In human gestational diabetes mellitus congenital malformations are related to pre-pregnancy body mass index and to severity of diabetes

被引:60
作者
García-Patterson, A
Erdozain, L
Ginovart, G
Adelantado, JM
Cubero, JM
Gallo, G
de Leiva, A
Corcoy, R
机构
[1] Autonomous Univ Barcelona, Hosp Holy Cross & St Paul, Dept Endocrinol & Nutr, Barcelona 08025, Spain
[2] Autonomous Univ Barcelona, Hosp Holy Cross & St Paul, Dept Pediat, Barcelona 08025, Spain
[3] Autonomous Univ Barcelona, Hosp Holy Cross & St Paul, Dept Obstet & Gynecol, Barcelona 08025, Spain
[4] Ctr Network Carlos III Hlth Inst, Madrid, Spain
关键词
gestational diabetes mellitus; congenital malformations; body mass index; hyperglycaemia;
D O I
10.1007/s00125-004-1337-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims/hypothesis. This study analysed the relationship between congenital malformations (CM) and severity of gestational diabetes mellitus. Methods. A cohort of 2060 infants of mothers with gestational diabetes was studied. Universal screening and 3(rd) Workshop-Conference criteria were used to diagnose gestational diabetes. The severity of diabetes was assessed on the basis of previous hyperglycaemia, blood glucose values in diagnostic OGTT, area under the glucose curve, gestational age and HbA(1)c at diagnosis, insulin requirements during pregnancy, and OGTT after delivery. Potentially confounding variables (age, pre-pregnancy BMI, smoking) were considered. The relationship of potential predictors with CM was analysed with several multivariate logistic regression analyses. Results. The rate of CM was 6% for minor and 3.8% for major malformations (1.4% heart, 0.8% renal/urinary, 0.7% skeletal, 0.3% hypospadias, 0.2% central nervous system, 0.2% cleft lip/palate, 0.1% digestive tract, 0.3% other). In the final models, forward logistic regression analysis identified pre-pregnancy BMI as the predictor of CM (area under receiver operating characteristic curve 0.616); in the backward analysis additional predictors were 1-h blood glucose in diagnostic OGTT and gestational age at diagnosis (area under receiver operating characteristic curve 0.646). Both BMI and severity of gestational diabetes were predictors of heart and minor CM, whereas BMI predicted renal/urinary CM and severity of diabetes predicted skeletal CM. Conclusions/interpretation. In these infants of mothers with gestational diabetes, severity of diabetes and pre-pregnancy BMI were predictors of CM, in accordance with the well-documented pathogenic role of BMI (in the general population) and hyperglycaemia (in diabetic pregnancy). BMI was the main predictor of more prevalent CM.
引用
收藏
页码:509 / 514
页数:6
相关论文
共 34 条
[1]  
Alberti KGMM, 1998, DIABETIC MED, V15, P539, DOI 10.1002/(SICI)1096-9136(199807)15:7<539::AID-DIA668>3.0.CO
[2]  
2-S
[3]   TRANS-PLACENTAL PASSAGE OF INSULIN COMPLEXED TO ANTIBODY [J].
BAUMAN, WA ;
YALOW, RS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (07) :4588-4590
[4]   ROLE OF HUMAN PLACENTA IN TRANSFER AND METABOLISM OF INSULIN [J].
BUSE, MG ;
BUSE, J ;
ROBERTS, WJ .
JOURNAL OF CLINICAL INVESTIGATION, 1962, 41 (01) :29-&
[5]   THE PATHOGENESIS OF CONGENITAL-MALFORMATIONS IN DIABETIC PREGNANCY [J].
ERIKSSON, UJ .
DIABETES-METABOLISM REVIEWS, 1995, 11 (01) :63-82
[6]   IS MATERNAL OBESITY A RISK FACTOR FOR OPEN NEURAL-TUBE DEFECTS [J].
HADDOW, JE ;
PALOMAKI, GE .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1995, 172 (01) :245-246
[7]   INTERNATIONAL CRITERIA FOR THE DIAGNOSIS OF DIABETES AND IMPAIRED GLUCOSE-TOLERANCE [J].
HARRIS, MI ;
HADDEN, WC ;
KNOWLER, WC ;
BENNETT, PH .
DIABETES CARE, 1985, 8 (06) :562-567
[8]   Effects of hyperinsulinemia and obesity on risk of neural tube defects among Mexican Americans [J].
Hendricks, KA ;
Nuno, OM ;
Suarez, L ;
Larsen, R .
EPIDEMIOLOGY, 2001, 12 (06) :630-635
[9]   Upstream AUGs in embryonic proinsulin mRNA control its low translation level [J].
Hernández-Sánchez, C ;
Mansilla, A ;
de la Rosa, EJ ;
Pollerberg, GE ;
Martínez-Salas, E ;
de Pablo, F .
EMBO JOURNAL, 2003, 22 (20) :5582-5592
[10]  
Heyner S., 1990, Current Topics in Developmental Biology, V24, P137, DOI 10.1016/S0070-2153(08)60086-1