Key result
In obese premenopausal women, peak GH secretion was inversely associated with HOMA-IR (R=-0.846, P=0.001), fasting insulin (R=-0.650, P=0.012), and LDL cholesterol (R=-0.692, P=0.006).
Why the study?
Is decreased growth hormone response to GHRH associated with cardiometabolic risk factors in premenopausal obese women?
Cross-Sectional
Is decreased growth hormone response to GHRH associated with cardiometabolic risk factors in premenopausal obese women?
In obese premenopausal women, a blunted growth hormone response to GHRH is strongly associated with insulin resistance and adverse lipid profiles, suggesting it may be a pituitary manifestation of metabolic syndrome.
Hypothesis-generating for GH dynamics in obese premenopausal women; leaves open causal contribution to cardiometabolic risk.
The aim of the present study was to evaluate the relationship between GHRH-induced GH secretion in obese premenopausal women and cardiovascular risk markers or insulin resistance. Premenopausal obese women, aged 35-52 years, were studied. GH secretion, IGF-I, serum cardiovascular risk markers, insulin, leptin, mid-waist and hip circumference, total body fat, and truncal fat were measured. Subjects were classified as meeting the criteria for GH deficiency (GHD) when peak GH after stimulation with GHRH was <or=3 microg/L. Mean total and LDL cholesterol, fasting insulin, and HOMA-IR were all higher, in subjects who would have been classified as GH-deficient compared with GH-sufficient. Peak GH secretion after stimulation was inversely associated with fasting insulin (R = -0.650, P = .012), HOMA-IR (R = -0.846, P = .001), total cholesterol (R = -0.532, P = .034), and LDL cholesterol (R = -0.692, P = .006) and positively associated with HDL cholesterol (R = 0.561, P = .037). These data strongly suggest a role for insulin resistance in the decreased GH secretion of obesity and that the blunted GH secretion of central obesity could be the pituitary expression of the metabolic syndrome.
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Cordido et al. (2010) conducted a cross-sectional in Obesity. Decreased GHRH-induced GH secretion (GH deficiency) vs. GH-sufficient was evaluated on Cardiovascular risk markers and insulin resistance. In obese premenopausal women, peak GH secretion was inversely associated with HOMA-IR (R=-0.846, P=0.001), fasting insulin (R=-0.650, P=0.012), and LDL cholesterol (R=-0.692, P=0.006).
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