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. 2022 Aug 8:11:e79798.
doi: 10.7554/eLife.79798.

Adiposity may confound the association between vitamin D and disease risk - a lifecourse Mendelian randomization study

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Adiposity may confound the association between vitamin D and disease risk - a lifecourse Mendelian randomization study

Tom G Richardson et al. Elife. .

Abstract

Background: Vitamin D supplements are widely prescribed to help reduce disease risk. However, this strategy is based on findings using conventional epidemiological methods which are prone to confounding and reverse causation.

Methods: In this short report, we leveraged genetic variants which differentially influence body size during childhood and adulthood within a multivariable Mendelian randomization (MR) framework, allowing us to separate the genetically predicted effects of adiposity at these two timepoints in the lifecourse.

Results: Using data from the Avon Longitudinal Study of Parents and Children (ALSPAC), there was strong evidence that higher childhood body size has a direct effect on lower vitamin D levels in early life (mean age: 9.9 years, range = 8.9-11.5 years) after accounting for the effect of the adult body size genetic score (beta = -0.32, 95% CI = -0.54 to -0.10, p=0.004). Conversely, we found evidence that the effect of childhood body size on vitamin D levels in midlife (mean age: 56.5 years, range = 40-69 years) is putatively mediated along the causal pathway involving adulthood adiposity (beta = -0.17, 95% CI = -0.21 to -0.13, p=4.6 × 10-17).

Conclusions: Our findings have important implications in terms of the causal influence of vitamin D deficiency on disease risk. Furthermore, they serve as a compelling proof of concept that the timepoints across the lifecourse at which exposures and outcomes are measured can meaningfully impact overall conclusions drawn by MR studies.

Funding: This work was supported by the Integrative Epidemiology Unit which receives funding from the UK Medical Research Council and the University of Bristol (MC_UU_00011/1).

Keywords: ALSPAC; Mendelian randomization; childhood adiposity; epidemiology; global health; human; lifecourse epidemiology; vitamin D.

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Conflict of interest statement

TR is employed part-time by Novo Nordisk on work outside of the work reported in this study, GP, GD No competing interests declared

Figures

Figure 1.
Figure 1.. Forest plots and schematic diagrams depicting the findings from this study.
(A) A forest plot illustrating the direct effect of childhood body size on circulating vitamin D levels measured during childhood (mean age: 9.9 years, n=3,800 participants) using data from the Avon Longitudinal Study of Parents and Children (ALSPAC) with the corresponding schematic diagram for this finding being located in panel (B). (C) A forest plot depicting the indirect effect of childhood body size on adulthood measured vitamin D levels using data from the UK Biobank study (mean age: 56.5 years, n=401,460 participants) as described in the schematic diagram presented in panel (D). MR – Mendelian randomization. All estimates underlying the forest plots can be found in Supplementary file 1.

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