The conventional inverse variance weighted method [14] was used to estimate the associations of genetically predicted 1 s.d. increase in each adiposity measure with odds ratio of gout and serum urate concentrations (in mg/dl). The weighted median and Mendelian randomization Egger (MR-Egger) regression methods were used as sensitivity analyses [14]. The weighted median method provides consistent estimates if at least 50% of the weight comes from valid instrumental variables [14]. The MR-Egger method can be used to identify and adjust for directional pleiotropy [14, 15]. Bias caused by pleiotropy is analogous to small study bias in a meta-analysis, where small studies with less precise estimates tend to report larger estimates than larger studies with more precise estimates. Heterogeneity between SNPs was tested by using the I2 statistic and Cochran’s Q test [16]. A threshold of statistical significance of P < 0.0125 (P = 0.05/4) was used to reflect testing of two adiposity measures (BMI and WHR adjusted for BMI) and two outcomes (gout and serum urate concentrations). Stata (version 14.1; StataCorp, College Station, TX, USA) was used for all analyses.
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