Background Associations between blood urate levels, blood pressure (BP), and kidney function have previously been reported in observational studies. However, causal inference between these three traits is challenging due to potentially bidirectional relationships. Method: We applied bidirectional univariable Mendelian randomization (UVMR) to assess the causal relationships between urate levels, BP, and kidney function, proxied by estimated glomerular filtration rate (eGFR), using genetic associations from UK Biobank and CKDGen. We performed multivariable MR (MVMR) to assess the independent effects of urate and BP on eGFR. Effect estimates are presented as standard deviation (SD) change in outcome (95% confidence interval) per SD increase in exposure. Results The UVMR analysis showed a bidirectional causal effect between urate and eGFR [urate on log(eGFR): beta=-0.10 (−0.22 to 0.02); log(eGFR) on urate: beta=−0.11 (−0.17 to −0.04)]. We also found bidirectional causal effects between urate and SBP [urate on SBP: beta=0.08 (0.04 to 0.11); SBP on urate: beta=0.13 (0.08 to 0.18)] and urate and DBP [urate on DBP: beta=0.09 (0.05 to 0.14); DBP on urate: beta=0.13 (0.08 to 0.18)]. However, there was weak evidence of a causal effect between BP and eGFR. MVMR results suggested the causal effect of urate on eGFR was independent of BP. Conclusion Our results provide evidence for bidirectional causal effects between urate and both eGFR and BP, suggesting urate control as a potential intervention to reduce BP and decline in kidney function in the general population, but little evidence of a causal relationship between BP and eGFR.
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Tang et al. (2024) studied this question.
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