Genetics of pancreatitis: a guide for clinicians

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This review discusses known genetic mutations predisposing carriers to chronic pancreatitis and their implications for clinicians, contributing to a better understanding of the disease's pathogenesis.

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Abstract

Chronic pancreatitis is an inflammatory disease of the pancreas leading to progressive fibrosis that presents with severe abdominal pain and may result in exocrine and/or endocrine insufficiency at later stages. Although alcohol is the strongest contributing factor for disease development, some patients feature none of the known classical risk factors and were consequently classified as having idiopathic or, in the presence of a positive family history, hereditary disease. Today, several mutations have been identified that predispose carriers to development of chronic pancreatitis. The genetic studies of the past decade have clearly contributed to a better understanding of the disease's pathogenesis. Currently known mutations associated with chronic pancreatitis and the implications for clinicians are discussed in this review.

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MeSH descriptors

Genetic Predisposition to Disease Pancreatitis, Chronic Practice Guidelines as Topic Chymotrypsin Chymotrypsin Cystic Fibrosis Transmembrane Conductance Regulator Cystic Fibrosis Transmembrane Conductance Regulator Female Gene Expression Regulation Genetic Predisposition to Disease Genetic Testing Humans Incidence Male Mutation Pancreatitis, Chronic Pancreatitis, Chronic Pancreatitis, Chronic Prognosis Risk Assessment

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