TY - JOUR
T1 - Obesity in IBD
T2 - Epidemiology, pathogenesis, disease course and treatment outcomes
AU - Singh, Siddharth
AU - Dulai, Parambir S.
AU - Zarrinpar, Amir
AU - Ramamoorthy, Sonia
AU - Sandborn, William J.
N1 - Funding Information:
S.S. is supported by the NIH/National Library of Medicine training grant T15LM011271, the American College of Gastroenterology Junior Faculty Development Award and the Crohn's and Colitis Foundation of American Career Development Award. P.S.D. is supported by the National Institute of Diabetes and Digestive and Kidney Diseases training grant 5T32DK007202. A.Z. has received support from NIH K08 DK102902, the American Association for the Study of Liver Diseases Liver Scholar Award, and the American Gastroenterological Association Microbiome Junior Investigator Research Award. The Authors thank L. J. Prokop, Senior Medical Librarian at Mayo Clinic, Rochester, USA, who assisted with a systematic literature review on this topic.
Publisher Copyright:
© 2017 Macmillan Publishers Limited, part of Springer Nature. All rights reserved.
PY - 2017/2/1
Y1 - 2017/2/1
N2 - Incidence of IBD is rising in parallel with overweight and obesity. Contrary to conventional belief, about 15-40% of patients with IBD are obese, which might contribute to the development of IBD. Findings from cross-sectional and retrospective cohort studies are conflicting on the effect of obesity on natural history and course of IBD. Most studies are limited by small sample size, low event rates, non-validated assessment of disease activity and lack robust longitudinal follow-up and have incomplete adjustment for confounding factors. The effect of obesity on the efficacy of IBD-related therapy remains to be studied, though data from other autoimmune diseases suggests that obesity results in suboptimal response to therapy, potentially by promoting rapid clearance of biologic agents leading to low trough concentrations. These data provide a rationale for using weight loss interventions as adjunctive therapy in patients with IBD who are obese. Obesity also makes colorectal surgery technically challenging and might increase the risk of perioperative complications. In this Review, we highlight the existing literature on the epidemiology of obesity in IBD, discuss its plausible role in disease pathogenesis and effect on disease course and treatment response, and identify high-priority areas of future research.
AB - Incidence of IBD is rising in parallel with overweight and obesity. Contrary to conventional belief, about 15-40% of patients with IBD are obese, which might contribute to the development of IBD. Findings from cross-sectional and retrospective cohort studies are conflicting on the effect of obesity on natural history and course of IBD. Most studies are limited by small sample size, low event rates, non-validated assessment of disease activity and lack robust longitudinal follow-up and have incomplete adjustment for confounding factors. The effect of obesity on the efficacy of IBD-related therapy remains to be studied, though data from other autoimmune diseases suggests that obesity results in suboptimal response to therapy, potentially by promoting rapid clearance of biologic agents leading to low trough concentrations. These data provide a rationale for using weight loss interventions as adjunctive therapy in patients with IBD who are obese. Obesity also makes colorectal surgery technically challenging and might increase the risk of perioperative complications. In this Review, we highlight the existing literature on the epidemiology of obesity in IBD, discuss its plausible role in disease pathogenesis and effect on disease course and treatment response, and identify high-priority areas of future research.
UR - http://www.scopus.com/inward/record.url?scp=85000416475&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85000416475&partnerID=8YFLogxK
U2 - 10.1038/nrgastro.2016.181
DO - 10.1038/nrgastro.2016.181
M3 - Review article
C2 - 27899815
AN - SCOPUS:85000416475
SN - 1759-5045
VL - 14
SP - 110
EP - 121
JO - Nature Reviews Gastroenterology and Hepatology
JF - Nature Reviews Gastroenterology and Hepatology
IS - 2
ER -