Neurodevelopmental outcome at 2 years in offspring of women randomised to metformin or insulin treatment for gestational diabetes

被引:55
|
作者
Wouldes, Trecia A. [1 ]
Battin, Malcolm [2 ]
Coat, Suzette [3 ]
Rush, Elaine C. [4 ]
Hague, William M. [5 ]
Rowan, Janet A. [6 ]
机构
[1] Fac Med & Hlth Sci, Dept Psychol Med, Private Bag 92019, Auckland 1142, New Zealand
[2] Auckland City Hosp, New Born Serv, Auckland, New Zealand
[3] Univ Adelaide, Robinson Res Inst, Adelaide, SA, Australia
[4] Auckland Univ Technol, Ctr Child Hlth Res, Auckland, New Zealand
[5] Univ Adelaide, Women & Childrens Hosp, Dept Obstet, Adelaide, SA, Australia
[6] Auckland City Hosp, Dept Obstet, Natl Womens Hlth, Auckland, New Zealand
基金
英国医学研究理事会;
关键词
AGE-CHILDREN BORN; SCHOOL-AGE; FOLLOW-UP; MELLITUS; MOTHERS; PREGNANCY; INFANTS;
D O I
10.1136/archdischild-2015-309602
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objective Gestational diabetes mellitus (GDM) is a common complication of pregnancy and is increasingly being treated with metformin that crosses the placenta rather than insulin, which does not. This study seeks to examine the neurodevelopment of offspring of women treated with metformin or insulin for GDM. Design We performed a prospective follow-up study of children whose mothers had been randomly assigned at 20-33 weeks gestation to treatment with metformin or insulin for GDM. Of the 211 children followed up at 2 years, 128 were from Auckland, New Zealand (64 metformin vs 64 insulin), and 83 from Adelaide, Australia (39 metformin vs 49 insulin). Neurodevelopment was examined with the Bayley Scales of Infant Development V.2 mental development index (MDI) and psychomotor development index (PDI). Clinical and demographic background characteristics were obtained at enrolment, birth and follow-up. Results No significant differences were found between treatment groups in clinical or demographic characteristics. The MDI and PDI composite scores were tested with general linear models. No significant differences were found between metformin and insulin, respectively, in New Zealand (MDI, M=83.6 vs 86.9 and PDI, M=83.4 vs M=85.2) or Australia (MDI, M=102.5 vs M=98.4 and PDI, M=105.6 vs M=99.9) and no interactions observed. The differences in neurodevelopmental outcomes between the Auckland and Adelaide cohorts were explained by parental ethnicity, infant birth weight >4000 g, neonatal hypoglycaemia, maternal glycaemia and smoking in the household. Conclusions This study provides additional data supporting the safety of metformin in the treatment of GDM.
引用
收藏
页码:F488 / F493
页数:6
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