INDICATIONS OF LOW SEX-HORMONE BINDING GLOBULIN (SHBG) IN YOUNG FEMALES WITH TYPE-1 DIABETES, AND AN INDEPENDENT ASSOCIATION TO MICROALBUMINURIA

Citation
S. Rudberg et B. Persson, INDICATIONS OF LOW SEX-HORMONE BINDING GLOBULIN (SHBG) IN YOUNG FEMALES WITH TYPE-1 DIABETES, AND AN INDEPENDENT ASSOCIATION TO MICROALBUMINURIA, Diabetic medicine, 12(9), 1995, pp. 816-822
Citations number
NO
Categorie Soggetti
Endocrynology & Metabolism","Medicine, General & Internal
Journal title
ISSN journal
07423071
Volume
12
Issue
9
Year of publication
1995
Pages
816 - 822
Database
ISI
SICI code
0742-3071(1995)12:9<816:IOLSBG>2.0.ZU;2-#
Abstract
Sex hormone binding globulin (SHBG) is normally decreased during puber ty and inversely related to insulin resistance. Microalbuminuria is ra re before puberty in Type 1 diabetes implicating that sex hormones may contribute to its development. We investigated SHBG levels in young f emales with >5 years of Type 1 diabetes, and the association to microa lbuminuria. Ten diabetic females with, and 15 without microalbuminuria , and 17 healthy controls in pubertal stage 4-5 were compared regardin g anthropometric data, fasting serum levels of SHBG, testosterone, ins ulin, insulin-like growth factor-1 (IGF-1), lipids and lipoproteins. M ultiple regression analyses were performed to study variables with ind ependent influences on SHBG and albumin excretion rate (AER), respecti vely, in Type 1 diabetes. SHBG was lower and testosterone/SHBG ratio h igher in normoalbuminuric females with diabetes than in controls. This was further emphasized in diabetic patients with microaibuminuria. IG F-1 was lower in Type 1 diabetes than in controls, and significantly d ecreased in microalbuminuric as compared to normoalbuminuric diabetic patients. IGF-1 was only correlated to SHBG in healthy controls. In Ty pe 1 diabetes, applying stepwise multiple regression analysis, insulin dose, BMI, and HbA(1C) had a significant and independent inverse infl uence on SHBG (r(2) = 0.77, p < 0.001). With log AER as the dependent variable, low SHBG, low IGF-1, HbA(1C), and age added to the regressio n (r(2) = 0.65, p=0.004), whereas BMI, insulin dose and blood pressure did not. In conclusion, SHBG is decreased in young females with Type 1 diabetes, influenced by increased insulin requirements, BMI and HbA( 1C). In turn, low SHBG seems to be independently associated to elevate d AER in these patients. Prospective studies are necessary to confirm our results.