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时机至关重要:发病年龄影响2型糖尿病患者长期视网膜病变风险,且独立于传统风险因素。

Timing is everything: age of onset influences long-term retinopathy risk in type 2 diabetes, independent of traditional risk factors.

作者信息

Wong Jencia, Molyneaux Lynda, Constantino Maria, Twigg Stephen M, Yue Dennis K

机构信息

Diabetes Centre, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia.

出版信息

Diabetes Care. 2008 Oct;31(10):1985-90. doi: 10.2337/dc08-0580. Epub 2008 Jul 15.

Abstract

OBJECTIVE

To test the hypothesis that age of type 2 diabetes onset influences inherent susceptibility to diabetic retinopathy, independent of disease duration and degree of hyperglycemia.

RESEARCH DESIGN AND METHODS

Retinopathy data from 624 patients with a type 2 diabetes duration of 20-30 years (group A) were analyzed by stratifying patients according to age of onset of diabetes and glycemic control. Retinopathy status was scored clinically as per a modified Early Treatment Diabetic Retinopathy Study (ETDRS) severity scale. To obviate possible bias due to a higher attrition from comorbidities in those with later-onset diabetes and retinopathy, 852 patients with type 2 diabetes of shorter duration (10-12 years, group B) were similarly studied.

RESULTS

Prevalence and severity of retinopathy was significantly higher in the younger-onset, group A patients. When further stratified according to mean A1C, retinopathy risk remained increased in younger-onset patients. The greatest impact was seen in those with a mean A1C >9% (odds ratio [OR] for retinopathy 16.6, 7.5, and 2.7 for age of diagnosis <45, 45-55, and >55 years, respectively, P = 0.003). By logistic regression, earlier type 2 diabetes onset is associated with increased retinopathy risk, independent of traditional risk factors (OR of retinopathy 1.9, 1.1, and 1 for age of onset <45, 45-55, and >55 years, respectively). Similar results were found in group B patients.

CONCLUSIONS

These data suggest an increased inherent susceptibility to diabetic retinopathy with earlier-onset type 2 diabetes. This further supports the importance of delaying development of diabetes and also implies a need for more stringent metabolic targets for younger individuals.

摘要

目的

检验2型糖尿病发病年龄会影响糖尿病视网膜病变的内在易感性这一假设,该易感性独立于疾病病程和高血糖程度。

研究设计与方法

对624例2型糖尿病病程为20 - 30年的患者(A组)的视网膜病变数据进行分析,根据糖尿病发病年龄和血糖控制情况对患者进行分层。视网膜病变状态根据改良的早期糖尿病视网膜病变研究(ETDRS)严重程度量表进行临床评分。为避免因发病较晚的糖尿病和视网膜病变患者合并症导致的更高损耗可能产生的偏差,对852例病程较短(10 - 12年)的2型糖尿病患者(B组)进行了类似研究。

结果

A组发病年龄较小的患者中,视网膜病变的患病率和严重程度显著更高。当根据平均糖化血红蛋白(A1C)进一步分层时,发病年龄较小的患者视网膜病变风险仍然增加。在平均A1C>9%的患者中影响最大(诊断年龄<45岁、45 - 55岁和>55岁的患者发生视网膜病变的比值比[OR]分别为16.6、7.5和2.7,P = 0.003)。通过逻辑回归分析,2型糖尿病发病较早与视网膜病变风险增加相关,独立于传统风险因素(发病年龄<45岁、45 - 55岁和>55岁的患者发生视网膜病变的OR分别为1.9、1.1和1)。在B组患者中也发现了类似结果。

结论

这些数据表明,2型糖尿病发病较早会增加糖尿病视网膜病变的内在易感性。这进一步支持了延缓糖尿病发生的重要性,也意味着需要为年轻个体设定更严格的代谢目标。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11e6/2551640/90be1397fadc/zdc0100872070001.jpg

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