Research Article

The Role of Inflammatory Biomarkers in Mediating the Effect of Inflammatory Bowel Disease on nonmalignant Digestive System Diseases: A Multivariable Mendelian Randomized Study

Table 2

Pleiotropy and heterogeneity test of the UC/CD IVs from nonmalignant digestive system diseases GWAS.

Pleiotropy testHeterogeneity test
MR-eggerMR-eggerIVW
InterceptSEPvalQQ_PvalQQ_Pval

UCAP−6.28E − 050.0090.9958.040.8258.040.85
IBS9.82E − 050.0080.9960.970.7460.970.77
GERD0.0010.0030.7039.300.1239.500.14
Cholelithiasis0.0100.0050.0599.760.009105.400.004
CeD0.0320.0380.41177.602.57E − 26183.276.06E − 27
IL-6−0.0070.0060.2392.810.0494.710.04
CRP−0.0040.0050.47162.552.10E − 19165.241.61E − 19
TNF-α0.0090.0080.2864.560.6365.720.62

CDAP−0.0070.0090.4495.590.4396.210.45
IBS0.0110.0070.1595.450.4497.630.41
GERD−1.70E − 040.0040.97103.611.76E − 09103.613.22E − 09
Cholelithiasis3.60E − 040.0060.95215.611.51E − 11215.622.30E − 11
CeD0.0260.0250.29125.166.16E − 15130.661.49E − 15
IL-6−0.0020.0040.6384.370.3284.610.34
CRP0.0040.0030.5550.760.000551.620.0006
TNF-α−0.0030.0110.76105.640.017105.770.02

IVW, inverse variance weighting; UC, ulcerative colitis; AP, acute pancreatitis; IBS, irritable bowel syndrome; GERD, gastroesophageal reflux disease; IL-6, interleukin 6; CRP, C-reactive protein; TNF-α, tumor necrosis factor-α; CD, Crohn’s disease; GWAS, genome-wide significant; CeD, celiac disease.