دورية أكاديمية

Variants in CPA1 are strongly associated with early onset chronic pancreatitis.

التفاصيل البيبلوغرافية
العنوان: Variants in CPA1 are strongly associated with early onset chronic pancreatitis.
المؤلفون: Witt, Heiko1, Beer, Sebastian2, Rosendahl, Jonas3, Chen, Jian-Min4, Chandak, Giriraj Ratan5, Masamune, Atsushi6, Bence, Melinda2, Szmola, Richárd7, Oracz, Grzegorz8, Macek, Milan9, Bhatia, Eesh10, Steigenberger, Sandra11, Lasher, Denise11, Bühler, Florence11, Delaporte, Catherine11, Tebbing, Johanna11, Ludwig, Maren11, Pilsak, Claudia11, Saum, Karolin11, Bugert, Peter12
المصدر: Nature Genetics. Oct2013, Vol. 45 Issue 10, p1216-1220. 5p. 5 Charts, 1 Graph.
مصطلحات موضوعية: *PANCREATITIS, *CARBOXYPEPTIDASES, *ENDOPLASMIC reticulum, *TRYPSIN, *CHYMOTRYPSIN, *GENETIC mutation
مستخلص: Chronic pancreatitis is an inflammatory disorder of the pancreas. We analyzed CPA1, encoding carboxypeptidase A1, in subjects with nonalcoholic chronic pancreatitis (cases) and controls in a German discovery set and three replication sets. Functionally impaired variants were present in 29/944 (3.1%) German cases and 5/3,938 (0.1%) controls (odds ratio (OR) = 24.9, P = 1.5 × 10−16). The association was strongest in subjects aged ≤10 years (9.7%; OR = 84.0, P = 4.1 × 10−24). In the replication sets, defective CPA1 variants were present in 8/600 (1.3%) cases and 9/2,432 (0.4%) controls from Europe (P = 0.01), 5/230 (2.2%) cases and 0/264 controls from India (P = 0.02) and 5/247 (2.0%) cases and 0/341 controls from Japan (P = 0.013). The mechanism by which CPA1 variants confer increased pancreatitis risk may involve misfolding-induced endoplasmic reticulum stress rather than elevated trypsin activity, as is seen with other genetic risk factors for this disease. [ABSTRACT FROM AUTHOR]
قاعدة البيانات: Academic Search Index