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Higher maternal adiposity reduces offspring birthweight if associated with a metabolically favourable profile.
Thompson, William D; Beaumont, Robin N; Kuang, Alan; Warrington, Nicole M; Ji, Yingjie; Tyrrell, Jessica; Wood, Andrew R; Scholtens, Denise M; Knight, Bridget A; Evans, David M; Lowe, William L; Santorelli, Gillian; Azad, Rafaq; Mason, Dan; Hattersley, Andrew T; Frayling, Timothy M; Yaghootkar, Hanieh; Borges, Maria Carolina; Lawlor, Deborah A; Freathy, Rachel M.
Affiliation
  • Thompson WD; Institute of Biomedical and Clinical Science, College of Medicine and Health, University of Exeter, Exeter, UK.
  • Beaumont RN; MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
  • Kuang A; Institute of Biomedical and Clinical Science, College of Medicine and Health, University of Exeter, Exeter, UK.
  • Warrington NM; Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Ji Y; University of Queensland Diamantina Institute, University of Queensland, Brisbane, QLD, Australia.
  • Tyrrell J; K.G. Jebsen Center for Genetic Epidemiology, Department of Public Health and Nursing, NTNU, Norwegian University of Science and Technology, Trondheim, Norway.
  • Wood AR; Institute of Biomedical and Clinical Science, College of Medicine and Health, University of Exeter, Exeter, UK.
  • Scholtens DM; Institute of Biomedical and Clinical Science, College of Medicine and Health, University of Exeter, Exeter, UK.
  • Knight BA; Institute of Biomedical and Clinical Science, College of Medicine and Health, University of Exeter, Exeter, UK.
  • Evans DM; Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Lowe WL; Institute of Biomedical and Clinical Science, College of Medicine and Health, University of Exeter, Exeter, UK.
  • Santorelli G; MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
  • Azad R; University of Queensland Diamantina Institute, University of Queensland, Brisbane, QLD, Australia.
  • Mason D; Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
  • Hattersley AT; Bradford Institute for Health Research, Bradford Royal Infirmary, Bradford, UK.
  • Frayling TM; Department of Biochemistry, Bradford Royal Infirmary, Bradford, UK.
  • Yaghootkar H; Bradford Institute for Health Research, Bradford Royal Infirmary, Bradford, UK.
  • Borges MC; Institute of Biomedical and Clinical Science, College of Medicine and Health, University of Exeter, Exeter, UK.
  • Lawlor DA; Institute of Biomedical and Clinical Science, College of Medicine and Health, University of Exeter, Exeter, UK.
  • Freathy RM; Institute of Biomedical and Clinical Science, College of Medicine and Health, University of Exeter, Exeter, UK.
Diabetologia ; 64(12): 2790-2802, 2021 12.
Article in En | MEDLINE | ID: mdl-34542646
ABSTRACT
AIMS/

HYPOTHESIS:

Higher maternal BMI during pregnancy is associated with higher offspring birthweight, but it is not known whether this is solely the result of adverse metabolic consequences of higher maternal adiposity, such as maternal insulin resistance and fetal exposure to higher glucose levels, or whether there is any effect of raised adiposity through non-metabolic (e.g. mechanical) factors. We aimed to use genetic variants known to predispose to higher adiposity, coupled with a favourable metabolic profile, in a Mendelian randomisation (MR) study comparing the effect of maternal 'metabolically favourable adiposity' on offspring birthweight with the effect of maternal general adiposity (as indexed by BMI).

METHODS:

To test the causal effects of maternal metabolically favourable adiposity or general adiposity on offspring birthweight, we performed two-sample MR. We used variants identified in large, published genetic-association studies as being associated with either higher adiposity and a favourable metabolic profile, or higher BMI (n = 442,278 and n = 322,154 for metabolically favourable adiposity and BMI, respectively). We then extracted data on the metabolically favourable adiposity and BMI variants from a large, published genetic-association study of maternal genotype and offspring birthweight controlling for fetal genetic effects (n = 406,063 with maternal and/or fetal genotype effect estimates). We used several sensitivity analyses to test the reliability of the results. As secondary analyses, we used data from four cohorts (total n = 9323 mother-child pairs) to test the effects of maternal metabolically favourable adiposity or BMI on maternal gestational glucose, anthropometric components of birthweight and cord-blood biomarkers.

RESULTS:

Higher maternal adiposity with a favourable metabolic profile was associated with lower offspring birthweight (-94 [95% CI -150, -38] g per 1 SD [6.5%] higher maternal metabolically favourable adiposity, p = 0.001). By contrast, higher maternal BMI was associated with higher offspring birthweight (35 [95% CI 16, 53] g per 1 SD [4 kg/m2] higher maternal BMI, p = 0.0002). Sensitivity analyses were broadly consistent with the main results. There was evidence of outlier SNPs for both exposures; their removal slightly strengthened the metabolically favourable adiposity estimate and made no difference to the BMI estimate. Our secondary analyses found evidence to suggest that a higher maternal metabolically favourable adiposity decreases pregnancy fasting glucose levels while a higher maternal BMI increases them. The effects on neonatal anthropometric traits were consistent with the overall effect on birthweight but the smaller sample sizes for these analyses meant that the effects were imprecisely estimated. We also found evidence to suggest that higher maternal metabolically favourable adiposity decreases cord-blood leptin while higher maternal BMI increases it. CONCLUSIONS/

INTERPRETATION:

Our results show that higher adiposity in mothers does not necessarily lead to higher offspring birthweight. Higher maternal adiposity can lead to lower offspring birthweight if accompanied by a favourable metabolic profile. DATA

AVAILABILITY:

The data for the genome-wide association studies (GWAS) of BMI are available at https//portals.broadinstitute.org/collaboration/giant/index.php/GIANT_consortium_data_files . The data for the GWAS of body fat percentage are available at https//walker05.u.hpc.mssm.edu .
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Adiposity / Genome-Wide Association Study Type of study: Clinical_trials / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Newborn / Pregnancy Language: En Journal: Diabetologia Year: 2021 Document type: Article Affiliation country: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Adiposity / Genome-Wide Association Study Type of study: Clinical_trials / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Newborn / Pregnancy Language: En Journal: Diabetologia Year: 2021 Document type: Article Affiliation country: United kingdom