Gastro-intestinal involvement in systemic sclerosis

The gastrointestinal (GI) tract can be involved in up to 90% of patients with systemic sclerosis (SSc) and is the leading cause of morbidity and third most common cause of mortality in these patients. The GI involvement can occur in the absence of cutaneous manifestations in 10% of patients. Vasculo...

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Main Authors: Saurabh Kedia, Anuj Chhaparia, Pramod Garg
Format: Article
Language:English
Published: SAGE Publishing 2017-01-01
Series:Indian Journal of Rheumatology
Subjects:
Online Access:http://www.indianjrheumatol.com/article.asp?issn=0973-3698;year=2017;volume=12;issue=6;spage=156;epage=166;aulast=Kedia
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author Saurabh Kedia
Anuj Chhaparia
Pramod Garg
author_facet Saurabh Kedia
Anuj Chhaparia
Pramod Garg
author_sort Saurabh Kedia
collection DOAJ
description The gastrointestinal (GI) tract can be involved in up to 90% of patients with systemic sclerosis (SSc) and is the leading cause of morbidity and third most common cause of mortality in these patients. The GI involvement can occur in the absence of cutaneous manifestations in 10% of patients. Vasculopathy, cellular and humoral immunity, and diffuse fibrosis are the principal pathogenetic mechanisms in SSc and begin with autoantibody-mediated neuronal damage followed by muscular damage and fibrosis. This leads to progressive dysmotility of the entire GI tract from mouth to anus and is responsible for the clinical manifestations including gastroesophageal reflux disease and dysphagia due to esophageal involvement, gastroparesis, small intestinal bacterial overgrowth and chronic intestinal pseudo-obstruction, and constipation due to colonic and fecal incontinence due to anorectal involvement. The clinical features resulting from the involvement of these organs often overlap and multiple areas may be involved simultaneously. The treatment remains mostly symptomatic because effective disease-modifying therapies are lacking. These patients are at a risk of malnutrition and nutritional screening, and thus rehabilitation is very important. Refractory cases require nutritional support in the form of enteral nutrition and/or home parenteral nutrition. Future research is needed in the pathogenesis, development of biomarkers for early identification of GI involvement at the asymptomatic stage, and targeted disease-modifying therapies, which can alter/halt the disease progression.
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spelling doaj-art-b7e4210d87d943cdb9ddf83a89e09f952025-02-03T12:00:10ZengSAGE PublishingIndian Journal of Rheumatology0973-36980973-37012017-01-01126156166Gastro-intestinal involvement in systemic sclerosisSaurabh KediaAnuj ChhapariaPramod GargThe gastrointestinal (GI) tract can be involved in up to 90% of patients with systemic sclerosis (SSc) and is the leading cause of morbidity and third most common cause of mortality in these patients. The GI involvement can occur in the absence of cutaneous manifestations in 10% of patients. Vasculopathy, cellular and humoral immunity, and diffuse fibrosis are the principal pathogenetic mechanisms in SSc and begin with autoantibody-mediated neuronal damage followed by muscular damage and fibrosis. This leads to progressive dysmotility of the entire GI tract from mouth to anus and is responsible for the clinical manifestations including gastroesophageal reflux disease and dysphagia due to esophageal involvement, gastroparesis, small intestinal bacterial overgrowth and chronic intestinal pseudo-obstruction, and constipation due to colonic and fecal incontinence due to anorectal involvement. The clinical features resulting from the involvement of these organs often overlap and multiple areas may be involved simultaneously. The treatment remains mostly symptomatic because effective disease-modifying therapies are lacking. These patients are at a risk of malnutrition and nutritional screening, and thus rehabilitation is very important. Refractory cases require nutritional support in the form of enteral nutrition and/or home parenteral nutrition. Future research is needed in the pathogenesis, development of biomarkers for early identification of GI involvement at the asymptomatic stage, and targeted disease-modifying therapies, which can alter/halt the disease progression.http://www.indianjrheumatol.com/article.asp?issn=0973-3698;year=2017;volume=12;issue=6;spage=156;epage=166;aulast=Kediaesophageal dysmotilityfecal incontinencefibrosisgastroparesispseudoobstruction
spellingShingle Saurabh Kedia
Anuj Chhaparia
Pramod Garg
Gastro-intestinal involvement in systemic sclerosis
Indian Journal of Rheumatology
esophageal dysmotility
fecal incontinence
fibrosis
gastroparesis
pseudoobstruction
title Gastro-intestinal involvement in systemic sclerosis
title_full Gastro-intestinal involvement in systemic sclerosis
title_fullStr Gastro-intestinal involvement in systemic sclerosis
title_full_unstemmed Gastro-intestinal involvement in systemic sclerosis
title_short Gastro-intestinal involvement in systemic sclerosis
title_sort gastro intestinal involvement in systemic sclerosis
topic esophageal dysmotility
fecal incontinence
fibrosis
gastroparesis
pseudoobstruction
url http://www.indianjrheumatol.com/article.asp?issn=0973-3698;year=2017;volume=12;issue=6;spage=156;epage=166;aulast=Kedia
work_keys_str_mv AT saurabhkedia gastrointestinalinvolvementinsystemicsclerosis
AT anujchhaparia gastrointestinalinvolvementinsystemicsclerosis
AT pramodgarg gastrointestinalinvolvementinsystemicsclerosis