National Institute of Diabetes and Digestive and Kidney Diseases, Phoenix, AZ.
University of Colorado, Aurora, CO.
Diabetes Care. 2022 Feb 1;45(2):436-443. doi: 10.2337/dc21-1688.
Type 2 diabetes (T2D) is a leading cause of end-stage kidney disease worldwide. Recent studies suggest a more aggressive clinical course of diabetic kidney disease in youth-onset compared with adult-onset T2D. We compared kidney structural lesions in youth- and adult-onset T2D to determine if youth onset was associated with greater early tissue injury.
Quantitative microscopy was performed on kidney tissue obtained from research kidney biopsies in 161 Pima Indians (117 women, 44 men) with T2D. Onset of T2D was established by serial oral glucose tolerance testing, and participants were stratified as youth onset (age <25 years) or adult onset (age ≥25 years). Associations between clinical and morphometric parameters and age at onset were tested using linear models.
At biopsy, the 52 participants with youth-onset T2D were younger than the 109 with adult-onset T2D (39.1 ± 9.9 vs. 51.4 ± 10.2 years; P < 0.0001), but their diabetes duration was similar (19.3 ± 8.1 vs. 17.0 ± 7.8 years; P = 0.09). Median urine albumin-to-creatinine ratio was higher in the youth-onset group (58 [25th-75th percentile 17-470] vs. 27 [13-73] mg/g; P = 0.02). Youth-onset participants had greater glomerular basement membrane (GBM) width (552 ± 128 vs. 490 ± 114 nm; P = 0.002) and mesangial fractional volume (0.31 ± 0.10 vs. 0.27 ± 0.08; P = 0.001) than adult-onset participants. Glomerular sclerosis percentage, glomerular volume, mesangial fractional volume, and GBM width were also inversely associated with age at diabetes onset as a continuous variable.
Younger age at T2D onset strongly associates with more severe kidney structural lesions. Studies are underway to elucidate the pathways underlying these associations.
2 型糖尿病(T2D)是全球终末期肾病的主要病因。最近的研究表明,与成人发病的 T2D 相比,青少年发病的糖尿病肾病具有更具侵袭性的临床病程。我们比较了青少年和成人发病的 T2D 的肾脏结构病变,以确定青少年发病是否与更大的早期组织损伤有关。
对 161 例皮马印第安人(117 名女性,44 名男性)的研究性肾脏活检组织进行了定量显微镜检查,这些人患有 T2D。通过连续口服葡萄糖耐量试验确定 T2D 的发病时间,参与者分为青少年发病(年龄<25 岁)或成人发病(年龄≥25 岁)。使用线性模型检验临床和形态计量学参数与发病年龄之间的关系。
在活检时,52 例青少年发病的 T2D 患者比 109 例成人发病的 T2D 患者年龄更小(39.1±9.9 岁比 51.4±10.2 岁;P<0.0001),但糖尿病病程相似(19.3±8.1 岁比 17.0±7.8 岁;P=0.09)。青少年发病组的尿白蛋白/肌酐比值中位数更高(58[25 至 75 百分位范围 17 至 470]比 27[13 至 73]mg/g;P=0.02)。与成人发病组相比,青少年发病组的肾小球基底膜(GBM)宽度(552±128nm 比 490±114nm;P=0.002)和系膜区体积分数(0.31±0.10 比 0.27±0.08;P=0.001)更大。肾小球硬化百分比、肾小球体积、系膜区体积分数和 GBM 宽度也与糖尿病发病年龄呈负相关。
T2D 发病年龄越小,肾脏结构病变越严重。目前正在进行研究以阐明这些关联的途径。