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Published on: August 8, 2022
Sex-Related Differences in Protein Expression in Sarcomere Mutation-Positive Hypertrophic Cardiomyopathy
Maike Schuldt1, Larissa M Dorsch1, Jaco C Knol2
1Amsterdam UMC, Department of Physiology, Amsterdam Cardiovascular Sciences, Vrije Universiteit Amsterdam, Amsterdam, Netherlands.
Insights
Proteomics reveal key cellular differences in hypertrophic cardiomyopathy (HCM) between sexes. Increased tubulin in women may explain severe diastolic dysfunction, while heat shock proteins may offer protection.
Area of Science:
- Cardiology
- Proteomics
- Molecular Biology
Background:
- Sex-differences in hypertrophic cardiomyopathy (HCM) presentation are known, with women experiencing more severe diastolic dysfunction.
- Cellular mechanisms driving these sex-differences in HCM remain largely unexplored.
Purpose of the Study:
- To investigate sex-differences at the protein level in cardiac tissue from hypertrophic cardiomyopathy (HCM) patients.
- To identify potential cellular mechanisms underlying the distinct clinical presentations of HCM in men and women.
Main Methods:
- Proteomic analysis of cardiac tissue from age-matched male and female HCM patients (n=13 each) undergoing myectomy.
- Comparison of HCM samples with non-failing controls (n=8).
- Validation of key protein changes using Western blot analysis.
Main Results:
- Only 46 differentially expressed proteins were found between male and female HCM samples.
- Female HCM patients showed increased levels of tubulin and heat shock proteins.
- Male HCM patients exhibited lower levels of translational proteins, and both sexes showed altered carbohydrate metabolism proteins compared to controls.
Conclusions:
- Elevated tubulin in women may contribute to more severe diastolic dysfunction in female hypertrophic cardiomyopathy (HCM) patients.
- Increased heat shock proteins in women might confer cardioprotection, potentially delaying disease onset.
- Reduced protein turnover in men could lead to damaged protein accumulation, impacting cellular function.
Abstract:
Background: Sex-differences in clinical presentation contribute to the phenotypic heterogeneity of hypertrophic cardiomyopathy (HCM) patients. While disease prevalence is higher in men, women present with more severe diastolic dysfunction and worse survival. Until today, little is known about the cellular differences underlying sex-differences in clinical presentation. Methods: To define sex-differences at the protein level, we performed a proteomic analysis in cardiac tissue obtained during myectomy surgery to relieve left ventricular outflow tract obstruction of age-matched female and male HCM patients harboring a sarcomere mutation (n = 13 in both groups). Furthermore, these samples were compared to 8 non-failing controls. Women presented with more severe diastolic dysfunction. Results: Out of 2099 quantified proteins, direct comparison of male, and female HCM samples revealed only 46 significantly differentially expressed proteins. Increased levels of tubulin and heat shock proteins were observed in female compared to male HCM patients. Western blot analyses confirmed higher levels of tubulin in female HCM samples. In addition, proteins involved in carbohydrate metabolism were significantly lower in female compared to male samples. Furthermore, we found lower levels of translational proteins specifically in male HCM samples. The disease-specificity of these changes were confirmed by a second analysis in which we compared female and male samples separately to non-failing control samples. Transcription factor analysis showed that sex hormone-dependent transcription factors may contribute to differential protein expression, but do not explain the majority of protein changes observed between male and female HCM samples. Conclusion: In conclusion, based on our proteomics analyses we propose that increased levels of tubulin partly underlie more severe diastolic dysfunction in women compared to men. Since heat shock proteins have cardioprotective effects, elevated levels of heat shock proteins in females may contribute to later disease onset in woman, while reduced protein turnover in men may lead to the accumulation of damaged proteins which in turn affects proper cellular function.
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