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Genetic and non-genetic risk factors for early-onset pancreatic cancer

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378041%3A_____%2F23%3A00581913" target="_blank" >RIV/68378041:_____/23:00581913 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11110/23:10458464 RIV/00216208:11120/23:43925300 RIV/00216208:11140/23:10458464 RIV/00064173:_____/23:43925300 and 2 more

  • Result on the web

    <a href="https://www.sciencedirect.com/science/article/pii/S1590865823005145?via%3Dihub" target="_blank" >https://www.sciencedirect.com/science/article/pii/S1590865823005145?via%3Dihub</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.dld.2023.02.023" target="_blank" >10.1016/j.dld.2023.02.023</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Genetic and non-genetic risk factors for early-onset pancreatic cancer

  • Original language description

    Background: Early-onset pancreatic cancer (EOPC) represents 5-10% of all pancreatic ductal adenocarcinoma (PDAC) cases, and the etiology of this form is poorly understood. It is not clear if established PDAC risk factors have the same relevance for younger patients. This study aims to identify genetic and non-genetic risk factors specific to EOPC. Methods: A genome-wide association study was performed, analysing 912 EOPC cases and 10 222 controls, divided into discovery and replication phases. Furthermore, the associations between a polygenic risk score (PRS), smoking, alcohol consumption, type 2 diabetes and PDAC risk were also assessed. Results: Six novel SNPs were associated with EOPC risk in the discovery phase, but not in the replication phase. The PRS, smoking, and diabetes affected EOPC risk. The OR comparing current smokers to never smokers was 2.92 (95% CI 1.69-5.04, P = 1.44 x 10 -4). For diabetes, the corresponding OR was 14.95 (95% CI 3.41-65.50, P = 3.58 x 10 -4). Conclusion: In conclusion, we did not identify novel genetic variants associated specifically with EOPC, and we found that established PDAC risk variants do not have a strong age-dependent effect. Furthermore, we add to the evidence pointing to the role of smoking and diabetes in EOPC. (c) 2023 The Authors. Published by Elsevier Ltd on behalf of Editrice Gastroenterologica Italiana S.r.l. This is an open access article under the CC BY-NC-ND license ( http://creativecommons.org/licenses/by-nc-nd/4.0/ )

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30101 - Human genetics

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2023

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Digestive and Liver Disease

  • ISSN

    1590-8658

  • e-ISSN

    1878-3562

  • Volume of the periodical

    55

  • Issue of the periodical within the volume

    10

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    9

  • Pages from-to

    1417-1425

  • UT code for WoS article

    001084748400001

  • EID of the result in the Scopus database

    2-s2.0-85151481167