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

Author:

Decina Caitlin S123,Hopkins Rhian1,Bowden Jack1,Shields Beverly M1,Lawlor Deborah A456,Warrington Nicole M237,Evans David M234ORCID,Freathy Rachel M14,Beaumont Robin N1ORCID

Affiliation:

1. Department of Clinical and Biomedical Sciences, Faculty of Health and Life Sciences, University of Exeter , Exeter, UK

2. University of Queensland Diamantina Institute, University of Queensland , Brisbane, Queensland, Australia

3. Institute for Molecular Bioscience, University of Queensland , Brisbane, Queensland, Australia

4. Medical Research Council Integrative Epidemiology Unit, University of Bristol , Bristol, UK

5. Population Health Science, Bristol Medical School, University of Bristol , Bristol, UK

6. Bristol NIHR Biomedical Research Centre , Bristol, UK

7. K.G. Jebsen Center for Genetic Epidemiology, Department of Public Health and Nursing, NTNU, Norwegian University of Science and Technology , Trondheim, Norway

Abstract

Abstract 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 × 10–75]. The MR causal effect estimate was directionally consistent, but smaller [–11 g (95% CI: –25, 3); PIVW = 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 × 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.

Funder

QUEX Institute

University of Exeter

University of Queensland

Wellcome Trust

Royal Society

Wellcome Senior Research Fellowship

British Heart Foundation

European Research Council

National Institute of Health

University of Bristol

Medical Research Council

British Heart Foundation Professor

Publisher

Oxford University Press (OUP)

Subject

General Medicine,Epidemiology

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