Laboratory of Investigation on Metabolism and Diabetes (Limed), Gastroenterological Diagnosis and Research Center (Gastrocentro), University of Campinas (Unicamp), Campinas, São Paulo, Brazil; Postgraduate Program in Child and Adolescent Health, Faculty of Medical Science, University of Campinas, (Unicamp), Campinas, São Paulo, Brazil.
Laboratory of Investigation on Metabolism and Diabetes (Limed), Gastroenterological Diagnosis and Research Center (Gastrocentro), University of Campinas (Unicamp), Campinas, São Paulo, Brazil; Postgraduate Program in Child and Adolescent Health, Faculty of Medical Science, University of Campinas, (Unicamp), Campinas, São Paulo, Brazil; School of Applied Sciences, University of Campinas, Limeira, São Paulo, Brazil.
Diabetes Res Clin Pract. 2018 Mar;137:72-82. doi: 10.1016/j.diabres.2017.12.013. Epub 2018 Jan 7.
Insulin resistance and beta-cell dysfunction manifest differently across racial/ethnic groups, and there is a lack of knowledge regarding the pathophysiology of type 2 diabetes mellitus (T2DM) for ethnically admixed adolescents. This study aimed to investigate the influence of adiposity and family history (FH) of T2DM on aspects of insulin sensitivity, beta-cell function, and hepatic insulin extraction in Brazilian adolescents.
A total of 82 normoglycemic adolescents were assessed. The positive FH of T2DM was defined as the presence of at least one known family member with T2DM. The hyperglycemic clamp test consisted of a 120-min protocol. Insulin secretion and beta-cell function were obtained from C-peptide deconvolution. Analysis of covariance considered pubertal stage as a covariate.
Both lean and overweight/obese adolescents had similar glycemic profiles and disposition indexes. Overweight/obese adolescents had about 1/3 the insulin sensitivity of lean adolescents (1.1 ± 0.2 vs. 3.4 ± 0.3 mg·kg·min·pmol ∗ 1000), which was compensated by an increase around 2.5 times in basal (130 ± 7 vs. 52 ± 10 pmol·l·min) and total insulin secretion (130,091 ± 12,230 vs. 59,010 ± 17,522 pmol·l·min), and in the first and second phases of insulin secretion; respectively (p < 0.001). This increase was accompanied by a mean reduction in hepatic insulin extraction of 35%, and a 2.7-time increase in beta-cell glucose sensitivity (p < 0.05). The positive FH of T2DM was not associated with derangements in insulin sensitivity, beta-cell function, and hepatic insulin extraction.
In an admixed sample of adolescents, the hyperglycemic clamp test demonstrated that adiposity had a strong influence, and FH of T2DM had no direct influence, in different aspects of glucose metabolism.
胰岛素抵抗和β细胞功能障碍在不同种族/民族群体中表现不同,对于族裔混合的青少年,关于 2 型糖尿病(T2DM)的病理生理学知识还很缺乏。本研究旨在探讨肥胖和 T2DM 家族史(FH)对巴西青少年胰岛素敏感性、β细胞功能和肝胰岛素摄取的影响。
共评估了 82 名血糖正常的青少年。T2DM 的阳性 FH 定义为至少有一名已知的 T2DM 家族成员。高血糖钳夹试验包括 120 分钟的方案。C 肽反卷积法获得胰岛素分泌和β细胞功能。协方差分析将青春期阶段作为协变量。
无论瘦或超重/肥胖的青少年,其血糖谱和处置指数都相似。超重/肥胖的青少年胰岛素敏感性约为瘦青少年的 1/3(1.1±0.2 对 3.4±0.3 mg·kg·min·pmol·1000),这通过基础胰岛素分泌增加约 2.5 倍(130±7 对 52±10 pmol·l·min)和总胰岛素分泌(130,091±12,230 对 59,010±17,522 pmol·l·min)得到补偿,并且在胰岛素分泌的第一和第二阶段也是如此(p<0.001)。这种增加伴随着肝胰岛素摄取平均减少 35%,β细胞葡萄糖敏感性增加 2.7 倍(p<0.05)。T2DM 的 FH 阳性与胰岛素敏感性、β细胞功能和肝胰岛素摄取的异常无关。
在混合样本的青少年中,高血糖钳夹试验表明肥胖对不同的血糖代谢方面有很大影响,而 T2DM 的 FH 没有直接影响。