Determinants of Small for Gestational Age in Women With Type 2 Diabetes in Pregnancy: Who Should Receive Metformin?

Author:

Feig Denice S.123ORCID,Zinman Bernard123ORCID,Asztalos Elizabeth4,Donovan Lois E.56,Shah Prakesh S.37,Sanchez J. Johanna48,Tomlinson George19,Murphy Kellie E.12310

Affiliation:

1. 1Department of Medicine, University of Toronto, Toronto, Ontario, Canada

2. 2Lunenfeld-Tanenbaum Research Institute, Toronto, Ontario, Canada

3. 3Sinai Health System, Mount Sinai Hospital, Toronto, Ontario, Canada

4. 4Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada

5. 6Departments of Medicine and Obstetrics & Gynecology, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada

6. 7Alberta Children’s Hospital Research Institute, Calgary, Alberta, Canada

7. 8Department of Paediatrics, University of Toronto, Toronto, Ontario, Canada

8. 5Sunnybrook Research Institute, Toronto, Ontario, Canada

9. 9Department of Medicine, University Health Network, Toronto, Ontario, Canada

10. 10Department of Obstetrics & Gynecology, University of Toronto, Toronto, Ontario, Canada

Abstract

OBJECTIVE In the MiTy (Metformin in Women With Type 2 Diabetes in Pregnancy) randomized trial of metformin versus placebo added to insulin, we found numerous benefits with metformin but identified an increased proportion of infants who were small for gestational age (SGA). We aimed to determine the predictors of SGA in order to individualize care. RESEARCH DESIGN AND METHODS Using logistic regression, we assessed baseline maternal characteristics as predictors of SGA. We compared maternal/neonatal outcomes in SGA metformin and placebo groups using the t, χ2, or Fisher exact test, as appropriate. RESULTS Among the 502 mothers, 460 infants were eligible for this study. There were 30 infants with SGA in the metformin group (12.9%) and 15 in the placebo group (6.6%) (P = 0.026). Among SGA infants, those in the metformin group were delivered significantly later than those in the placebo group (37.2 vs. 35.3 weeks; P = 0.038). In adjusted analyses, presence of a comorbidity (chronic hypertension and/or nephropathy) (odds ratio [OR] 3.05; 95% CI 1.58–5.81) and metformin use (OR 2.26; 95% CI 1.19–4.74) were predictive of SGA. The absolute risk of SGA was much higher in women receiving metformin with comorbidity compared with women receiving metformin without comorbidity (25.0% vs. 9.8%). CONCLUSIONS In this study, we observed a high percentage of SGA births among women with type 2 diabetes and chronic hypertension and/or nephropathy who were treated with metformin. Therefore, with the aim of reducing SGA, it is reasonable to be cautious in our use of metformin in those with type 2 diabetes and chronic hypertension or nephropathy in pregnancy.

Publisher

American Diabetes Association

Subject

Advanced and Specialized Nursing,Endocrinology, Diabetes and Metabolism,Internal Medicine

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