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Sex-based differences in cardiac ischaemic injury and protection: therapeutic implications
1Institute of Physiology, Academy of Sciences of the Czech Republic, Prague, Czech Republic.
Insights
Ischaemic heart disease (IHD) risk differs between sexes, with women experiencing increased incidence post-menopause. Understanding these sex-specific differences is crucial for developing targeted therapies to improve outcomes for women with IHD.
Area of Science:
- Cardiovascular Science
- Endocrinology
- Sex Differences in Medicine
Background:
- Ischaemic heart disease (IHD) is a leading cause of mortality globally.
- Premenopausal women exhibit lower IHD risk than men, with incidence rising post-menopause, suggesting hormonal influence.
- Female sex is associated with improved cardiac remodeling following ischaemia/reperfusion injury.
Purpose of the Study:
- To explore the complex sex-related differences in cardiac tolerance to ischaemia.
- To investigate the role of sex hormones, particularly oestrogens, in these differences.
- To highlight the need for female-specific therapeutic strategies in IHD management.
Main Methods:
- Review of epidemiological studies on IHD incidence and sex differences.
- Analysis of experimental data on sex-specific cardiac responses to ischaemia/reperfusion.
- Examination of clinical trial outcomes regarding oestrogen replacement therapy.
Main Results:
- Oestrogen levels significantly influence IHD risk, with declining levels post-menopause correlating with increased incidence.
- While oestrogen may offer protection, clinical trials indicate potential harm with hormone replacement therapy in postmenopausal women.
- Sex-related disparities exist in the management and outcomes of acute coronary syndrome in women.
Conclusions:
- The mechanisms underlying sex differences in cardiac ischaemic tolerance are complex, involving both genomic and non-genomic effects of sex hormones.
- Current therapeutic strategies for IHD may not be optimal for women due to unaddressed sex-specific factors.
- Urgent research is needed to develop personalized, evidence-based treatments for women to reduce IHD mortality and improve quality of life.
Abstract:
Ischaemic heart disease (IHD) is the most frequent cause of mortality among men and women. Many epidemiological studies have demonstrated that premenopausal women have a reduced risk for IHD compared with their male counterparts. The incidence of IHD in women increases after menopause, suggesting that IHD is related to declining oestrogen levels. Experimental observations have confirmed the results of epidemiological studies investigating sex-specific differences in cardiac tolerance to ischaemia. Female sex appears also to favourably influence cardiac remodelling after ischaemia/reperfusion injury. Furthermore, sex-related differences in ischaemic tolerance of the adult myocardium can be influenced by interventions during the early phases of ontogenetic development. Detailed mechanisms of these sex-related differences remain unknown; however, they involve the genomic and non-genomic effects of sex steroid hormones, particularly the oestrogens, which have been the most extensively studied. Although the protective effects of oestrogen have many potential therapeutic implications, clinical trials have shown that oestrogen replacement in postmenopausal women may actually increase the incidence of IHD. The results of these trials have illustrated the complexity underlying the mechanisms involved in sex-related differences in cardiac tolerance to ischaemia. Sex-related differences in cardiac sensitivity to ischaemia/reperfusion injury may also influence therapeutic strategies in women with acute coronary syndrome. Women undergo coronary intervention less frequently and a lower proportion of women receive evidence-based therapy compared with men. Although our understanding of this important topic has increased in recent years, there is an urgent need for intensive experimental and clinical research to develop female-specific therapeutic strategies. Only then we will be able to offer patients better evidence-based treatment, a better quality of life and lower mortality.
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