4.5 Article

Associations of maternal weight status prior and during pregnancy with neonatal cardiometabolic markers at birth: the Healthy Start study

Journal

INTERNATIONAL JOURNAL OF OBESITY
Volume 39, Issue 10, Pages 1437-1442

Publisher

SPRINGERNATURE
DOI: 10.1038/ijo.2015.109

Keywords

-

Funding

  1. National Institute of Diabetes and Digestive and Kidney Diseases Awards [R01-DK076648]
  2. Nutrition and Obesity Research Center Metabolic Core lab [P30-DK048520]
  3. National Institute of Child Health and Development [T32-HD007186]
  4. NIH/National Center for Advancing Translational Sciences Colorado Clinical and Translational Science Institute [UL1 TR001082]
  5. [F32-DK101179]

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BACKGROUND: Maternal obesity increases adult offspring risk for cardiovascular disease; however, the role of offspring adiposity in mediating this association remains poorly characterized. OBJECTIVE: To investigate the associations of maternal pre-pregnant body mass index (maternal BMI) and gestational weight gain (GWG) with neonatal cardiometabolic markers independent of fetal growth and neonatal adiposity. METHODS: A total of 753 maternal-infant pairs from the Healthy Start study, a large multiethnic pre-birth observational cohort were used. Neonatal cardiometabolic markers included cord blood glucose, insulin, glucose-to-insulin ratio (Glu/Ins), total and high-density lipoprotein cholesterol (HDL-c), triglycerides, free fatty acids and leptin. Maternal BMI was abstracted from medical records or self-reported. GWG was calculated as the difference between the first pre-pregnant weight and the last weight measurement before delivery. Neonatal adiposity (percent fat mass) was measured within 72 h of delivery using whole-body air-displacement plethysmography. RESULTS: In covariate adjusted models, maternal BMI was positively associated with cord blood insulin (P = 0.01) and leptin (P < 0.001) levels, and inversely associated with cord blood HDL-c (P = 0.05) and Glu/Ins (P = 0.003). Adjustment for fetal growth or neonatal adiposity attenuated the effect of maternal BMI on neonatal insulin, rendering the association nonsignificant. However, maternal BMI remained associated with higher leptin (P < 0.0011), lower HDL-c (P = 0.02) and Glu/Ins (P = 0.05), independent of neonatal adiposity. GWG was positively associated with neonatal insulin (P = 0.02), glucose (P = 0.03) and leptin levels (P < 0.001) and negatively associated with Glu/Ins (P = 0.006). After adjusting for neonatal adiposity, GWG remained associated with higher neonatal glucose (P = 0.02) and leptin levels (P = 0.02) and lower Glu/Ins (P = 0.048). CONCLUSIONS: Maternal weight prior and/or during pregnancy is associated with neonatal cardiometabolic makers including leptin, glucose and HDL-c at delivery, independent of neonatal adiposity. Our results suggest that intrauterine exposure to maternal obesity influences metabolic processes beyond fetal growth and fat accretion.

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