Microscopic colitis.


Journal

Nature reviews. Disease primers
ISSN: 2056-676X
Titre abrégé: Nat Rev Dis Primers
Pays: England
ID NLM: 101672103

Informations de publication

Date de publication:
10 06 2021
Historique:
accepted: 30 04 2021
entrez: 11 6 2021
pubmed: 12 6 2021
medline: 26 11 2021
Statut: epublish

Résumé

Microscopic colitis (MC) is an inflammatory disease of the large intestine associated with urgent watery diarrhoea. MC may occur in people of all ages, although the disease primarily affects older women. Once believed to be rare, MC is now known to be a common cause of chronic watery diarrhoea in high-income countries, affecting 1 in 115 women and 1 in 286 men during their lifetime in Swedish population-based estimates. An inappropriate immune response to disturbances in the gut microenvironment is implicated in the pathogenesis of MC. Evidence also supports an underlying genetic basis for disease. The diagnosis of MC relies on clinical symptoms and microscopic assessment of colonic biopsy samples. MC is categorized histologically into collagenous colitis, lymphocytic colitis and their incomplete forms. The mainstay of treatment includes the use of budesonide, with or without adjunctive therapies, and withdrawal of offending drugs. Emerging studies suggest a role for biologicals and immunosuppressive therapies for the management of budesonide-refractory or budesonide-dependent disease. MC can have a substantial negative effect on patient quality of life. The outlook for MC includes a better understanding of the immune response, genetics and the microbiome in disease pathogenesis along with progress in disease management through robust clinical trials.

Identifiants

pubmed: 34112810
doi: 10.1038/s41572-021-00273-2
pii: 10.1038/s41572-021-00273-2
doi:

Substances chimiques

Budesonide 51333-22-3

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

39

Subventions

Organisme : NIA NIH HHS
ID : R01 AG068390
Pays : United States

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Auteurs

Kristin E Burke (KE)

Gastroenterology Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA. keburke@mgh.harvard.edu.
Clinical and Translational Epidemiology Unit, Massachusetts General Hospital, Boston, MA, USA. keburke@mgh.harvard.edu.

Mauro D'Amato (M)

Gastrointestinal Genetics Lab, CIC bioGUNE, Basque Research and Technology Alliance (BRTA), Derio, Spain.
Ikerbasque, Basque Foundation for Science, Bilbao, Spain.

Siew C Ng (SC)

Department of Medicine and Therapeutics, State Key Laboratory of Digestive Disease, LK Institute of Health Science, The Chinese University of Hong Kong, Shatin, NT, Hong Kong, China.

Darrell S Pardi (DS)

Division of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.

Jonas F Ludvigsson (JF)

Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden.
Department of Paediatrics, Örebro University Hospital, Örebro University, Örebro, Sweden.

Hamed Khalili (H)

Gastroenterology Unit, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA. hkhalili@mgh.harvard.edu.
Clinical and Translational Epidemiology Unit, Massachusetts General Hospital, Boston, MA, USA. hkhalili@mgh.harvard.edu.
Institute of Environmental Medicine, Nutrition Epidemiology, Karolinska Institutet, Solna, Sweden. hkhalili@mgh.harvard.edu.

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