4.7 Article

Analysis of Continuous Glucose Monitoring in Pregnant Women With Diabetes: Distinct Temporal Patterns of Glucose Associated With Large-for-Gestational-Age Infants

Journal

DIABETES CARE
Volume 38, Issue 7, Pages 1319-1325

Publisher

AMER DIABETES ASSOC
DOI: 10.2337/dc15-0070

Keywords

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Funding

  1. Ipswich Diabetes Centre Charity Research Fund
  2. Higher Education Funding Council for England
  3. National Institute for Health Research (Career Development Fellowship) [CDF-2013-06-035]
  4. European Foundation for the Study of Diabetes and LifeScan
  5. Rigshospitalet's Research Foundation
  6. Capital Region of Denmark
  7. Medical Faculty Foundation of Copenhagen University
  8. Aase and Ejnar Danielsen's Foundation
  9. Master Joiner Sophus Jacobsen and wife Astrid Jacobsen's Foundation
  10. Novo Nordisk Foundation
  11. National Institute for Health Research [CDF-2013-06-035, PDF/01/036] Funding Source: researchfish
  12. Novo Nordisk Fonden [NNF14OC0009275] Funding Source: researchfish

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OBJECTIVEContinuous glucose monitoring (CGM) is increasingly used to assess glucose control in diabetes. The objective was to examine how analysis of glucose data might improve our understanding of the role temporal glucose variation has on large-for-gestational-age (LGA) infants born to women with diabetes.RESEARCH DESIGN AND METHODSFunctional data analysis (FDA) was applied to 1.68 million glucose measurements from 759 measurement episodes, obtained from two previously published randomized controlled trials of CGM in pregnant women with diabetes. A total of 117 women with type 1 diabetes (n = 89) and type 2 diabetes (n = 28) who used repeated CGM during pregnancy were recruited from secondary care multidisciplinary obstetric clinics for diabetes in the U.K. and Denmark. LGA was defined as birth weight 90th percentile adjusted for sex and gestational age.RESULTSA total of 54 of 117 (46%) women developed LGA. LGA was associated with lower mean glucose (7.0 vs. 7.1 mmol/L; P < 0.01) in trimester 1, with higher mean glucose in trimester 2 (7.0 vs. 6.7 mmol/L; P < 0.001) and trimester 3 (6.5 vs. 6.4 mmol/L; P < 0.01). FDA showed that glucose was significantly lower midmorning (0900-1100 h) and early evening (1900-2130 h) in trimester 1, significantly higher early morning (0330-0630 h) and throughout the afternoon (1130-1700 h) in trimester 2, and significantly higher during the evening (2030-2330 h) in trimester 3 in women whose infants were LGA.CONCLUSIONSFDA of CGM data identified specific times of day that maternal glucose excursions were associated with LGA. It highlights trimester-specific differences, allowing treatment to be targeted to gestational glucose patterns.

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