Abstract
Background
Cystic fibrosis transmembrane conductance regulator IVS8-5T gene variation appears
to be associated with a higher risk of chronic pancreatitis (CP); however, there is
inconsistency between previous reported studies. Here, we performed a meta-analysis
to investigate this relationship.
Materials and Methods
PubMed and WANFANG databases were searched for the case-control studies that contained
Patients with CP with IVS8-5T variation. Odd ratios (ORs) and 95% confidence intervals
(CIs) were calculated to assess the relevance of IVS8-5T gene variation and CP.
Results
Analysis showed that the frequency of the 5T allele was significantly higher in CP
subjects than that in control subjects (OR = 1.43, 95% CI: 1.13–1.81, I2 = 1.2%). Based on the subgroup analysis stratified by etiology, the 5T allele was
associated with a higher risk of idiopathic chronic pancreatitis (ICP) (OR = 1.80,
95% CI: 1.18-2.76, I2 = 0.0%) and not alcoholic CP (OR = 2.14, 95% CI: 0.98-4.66, I2 = 0.0%). Further study indicated that the 5T allele was related to higher ICP prevalence
in the European population (OR = 1.79, 95% CI: 1.06-3.03, I2 = 0.0%). In contrast, there was no significant difference between ICP subjects and
healthy controls within the Asian population (OR = 1.84, 95% CI: 0.91-3.72, I2 = 38.0%).
Conclusions
Cystic fibrosis transmembrane conductance regulator IVS8-5T is a risk factor in patients
with CP. IVS8-5T variation may play a significant role in the occurrence of ICP, especially
in the European population.
Key Indexing Terms
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Article info
Publication history
Published online: April 25, 2020
Accepted:
April 17,
2020
Received:
November 6,
2019
Footnotes
Funding: This work was supported by the Nature Science Foundations of Guangxi Province (Grant number: 2016GXNSFDA380010), National Natural Science Foundation of China (Grant number: 81774171).
Disclosures: The authors declare that there are no conflicts of interest regarding the publication of this paper.
Identification
Copyright
© 2020 Southern Society for Clinical Investigation. Published by Elsevier Inc. All rights reserved.