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Deterioration of Glycemic Control in Youth-Onset Type 2 Diabetes: What Are the Early and Late Predictors?青少年起病 2 型糖尿病患者血糖控制恶化:哪些是早期和晚期的预测因素?
J Clin Endocrinol Metab. 2022 Jul 14;107(8):e3384-e3394. doi: 10.1210/clinem/dgac254.
2
Understanding Metabolic Memory: The Prolonged Influence of Glycemia During the Diabetes Control and Complications Trial (DCCT) on Future Risks of Complications During the Study of the Epidemiology of Diabetes Interventions and Complications (EDIC).理解代谢记忆:糖尿病控制与并发症试验(DCCT)期间血糖水平对糖尿病干预与并发症流行病学研究(EDIC)中未来并发症风险的长期影响。
Diabetes Care. 2021 Sep 21;44(10):2216-24. doi: 10.2337/dc20-3097.
3
Long-Term Complications in Youth-Onset Type 2 Diabetes.青少年 2 型糖尿病的长期并发症。
N Engl J Med. 2021 Jul 29;385(5):416-426. doi: 10.1056/NEJMoa2100165.
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The First Genome-Wide Association Study for Type 2 Diabetes in Youth: The Progress in Diabetes Genetics in Youth (ProDiGY) Consortium.第一型糖尿病的全基因组关联研究:青少年糖尿病遗传学研究(ProDiGY)联盟。
Diabetes. 2021 Apr;70(4):996-1005. doi: 10.2337/db20-0443. Epub 2021 Jan 21.
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Association Between Fasting Glucose Variability in Young Adulthood and the Progression of Coronary Artery Calcification in Middle Age.青年期空腹血糖变异性与中年冠状动脉钙化进展的关系。
Diabetes Care. 2020 Oct;43(10):2574-2580. doi: 10.2337/dc20-0838. Epub 2020 Jul 30.
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Visit-to-visit variability of glycemia and vascular complications: the Hoorn Diabetes Care System cohort.血糖的随访间变异性与血管并发症:霍恩糖尿病护理系统队列研究。
Cardiovasc Diabetol. 2019 Dec 12;18(1):170. doi: 10.1186/s12933-019-0975-1.
7
Glycaemic variability in diabetes: clinical and therapeutic implications.糖尿病患者的血糖变异性:临床和治疗意义。
Lancet Diabetes Endocrinol. 2019 Mar;7(3):221-230. doi: 10.1016/S2213-8587(18)30136-0. Epub 2018 Aug 13.
8
The Legacy Effect in Type 2 Diabetes: Impact of Early Glycemic Control on Future Complications (The Diabetes & Aging Study).2 型糖尿病的遗留效应:早期血糖控制对未来并发症的影响(糖尿病与衰老研究)。
Diabetes Care. 2019 Mar;42(3):416-426. doi: 10.2337/dc17-1144. Epub 2018 Aug 13.
9
Haemoglobin A1c variability is a strong, independent predictor of all-cause mortality in patients with type 2 diabetes.糖化血红蛋白变异性是 2 型糖尿病患者全因死亡率的一个强有力的独立预测指标。
Diabetes Obes Metab. 2018 Aug;20(8):1885-1893. doi: 10.1111/dom.13306. Epub 2018 Apr 19.
10
Treatment of type 2 diabetes mellitus in elderly patients.老年2型糖尿病的治疗
Rev Clin Esp (Barc). 2018 Mar;218(2):74-88. doi: 10.1016/j.rce.2017.12.003. Epub 2018 Feb 1.

基于血糖控制持久性的 2 型糖尿病年轻成人的长期结局:来自 TODAY 队列研究的结果。

Long-term Outcomes Among Young Adults With Type 2 Diabetes Based on Durability of Glycemic Control: Results From the TODAY Cohort Study.

出版信息

Diabetes Care. 2022 Nov 1;45(11):2689-2697. doi: 10.2337/dc22-0784.

DOI:10.2337/dc22-0784
PMID:36190810
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9679266/
Abstract

OBJECTIVE

To examine the effect of different patterns of durable glycemic control on the development of comorbidities among youth with type 2 diabetes (T2D) and to assess the impact of fasting glucose (FG) variability on the clinical course of T2D.

RESEARCH DESIGN AND METHODS

From the Treatment Options for Type 2 Diabetes in Adolescents and Youth (TODAY) study, 457 participants (mean age, 14 years) with mean diabetes duration <2 years at entry and a minimum study follow-up of 10 years were included in these analyses. HbA1c, FG concentrations, and β-cell function estimates from oral glucose tolerance tests were measured longitudinally. Prevalence of comorbidities by glycemic control status after 10 years in the TODAY study was assessed.

RESULTS

Higher baseline HbA1c concentration, lower β-cell function, and maternal history of diabetes were strongly associated with loss of glycemic control in youth with T2D. Higher cumulative HbA1c concentration over 4 years and greater FG variability over a year within 3 years of diagnosis were related to higher prevalence of dyslipidemia, nephropathy, and retinopathy progression over the subsequent 10 years. A coefficient of variability in FG ≥8.3% predicted future loss of glycemic control and development of comorbidities.

CONCLUSIONS

Higher baseline HbA1c concentration and FG variability during year 1 accurately predicted youth with T2D who will experience metabolic decompensation and comorbidities. These values may be useful tools for clinicians when considering early intensification of therapy.

摘要

目的

研究不同持久血糖控制模式对 2 型糖尿病(T2D)青少年合并症发展的影响,并评估空腹血糖(FG)变异性对 T2D 临床病程的影响。

研究设计和方法

在青少年 2 型糖尿病治疗选择(TODAY)研究中,纳入了 457 名参与者(平均年龄 14 岁),他们在入组时的糖尿病病程<2 年,且至少有 10 年的研究随访。HbA1c、FG 浓度和口服葡萄糖耐量试验的β细胞功能估计值进行了纵向测量。在 TODAY 研究中,评估了 10 年后按血糖控制状态的合并症患病率。

结果

基线 HbA1c 浓度较高、β细胞功能较低和母亲有糖尿病病史与 T2D 青少年血糖控制的丧失密切相关。4 年内累积 HbA1c 浓度较高和诊断后 3 年内 1 年内 FG 变异性较大与随后 10 年内血脂异常、肾病和视网膜病变进展的发生率较高相关。FG 变异系数≥8.3%预测未来血糖控制丧失和合并症的发生。

结论

基线时较高的 HbA1c 浓度和 1 年内的 FG 变异性准确预测了将经历代谢失代偿和合并症的 T2D 青少年。这些值可能是临床医生在考虑早期强化治疗时的有用工具。