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ABSTRACT: Background
Excessive alcohol consumption has long been known to be the primary cause of chronic pancreatitis (CP) but genetic risk factors have been increasingly identified over the past 25 years. The scale and scope of gene-alcohol interactions in CP nevertheless remain unclear.Methods
All studies that had obtained genetic variant data concurrently on alcoholic CP (ACP) patients, non-ACP (NACP) patients and normal controls were collated. Employing normal controls as a common baseline, paired ORACP and ORNACP (odds ratios associated with ACP and NACP, respectively) values were calculated and used to assess gene-alcohol interactions.Results
Thirteen variants involving PRSS1, SPINK1, CTRC, CLDN2, CPA1, CEL
SUBMITTER: Chen JM
PROVIDER: S-EPMC8064432 | biostudies-literature | 2021 Mar
REPOSITORIES: biostudies-literature