American Journal of Obstetrics & Gynecology
Volume 182, Issue 2 , Pages 313-320, February 2000

Patterns of congenital anomalies and relationship to initial maternal fasting glucose levels in pregnancies complicated by type 2 and gestational diabetes☆☆

  • Ute M. Schaefer-Graf, MD

      Affiliations

    • Department of Obstetrics and Gynecology Los Angeles, California
    • University of Southern California School of Medicine, and the Department of Perinatal Medicine, Hospital Neukoelln, and the Department of Obstetrics, Charitè Campus Virchow-Klinikum, Humboldt University. Los Angeles, California
  • ,
  • Thomas A. Buchanan, MD

      Affiliations

    • Department of Obstetrics and Gynecology Los Angeles, California
    • Department of Medicine Los Angeles, California
  • ,
  • Anny Xiang, PhD

      Affiliations

    • Department of Preventive Medicine Los Angeles, California
  • ,
  • Giuliana Songster, MD

      Affiliations

    • Department of Obstetrics and Gynecology Los Angeles, California
  • ,
  • Martin Montoro, MD

      Affiliations

    • Department of Obstetrics and Gynecology Los Angeles, California
  • ,
  • Siri L. Kjos, MD

      Affiliations

    • Department of Obstetrics and Gynecology Los Angeles, California

Received 26 March 1999; received in revised form 2 August 1999; accepted 23 September 1999.

Abstract 

Objectives: We sought to determine the types of congenital anomalies affecting infants of women with gestational diabetes mellitus or type 2 diabetes and to examine the relationship between those malformation types and measures of initial glycemia of women at entry into prenatal care with type 2 diabetes or at time of diagnosis in women with gestational diabetes mellitus. Study Design: A total of 4180 pregnancies complicated by gestational diabetes mellitus (n = 3764) or type 2 diabetes (n = 416) that were delivered after 20 weeks of gestation were reviewed for the presence of congenital malformations diagnosed before hospital discharge. Anomalies were categorized as being absent, minor, major, genetic syndromes, or aneuploidies. Major anomalies were further categorized by the number and type of affected organ systems. In addition to maternal clinical and historical parameters, the initial fasting serum glucose either from the diagnostic glucose tolerance test (gestational diabetes mellitus) or at entry to prenatal care (type 2 diabetes) and the initial glycosylated hemoglobin before insulin therapy were examined for a relationship to anomalies. Results: The initial fasting serum glucose and glycosylated hemoglobin levels were significantly higher in pregnancies with major (n = 143) and minor (n = 112) anomalies and genetic syndromes (n = 9) compared with pregnancies with no anomalies (n = 3895). Of those pregnancies with major anomalies, the most commonly affected organ systems were the cardiac (37.6%), musculoskeletal (14.7%), and central nervous systems (9.8%) and anomalies involving multiple organ systems (16%). There was no increased predominance of any specific organ system involvement seen with increasing fasting serum glucose levels in pregnancies with major congenital anomalies. Pregnancies with major anomalies affecting multiple organ systems had significantly higher initial fasting serum glucose levels (166 ± 64 mg/dL) compared with pregnancies in which one organ system was affected (141 ± 55 mg/dL, P < .04) or no organ systems were affected (115 ± 38 mg/dL, P < .0001). Conclusion: Congenital anomalies in offspring of women with gestational and type 2 diabetes affect the same organ systems that have been previously described in pregnancies complicated by type 1 diabetes. Increasing hyperglycemia at diagnosis or presentation for care was associated with an increasing risk of anomalies in general and with anomalies involving multiple organ systems without a preferential increase in involvement of specific organ system. (Am J Obstet Gynecol 2000;182:313-20.)

Keywords:  Type 2 diabetes mellitus, gestational diabetes mellitus, congenital anomaly, fasting serum glucose, organ system

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 Supported in part by grant M 01-RR43 from the General Clinical Research Center Branch, National Center for Research Resources, and the US National Institutes of Health.

☆☆ Reprint requests: Siri L. Kjos, MD, Department of Obstetrics and Gynecology, University of Southern California School of Medicine, Women and Children’s Hospital, 1240 North Mission Rd, Rm L1017, Los Angeles, CA 90033.

PII: S0002-9378(00)70217-1

American Journal of Obstetrics & Gynecology
Volume 182, Issue 2 , Pages 313-320, February 2000