Causal relationship between inflammatory bowel disease and erythema nodosum: A two‐sample bidirectional Mendelian randomization study

Abstract

AbstractBackgroundPrevious studies have demonstrated the coexistence of erythema nodosum (EN) and inflammatory bowel disease (IBD), while the exact etiology of the co‐occurrence of the two disorders remains uncertain.MethodsA bidirectional two‐sample Mendelian randomization (MR) design was employed to determine the causal link between EN and IBD. Genetic variations associated with Crohn's disease (CD) and ulcerative colitis (UC) were derived from accessible genome‐wide association studies pertaining to European ancestry. The FinnGen database was used to find the genetic variations containing EN. In the forward model, IBD was identified as the exposure, whereas in the reverse model, EN was identified as the exposure. The causal link between IBD and EN was examined using a range of different analysis techniques, the primary one being the inverse variance weighted (IVW) method, including inverse variance weighted‐fixed effects (IVW‐FE) and inverse‐variance weighted‐multiplicative random effects (IVW‐MRE). To strengthen the results, assessments of sensitivity, heterogeneity, and pleiotropy were also conducted.ResultsMR results showed that IBD increased the risk of EN (IVW‐MRE: OR = 1.242, 95% CI = 1.068–1.443, p = 0.005). Furthermore, there was a strong correlation found between CD and a higher risk of EN (IVW‐FE: OR = 1.250, 95% CI = 1.119–1.396, p = 8.036 × 10−5). However, UC did not appear to be linked to EN (IVW‐FE: OR = 1.104, 95% CI = 0.868–1.405, p = 0.421). The reverse MR analysis findings did not imply that EN was linked to IBD. Horizontal pleiotropy did not appear to exist, and the robustness of these findings was confirmed.ConclusionThe current investigation found that in European populations, IBD and its subtype CD could raise the incidence of EN.