PREDICTION OF PERSISTENT CARBOHYDRATE INTOLERANCE IN PATIENTS WITH GESTATIONAL DIABETES

被引:37
作者
LAM, KSL
LI, DF
LAUDER, IJ
LEE, CP
KUNG, AWC
MA, JTC
机构
[1] UNIV HONG KONG,DEPT MED,HONG KONG,HONG KONG
[2] UNIV HONG KONG,DEPT OBSTET & GYNAECOL,HONG KONG,HONG KONG
[3] UNIV HONG KONG,DEPT STAT,HONG KONG,HONG KONG
关键词
GESTATIONAL DIABETES-MELLITUS; ORAL GLUCOSE TOLERANCE TEST; POSTPARTUM GLUCOSE TOLERANCE; PREDICTION; LOGISTIC DISCRIMINATION;
D O I
10.1016/0168-8227(91)90075-O
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A 12-month prospective study was carried out in 120 Chinese patients with gestational diabetes who were found to have persistent carbohydrate intolerance at 6 weeks postpartum. The 75 g OGTT and WHO diagnostic criteria were employed for both antepartum and postpartum assessment. By 12 months, persistent carbohydrate intolerance was found in 13.3% of the patients only, 6 patients were diabetic while 10 had impaired glucose tolerance. Of those whose carbohydrate tolerance reverted to normal, 85% did so within the first 6 months. The clinical variables were analysed by multiple discriminant analysis using the logistic model. Five prognostic variables which were predictive of persistent carbohydrate intolerance at 12 months were identified. In order of decreasing predictive value, these included a high fasting glucose during pregnancy and at the first postnatal visit, a high antepartum 2 h blood glucose, the requirement of insulin during pregnancy, and a high postpartum 2 h blood glucose. Macrosomia, gestational age at diagnosis and a family history of diabetes were not predictive of persistent carbohydrate intolerance. Multiparity, maternal age and body mass index were of marginal significance only. The fitted logistic model provides a mechanism to estimate the probability of persistent carbohydrate intolerance. Such information will be helpful in patient counselling and in the efficient planning of postpartum medical follow-up.
引用
收藏
页码:181 / 186
页数:6
相关论文
共 20 条
  • [1] SEPARATE SAMPLE LOGISTIC DISCRIMINATION
    ANDERSON, JA
    [J]. BIOMETRIKA, 1972, 59 (01) : 19 - 35
  • [2] [Anonymous], 1985, DIABETOLOGIA, V28, P615, DOI [10.1007/BF00290267, DOI 10.1007/BF00290267]
  • [3] Cox D.R., 1974, THEORETICAL STAT
  • [4] Cox D.R., 1989, ANAL BINARY DATA, V32
  • [5] DAVID AP, 1976, BIOMETRICS, V32, P647
  • [6] Duncan JM, 1882, T OBSTET SOC LONDON, V24, P256, DOI DOI 10.1172/JCI24531
  • [7] GESTATIONAL DIABETES - INFANT MALFORMATIONS AND SUBSEQUENT MATERNAL GLUCOSE-TOLERANCE
    FARRELL, J
    FORREST, JM
    STOREY, GNB
    YUE, DK
    SHEARMAN, RP
    TURTLE, JR
    [J]. AUSTRALIAN & NEW ZEALAND JOURNAL OF OBSTETRICS & GYNAECOLOGY, 1986, 26 (01) : 11 - 16
  • [8] FREINKEL N, 1985, ADV EXP MED BIOL, V189, P47
  • [9] THE LONG-TERM FOLLOW-UP OF WOMEN WITH GESTATIONAL DIABETES
    GRANT, PT
    OATS, JN
    BEISCHER, NA
    [J]. AUSTRALIAN & NEW ZEALAND JOURNAL OF OBSTETRICS & GYNAECOLOGY, 1986, 26 (01) : 17 - 22
  • [10] LI, 1987, BR J OBSTET GYNAECOL, V97, P847