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

Table 3.

Results of mendelian randomization between genetically predicted body mass index (exposure) and thyrotropin (outcome)

Analysis type NSNV β SE P Q Q_P Egger intercept Intercept_P
IVW, fixed Model 1 918 .031 0.012 .010 1111.565 9.689 × 10–6 7.863 × 10–4 .191
Model 2 903 .038 0.012 .002 1079.502 3.938 × 10–5 4.062 × 10–4 .519
IVW, random Model 1 918 .031 0.013 .020 1111.565 9.689 × 10–6 7.863 × 10–4 .191
Model 2 903 .038 0.013 .004 1079.502 3.938 × 10–5 4.062 × 10–4 .519
MR-Egger Model 1 918 –.021 0.042 .612 1109.488 1.060 × 10–5 7.863 × 10–4 .191
Model 2 903 .011 0.045 .807 1079.004 3.738 × 10–5 4.062 × 10–4 .519

Model 1, crude; Model 2, SNVs associated with confounding factors (thyroid antibodies, thyroxine, or triiodothyronine) were all 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]).