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Diabetes Care, Vol 19, Issue 10 1045-1050, Copyright © 1996 by American Diabetes Association
Sex hormones and DHEA-SO4 in relation to ischemic heart disease mortality in diabetic subjects. The Wisconsin Epidemiologic Study of Diabetic Retinopathy
SM Haffner, SE Moss, BE Klein and R Klein
Department of Medicine, University of Texas Health Science Center, San Antonio 78284-7873, USA.
OBJECTIVE: Sex hormones are associated with atherogenic changes in
lipoproteins and changes in glucose and insulin metabolism, yet few data
are available on the relationship of sex hormones and
dehydroepiandrosterone sulfate (DHEA-SO4) to ischemic heart disease (IHD)
in diabetic subjects, a group with very high levels of IHD. RESEARCH DESIGN
AND METHODS: We examined the relation of total and free testosterone, sex
hormone binding globulin, estrone, estradiol, and DHEA-SO4 to the 5-year
IHD mortality in the older-onset diabetic subjects in the Wisconsin
Epidemiologic Study of Diabetic Retinopathy (WESDR) in a matched diabetic
subject-control design (two control subjects for every diabetic subject).
RESULTS: In men (n = 123), none of the sex hormones or DHEA-SO4
significantly predicted IHD mortality. In women (n = 120), lower levels of
DHEA-SO4 (P < 0.01) and total testosterone (P = 0.07) predicted IHD
mortality. These results were essentially unchanged after adjustment for
duration of diabetes, GHb, diuretic use, and serum creatinine, which are
major predictors of IHD mortality in the WESDR. Finding lower testosterone
levels in diabetic subjects of IHD in women is contrary to data on risk
factors, which suggests that increased androgen activity may be associated
with worse IHD risk factors. CONCLUSIONS: This study suggests that
alterations in sex hormones and DHEA-SO4 are unlikely to explain a major
proportion of the variation in IHD mortality in diabetic subjects.

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Copyright © 1996 by the American Diabetes Association.
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