The Impact Of Anti-Tnf Alpha Agents On Weight-Related Changes: New Insights From A Real-World Pharmacovigilance Study Using The Fda Adverse Event Reporting System (Faers) Database

Introduction Studies in patients with immune-mediated inflammatory diseases (IMIDs) have inconsistently suggested that anti-TNF alpha therapy may be associated with excessive weight gain. Areas covered We performed a nested case/non-case analysis to investigate the anti-TNF-alpha inhibitor-associated body-changes in the US Food and Drug Administration (FDA) Adverse Event Reporting System (FAERS) database. The risk was expressed as a measure of disproportionality using the reporting odds ratio (ROR) while adjusting for sex, drugs known to cause weight gain and reporter type. We also performed a time-to-onset (TTO) analysis of body weight-related events. Results Infliximab was the most commonly involved TNF-alpha inhibitor in body weight-related changes, reaching an aROR of 1.42 (95%CI:1. 26; 1.59). An increased risk was especially found in patients affected by rheumatic disorders, both in the adult and pediatric population. The median TTO after the start of anti- TNF alpha therapy was about 6-7 months for both children and adults. Conclusions Given the potential effect of these agents on the excess weight gain in IMIDs patients, continuous attention for this side effect with appropriate counseling regarding lifestyle modifications are warranted, especially in those at high risk for obesity.