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The role of adipose tissue in the pathogenesis of Crohn's disease. | LitMetric

The role of adipose tissue in the pathogenesis of Crohn's disease.

Pharmacol Rep

Department of Biochemistry, Faculty of Medicine, Medical University of Lodz, Łódź, Poland; Department of General and Colorectal Surgery, Faculty of Military Medicine, Medical University of Lodz, Łódź, Poland. Electronic address:

Published: February 2019

AI Article Synopsis

  • * The study aims to explore how adipose tissue, particularly intra-abdominal white adipose tissue (WAT), contributes to the development and progression of CD, given the known association between body fat distribution changes and the disease.
  • * The review emphasizes the need for more research on the roles of WAT and its secreted substances (adipokines) in influencing inflammatory and fibrotic reactions in individuals with CD.

Article Abstract

Crohn's disease (CD) is a chronic, immune system-mediated inflammatory disease affecting gastrointestinal (GI) tract. The pathogenesis of the intestinal lesions is not entirely explained and understood: excessive activation of the immune system may come as a result of the interaction of environmental, genetic and infectious factors and the mediation of abnormal intestinal flora. The main objective of the current study is to further identify the role of adipose tissue in the pathogenesis of CD. Alterations in body fat distribution, accumulation of intra-abdominal white adipose tissue (WAT) and mesenteric obesity are well-known features of CD. Up to date, data concerning the role of WAT in the pathogenesis of CD is limited with only a few studies on the relationship between WAT and the course of the disease, as well as pro- and anti-inflammatory cytokine profile and general immune system functioning. In this review, we focus on the importance of physiological and pathophysiological WAT functions and secreted adipokines, which seem to have a vital role in the inflammatory and fibrotic processes in CD sufferers.

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Source
http://dx.doi.org/10.1016/j.pharep.2018.09.011DOI Listing

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