Abstract | CONTEXT: CASE REPORT: A 43-year-old man with a history of heavy alcohol drinking presented with recurrent abdominal pain. Alcoholic pancreatitis was diagnosed and responded well to pancreatic stricture dilatation with stent insertion. Sequencing analysis revealed that he was heterozygous for a novel transition c.206C>T in exon 4 of the SPINK1 gene, resulting in the substitution of threonine for isoleucine at codon 69 (T69I). Evidence supporting its etiologic role includes the alteration of the polarity of the amino acid change, its revolutionary conservation among mammals and its absence in 100 ethnic-matched control alleles. CONCLUSIONS: We identified a novel SPINK1 mutation, c.206C>T (T69I), in a Thai patient with alcoholic pancreatitis. This extends the total number of confirmed SPINK1 mutations and polymorphisms to more than 30. It also supports a previous observation that the SPINK1 gene is a susceptibility locus for alcoholic pancreatitis.
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Authors | Rungsun Rerknimitr, Vorasuk Shotelersuk, Patinut Buranasupkajorn, Wanee Plengpanich, Thiti Snabboon |
Journal | JOP : Journal of the pancreas
(JOP)
Vol. 9
Issue 1
Pg. 33-6
(Jan 08 2008)
ISSN: 1590-8577 [Electronic] Italy |
PMID | 18182741
(Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Carrier Proteins
- SPINK1 protein, human
- Trypsin Inhibitor, Kazal Pancreatic
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Topics |
- Adult
- Amino Acid Sequence
- Carrier Proteins
(genetics)
- Chronic Disease
- Female
- Genetic Predisposition to Disease
- Humans
- Male
- Middle Aged
- Molecular Sequence Data
- Pancreatitis, Alcoholic
(diagnostic imaging, genetics)
- Point Mutation
- Thailand
- Tomography, X-Ray Computed
- Trypsin Inhibitor, Kazal Pancreatic
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