Obesity is associated with reduced growth hormone (GH) secretion. Reduced GH secretion in obesity is associated with increased cardiovascular disease risk. However, it is not yet known how reduced GH increases cardiovascular disease risk in obesity. The investigators hypothesize that reduced GH contributes to dysfunction of the mitochondria. Therefore, the investigators hypothesize that treatment of obese subjects with reduced GH secretion with GH will improve mitochondrial function and that this improvement in mitochondrial function will contribute, in part, to the effects of GH to improve metabolic parameters in obesity. The investigators propose to study skeletal muscle mitochondria in obese subjects with reduced GH secretion using magnetic resonance spectroscopy and muscle biopsies before and after treatment with GH.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
15
Growth hormone 0.4 mg once daily (titrated to IGF-1) by sub-cutaneous injection for 12 weeks.
Massachusetts General Hospital
Boston, Massachusetts, United States
Phosphocreatine Recovery
The primary objective of this study is to determine the effects of growth hormone on mitochondrial function as assessed by 31P-MRS in obese subjects with reduced GH secretion. Mitochondrial function was represented by ViPCr, a measure of phosphocreatine recovery after sub-maximal exercise. Univariate regression analyses was performed to assess the relationship between the change in skeletal muscle IGF-1 mRNA after 12 weeks treatment with rhGH to change in ViPCr.
Time frame: 12-weeks
Change in Circulating IGF-1 Concentration
Change in circulating IGF-1 from Baseline to 12-weeks is reported.
Time frame: Baseline and 12-weeks
Change in Skeletal Muscle IGF-1 Gene Expression
Change in skeletal muscle IGF-1 gene mRNA expression from Baseline to 12-weeks is reported.
Time frame: Baseline and 12-weeks
Change in Body Composition
Change in waist circumference from Baseline to 12-weeks is reported.
Time frame: Baseline and 12-weeks
Change in Inflammatory Marker
Change in high sensitivity C-reactive protein (hsCRP) from Baseline to 12-weeks is reported.
Time frame: Baseline and 12-weeks
Change in Insulin Sensitivity
Change in fasting glucose from Baseline to 12-weeks is reported.
Time frame: Baseline and 12-weeks
Change in Phosphocreatine Recovery
Change in phosphocreatine recovery, represented by ViPCr, from Baseline to 12-weeks is reported.
Time frame: Baseline and 12-weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.