Meta-analysis of the impact of SPINK1 p.N34S gene variation in Caucasic patients with chronic pancreatitis. An update

被引:21
作者
Di Leo, Milena [1 ]
Bianco, Margherita [2 ]
Zuppardo, Raffaella Alessia [1 ]
Guslandi, Mario [1 ]
Calabrese, Federica [1 ]
Mannucci, Alessandro [1 ]
Neri, Tauro Maria [3 ]
Testoni, Pier Alberto [1 ]
Leandro, Gioacchino [2 ,4 ]
Cavestro, Giulia Martina [1 ]
机构
[1] Univ Vita Salute San Raffaele, IRCCS San Raffaele Sci Inst, Div Expt Oncol, Gastroenterol & Gastrointestinal Endoscopy Unit, Milan, Italy
[2] Gastroenterol Hosp S De Bellis IRCCS, Gastroenterol Unit 1, Castellana Grotte, BA, Italy
[3] Univ Hosp Parma, Mol Genet Lab, Diagnost Dept, Unit Med Genet, Parma, Italy
[4] UCL, Inst Digest & Liver Hlth, London, England
关键词
Alcohol; Genetic pancreatitis; PSTI; TATI; SERINE-PROTEASE INHIBITOR; KAZAL TYPE-1 SPINK1; IDIOPATHIC CHRONIC-PANCREATITIS; CATIONIC TRYPSINOGEN PRSS1; N34S MUTATION; CFTR GENE; RECURRENT ACUTE; RISK; POLYMORPHISMS; VARIANTS;
D O I
10.1016/j.dld.2017.04.023
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: SPINKI p.N34S gene variation is one of the endogenous factors which seem to be associated with chronic pancreatitis (CP). However, in literature there is no clear agreement regarding its contribution in different ethnicity and CP etiologies. Aim: To investigate the role of SPINKI p.N34S gene variation in CP patients with European origin by means of meta-analysis. Methods: Literature search was conducted and case-control studies evaluating Caucasian population, published between May 2007 and May 2015, were included. We also included Caucasian selected studies analyzed in previous meta-analysis. We carried out meta-analysis including all selected studies. After that, we performed two additional meta-analyses considering the incidence of SPINKI p.N34S gene variation in alcoholic or in idiopathic CP patients vs control group. Results: Twenty-five studies were included and the total number of subjects was 8800 (2981 cases and 5819 controls). The presence of p.N34S variation increased nine times the overall CP risk in population of European origin [OR 9.695 (CI 95% 7.931-11.851)]. Also, the contribution of SPINKI in idiopathic pancreatitis [OR 13.640 (CI 95% 8.858-21.002)] was found to be higher than in alcoholic CP [5.283 (CI 95% 3.449-8.092)]. Conclusion: The association between SPINKI p.N34S gene variation and CP is confirmed. Also, we confirmed that the idiopathic etiology needs a better definition by means of genetic analysis. (C) 2017 Editrice Gastroenterologica Italiana S.r.l. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:847 / 853
页数:7
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