4.7 Article

Investigating a possible causal relationship between maternal serum urate concentrations and offspring birthweight: a Mendelian randomization study

期刊

出版社

OXFORD UNIV PRESS
DOI: 10.1093/ije/dyac186

关键词

Birthweight; serum urate; Mendelian randomization; blood pressure; genetics

资金

  1. UK Biobank [7036]
  2. National Institute of Health Research (NIHR) Exeter Clinical Research Facility
  3. South West NHS Research and Development
  4. Exeter NHS Research and Development
  5. Darlington Trust
  6. Peninsula NIHR Clinical Research Facility at the University of Exeter
  7. Wellcome Trust
  8. Royal Society [104150/Z/14/Z]
  9. MRC Clinical Research Infrastructure award (MRC) [MR/M008924/1]

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The study revealed that higher maternal urate levels are associated with lower offspring birthweight and the causal effect of maternal urate on offspring birthweight is small. Additionally, higher urate levels are causally associated with higher systolic blood pressure, but the relationship between urate levels and offspring birthweight may be confounded.
Background Higher urate levels are associated with higher systolic blood pressure (SBP) in adults, and in pregnancy with lower offspring birthweight. Mendelian randomization (MR) analyses suggest a causal effect of higher urate on higher SBP and of higher maternal SBP on lower offspring birthweight. If urate causally reduces birthweight, it might confound the effect of SBP on birthweight. We therefore tested for a causal effect of maternal urate on offspring birthweight. Methods We tested the association between maternal urate levels and offspring birthweight using multivariable linear regression in the Exeter Family Study of Childhood Health (EFSOCH; n = 872) and UK Biobank (UKB; n = 133 187). We conducted two-sample MR to test for a causal effect of maternal urate [114 single-nucleotide polymorphisms (SNPs); n = 288 649 European ancestry] on offspring birthweight (n = 406 063 European ancestry; maternal SNP effect estimates adjusted for fetal effects). We assessed a causal relationship between urate and SBP using one-sample MR in UKB women (n = 199 768). Results Higher maternal urate was associated with lower offspring birthweight with similar confounder-adjusted magnitudes in EFSOCH [22 g lower birthweight per 1-SD higher urate (95% CI: -50, 6); P = 0.13] and UKB [-28 g (95% CI: -31, -25); P = 1.8 x 10(-75)]. The MR causal effect estimate was directionally consistent, but smaller [-11 g (95% CI: -25, 3); P-IVW = 0.11]. In women, higher urate was causally associated with higher SBP [1.7 mmHg higher SBP per 1-SD higher urate (95% CI: 1.4, 2.1); P = 7.8 x 10(-22)], consistent with that previously published in women and men. Conclusion The marked attenuation of the MR result of maternal urate on offspring birthweight compared with the multivariable regression result suggests previous observational associations may be confounded. The 95% CIs of the MR result included the null but suggest a possible small effect on birthweight. Maternal urate levels are unlikely to be an important contributor to offspring birthweight.

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