Söderberg S, Ahrén B, Eliasson M, Dinesen B, Brismar K, Olsson T
Department of Medicine, Umeå University Hospital, Sweden.
Eur J Endocrinol. 2001 Mar;144(3):283-90. doi: 10.1530/eje.0.1440283.
Hyperleptinaemia and hyperinsulinaemia interrelate to insulin-like growth factor binding protein 1 (IGFBP-1), and disturbances in the growth hormone-IGF-I axis are linked to obesity and cardiovascular diseases. However, whether the association between leptin and the GH-IGF-I axis is altered with increasing obesity is not known. We therefore examined the relationship between leptin, IGF-I, IGFBP-1, insulin and proinsulin in men and women with or without obesity in a population study.
Healthy subjects (n=158; 85 men and 73 pre- and postmenopausal women) from the Northern Sweden MONICA (Monitoring of Trends and Determinants in Cardiovascular Disease) population were studied with a cross-sectional design.
Anthropometric measurements (body mass index (BMI) and waist circumference) and oral glucose tolerance tests were performed. Radioimmunoassays were used for the analyses of leptin, IGF-I and IGFBP-1, and ELISAs for specific insulin and proinsulin.
Leptin inversely correlated to IGFBP-1 in non-obese men (P<0.05) and obese postmenopausal women (P<0.05). In contrast, leptin did not correlate to IGF-I. IGFBP-1 was also significantly associated with proinsulin in non-obese men (P<0.01) and non-obese premenopausal women (P<0.05). The association between leptin and IGFBP-1 was lost after adjustment for insulin. In multivariate analyses taking measures of adiposity into account, low proinsulin, and IGF-I in combination with old age, but not leptin, predicted high IGFBP-1 levels.
Leptin was inversely associated with IGFBP-1 in non-obese men and obese postmenopausal women, and proinsulin was inversely associated with IGFBP-1 in non-obese men and premenopausal women. However, these associations were lost with increasing central obesity in men and premenopausal women and after control for insulin. Therefore, this study suggests (i) that leptin is of minor importance for regulation of IGFBP-1 levels and (ii) that the insulin resistance syndrome is characterised by an altered relationship between leptin, IGFBP-1 and insulin.
高瘦素血症和高胰岛素血症与胰岛素样生长因子结合蛋白1(IGFBP - 1)相互关联,生长激素 - IGF - I轴的紊乱与肥胖症和心血管疾病相关。然而,随着肥胖程度增加,瘦素与生长激素 - IGF - I轴之间的关联是否改变尚不清楚。因此,我们在一项人群研究中考察了有或无肥胖的男性和女性中瘦素、IGF - I、IGFBP - 1、胰岛素和胰岛素原之间的关系。
采用横断面设计,对来自瑞典北部心血管疾病趋势和决定因素监测(MONICA)人群的健康受试者(n = 158;85名男性以及73名绝经前和绝经后女性)进行了研究。
进行人体测量(体重指数(BMI)和腰围)以及口服葡萄糖耐量试验。采用放射免疫分析法分析瘦素、IGF - I和IGFBP - 1,采用酶联免疫吸附测定法分析特异性胰岛素和胰岛素原。
在非肥胖男性(P < 0.05)和肥胖绝经后女性(P < 0.05)中,瘦素与IGFBP - 1呈负相关。相比之下,瘦素与IGF - I无相关性。在非肥胖男性(P < 0.01)和非肥胖绝经前女性(P < 0.05)中,IGFBP - 1也与胰岛素原显著相关。校正胰岛素后,瘦素与IGFBP - 1之间的关联消失。在多变量分析中,综合考虑肥胖指标后,低胰岛素原、IGF - I与老年因素(而非瘦素)可预测高IGFBP - 1水平。
在非肥胖男性和肥胖绝经后女性中,瘦素与IGFBP - 1呈负相关;在非肥胖男性和绝经前女性中,胰岛素原与IGFBP - 1呈负相关。然而,在男性和绝经前女性中,随着中心性肥胖增加以及校正胰岛素后,这些关联消失。因此,本研究表明:(i)瘦素对IGFBP - 1水平的调节作用较小;(ii)胰岛素抵抗综合征的特征是瘦素、IGFBP - 1和胰岛素之间的关系发生改变。