4.7 Article

Obesity-susceptibility loci have a limited influence on birth weight: a meta-analysis of up to 28,219 individuals

Journal

AMERICAN JOURNAL OF CLINICAL NUTRITION
Volume 93, Issue 4, Pages 851-860

Publisher

ELSEVIER SCIENCE INC
DOI: 10.3945/ajcn.110.000828

Keywords

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Funding

  1. Medical Research Council UK [74882]
  2. Cancer Research UK
  3. The Danish Heart Foundation
  4. The Danish Medical Research Council Health Foundation
  5. The Danish Council for Sports Research
  6. The Foundation in Memory of Asta Florida Bolding Renee Andersen
  7. The Faculty of Health Sciences, University of Southern Denmark
  8. The Estonian Science Foundation [3277, 5209]
  9. Wellcome Trust [076467]
  10. MRC [MC_U106179472, MC_U106188470, MC_U106179473, G0701863] Funding Source: UKRI
  11. Medical Research Council [G1000143, U1475000001, MC_U106179473, MC_U106179472, MC_U106179471, MC_U106188470, G0701863, MC_UP_A620_1014, G0401527] Funding Source: researchfish
  12. National Institute for Health Research [NF-SI-0508-10082] Funding Source: researchfish

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Background: High birth weight is associated with adult body mass index (BMI). We hypothesized that birth weight and BMI may partly share a common genetic background. Objective: The objective was to examine the associations of 12 established BMI variants in or near the NEGR1, SEC16B, TMEM18, ETV5, GNPDA2, BDNF, MTCH2, BCDIN3D, SH2B1, FTO, MC4R, and KCTD15 genes and their additive score with birth weight. Design: A meta-analysis was conducted with the use of 1) the European Prospective Investigation into Cancer and Nutrition (EPIC)-Norfolk, Hertfordshire, Fenland, and European Youth Heart Study cohorts (n(max) = 14,060); 2) data extracted from the Early Growth Genetics Consortium meta-analysis of 6 genome-wide association studies for birth weight (n(max) = 10,623); and 3) all published data (n(max) = 14,837). Results: Only the MTCH2 and FTO loci showed a nominally significant association with birth weight. The BMI-increasing allele of the MTCH2 variant (rs10838738) was associated with a lower birth weight (beta +/- SE: 213 +/- 5 g/allele; P = 0.012; n = 23,680), and the BMI-increasing allele of the FTO variant (rs1121980) was associated with a higher birth weight (beta +/- SE: 11 +/- 4 g/allele; P = 0.013; n = 28,219). These results were not significant after correction for multiple testing. Conclusions: Obesity-susceptibility loci have a small or no effect on weight at birth. Some evidence of an association was found for the MTCH2 and FTO loci, ie, lower and higher birth weight, respectively. These findings may provide new insights into the underlying mechanisms by which these loci confer an increased risk of obesity. Am J Clin Nutr 2011;93:851-60.

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