弹性蛋白衍生肽与微血管并发症发生的关系

George Nicoloff , S. Baydanoff , N. Stanimorova , Ch. Petrova , P. Cristova
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引用次数: 20

摘要

采用酶联免疫吸附试验(ELISA)检测28例1型(胰岛素依赖型)糖尿病患儿(平均年龄11.6±2.8岁,糖尿病病程5.1±2.5年)血清弹性蛋白衍生肽(EDP)水平。这些儿童均无血管并发症的临床或实验室证据。研究人员对这些儿童进行了为期6年的随访,并将24名年龄和性别相近的健康儿童作为对照组。调查期间,有10例糖尿病患者出现EDP水平升高,其中9例糖尿病病程超过5年,1例少于5年。其中7例出现糖尿病微血管并发症。本组中,EDP与年龄独立相关(r=。39, P=.047),视网膜病变(r=。48, P= 0.034),晚期糖基化终产物(AGE)抗体(r= 0.034)。52岁的P = .018)。这项初步研究的数据还不够强大,不足以表明EDP是微血管并发症后续发展的有用预测指标。这可能是由于受试者数量少,研究持续时间短,测量EDP或终点的方式,或测量EDP的频率。需要在更大的人群中进行更长期的前瞻性研究,以确定EDP作为糖尿病微血管并发症发展的早期标志物的作用。
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Relationship between elastin-derived peptides and the development of microvascular complications

Levels of elastin-derived peptides (EDP) were determined by enzyme-linked immunosorbent assay (ELISA) in sera of 28 children with Type 1 (insulin-dependent) diabetes mellitus (mean age 11.6±2.8 years, diabetes duration 5.1±2.5 years). None of the children had clinical or laboratory evidence of vascular complications. The children were followed over a period of 6 years, and 24 healthy children of similar age and sex served as a control group. During the investigative period, 10 diabetic patients had increased EDP levels, with 9 having been diabetic for more than 5 years and 1 patient less than 5 years. Seven of these patients developed diabetic microvascular complications. In this group, EDP were independently associated with age (r=.39, P=.047), retinopathy (r=.48, P=.034), and antibodies to advanced glycation endproducts (AGE) (r=.52, P=.018). The data of this pilot study are not strong enough to appear that EDP are a useful predictor of subsequent development of microvascular complications. This may be due to the small number of subjects, short duration of the study, manner in which EDP or the endpoints were measured, or frequency of which EDP measurements were made. Further prospective and longer studies of larger populations are needed to identify the role of EDP as an early marker for the development of diabetic microvascular complications.

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