Genetic Mutations in a Spanish Population with Chronic Pancreatitis

被引:10
作者
Mora, Josefina [2 ]
Comas, Laia [2 ]
Ripoll, Elia [2 ]
Goncalves, Patricia [1 ]
Queralto, Josep M. [2 ]
Gonzalez-Sastre, Francesc [2 ]
Farre, Antoni [1 ]
机构
[1] Hosp Santa Creu & Sant Pau, Dept Gastroenterol, ES-08025 Barcelona, Spain
[2] Hosp Santa Creu & Sant Pau, Dept Clin Chem, ES-08025 Barcelona, Spain
关键词
Genetic mutations; Chronic pancreatitis; Idiopathic chronic pancreatitis; Alcohol-related pancreatitis; Hereditary pancreatitis; SERINE-PROTEASE INHIBITOR; CATIONIC TRYPSINOGEN GENE; CYSTIC-FIBROSIS GENE; TYPE-1; SPINK1; GENE; KAZAL TYPE-1; HEREDITARY PANCREATITIS; N34S MUTATION; ALCOHOL; RISK; DEFICIENCY;
D O I
10.1159/000181177
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: Mutations in the PRSS1 and the SPINK1 genes have variably been associated with alcohol-related, idiopathic and hereditary chronic pancreatitis (CP). The aim of this study was to determine for the first time the significance of PRSS1, SPINK1 mutations and genetic variants of AAT in a group of Spanish patients with CP. Methods: 104 consecutive patients with CP were included, as well as 84 healthy control subjects. The R122H and N29I mutations in the PRSS1 gene, the N34S mutation in the SPINK1 gene and PiS and PiZ mutations in the AAT gene were analyzed by RFLP-PCR methods. Results: No R122H mutation was found in the PRSS1 gene, and N29I mutation was detected in 7.7% of CP patients. A N29I mutation was observed in 3.9% of patients with alcohol-related pancreatitis (ACP). A total of 5.8% of CP patients were identified with the N34S mutation. Genotype MS, SS and MZ were detected in 18.3, 3.8 and 1.3% of CP patients, respectively. Conclusion: The percentage of N29I mutations in ACP patients was higher than that reported in other studies, while the percentage of N34S and AAT mutations in ACP and idiopathic CP patients was similar. Copyright (C) 2009 S. Karger AG, Basel and IAP
引用
收藏
页码:644 / 651
页数:8
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