Divergent Roles of SPINK1 and PRSS2 Variants in Tropical Calcific Pancreatitis

被引:10
作者
Sundaresan, Santhosh [2 ]
Chacko, Ashok [2 ]
Dutta, Amit K. [2 ]
Bhatia, Eesh [3 ]
Witt, Heiko [4 ]
Morsche, Rene H. M. Te
Jansen, Jan B. M. J.
Drenth, Joost P. H. [1 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Med,Div Gastroenterol & Hepatol, Univ Med Ctr St Radboud, NL-6500 HB Nijmegen, Netherlands
[2] Christian Med Coll & Hosp, Dept Gastrointestinal Sci, Vellore 632004, Tamil Nadu, India
[3] Sanjay Gandhi Postgrad Inst Med Sci, Dept Endocrinol, Lucknow, Uttar Pradesh, India
[4] Free Univ Berlin, Klinikum Rudolf Virchow, Charite, Dept Gastroenterol, D-1000 Berlin, Germany
关键词
Tropical calcific pancreatitis; SPINK1; PRSS2; CTRC sequencing; CATIONIC TRYPSINOGEN GENE; SERINE-PROTEASE INHIBITOR; DIABETES-MELLITUS; KAZAL TYPE-1; MUTATIONS; BANGLADESH; DEGRADATION;
D O I
10.1159/000178885
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: Tropical calcific pancreatitis (TCP) refers to a type of idiopathic pancreatitis prevalent in Asia. The trypsin inhibitor (SPINK1) N34S variant partially explains the genetic susceptibility to TCP. As anionic trypsinogen (PRSS2) G191R protects against chronic pancreatitis in Europeans, we investigated whether this variant protects from TCP in Indians. Methods: We enrolled 174 patients and 794 controls from two Indian tertiary care referral hospitals. We analyzed PRSS2 and SPINK1 variants by melting curve analysis, allele-specific discrimination assay, and sequencing. Results: G191R was detected in 1 TCP patient (0.6%) compared to 13 controls (1.6%; OR 0.27, 95% CI 0.03-2.1; p = 0.33). SPINK1 N34S was enriched in the TCP population 67/174 (38.5%) compared to controls 10/234 (4.3%; OR 14, 95% CI 6.9-28.3; p < 0.001). Conclusion: G191R PRSS2 is a rare allele in the Indian population and the data suggest a nonsignificant trend towards a protective effect. N34S SPINK1 represents the major genetic risk factor in TCP. Copyright (C) 2008 S. Karger AG, Basel and IAP
引用
收藏
页码:145 / 149
页数:5
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