Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/73773
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Type: Journal article
Title: The interaction between the maternal BMI and angiogenic gene polymorphisms associates with the risk of spontaneous preterm birth
Author: Andraweera, P.
Dekker, G.
Thompson, S.
North, R.
McCowan, L.
Roberts, C.
Citation: Molecular Human Reproduction, 2012; 18(9):459-465
Publisher: Oxford Univ Press
Issue Date: 2012
ISSN: 1360-9947
1460-2407
Statement of
Responsibility: 
Prabha H. Andraweera, Gustaaf A. Dekker, Steven D. Thompson, Robyn A. North, Lesley M.E. McCowan and Claire T. Roberts on behalf of the SCOPE Consortium
Abstract: Obesity is associated with an increased level of inflammation. Interactions between inflammatory and angiogenic pathways are implicated in the major pregnancy disorders. The aim of this study was to investigate whether functional polymorphisms in angiogenesis-regulating genes (VEGFA rs699947, VEGFA rs3025039, KDR rs2071559 and ANGPT1 rs2507800) interact with the maternal BMI to modify the risk of a spontaneous preterm birth (sPTB). We conducted a nested case–control study of 1190 nulliparous Caucasian women (107 sPTBs and 1083 controls). Spontaneous PTB was defined as spontaneous preterm labour or a preterm premature rupture of membranes resulting in a preterm birth at <37 weeks of gestation. DNA was extracted from the peripheral blood and genotyped using the Sequenom MassARRAY system. Among overweight or obese women (BMI ≥25), the VEGFA rs699947 AA genotype was associated with a higher risk of sPTBs [odds ratio (OR) = 2.4, 95% confidence interval (CI): 1.4–4.6, P = 0.001] and a significant interaction between the BMI and the polymorphism was detected (OR = 4.2, 95% CI: 1.7–10.9, P = 0.003). Among women with a BMI < 25, ANGPT1 rs2507800 AA genotype was associated with a higher risk of sPTB (OR = 2.3, 95% CI: 1.2–4.4, P = 0.02) and a significant interaction between BMI and the polymorphism was detected (OR = 3.3, 95% CI: 1.1–9.3, P = 0.02). All results remained significant after adjusting for potential confounding factors. The maternal BMI interacts with angiogenesis-regulating gene polymorphisms to modify the risk of sPTBs. Trial Registry Name: Screening nulliparous women to identify the combinations of clinical risk factors and/or biomarkers required to predict pre-eclampsia, small-for-gestational-age babies and spontaneous preterm birth (https://www.anzctr.org.au). Registration number: ACTRN12607000551493.
Keywords: SCOPE Consortium; Humans; Pregnancy Complications; Premature Birth; Obesity; Inflammation; Vascular Endothelial Growth Factor Receptor-2; Angiopoietin-1; Vascular Endothelial Growth Factor A; Body Mass Index; Odds Ratio; Risk Factors; Case-Control Studies; Pregnancy; Neovascularization, Physiologic; Genotype; Polymorphism, Single Nucleotide; Adult; Female
Rights: © The Author 2012.
RMID: 0020121953
DOI: 10.1093/molehr/gas016
Appears in Collections:Obstetrics and Gynaecology publications

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