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慢性胰腺炎患者CFTR和PSTI基因的种系突变。

Germline mutations in CFTR and PSTI genes in chronic pancreatitis patients.

作者信息

Gaia Ezio, Salacone Paola, Gallo Monica, Promis Gianni Gerbino, Brusco Alfredo, Bancone Claudia, Carlo Arduino

机构信息

Struttura Complessa di Gastroenterologia, Dipartimento di Clinica Medica, Azienda Ospedaliera San Luigi Gonzaga, Torino, Italy.

出版信息

Dig Dis Sci. 2002 Nov;47(11):2416-21. doi: 10.1023/a:1020579119691.

Abstract

Mutations in the cationic trypsinogen, cystic fibrosis transmembrane conductance regulator (CFTR) and pancreatic secretory trypsinogen inhibitor (PSTI) genes have recently been associated with chronic pancreatitis. This paper investigates the frequency of CFTR and PSTI gene mutation in patients with idiopathic and alcoholic chronic pancreatitis, the clinical course of patients with these two kinds of disease, and examines the clinical differences between carriers and noncarriers of mutation. In idiopathic pancreatitis a significant increase was found in mutation frequency both in the CFTR gene (13%) and N34S mutation in the PSTI gene (3.9%), as well as an increase in familial disposition to pancreatic disorders. In alcohol-induced pancreatitis an increase in calcification, exocrine insufficiency, and diabetes mellitus was observed. In conclusions, mutations in the genes investigated are involved in causing idiopathic pancreatitis. Such mutations have no connection either with the age at onset or the clinical course of the disease.

摘要

阳离子胰蛋白酶原、囊性纤维化跨膜传导调节因子(CFTR)和胰腺分泌性胰蛋白酶原抑制剂(PSTI)基因的突变最近被认为与慢性胰腺炎有关。本文研究特发性和酒精性慢性胰腺炎患者中CFTR和PSTI基因突变的频率、这两种疾病患者的临床病程,并考察突变携带者与非携带者之间的临床差异。在特发性胰腺炎中,发现CFTR基因的突变频率显著增加(13%),PSTI基因的N34S突变频率也增加(3.9%),同时胰腺疾病的家族易感性增加。在酒精性胰腺炎中,观察到钙化、外分泌功能不全和糖尿病有所增加。总之,所研究的基因中的突变参与了特发性胰腺炎的发病。此类突变与发病年龄或疾病的临床病程均无关联。

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