INCREASED ERYTHROCYTE AGGREGATION IN INSULIN-DEPENDENT DIABETES-MELLITUS AND ITS RELATIONSHIP TO PLASMA FACTORS - A MULTIVARIATE-ANALYSIS

被引:42
作者
ZIEGLER, O
GUERCI, B
MULLER, S
CANDILOROS, H
MEJEAN, L
DONNER, M
STOLTZ, JF
DROUIN, P
机构
[1] UNIV NANCY 1,CHU,HOP JEANNE ARC,MED SERV G,F-54201 TOUL,FRANCE
[2] UNIV NANCY 1,HOP JEANNE ARC,DEPT NUTR & MALAD METAB,TOUL,FRANCE
[3] INSERM,U284,F-54511 VANDOEUVRE NANCY,FRANCE
[4] INSERM,U308,F-54013 NANCY,FRANCE
来源
METABOLISM-CLINICAL AND EXPERIMENTAL | 1994年 / 43卷 / 09期
关键词
D O I
10.1016/0026-0495(94)90063-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Red blood cell aggregation in vitro (kinetics and shear resistance) was studied in 13 healthy controls and 13 type (insulin-dependent) diabetic patients free of severe degenerative complications who were matched for age, sex, and body mass index. Measurements were performed with a device that analyzes the laser light backscattered by a blood suspension. Both the velocity of rouleau formation and the cohesion of the rouleau network were significantly increased in diabetic patients. Plasma viscosity and whole-blood viscosity measured at low shear rate (0.95 s(-1)) were also significantly elevated in the diabetic group. Multivariate analyses of the whole population sample and the diabetic patients confirmed the influence of plasma proteins on the kinetics of aggregation. Fibrinogen levels, which were close to normal, affected mainly the shear resistance of the aggregates. Triglyceride and apolipoprotein (ape) B levels and indexes of metabolic control or protein glycation (fasting blood glucose and fructosamine) also appeared to influence markedly both the kinetics of rouleau formation and the cohesion of the rouleau networks. These theological abnormalities occurred in diabetic patients before the appearance of any severe degenerative complications. We suggest that these theological abnormalities are linked to plasma or erythrocyte factors, and are not due to angiopathy. Copyright (C) 1994 by W.B. Saunders Company
引用
收藏
页码:1182 / 1186
页数:5
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