Table 5.
Exposure | Outcome | Method | IV | β | SE | p value |
---|---|---|---|---|---|---|
Fasting GIPa | CAD | Wald ratio (2SMR) | rs1800437 | 0.51 | 0.165 | 0.002 |
Fasting GIPa | MI | Wald ratio (2SMR) | rs1800437 | 0.46 | 0.186 | 0.013 |
Fasting GIPb | CAD | Wald ratio (2SMR) | rs1800437 | 0.42 | 0.129 | 0.001 |
CADc | Fasting GIP | IVW | 114 SNPs | −0.042 | 0.029 | 0.148 |
CADc | Fasting GIP | MR Egger | 114 SNPs | −0.039 | 0.074 | 0.595 |
aData from CARDIoGRAMplusC4D for CAD (n = 184,305; 60,801 cases, 123,504 controls) and myocardial infarction (n = 171,875; 43,676 cases, 128,199 controls)
bData for CAD from UK Biobank (n = 296,525; 34,541 cases, 61,984 controls)
cLoci from CARDiOGRAMplusC4D and UK Biobank were used for constructing the instrumental variable. The summary data for the outcome (fasting GIP) was acquired from the MDC-CC cohort. Out of 147 SNPs in CARDiOGRAMplusC4D and UK Biobank (ESM Table 1) with p < 5 × 10−8 and r2 measure of linkage disequilibrium <0.2, 116 SNPs were selected with available information in MDC-CC (ESM Table 2). An additional two SNPs (rs472109, rs4754698) were removed from analysis for being palindromic with intermediate allele frequencies
IV, instrumental variable; MI, myocardial infarction