GOS Institute of Child Health, University College London (UCL), London, UK.
Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Pediatr Diabetes. 2019 Nov;20(7):821-831. doi: 10.1111/pedi.12897. Epub 2019 Jul 29.
Not much is known about glycaemic-control trajectories in childhood-onset type 2 diabetes (T2D). We investigated characteristics of children and young people (CYP) with T2D and inequalities in glycemic control.
We studied 747 CYP with T2D, <19 years of age in 2009-2016 (from the total population-based National Pediatric Diabetes Audit [>95% diabetes cases in England/Wales]). Linear mixed-effects modeling was used to assess socioeconomic and ethnic differences in longitudinal glycated hemoglobin (HbA ) trajectories during 4 years post-diagnosis (3326 HbA data points, mean 4.5 data points/subject). Self-identified ethnicity was grouped into six categories. Index of Multiple Deprivation (a small geographical area-level deprivation measure) was grouped into SES quintiles for analysis.
Fifty-eight percent were non-White, 66% were female, and 41% were in the most disadvantaged SES quintile. Mean age and HbA at diagnosis were 13.4 years and 68 mmol/mol, respectively. Following an initial decrease between diagnosis and end of year 1 (-15.2 mmol/mol 95%CI, -19.2, -11.2), HbA trajectories increased between years 1 and 3 (10 mmol/mol, 7.6, 12.4), followed by slight gradual decrease subsequently (-1.6 mmol/mol, -2, -1.1). Compared to White CYP, Pakistani children had higher HbA at diagnosis (13.2 mmol/mol, 5.6-20.9). During follow-up, mixed-ethnicity and Pakistani CYP had poorer glycemic control. Compared to children in the most disadvantaged quintile, those in the most advantaged had lower HbA at diagnosis (-6.3 mmol, -12.6, -0.1). Differences by SES remained during follow-up. Mutual adjustment for SES and ethnicity did not substantially alter the above estimates.
About two-thirds of children with childhood-onset T2D were non-White, female adolescents, just under half of whom live in the most disadvantaged areas of England and Wales. Additionally, there are substantial socioeconomic and ethnic inequalities in diabetes control.
对于儿童期 2 型糖尿病(T2D)患者的血糖控制轨迹,我们知之甚少。我们研究了 T2D 患儿和青少年(CYP)的特征以及血糖控制方面的不平等现象。
我们研究了 2009 年至 2016 年期间在英格兰/威尔士进行的基于人群的国家儿科糖尿病审计(>95%的糖尿病病例)中年龄<19 岁的 747 名 T2D CYP。使用线性混合效应模型评估了社会经济和种族差异对诊断后 4 年(3326 个糖化血红蛋白 [HbA ]数据点,平均每个受试者 4.5 个数据点)纵向 HbA 轨迹的影响。自我认定的种族分为六类。指数的多重剥夺(一个小的地理区域水平剥夺措施)分为 SES 五分位数进行分析。
58%是非白人,66%是女性,41%处于社会经济地位最不利的五分位数。平均年龄和诊断时的 HbA 分别为 13.4 岁和 68mmol/mol。在诊断后和第 1 年年末之间,HbA 轨迹最初下降(-15.2mmol/mol,95%CI-19.2,-11.2),然后在第 1 年至第 3 年之间增加(10mmol/mol,7.6,12.4),随后逐渐缓慢下降(-1.6mmol/mol,-2,-1.1)。与白人 CYP 相比,巴基斯坦儿童的诊断时 HbA 更高(13.2mmol/mol,5.6-20.9)。在随访期间,混合种族和巴基斯坦 CYP 的血糖控制较差。与处于最不利五分位的儿童相比,处于最有利五分位的儿童诊断时的 HbA 较低(-6.3mmol,-12.6,-0.1)。SES 差异在随访期间仍然存在。SES 和种族的相互调整并没有实质性地改变上述估计值。
大约三分之二的儿童期 T2D 患儿是非白人、青春期女性,其中近一半居住在英格兰和威尔士最贫困的地区。此外,糖尿病控制方面存在着巨大的社会经济和种族不平等现象。