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

Table 1.

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

Analysis type NSNV β SE P Q Q_P Egger intercept Intercept_P
IVW, fixed Model 1 65 .011 0.005 .011 127.351 4.292 × 10–6 0.001 .231
Model 2 48 .008 0.005 .144 79.911 .002 3.859 × 10–4 .675
IVW, random Model 1 65 .011 0.006 .073 127.351 4.292 × 10–6 0.001 .231
Model 2 48 .008 0.007 .263 79.911 .002 3.859 × 10–4 .675
MR-Egger Model 1 65 –.005 0.015 .727 124.456 6.377 × 10–6 0.001 .231
Model 2 48 .001 0.016 .935 79.602 .002 3.859 × 10–4 .675

Model 1, crude; Model 2, SNVs associated with confounding factors (blood pressure, blood lipids, or blood glucose) 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 variation (formerly single-nucleotide polymorphism [SNP]).