients > or =50 years of age and with resting outflow obstruction (p < 0.005). Hypertrophic cardiomyopathy-related mortality and risk of sudden death were similar in men and women.
Conclusions:
Women with HCM were under-represented, older, and more symptomatic than men, and showed higher risk of progression to advanced heart failure or death, often associated with outflow obstruction. These gender-specific differences suggest that social, endocrine, or genetic factors may affect the diagnosis and clinical course of HCM. A heightened suspicion for HCM in women may allow for timely implementation of treatment strategies, including relief of obstruction and prevention of sudden death or stroke.
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