Alimentary Pharmacology & Therapeutics · 2018 · 91 citations · 20 references
MedicinePharmacotherapySurgeryClinical PharmacologyGastroenterologyGastrointestinal PharmacotherapyCrohn Disease PharmacotherapyInflammatory Bowel DiseaseUlcerative Colitis PharmacotherapyWeight LossWeight ManagementClinical RemissionCohort Study InvestigationInflammatory Bowel Disease Activity AssessmentInflammatory Bowel Disease TherapyObesity As A Selection CriterionPrimary Outcome AnalysisTreatment Discontinuation RatesTreatment Regimen Modification
BACKGROUND: Though pharmacokinetic studies suggest accelerated biologic drug clearance with increasing body weight, evidence of obesity's impact on clinical outcomes in biologic-treated patients with ulcerative colitis (UC) is inconsistent. AIM: To evaluate the impact of obesity on real world response to biological therapy in patients with UC. METHODS: In a single-centre retrospective cohort study between 2011-2016 of biologic-treated patients with UC, we evaluated treatment response by baseline body mass index (BMI). Primary outcome was treatment failure (composite outcome of IBD-related surgery/hospitalisation or treatment modification including dose escalation, treatment discontinuation or addition of corticosteroids); secondary outcomes were risk of IBD-related surgery/hospitalisation and endoscopic remission. We conducted multivariate Cox proportional hazard analyses to evaluate the independent impact of BMI on clinical outcomes. Stratified analysis by weight-based regimens (infliximab) or fixed-dose regimens (adalimumab, golimumab, vedolizumab, certolizumab pegol) was performed. RESULTS: increase in BMI was associated with 4% increase in the risk of treatment failure (adjusted hazard ratio [aHR], 1.04 [95% CI, 1.00-1.08]) and 8% increase in the risk of surgery/hospitalisation (aHR, 1.08 [1.02-1.14]). The effect on treatment failure was seen in patients on weight-based dosing regimens or fixed-dose therapies. CONCLUSION: BMI is independently associated with increased risk of treatment failure in biologic-treated patients with UC, independent of dosing regimen.
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Marie Ng, Tom Fleming, Margaret S. Robinson et al. · The Lancet · 2014 · 12.1K citations · Full text