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. 2021 Mar 23;106(10):e4251–e4259. doi: 10.1210/clinem/dgab183

Table 4.

Results of mendelian randomization between genetically predicted obesity (exposure) and thyrotropin (outcome)

Analysis type NSNV β SE P Q Q_P Egger intercept Intercept_P
IVW, fixed Model 1 5 –.008 0.012 .514 5.284 .259 9.178 × 10–4 .970
Model 2 4 .003 0.009 .731 1.462 .481 –0.002 .922
IVW, random Model 1 5 –.008 0.013 .570 5.284 .259 9.178 × 10–4 .970
Model 2 4 .003 0.013 .809 1.462 .481 –0.002 .922
MR-Egger Model 1 5 –.012 0.117 .923 5.281 .152 9.178 × 10–4 .970
Model 2 4 .013 0.089 .899 1.474 .688 –0.002 .922

Model 1, crude; Model 2, rs571312 associated with confounding factor (thyroxine level) was excluded by the phenome-wide association study. Q and Q_P represent the Cochran Q value and corresponding P value for estimated heterogeneity; Egger intercept and intercept_P represent estimated pleiotropy effect and corresponding P value.

Abbreviations: IVW, inverse variant weighted; MR, mendelian randomization; SNV, single-nucleotide variations (formerly single-nucleotide polymorphisms [SNPs]).