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Diabetes and Vascular Disease Research
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Rosiglitazone increases bioactive testosterone and reduces waist circumference in hypogonadal men with type 2 diabetes

Dheeraj Kapoor

The Robert Hague Centre for Diabetes and Endocrinology, Barnsley NHS Foundation Trust Hospital, Gawber Road, Barnsley, S75 2EP, UK.

Kevin S Channer

Department of Cardiology, Royal Hallamshire Hospital, Glossop Road, Sheffield, S10 2JP, UK.

T Hugh Jones

The Robert Hague Centre for Diabetes and Endocrinology, Barnsley NHS Foundation Trust Hospital, Gawber Road, Barnsley, S75 2EP, UK.

The purpose of this study was to assess the effect of rosiglitazone on bioavailable, free and total testosterone levels in hypogonadal men with type 2 diabetes. Sixteen type 2 diabetic men with hypogonadism were studied before and after administration of rosiglitazone (8 mg/day) for six months, with assessments performed every two months on two consecutive days. We measured testosterone and sex hormone binding globulin (SHBG), visceral adiposity, high-sensitivity CRP (hs-CRP), lipids, microalbuminuria and blood pressure.

There was a significant increase in free (p=0.01), bioavailable (p=0.007) and total testosterone (p=0.002), as well as SHBG (p=0.03) levels, with rosiglitazone treatment. Waist circumference and waist/hip ratio decreased with the improvement in insulin sensitivity and glycaemic control (p=0.01). There was also a significant reduction in hs-CRP (p=0.02) and urinary albumin excretion. No significant effect on blood pressure or the ratio of low-density lipoprotein cholesterol to high-density lipoprotein cholesterol (LDL to HDL) was seen.

In conclusion, the insulin-sensitiser rosiglitazone increases bioavailable, free and total testosterone and SHBG levels in hypogonadal men with type 2 diabetes.

Key Words: hypogonadism • men • rosiglitazone • testosterone • type 2 diabetes

Diabetes and Vascular Disease Research, Vol. 5, No. 2, 135-137 (2008)
DOI: 10.3132/dvdr.2008.022


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Endocr. Rev.Home page
H. M. Scott, J. I. Mason, and R. M. Sharpe
Steroidogenesis in the Fetal Testis and Its Susceptibility to Disruption by Exogenous Compounds
Endocr. Rev., December 1, 2009; 30(7): 883 - 925.
[Abstract] [Full Text] [PDF]