TY - JOUR
T1 - Testosterone, sex hormone-binding globulin, and the development of type 2 diabetes in middle-aged men
T2 - Prospective results from the Massachusetts Male Aging Study
AU - Stellato, Rebecca K.
AU - Feldman, Henry A.
AU - Hamdy, Osama
AU - Horton, Edward S.
AU - Mckinlay, John B.
PY - 2000
Y1 - 2000
N2 - OBJECTIVE - The objective was to examine prospectively the association between low testosterone and sex hormone-binding globulin (SHBG) levels and the subsequent development of type 2 diabetes in men. RESEARCH DESIGN AND METHODS - Analyses were conducted on the cohort of the Massachusetts Male Aging Study, a population-based random sample of men aged 40-70. Of the 1,709 men enrolled in 1987-1989 (T1), 1,156 were followed up 7-10 years later (T2). Testosterone and SHBG levels at T1 were used to predict new cases of diabetes between T1 and T2. RESULTS - After controlling for potential confounders, diabetes at follow-up was predicted jointly and independently by lower baseline levels of free testosterone and SHBG. The odds ratio for future diabetes was 1.58 for a decrease of 1SD in free testosterone (4 ng/dl) and 1.89 for a 1SD decrease in SHBG (16 nmol/l), both significant at P < 0.02. CONCLUSIONS - Our prospective findings are consistent with previous, mainly cross-sectional reports, suggesting that low levels of testosterone and SHBG play some role in the development of insulin resistance and subsequent type 2 diabetes.
AB - OBJECTIVE - The objective was to examine prospectively the association between low testosterone and sex hormone-binding globulin (SHBG) levels and the subsequent development of type 2 diabetes in men. RESEARCH DESIGN AND METHODS - Analyses were conducted on the cohort of the Massachusetts Male Aging Study, a population-based random sample of men aged 40-70. Of the 1,709 men enrolled in 1987-1989 (T1), 1,156 were followed up 7-10 years later (T2). Testosterone and SHBG levels at T1 were used to predict new cases of diabetes between T1 and T2. RESULTS - After controlling for potential confounders, diabetes at follow-up was predicted jointly and independently by lower baseline levels of free testosterone and SHBG. The odds ratio for future diabetes was 1.58 for a decrease of 1SD in free testosterone (4 ng/dl) and 1.89 for a 1SD decrease in SHBG (16 nmol/l), both significant at P < 0.02. CONCLUSIONS - Our prospective findings are consistent with previous, mainly cross-sectional reports, suggesting that low levels of testosterone and SHBG play some role in the development of insulin resistance and subsequent type 2 diabetes.
UR - http://www.scopus.com/inward/record.url?scp=0034106347&partnerID=8YFLogxK
U2 - 10.2337/diacare.23.4.490
DO - 10.2337/diacare.23.4.490
M3 - Article
C2 - 10857940
AN - SCOPUS:0034106347
SN - 0149-5992
VL - 23
SP - 490
EP - 494
JO - Diabetes Care
JF - Diabetes Care
IS - 4
ER -