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Coronary heart disease in women: why the disproportionate risk?
1The Conway Institute, University College Dublin, Belfield, Dublin 4, Ireland. helen.colhoun@ucd.ie
Insights
Diabetic women face higher coronary heart disease (CHD) risks than men. Unlike diabetic men, diabetic women do not benefit from a cardioprotective lipid profile, necessitating early risk factor intervention.
Area of Science:
- Cardiovascular disease
- Endocrinology
- Diabetes mellitus
Background:
- Women with diabetes have a disproportionately higher risk of coronary heart disease (CHD) compared to men.
- This disparity is partly explained by more unfavorable CHD risk factor patterns in women with type 2 diabetes.
Purpose of the Study:
- To investigate the factors contributing to the increased CHD risk in women with diabetes, particularly comparing type 1 and type 2 diabetes.
- To understand the role of lipid profiles, blood pressure, and body fat distribution in this elevated risk.
Main Methods:
- Comparative analysis of CHD risk factors in diabetic men and women across different diabetes types (type 1 and type 2).
- Review of existing evidence on lipid profiles, blood pressure, and body fat distribution in diabetic populations.
Main Results:
- In type 2 diabetes, adverse risk factor patterns explain much of the higher CHD risk in women.
- In type 1 diabetes, men exhibit a cardioprotective lipid profile, but women do not. Women also show evidence of altered body fat distribution and higher blood pressure.
- The potential link to increased insulin resistance in type 1 diabetic women is suggested but remains debated.
Conclusions:
- The usual cardioprotective effect of being female does not extend to women with diabetes.
- Early and aggressive risk factor intervention is crucial for diabetic women to mitigate their elevated CHD risk.
Abstract:
Women with diabetes experience much greater relative risks of coronary heart disease (CHD) compared with the nondiabetic population than do men with diabetes. In type 2 diabetes, much of the greater elevation in risk in women is explained by a more adverse pattern of known CHD risk factors. In type 1 diabetes the picture is less clear, but current evidence suggests that a cardioprotective lipid profile is found in type 1 diabetic men, thus reducing the effect of diabetes on CHD, but that in women this is not the case. Also, in type 1 diabetic women there is some evidence of altered body fat distribution and a greater elevation in blood pressure. Whether these reflect a greater degree of insulin resistance in type 1 women, and what the origin of this might be, remains controversial. The practical consequence is that clinicians need to be aware that the usual cardioprotective effect of sex does not apply in diabetic women and that risk factor intervention is needed at an early age.
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