Association Between Low Sex Hormone-Binding Globulin and Increased Risk of Type 2 Diabetes Is Mediated by Increased Visceral and Liver Fat: Results From Observational and Mendelian Randomization Analyses.

Diabetes Pub Date : 2024-11-01 DOI:10.2337/db23-0982
Theresa A Stangl, Chantal M Wiepjes, Roelof A J Smit, Astrid van Hylckama Vlieg, Hildo J Lamb, Jeroen H P M van der Velde, Esther Winters-van Eekelen, Sebastiaan C Boone, Martijn C G J Brouwers, Frits R Rosendaal, Martin den Heijer, Annemieke C Heijboer, Renée de Mutsert
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Abstract

The aim of this study was to investigate the associations among sex hormone-binding globulin (SHBG), visceral adipose tissue (VAT), liver fat content, and risk of type 2 diabetes (T2D). In the Netherlands Epidemiology of Obesity study, 5,690 women (53%) and men (47%) without preexisting diabetes were included and followed for incident T2D. SHBG concentrations were measured in all participants, VAT was measured using MRI, and liver fat content was measured using proton magnetic resonance spectroscopy in a random subset of 1,822 participants. We examined associations between SHBG and liver fat using linear regression and bidirectional Mendelian randomization analyses and between SHBG and T2D using Cox regression adjusted for confounding and additionally for VAT and liver fat to examine mediation. Mean age was 56 (SD 6) years, mean BMI was 30 (SD 4) kg/m2, median SHBG was 47 (interquartile range [IQR] 34-65) nmol/L in women and 34 (26-43) nmol/L in men, and median liver fat was 3.4% (IQR 1.6-8.2%) in women and 6.0% (2.9-13.5%) in men. Compared with the highest SHBG quartile, liver fat was 2.9-fold (95% CI 2.4, 3.4) increased in women and 1.6-fold (95% CI 1.3, 1.8) increased in men, and the hazard ratio of T2D was 4.9 (95% CI 2.4, 9.9) in women and 1.8 (1.1, 2.9) in men. Genetically predicted SHBG was associated with liver fat content (women: SD -0.45 [95% CI -0.55, -0.35]; men: natural logarithm, -0.25 [95% CI -0.34, -0.16]). VAT and liver fat together mediated 43% (women) and 60% (men) of the SHBG-T2D association. To conclude, in a middle-aged population with overweight, the association between low SHBG and increased risk of T2D was, for a large part, mediated by increased VAT and liver fat.

Article highlights:

性激素结合球蛋白低与 2 型糖尿病风险增加之间的关联是由内脏和肝脏脂肪增加介导的:观察性分析和孟德尔随机分析的结果。
本研究旨在探讨性激素结合球蛋白(SHBG)、内脏脂肪(VAT)、肝脏脂肪含量与 2 型糖尿病风险之间的关系。在荷兰肥胖症流行病学研究中,5690 名女性(53%)和男性未患糖尿病,研究人员对他们进行了随访,以了解他们是否患有 2 型糖尿病。所有研究人员的SHBG浓度都进行了测量,1822名研究人员的VAT用核磁共振成像进行了测量,肝脏脂肪含量用质子核磁共振光谱进行了测量。我们通过线性回归和双向孟德尔随机分析研究了SHBG与肝脏脂肪之间的关系,通过Cox回归研究了SHBG与2型糖尿病之间的关系,并对混杂因素进行了调整,此外还对VAT和肝脏脂肪进行了调整,以研究两者之间的中介关系。平均(标清)年龄为56(6)岁,体重指数为30(4)kg/m2,SHBG中位数(IQR)为女性47(34,65)nmol/L,男性34(26,43)nmol/L,肝脏脂肪中位数(IQR)为女性3.4(1.6,8.2)%,男性6.0(2.9,13.5)%。与SHBG最高的四分位数相比,女性肝脏脂肪增加了2.9倍(95%CI:2.4,3.4),男性增加了1.6倍(95%CI:1.3,1.8),女性患2型糖尿病的危险比(95%CI)为4.9(2.4,9.9),男性为1.8(1.1,2.9)。基因预测的 SHBG 与肝脏脂肪含量有关(女性:SD(95%CI)-1.5,男性:SD(95%CI)-1.5):SD(95%CI)-0.45(-0.55,-0.35),男性:ln(95%CI)-0.25(-0.34,-0.16))。在SHBG与2型糖尿病的关系中,43%(女性)和60%(男性)的脂肪是由VAT和肝脏脂肪共同介导的。总之,在超重的中年人群中,低SHBG与2型糖尿病风险增加之间的关系在很大程度上是由脂肪体积和肝脏脂肪的增加介导的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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