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Relation of FTO gene variants to fetal growth trajectories: Findings from the Southampton Women's survey.
Barton, S J; Mosquera, M; Cleal, J K; Fuller, A S; Crozier, S R; Cooper, C; Inskip, H M; Holloway, J W; Lewis, R M; Godfrey, K M.
Afiliación
  • Barton SJ; MRC Lifecourse Epidemiology Unit, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK. Electronic address: S.J.Barton@soton.ac.uk.
  • Mosquera M; Institute of Developmental Sciences, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK; Department of Physiological Sciences, Faculty of Health, University of Valle, Cali, Colombia.
  • Cleal JK; Institute of Developmental Sciences, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK.
  • Fuller AS; MRC Lifecourse Epidemiology Unit, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK.
  • Crozier SR; MRC Lifecourse Epidemiology Unit, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK.
  • Cooper C; MRC Lifecourse Epidemiology Unit, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK; NIHR Musculoskeletal Biomedical Research Unit, University of Oxford, Oxford, OX1 2JD, UK.
  • Inskip HM; MRC Lifecourse Epidemiology Unit, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK.
  • Holloway JW; Human Genetics and Genomic Medicine, Human Development & Health, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK.
  • Lewis RM; Institute of Developmental Sciences, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK.
  • Godfrey KM; MRC Lifecourse Epidemiology Unit, Faculty of Medicine, University of Southampton, Southampton SO16 6YD, UK; NIHR Southampton Biomedical Research Centre, University of Southampton and University Hospital Southampton NHS Foundation Trust, Southampton, SO16 6YD, UK.
Placenta ; 38: 100-6, 2016 Feb.
Article en En | MEDLINE | ID: mdl-26907388
ABSTRACT

INTRODUCTION:

Placental function is an important determinant of fetal growth, and fetal growth influences obesity risk in childhood and adult life. Here we investigated how FTO and MC4R gene variants linked with obesity relate to patterns of fetal growth and to placental FTO expression.

METHODS:

Southampton Women's Survey children (n = 1990) with measurements of fetal growth from 11 to 34 weeks gestation were genotyped for common gene variants in FTO (rs9939609, rs1421085) and MC4R (rs17782313). Linear mixed-effect models were used to analyse relations of gene variants with fetal growth.

RESULTS:

Fetuses with the rs9939609 AA FTO genotype had faster biparietal diameter and head circumference growth velocities between 11 and 34 weeks gestation (by 0.012 (95% CI 0.005 to 0.019) and 0.008 (0.002-0.015) standard deviations per week, respectively) compared to fetuses with the TT FTO genotype; abdominal circumference growth velocity did not differ between genotypes. FTO genotype was not associated with placental FTO expression, but higher placental FTO expression was independently associated with larger fetal size and higher placental ASCT2, EAAT2 and y + LAT2 amino acid transporter expression. Findings were similar for FTO rs1421085, and the MC4R gene variant was associated with the fetal growth velocity of head circumference.

DISCUSSION:

FTO gene variants are known to associate with obesity but this is the first time that the risk alleles and placental FTO expression have been linked with fetal growth trajectories. The lack of an association between FTO genotype and placental FTO expression adds to emerging evidence of complex biology underlying the association between FTO genotype and obesity.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Desarrollo Fetal / Dioxigenasa FTO Dependiente de Alfa-Cetoglutarato Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male / Newborn / Pregnancy País/Región como asunto: Europa Idioma: En Revista: Placenta Año: 2016 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Desarrollo Fetal / Dioxigenasa FTO Dependiente de Alfa-Cetoglutarato Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male / Newborn / Pregnancy País/Región como asunto: Europa Idioma: En Revista: Placenta Año: 2016 Tipo del documento: Article