Why the study?
Patients with type 2 diabetes have an increased risk of ischemic and non-ischemic heart disease, prompting evaluation of sex differences in microvascular function and myocardial extracellular fibrosis.
Are there sex-related differences in microvascular function and myocardial extracellular fibrosis in patients with type 2 diabetes?
Are there sex-related differences in microvascular function and myocardial extracellular fibrosis in patients with type 2 diabetes?
Women with type 2 diabetes exhibit distinct mechanisms of microvascular dysfunction and myocardial remodeling compared to men, highlighting the need for sex-specific risk stratification in diabetic cardiomyopathy.
Sex-specific MBF and ECV patterns in T2D warrant cautious consideration in cardiac phenotyping; leaves open mechanistic and outcome links.
Aims It is well known that patients with type 2 diabetes (T2D) have an increased risk of both ischemic and non-ischemic heart disease. We studied sex differences in the microvascular function and myocardial extracellular fibrosis that underlie cardiac dysfunction. Methods In a cross-sectional echocardiography and cardiovascular magnetic resonance imaging study, myocardial extracellular volume fraction (ECV), myocardial blood flow at rest (MBF rest ) and during adenosine-induced stress (MBF stress ), and the myocardial perfusion reserve (MPR) were determined in 221 patients with T2D without ischemic heart disease and 25 age-matched controls. We investigated sex-related differences in MBF, MPR, ECV, and diastolic and systolic function. Results Both in unadjusted analyses and after multiple linear regression analyses adjusted for known confounders, women with T2D had higher MBF rest , MBF stress, and ECV than men. The differences in microvascular function resulted in T2D men and women both having lower MPR compared to healthy controls, but the underlying causes differed . Female sex associated with lower lateral e' and higher E/e' independently of MBF stress and ECV. Conclusions These findings highlight distinct sex-specific mechanisms of microvascular dysfunction and myocardial remodeling in T2D. Recognizing these differences may be critical for improving risk stratification and guiding targeted preventive strategies in diabetic cardiomyopathy.
No takes yet. Share an insight, caveat, or question.
Ell et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: