Abstract | BACKGROUND & AIMS: METHODS: Patients and controls were screened by means of previously described quantitative fluorescent multiplex polymerase chain reaction and/or genotyping of the microsatellite marker rs3222967. RESULTS: The approximately 605 kilobase triplication and a novel duplication (confirmed by fluorescence in situ hybridization) of the trypsinogen locus were detected in 10 and 2 of 202 ICP patients, respectively (age of disease onset, <or=20 years) but were absent in 282 French controls. In addition, the duplication mutation was found in 2 of 1044 ICP patients whose age of disease onset was >20 years. However, the 2 trypsinogen copy number mutations were observed in neither 103 FCP patients nor 268 Indian TCP patients. CONCLUSIONS: Our findings revealed the molecular basis of 6% of the young ICP patients and further demonstrated that chronic pancreatitis is a genomic disorder. Our findings also add to the mounting evidence showing that trypsinogen gene mutations do not appear to play an important role in the pathogenesis of TCP in the Indian population. Finally, a dividend of this study is that we have provided convincing evidence to show that all 5 previously described copy number variations involving PRSS1 or/and PRSS2 are artifacts.
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Authors | Emmanuelle Masson, Cédric Le Maréchal, Giriraj R Chandak, Jérôme Lamoril, Stephane Bezieau, Swapna Mahurkar, Seema Bhaskar, D Nageshwar Reddy, Jian-Min Chen, Claude Férec |
Journal | Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association
(Clin Gastroenterol Hepatol)
Vol. 6
Issue 1
Pg. 82-8
(Jan 2008)
ISSN: 1542-7714 [Electronic] United States |
PMID | 18063422
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Genetic Markers
- Trypsinogen
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Topics |
- Adolescent
- Adult
- Case-Control Studies
- Child
- Female
- France
- Gene Dosage
- Genetic Markers
- Humans
- In Situ Hybridization, Fluorescence
- India
- Male
- Middle Aged
- Mutation
- Pancreatitis, Chronic
(genetics)
- Polymerase Chain Reaction
- Trypsinogen
(genetics)
- White People
(genetics)
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