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 × 10-4). For diabetes, the corresponding OR was 14.95 (95% CI 3.41-65.50, P = 3.58 × 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.

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

Gentiluomo, Manuel
Co-primo
Writing – Original Draft Preparation
;
Landi, Stefano;Morelli, Luca;Boggi, Ugo;Campa, Daniele
Ultimo
Writing – Original Draft Preparation
2023-01-01

Abstract

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 × 10-4). For diabetes, the corresponding OR was 14.95 (95% CI 3.41-65.50, P = 3.58 × 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.
2023
Nodari, Ylenia; Gentiluomo, Manuel; Mohelnikova-Duchonova, Beatrice; Kreivenaite, Edita; Milanetto, Anna Caterina; Skieceviciene, Jurgita; Landi, Stefano; Lawlor, Rita T; Petrone, Maria Chiara; Arcidiacono, Paolo Giorgio; Lovecek, Martin; Gazouli, Maria; Bijlsma, Maarten F; Morelli, Luca; Kiudelis, Vytautas; Tacelli, Matteo; Zanette, Dalila Lucíola; Soucek, Pavel; Uzunoglu, Faik; Kaaks, Rudolf; Izbicki, Jakob; Boggi, Ugo; Pezzilli, Raffaele; Mambrini, Andrea; Pasquali, Claudio; van Laarhoven, Hanneke W; Katzke, Verena; Cavestro, Giulia Martina; Sperti, Cosimo; Loos, Martin; Latiano, Anna; Erőss, Bálint; Oliverius, Martin; Johnson, Theron; Basso, Daniela; Neoptolemos, John P; Aoki, Mateus Nóbrega; Greenhalf, William; Vodicka, Pavel; Archibugi, Livia; Vanella, Giuseppe; Lucchesi, Maurizio; Talar-Wojnarowska, Renata; Jamroziak, Krzysztof; Saeedi, Mohammed Al; van Eijck, Casper H J; Kupcinskas, Juozas; Hussein, Tamás; Puzzono, Marta; Bunduc, Stefania; Götz, Mara; Carrara, Silvia; Szentesi, Andrea; Tavano, Francesca; Moz, Stefania; Hegyi, Péter; Luchini, Claudio; Capurso, Gabriele; Perri, Francesco; Ermini, Stefano; Theodoropoulos, George; Capretti, Giovanni; Palmieri, Orazio; Ginocchi, Laura; Furbetta, Niccolò; Canzian, Federico; Campa, Daniele
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/1179127
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