CYCLOSPORINE-A DOES NOT DELAY INSULIN DEPENDENCY IN ASYMPTOMATIC IDDM PATIENTS

被引:10
作者
RAKOTOAMBININA, B
TIMSIT, J
DESCHAMPS, I
LABORDE, K
JOS, J
BOITARD, C
ASSAN, R
ROBERT, JJ
机构
[1] HOP NECKER ENFANTS MALAD,DEPT PEDIAT DIABETOL,UNITE DIABET ENFANT,F-75015 PARIS,FRANCE
[2] HOP NECKER ENFANTS MALAD,INSERM,U30,F-75015 PARIS,FRANCE
[3] HOP NECKER ENFANTS MALAD,DEPT CLIN IMMUNOL,DIABETOL UNIT,F-75015 PARIS,FRANCE
[4] HOP NECKER ENFANTS MALAD,INSERM,U25,F-75015 PARIS,FRANCE
[5] HOP BICHAT,DEPT DIABETOL,F-75877 PARIS,FRANCE
关键词
D O I
10.2337/diacare.18.11.1487
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE - To measure the effects of cyclosporin A (CyA) with no insulin therapy on glucose tolerance and beta-cell function in the preclinical phase of insulin-dependent diabetes mellitus (IDDM). RESEARCH DESIGN AND METHODS- beta-cell responses to the intravenous glucose tolerance test (IVGTT), hyperglycemic clamp, intravenous arginine, and intravenous glucagon were evaluated before and after a 6-month course of CyA in seven patients (mean age 19.6 years) with asymptomatic IDDM. RESULTS - Initial insulin secretary responses were severely decreased when the patients were compared with eight healthy control subjects: IVGTT (1 + 3 min): 106 +/- 16 vs. 884 +/- 190 pmol/l (P < 0.001); hyperglycemic clamp: 102 +/- 16 vs. 310 +/- 42 pmol/l(P < 0.001); intravenous arginine: 346 +/- 72 vs. 1104 +/- 168 pmol/l (P < 0.01); and intravenous glucagon: 170 +/- 37 vs. 247 +/- 35 pmol/l(NS). The beta-cell responses remained markedly abnormal after 6 months of CyA, although the response to intravenous glucose and oral glucose tolerance tests improved in three subjects. All the patients became insulin-dependent after 5-36 months. CONCLUSIONS - CyA alone is not a suitable treatment for asymptomatic IDDM. Earlier identification of subjects with substantial beta-cell secretory capacity and newer nontoxic intervention strategies are required for the prevention of IDDM.
引用
收藏
页码:1487 / 1490
页数:4
相关论文
共 10 条
[1]  
[Anonymous], 1988, DIABETES, V37, P1574, DOI 10.2337/diabetes.37.11.15742903105
[2]   PLASMA-C-PEPTIDE LEVELS AND CLINICAL REMISSIONS IN RECENT-ONSET TYPE-I DIABETIC-PATIENTS TREATED WITH CYCLOSPORINE-A AND INSULIN [J].
ASSAN, R ;
FEUTREN, G ;
SIRMAI, J ;
LABORIE, C ;
BOITARD, C ;
VEXIAU, P ;
DUROSTU, H ;
RODIER, M ;
FIGONI, M ;
VAGUE, P ;
HORS, J ;
BACH, JF .
DIABETES, 1990, 39 (07) :768-774
[3]   ANALYSIS OF METABOLIC PROGRESSION TO TYPE-I DIABETES IN ICA+ RELATIVES OF PATIENTS WITH TYPE-I DIABETES [J].
BLEICH, D ;
JACKSON, RA ;
SOELDNER, JS ;
EISENBARTH, GS .
DIABETES CARE, 1990, 13 (02) :111-118
[4]   LIMITED DURATION OF REMISSION OF INSULIN DEPENDENCY IN CHILDREN WITH RECENT OVERT TYPE-I DIABETES TREATED WITH LOW-DOSE CYCLOSPORINE [J].
BOUGNERES, PF ;
LANDAIS, P ;
BOISSON, C ;
CAREL, JC ;
FRAMENT, N ;
BOITARD, C ;
CHAUSSAIN, JL ;
BACH, JF .
DIABETES, 1990, 39 (10) :1264-1272
[5]  
CAREL JC, 1995, DIABETES, V44, pA136
[6]   DIAGNOSIS OF PRE-TYPE-1 DIABETES [J].
CHASE, HP ;
VOSS, MA ;
BUTLERSIMON, N ;
HOOPS, S ;
OBRIEN, D ;
DOBERSEN, MJ .
JOURNAL OF PEDIATRICS, 1987, 111 (06) :807-812
[7]  
FEUTREN G, 1986, LANCET, V2, P119
[8]  
FEUTREN G, 1993, NEW ENGL J MED, V326, P1654
[9]  
Skyler JS, 1993, DIABETES REV, V1, P15
[10]  
Weiner H L, 1993, Autoimmunity, V15 Suppl, P6, DOI 10.3109/08916939309008850