FOLLOW-UP OF WOMEN WITH PREVIOUS GDM - INSULIN, C-PEPTIDE, AND PROINSULIN RESPONSES TO ORAL GLUCOSE-LOAD

被引:68
作者
PERSSON, B
HANSON, U
HARTLING, SG
BINDER, C
机构
[1] HAGEDORN RES LAB,DK-2820 GENTOFTE,DENMARK
[2] HVIDOVRE UNIV HOSP,HVIDOVRE,DENMARK
[3] ST GORANS UNIV HOSP,DEPT PEDIAT,S-11281 STOCKHOLM,SWEDEN
[4] KAROLINSKA INST,KAROLINSKA HOSP,DEPT OBSTET & GYNECOL,S-10401 STOCKHOLM 60,SWEDEN
[5] STENO MEM HOSP,DK-2820 GENTOFTE,DENMARK
关键词
D O I
10.2337/diab.40.2.S136
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Gestational diabetes mellitus (GDM) is a strong predictor of glucose intolerance later in life. Former GDM (n = 145) and control (n = 41) subjects were studied 3-4 yr after the index pregnancy. They were subjected to a 75-g oral glucose tolerance test (OGTT) with measurements of insulin, C-peptide, and proinsulin in the basal state and every 30 min for 180 min. In the former GDM group, 5 subjects (3.4%) had developed non-insulin-dependent diabetes mellitus (NIDDM), and 32 (22%) had developed impaired glucose tolerance (IGT; by World Health Organization criteria). In the control group, 2 (4%) had IGT. In the GDM group, IGT or NIDDM was significantly associated with obesity (body mass index [BMI] greater-than-or-equal-to 25 kg/m2) and earlier diagnosis of GDM during pregnancy (P < 0.001). Nonobese (BMI < 25 kg/m2) GDM subjects with normal glucose tolerance at follow-up had significantly higher mean glucose (P < 0.01), insulin (P < 0.05), and proinsulin (P < 0.001) values during the OGTT than control subjects, whereas there was no significant difference in C-peptide values. A comparison between control subjects with normal OGTT and BMI < 25 kg/m2 (n = 39) and GDM subjects (n = 39) selected to have a comparable area under the glucose curve, BMI, and age demonstrated no group differences in glucose, C-peptide, or insulin levels, whereas the proinsulin levels were significantly higher (P < 0.001) during the glucose load. The molar ratio between proinsulin and insulin was also significantly higher among the former GDM subjects. We speculate that an elevated proinsulin-insulin ratio in women with previous GDM could be a marker for later development of NIDDM.
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收藏
页码:136 / 141
页数:6
相关论文
共 23 条
[1]   SUBCLINICAL ABNORMALITIES OF GLUCOSE-METABOLISM IN SUBJECTS WITH PREVIOUS GESTATIONAL DIABETES [J].
CATALANO, PM ;
BERNSTEIN, IM ;
WOLFE, RR ;
SRIKANTA, S ;
TYZBIR, E ;
SIMS, EAH .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1986, 155 (06) :1255-1262
[2]   DIRECT MEASUREMENT OF PLASMA PROINSULIN IN NORMAL AND DIABETIC SUBJECTS [J].
DUCKWORT.WC ;
KITABCHI, AE ;
HEINEMAN.M .
AMERICAN JOURNAL OF MEDICINE, 1972, 53 (04) :418-&
[3]   GLUCOSE-TOLERANCE, INSULIN RELEASE, AND INSULIN SENSITIVITY IN NORMAL-WEIGHT WOMEN WITH PREVIOUS GESTATIONAL DIABETES-MELLITUS [J].
EFENDIC, S ;
HANSON, U ;
PERSSON, B ;
WAJNGOT, A ;
LUFT, R .
DIABETES, 1987, 36 (04) :413-419
[4]   CARBOHYDRATE-METABOLISM IN PREGNANCY .1. DIURNAL PLASMA GLUCOSE PROFILE IN NORMAL AND DIABETIC WOMEN [J].
GILLMER, MDG ;
BEARD, RW ;
BROOKE, FM ;
OAKLEY, NW .
BRITISH MEDICAL JOURNAL, 1975, 3 (5980) :399-402
[5]  
GORDEN P, 1974, DIABETOLOGIA, V10, P459
[6]  
Hadden D R, 1985, Diabetes, V34 Suppl 2, P8
[7]   ELEVATED PROINSULIN IN HEALTHY SIBLINGS OF IDDM PATIENTS INDEPENDENT OF HLA IDENTITY [J].
HARTLING, SG ;
LINDGREN, F ;
DAHLQVIST, G ;
PERSSON, B ;
BINDER, C .
DIABETES, 1989, 38 (10) :1271-1274
[8]   ELISA FOR HUMAN PROINSULIN [J].
HARTLING, SG ;
DINESEN, B ;
KAPPELGARD, AM ;
FABER, OK ;
BINDER, C .
CLINICA CHIMICA ACTA, 1986, 156 (03) :289-297
[9]   EVIDENCE OF BETA-CELL DYSFUNCTION WHICH DOES NOT LEAD ON TO DIABETES - A STUDY OF IDENTICAL-TWINS OF INSULIN-DEPENDENT DIABETICS [J].
HEATON, DA ;
MILLWARD, BA ;
GRAY, P ;
TUN, Y ;
HALES, CN ;
PYKE, DA ;
LESLIE, RDG .
BRITISH MEDICAL JOURNAL, 1987, 294 (6565) :145-146
[10]   INCREASED PROINSULIN LEVELS AS AN EARLY INDICATOR OF B-CELL DYSFUNCTION IN NON-DIABETIC TWINS OF TYPE-1 (INSULIN-DEPENDENT) DIABETIC-PATIENTS [J].
HEATON, DA ;
MILLWARD, BA ;
GRAY, IP ;
TUN, Y ;
HALES, CN ;
PYKE, DA ;
LESLIE, RDG .
DIABETOLOGIA, 1988, 31 (03) :182-184