Maternal obesity, diabetes mellitus and cord blood biomarkers in large-for-gestational age infants

Article type: Research Article

Authors: Mestan, Karen | Ouyang, Fengxiu | Matoba, Nana | Pearson, Colleen | Ortiz, Katherin | Wang, Xiaobin

Affiliations: Division of Neonatology, Children's Memorial Hospital, and Department of Pediatrics, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA | Mary Ann and J. Milburn Smith Child Health Research Program, Children's Memorial Hospital and Children's Memorial Research Center, and Department of Pediatrics, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA | Department of Pediatrics, Boston University School of Medicine and Boston Medical Center, Boston, MA, USA

Note: [] Correspondence: Karen Mestan, MD, Division of Neonatology, Children's Memorial Hospital, 2300 Children's Plaza, Box 45 Chicago, IL 60614, USA. Tel.: +1 773 880 4536; Fax: +1 773 880 3061; E-mail: [email protected]

Abstract: Infants born large-for-gestational age (LGA) are at risk for early childhood obesity. The aims of this study were to investigate factors associated with LGA status and their relationship to inflammatory biomarkers that have been implicated in the LGA infant at birth. Included were 364 mother-infant pairs enrolled as part of an ongoing longitudinal cohort study of infant birth weight being conducted at Boston Medical Center (BMC). LGA was defined as birth weight (BW) ⩾ 90th percentile of the reference population at BMC (N=45). Appropriate-for-gestational age (AGA) was defined as BW<90th and >10th percentile (N=319). Cord blood IL-6, IL-8, TNF-alpha and RANTES levels were analyzed from a larger panel of immune biomarkers measured using multiplex immunoassay. Multivariate regression models were used to determine the associations between LGA status, maternal BMI and diabetes (DM), which included either gestational or type 2 diabetes (T2DM), and cord blood biomarkers, with adjustment for important demographic and clinical variables. Maternal pre-pregnancy BMI within the obesity range (⩾30 kg/m^{2}), as well as DM, were each associated with increased risk of LGA (OR=2.64, 95%CI 1.31–6.20; OR=5.58, 95%CI 2.06–15.13, respectively). Among the 4 biomarkers, only RANTES (regulated on activation, normal T cell express and secreted upon uptake), which is a chemokine secreted by white adipose tissue, was significantly increased in LGA infants (beta-coefficient =0.37; 95%CI: 0.09, 0.65; P<0.01). This association remained essentially unchanged after adjustment for maternal DM and BMI (beta-coefficient=0.37; 95%: 0.08, 0.65; P=0.01). Ponderal index (PI=BWx100/length^{3}) was also positively correlated with RANTES. Cord blood RANTES is selectively elevated with fetal macrosomia, independent of maternal factors. Further investigation of RANTES as a marker of LGA and future childhood health is warranted.

Keywords: Birth weight, large-for-gestational age, cord blood, inflammation, obesity, diabetes

DOI: 10.3233/JPB-2010-0023

Journal: Journal of Pediatric Biochemistry, vol. 1, no. 3, pp. 217-224, 2010/2011