TY - JOUR
T1 - Low sex hormone binding globulin is a potential marker for the metabolic syndrome in different ethnic groups
AU - Heald, A. H.
AU - Anderson, S. G.
AU - Ivison, F.
AU - Riste, L.
AU - Laing, I.
AU - Cruickshank, J. K.
AU - Gibson, J. M.
PY - 2005/10
Y1 - 2005/10
N2 - Hepatic sex-hormone binding globulin (SHBG) production is down-regulated by insulin and low levels reflect insulin resistance. Because insulin resistance is closely related to the development of cardiovascular disease in different ethnic groups we examined ethnic variation in SHBG across populations with different baseline cardiovascular risk and metabolic syndrome prevalence. Participants were population-based, of European (n = 142), Pakistani (n = 130), and African-Caribbean (AfC) origin (n = 193). SHBG, fasting lipids, and glucose concentrations plus insulin sensitivity (HOMA-S) were determined. Age adjusted SHBG was significantly lower in both Pakistani men and women. Circulating SHBG levels were lower in those with impaired vs. normal glucose homeostasis. SHBG correlated positively with HOMA-S (ρ = 0.28, p <0.001), and negatively with WHR (ρ = -0.38, p <0.001), BMI (r = -0.30, p <0.001), and diastolic blood pressure (ρ = -0.14, p <0.01) across all ethnic groups. In multivariate logistic regression analysis a low SHBG increased the likelihood of the metabolic syndrome (odds ratio [OR] = 0.42 [0.21 -0.82], p = 0.01) as did higher fasting NEFA (OR 1.47 [1.04-2.08], p = 0.03), low IGFBP-1 concentrations (OR 0.6 [0.44-0.81], p = 0.001), age (OR 1.05 [1.02-1.09], p = 0.003), and Pakistani ethnicity (p = 0.001) in a model which also contained gender, InCRP, IGF-I, and IGF-II. As ethnic differences in SHBG level closely parallel differences in insulin resistance. Its measurement may be useful in identifying individuals at particular risk of the metabolic syndrome, for early intervention. © J. A. Barth Verlag in Georg Thieme Verlag KG.
AB - Hepatic sex-hormone binding globulin (SHBG) production is down-regulated by insulin and low levels reflect insulin resistance. Because insulin resistance is closely related to the development of cardiovascular disease in different ethnic groups we examined ethnic variation in SHBG across populations with different baseline cardiovascular risk and metabolic syndrome prevalence. Participants were population-based, of European (n = 142), Pakistani (n = 130), and African-Caribbean (AfC) origin (n = 193). SHBG, fasting lipids, and glucose concentrations plus insulin sensitivity (HOMA-S) were determined. Age adjusted SHBG was significantly lower in both Pakistani men and women. Circulating SHBG levels were lower in those with impaired vs. normal glucose homeostasis. SHBG correlated positively with HOMA-S (ρ = 0.28, p <0.001), and negatively with WHR (ρ = -0.38, p <0.001), BMI (r = -0.30, p <0.001), and diastolic blood pressure (ρ = -0.14, p <0.01) across all ethnic groups. In multivariate logistic regression analysis a low SHBG increased the likelihood of the metabolic syndrome (odds ratio [OR] = 0.42 [0.21 -0.82], p = 0.01) as did higher fasting NEFA (OR 1.47 [1.04-2.08], p = 0.03), low IGFBP-1 concentrations (OR 0.6 [0.44-0.81], p = 0.001), age (OR 1.05 [1.02-1.09], p = 0.003), and Pakistani ethnicity (p = 0.001) in a model which also contained gender, InCRP, IGF-I, and IGF-II. As ethnic differences in SHBG level closely parallel differences in insulin resistance. Its measurement may be useful in identifying individuals at particular risk of the metabolic syndrome, for early intervention. © J. A. Barth Verlag in Georg Thieme Verlag KG.
KW - Insulin resistance
KW - Metabolic syndrome
KW - SHBG
U2 - 10.1055/s-2005-865807
DO - 10.1055/s-2005-865807
M3 - Article
SN - 0947-7349
VL - 113
SP - 522
EP - 528
JO - Experimental and Clinical Endocrinology and Diabetes
JF - Experimental and Clinical Endocrinology and Diabetes
IS - 9
ER -