Key result
In midlife women, higher sex hormone binding globulin was inversely related to total carotid plaque area, whereas higher free testosterone was associated with greater area.
Why the study?
Endogenous sex hormones may contribute to cardiovascular disease in women, but few studies have evaluated sex steroids in relation to carotid plaque burden and characteristics.
Are endogenous sex hormones associated with carotid plaque burden and characteristics in midlife women?
Cross-Sectional (n=141)
Are endogenous sex hormones associated with carotid plaque burden and characteristics in midlife women?
Endogenous sex hormones, specifically SHBG, free testosterone, and estrone, are associated with carotid plaque burden and echogenicity in midlife women, suggesting distinct roles in plaque development.
Answers are grounded in this paper and cite their sources.
Should not yet inform clinical vascular risk assessment in midlife women; leaves open causal roles for SHBG and testosterone in plaque.
CONTEXT: Endogenous sex hormones may be involved in the pathogenesis of cardiovascular disease (CVD) in women. Carotid plaque characteristics, such as echogenicity, an ultrasound measure that reflects plaque composition, may identify unstable plaques that are more likely to rupture, precipitating a CVD event. However, few studies have considered sex steroids in relation to carotid plaque and its characteristics. OBJECTIVE: To evaluate estrone (E1), estradiol (E2), testosterone (T), sex hormone binding globulin (SHBG), and free T (FT) in relation to carotid plaque in women. DESIGN, SETTING, AND PARTICIPANTS: In MsHeart, a cross-sectional study of 304 women aged 40 to 60 years, participants underwent a carotid artery ultrasound assessment. The current analysis included MsHeart participants with carotid plaque (n = 141, 46%). E1, E2, and T were assayed using liquid chromatography-tandem mass spectrometry; FT was estimated using ensemble allostery models. Regression models were adjusted for sociodemographic characteristics and CVD risk factors. MAIN OUTCOMES: Carotid plaque burden (number of plaques, total plaque area [TPA]) and characteristics (calcification, echogenicity) were determined using semi-automated software. RESULTS: SHBG was inversely related to TPA (odds ratio [OR] 0.39; 95% confidence interval [CI] 0.21, 0.74; multivariable) and higher FTs were associated with greater TPA (OR 2.89; 95% CI 1.31, 6.37; multivariable). Higher E1 was related to echogenicity (OR 2.31; 95% CI 1.26, 4.33; multivariable), characteristic of more stable plaque. CONCLUSIONS: SHBG and FT are related to TPA while E1 is related to plaque echogenicity, suggesting these hormones have different roles in the development of carotid plaque. Our findings highlight the importance of sex hormones in the development of carotid plaque in midlife women.
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Cortés et al. (2020) conducted a cross-sectional in Carotid plaque (n=141). Endogenous sex hormones (SHBG, free testosterone, estrone) was evaluated on Carotid plaque burden (total plaque area) and characteristics (OR 0.39, 95% CI 0.21-0.74). In midlife women, higher sex hormone binding globulin was inversely related to total carotid plaque area, whereas higher free testosterone was associated with greater area.
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