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Longitudinal relation between limited joint mobility height insulin-like growth factor 1 levels and risk of developing microalbuminuria: the Oxford Regional Prospective Study

机译:有限的关节活动度身高胰岛素样生长因子1水平和发生微量白蛋白尿的风险之间的纵向关系:牛津地区前瞻性研究

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摘要

>Aims: To determine risk factors for development of microalbuminuria (MA) in relation to detection of limited joint mobility (LJM+) of the interphalangeal joints in a longitudinal cohort of type 1 diabetic (T1DM) subjects. >Results: After a median follow up of 10.9 years, 162 subjects (35.1%) developed LJM at median age 13.0 years and duration 5.2 years. More subjects developed LJM after compared to before puberty (67.6 v 32.4%). In LJM+ compared to LJM– subjects, HbA1c (mean 10.1 (SD 1.6) v 9.6 (1.4) %)) and ACR levels (median 1.1 (range 0.2–242.9) v 0.9 (0.4–70.7) mg/mmol) were higher, and in a Cox model probability of developing LJM was related to puberty and higher HbA1c levels. ACR levels were higher after detection of LJM compared to before (median 1.2 (range 0.4–102.6) v 0.8 (0.2–181.9) mg/mmol). Probability of developing MA was related to puberty, HbA1c, female sex, and presence of LJM (a 1.9-fold increased risk). Both LJM and MA were associated with lower height SDS (LJM: mean 0.0 (SD 1.0) v 0.2 (1.1); MA: 0.0 (1.0) v 0.2 (SD 1.0)) and lower IGF-1 levels. >Conclusion: The development of LJM was associated with an increased risk of microalbuminuria, independent of glycaemic control. Risk for both microalbuminuria and LJM was associated with puberty, reduced growth, and reduced IGF-1 levels, and may indicate underlying shared pathogenic mechanisms.
机译:>目标:确定与1型糖尿病(T1DM)受试者纵向队列中指间关节的有限关节活动度(LJM +)的检测有关的发展微量白蛋白尿(MA)的危险因素。 >结果:中位随访时间为10.9年后,有162名受试者(35.1%)在中位年龄为13.0岁,病程为5.2年时发生了LJM。与青春期之前相比,更多的受试者发生了LJM(67.6 v 32.4%)。与LJM–受试者相比,LJM +受试者的HbA1c(平均10.1(SD 1.6)v 9.6(1.4)%)和ACR水平(中位数1.1(0.2–242.9)v 0.9(0.4–70.7)mg / mmol)更高,在Cox模型中,发生LJM的可能性与青春期和HbA1c水平升高有关。检测到LJM后的ACR水平高于之前(中位数1.2(范围0.4–102.6)v 0.8(0.2–181.9)mg / mmol)。发生MA的可能性与青春期,HbA1c,女性和LJM的存在有关(风险增加1.9倍)。 LJM和MA均与较低身高的SDS(LJM:平均值0.0(SD 1.0)v 0.2(1.1); MA:0.0(1.0)v 0.2(SD 1.0))和较低的IGF-1水平相关。 >结论: LJM的发展与微白蛋白尿风险增加有关,而与血糖控制无关。微量白蛋白尿和LJM的风险与青春期,生长减少和IGF-1水平降低有关,并且可能表明潜在的共有致病机制。

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