原发性胰岛素依赖(I型)与继发性胰岛素依赖(II型)糖尿病患者胰岛素抗体的比较研究

Medecine interne Pub Date : 1989-10-01
C Ionescu-Tîrgovişte, Z Mirodon, D Cheţa, E Sântu, M Simionescu, A Nicolau, I Mincu
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摘要

采用RIA法测定404例胰岛素治疗糖尿病患者的胰岛素抗体(%结合),分为两组:(A)原发性胰岛素依赖患者(I型糖尿病):300例,170例,130例,平均年龄+/- SD 29.2 +/- 7.5年,疾病和胰岛素治疗时间7.7 +/- 6年;(B) II型糖尿病需要胰岛素(继发性胰岛素依赖)患者:104例,男47例,女57例,年龄53.4 +/- 9.2年,糖尿病病程13.1 +/- 8.3年,胰岛素治疗病程3.1 +/- 2.1年。两组患者使用相同类型的胰岛素制剂。297例均为(A)组,同时测定空腹c肽。继发性胰岛素依赖患者的胰岛素抗体滴度显著(p < 0.001)高于原发性胰岛素依赖患者(22.96 +/- 15.1% vs 10.25 +/- 9.89),尽管后者的胰岛素治疗时间较长;58例结合能力小于10%的1型糖尿病患者的c肽均值显著低于11例结合能力大于20%的1型糖尿病患者(0.091 +/- 0.57 vs 0.273 +/- 0.37 pmol/ml) (p < 0.001);胰岛素抗体与代谢控制、胰岛素需求或慢性并发症之间没有相关性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative study of insulin antibodies in diabetic patients with primary insulin-dependence (type I) and secondary insulin-dependence (type II).

Insulin antibodies (% binding) were determined by RIA method in 404 insulin-treated diabetic patients divided into two groups: (A) primary insulin-dependent patients (Type I diabetes): 300 cases, 170 M, 130 F, mean age +/- SD 29.2 +/- 7.5 yrs, disease and insulin treatment duration 7.7 +/- 6 yrs: (B) Type II diabetic patients needing insulin (secondary insulin-dependence): 104 cases, 47 M, 57 F, aged 53.4 +/- 9.2 yrs, duration of diabetes 13.1 +/- 8.3 yrs, and of insulin treatment 3.1 +/- 2.1 yrs. Both groups of patients were with the same types of insulin preparations. In 297 cases, all belonging to group (A), fasting C-peptide was also determined. The titre of insulin antibodies was significantly (p less than 0.001) higher in patients with secondary insulin dependence than in those with primary insulin dependence (22.96 +/- 15.1% vs 10.25 +/- 9.89) in spite of the longer duration of insulin treatment in the later group; the mean C-peptide value found in 58 Type I diabetic patients with a binding capacity less than 10% was significantly lower (p less than 0.001) than that found in 11 Type I diabetic cases with a binding capacity greater than 20% (0.091 +/- 0.57 vs 0.273 +/- 0.37 pmol/ml); no correlation was found between insulin antibodies and metabolic control, insulin requirements or chronic complications.

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