Pancreatitis-Associated Genes and Pancreatic Cancer Risk

OBJECTIVE: The aim of this study was to evaluate the connection between pancreatic cancer (PC) and genetic variants associated with chronic pancreatitis via systematic review and meta-analysis. METHODS: The data search was performed in 3 major databases (PubMed, EMBASE, and Cochrane Library). The se...

Teljes leírás

Elmentve itt :
Bibliográfiai részletek
Szerzők: Cazacu Irina Mihaela
Borbásné Farkas Kornélia
Garami András
Balaskó Márta
Mosdósi Bernadett
Alizadeh Hussain
Gyöngyi Zoltán
Rakonczay Zoltán, ifj
Vigh Éva
Habon Tamás
Czopf László
Erőss Bálint Mihály
Sahin-Tóth Miklós
Hegyi Péter
Dokumentumtípus: Cikk
Megjelent: 2018
Sorozat:PANCREAS 47 No. 9
doi:10.1097/MPA.0000000000001145

mtmt:3407223
Online Access:http://publicatio.bibl.u-szeged.hu/15409
Leíró adatok
Tartalmi kivonat:OBJECTIVE: The aim of this study was to evaluate the connection between pancreatic cancer (PC) and genetic variants associated with chronic pancreatitis via systematic review and meta-analysis. METHODS: The data search was performed in 3 major databases (PubMed, EMBASE, and Cochrane Library). The selected studies have looked into the presence of the pancreatitis-associated genes in patients with PC and in control subjects, the outcome being the frequency of the mutations in the 2 groups. For the binary outcomes, pooled odds ratio (OR) and 95% confidence interval (CI) were calculated. RESULTS: Ten articles proved to be eligible for the qualitative synthesis, and 8 articles were suitable for statistical analysis. Six case-control studies, comprising 929 PC cases and 1890 control subjects for serine protease inhibitor Kazal type 1 (SPINK1) mutations, and 5 case-control studies, comprising 1674 PC cases and 19,036 control subjects for CFTR mutations, were enrolled in our analysis. SPINK1 mutations showed no association with PC (OR, 1.52; 95% CI, 0.67-3.45; P = 0.315), whereas mutations in CFTR modestly increased the risk of PC (OR, 1.41; 95% CI, 1.07-1.84; P = 0.013). CONCLUSION: Our meta-analysis showed that mutations in CFTR modestly increase the risk of PC, whereas no association was found between SPINK1 and PC.This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
Terjedelem/Fizikai jellemzők:1078-1086
ISSN:0885-3177