This study will compare growth hormone levels and cardiovascular risk markers in normal weight and overweight women and men. In women and men with increased abdominal weight, growth hormone (GH) versus placebo will be administered and effects on cardiovascular risk, insulin resistance and body composition will be measured.
The purpose of this study is to measure growth hormone levels in women and men who are normal weight, overweight, and obese. Growth hormone levels will be correlated with body weight, body composition, and markers of cardiovascular risk. In overweight or obese women and men with increased visceral adiposity and below average IGF-1 levels, growth hormone versus placebo will be given for 6 months. Effects of growth hormone treatment on weight, body composition, insulin resistance, lipids, and cardiovascular risk markers will then be assessed. Study subjects will be followed for an additional six months for these endpoints.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
142
Participants will give themselves injections of growth hormone every night for 6 months.
Participants will give themselves injections of placebo growth hormone every night for 6 months.
Massachusetts General Hospital
Boston, Massachusetts, United States
HsCRP
6 month change in HsCRP (primary cardiovascular risk endpoint)
Time frame: Measured at baseline and month 6
Total Abdominal Fat
6 month change in total abdominal fat (primary body composition endpoint)
Time frame: Measured at baseline and month 6
Abdominal Fat
6 month change in visceral abdominal fat (primary body composition endpoint)
Time frame: Measured at baseline and month 6
Measure of Insulin Resistance
6 month change in 2-hour glucose (primary insulin resistance endpoint)
Time frame: Measured at baseline and month 6
Insulin-like Growth Factor-1 (IGF-1) Levels
6-month change in IGF-1 levels
Time frame: Measured at baseline and month 6
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