Department of Pediatrics, The Johns Hopkins University School of Medicine, Baltimore, Maryland.
Department of Physiology, The Johns Hopkins University School of Medicine, Baltimore, Maryland.
Am J Physiol Endocrinol Metab. 2021 Jun 1;320(6):E1044-E1052. doi: 10.1152/ajpendo.00626.2020. Epub 2021 Apr 26.
Obesity and type 2 diabetes are rapidly increasing in the adolescent population. We sought to determine whether adipokines, specifically leptin, C1q/TNF-related proteins 1 (CTRP1) and CTRP9, and the hepatokine fibroblast growth factor 21 (FGF21), are associated with obesity and hyperglycemia in a cohort of lean and obese adolescents, across the spectrum of glycemia. In an observational, longitudinal study of lean and obese adolescents, we measured fasting laboratory tests, oral glucose tolerance tests, and adipokines including leptin, CTRP1, CTRP9, and FGF21. Participants completed baseline and 2-year follow-up study visits and were categorized as lean (LC, lean control; = 30), obese normoglycemic (ONG; = 61), and obese hyperglycemic (OHG; = 31) adolescents at baseline and lean ( = 8), ONG ( = 18), and OHG ( = 4) at follow-up. Groups were compared using ANOVA and regression analysis, and linear mixed effects modeling was used to test for differences in adipokine levels across baseline and follow-up visits. Results showed that at baseline, leptin was higher in all obese groups ( < 0.001) compared with LC. FGF21 was higher in OHG participants compared with LC ( < 0.001) and ONG ( < 0.001) and positively associated with fasting glucose ( < 0.001), fasting insulin ( < 0.001), Homeostasis Model Assessment-Insulin Resistance Index (HOMA-IR; < 0.001), and hemoglobin A1c (HbA1c; = 0.01). CTRP1 was higher in OHG compared with ONG ( = 0.03). CTRP9 was not associated with obesity or hyperglycemia in this pediatric cohort. At 2 years, leptin decreased in ONG ( = 0.003) and FGF21 increased in OHG ( = 0.02), relative to lean controls. Altered adipokine levels are associated with the inflammatory milieu in obese youth with and without hyperglycemia. In adolescence, the novel adipokine CTRP1 was elevated with hyperglycemia, whereas CTRP9 was unchanged in this cohort. Leptin is higher in obese adolescents and FGF21 is higher in obese hyperglycemic adolescents. The novel adipokine CTRP1 is higher in obese hyperglycemic adolescents, whereas CTRP9 was unchanged in this adolescent cohort.
肥胖和 2 型糖尿病在青少年人群中迅速增加。我们旨在确定脂肪因子,特别是瘦素、C1q/TNF 相关蛋白 1(CTRP1)和 CTRP9,以及肝源细胞因子成纤维细胞生长因子 21(FGF21),是否与瘦素和肥胖青少年的肥胖和高血糖有关,涵盖了血糖谱的范围。在一项对瘦素和肥胖青少年的观察性、纵向研究中,我们测量了空腹实验室检查、口服葡萄糖耐量试验以及包括瘦素、CTRP1、CTRP9 和 FGF21 在内的脂肪因子。参与者完成了基线和 2 年随访研究访问,并在基线时被归类为瘦(LC,瘦对照组;n = 30)、肥胖正常血糖(ONG;n = 61)和肥胖高血糖(OHG;n = 31)青少年,在随访时被归类为瘦(n = 8)、ONG(n = 18)和 OHG(n = 4)。使用方差分析和回归分析比较组间差异,使用线性混合效应模型测试脂肪因子水平在基线和随访访问期间的差异。结果表明,在基线时,所有肥胖组的瘦素水平均高于 LC 组( < 0.001)。OHG 组的 FGF21 水平高于 LC 组( < 0.001)和 ONG 组( < 0.001),与空腹血糖( < 0.001)、空腹胰岛素( < 0.001)、稳态模型评估-胰岛素抵抗指数(HOMA-IR; < 0.001)和糖化血红蛋白(HbA1c; = 0.01)呈正相关。OHG 组的 CTRP1 水平高于 ONG 组( = 0.03)。在这个儿科队列中,CTRP9 与肥胖或高血糖无关。在 2 年时,ONG 组的瘦素水平下降( = 0.003),OHG 组的 FGF21 水平升高( = 0.02),与瘦对照组相比。在肥胖伴或不伴高血糖的青少年中,脂肪因子水平的改变与炎症环境有关。在青春期,新型脂肪因子 CTRP1 在高血糖时升高,而在该队列中,CTRP9 不变。肥胖青少年的瘦素水平较高,肥胖高血糖青少年的 FGF21 水平较高。新型脂肪因子 CTRP1 在肥胖高血糖青少年中升高,而在该青少年队列中,CTRP9 不变。