Title of article :
Sex hormones, sex hormone binding globulin, and abdominal aortic calcification in women and men in the multi-ethnic study of atherosclerosis (MESA)
Author/Authors :
Erin D. Michos، نويسنده , , Dhananjay Vaidya، نويسنده , , Susan M. Gapstur، نويسنده , , Pamela J. Schreiner، نويسنده , , Sherita H. Golden، نويسنده , , Nathan D. Wong، نويسنده , , Michael H. Criqui، نويسنده , , Pamela Ouyang، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2008
Pages :
7
From page :
432
To page :
438
Abstract :
Background Conflicting findings exist regarding the associations of sex hormones with subclinical atherosclerosis. Methods This is a substudy from MESA of 881 postmenopausal women and 978 men who had both abdominal aortic calcification (AAC) quantified by computed tomography and sex hormone levels assessed [Testosterone (T), estradiol (E2), dehydroepiandrosterone (DHEA), and sex hormone binding globulin (SHBG)]. We examined the association of sex hormones with presence and extent of AAC. Results For women, SHBG was inversely associated with both AAC presence [OR = 0.62, 95% CI 0.42–0.91 for 1 unit greater log(SHBG) level] and extent [0.29 lower log(AAC) for 1 unit greater log(SHBG) level, β = −0.29 (95% CI −0.57 to −0.006)] adjusting for age, race, hypertension, smoking, diabetes, BMI, physical activity, and other sex hormones. After further adjustment for total and HDL-cholesterol, SHBG was not associated with ACC presence or extent. In men, there was no association between SHBG and AAC. In both men and women, neither T, E2, nor DHEA was associated with AAC presence or extent. Conclusion After adjustment for non-lipid cardiovascular risk factors, SHBG levels are inversely associated with both the presence and severity of AAC in women but not in men, which may be accounted for by HDL.
Keywords :
Sex hormone binding globulin , Subclinical Atherosclerosis , Abdominal aortic calcification , sex hormones
Journal title :
Atherosclerosis
Serial Year :
2008
Journal title :
Atherosclerosis
Record number :
633164
Link To Document :
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