Sokooti Sara, Dam Wendy A, Szili-Torok Tamas, Gloerich Jolein, van Gool Alain J, Post Adrian, de Borst Martin H, Gansevoort Ron T, Heerspink Hiddo J L, Dullaart Robin P F, Bakker Stephan J L
Department of Internal Medicine, Division of Nephrology, University Medical Center Groningen, University of Groningen, 9713 GZ Groningen, The Netherlands.
Translational Metabolic Laboratory, Department of Laboratory Medicine, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
J Pers Med. 2022 Jul 12;12(7):1131. doi: 10.3390/jpm12071131.
Fasting proinsulin levels may serve as a marker of β-cell dysfunction and predict type 2 diabetes (T2D) development. Kidneys have been found to be a major site for the degradation of proinsulin. We aimed to evaluate the predictive value of proinsulin for the risk of incident T2D added to a base model of clinical predictors and examined potential effect modification by variables related to kidney function. Proinsulin was measured in plasma with U-PLEX platform using ELISA immunoassay. We included 5001 participants without T2D at baseline and during a median follow up of 7.2 years; 271 participants developed T2D. Higher levels of proinsulin were associated with increased risk of T2D independent of glucose, insulin, C-peptide, and other clinical factors (hazard ratio (HR): 1.28; per 1 SD increase 95% confidence interval (CI): 1.08-1.52). Harrell's C-index for the Framingham offspring risk score was improved with the addition of proinsulin ( = 0.019). Furthermore, we found effect modification by hypertension ( = 0.019), eGFR ( = 0.020) and urinary albumin excretion ( = 0.034), consistent with an association only present in participants with hypertension or kidney dysfunction. Higher fasting proinsulin level is an independent predictor of incident T2D in the general population, particularly in participants with hypertension or kidney dysfunction.
空腹胰岛素原水平可作为β细胞功能障碍的标志物,并预测2型糖尿病(T2D)的发生。肾脏已被发现是胰岛素原降解的主要部位。我们旨在评估胰岛素原对临床预测指标基础模型中新增的T2D发病风险的预测价值,并研究与肾功能相关变量的潜在效应修正作用。使用酶联免疫吸附测定法在U-PLEX平台上检测血浆中的胰岛素原。我们纳入了5001名基线时无T2D且中位随访7.2年的参与者;271名参与者发生了T2D。较高的胰岛素原水平与T2D风险增加相关,独立于血糖、胰岛素、C肽和其他临床因素(风险比(HR):1.28;每增加1个标准差,95%置信区间(CI):1.08 - 1.52)。加入胰岛素原后,弗雷明汉后代风险评分的Harrell's C指数有所改善( = 0.019)。此外,我们发现高血压( = 0.019)、估算肾小球滤过率(eGFR)( = 0.020)和尿白蛋白排泄( = 0.034)存在效应修正,这与仅在高血压或肾功能不全参与者中存在的关联一致。较高的空腹胰岛素原水平是一般人群中T2D发病的独立预测指标,尤其是在高血压或肾功能不全的参与者中。