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早发性胰腺癌的遗传和非遗传风险因素。

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

机构信息

Department of Biology, University of Pisa, Pisa, Italy.

Department of Oncology, Faculty of Medicine and Dentistry, Palacký University, Olomouc, Czech Republic.

出版信息

Dig Liver Dis. 2023 Oct;55(10):1417-1425. doi: 10.1016/j.dld.2023.02.023. Epub 2023 Mar 25.

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

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.

摘要

背景

早发性胰腺癌(EOPC)占所有胰腺导管腺癌(PDAC)病例的 5-10%,其病因尚不清楚。目前尚不清楚已确定的 PDAC 危险因素对年轻患者是否具有相同的相关性。本研究旨在确定 EOPC 特有的遗传和非遗传风险因素。

方法

进行了全基因组关联研究,分析了 912 例 EOPC 病例和 10222 例对照,分为发现和复制阶段。此外,还评估了多基因风险评分(PRS)、吸烟、饮酒、2 型糖尿病与 PDAC 风险之间的关联。

结果

在发现阶段,有 6 个新的 SNP 与 EOPC 风险相关,但在复制阶段没有相关性。PRS、吸烟和糖尿病影响 EOPC 风险。与从不吸烟者相比,当前吸烟者的 OR 为 2.92(95%CI 1.69-5.04,P=1.44×10)。对于糖尿病,相应的 OR 为 14.95(95%CI 3.41-65.50,P=3.58×10)。

结论

总之,我们没有发现与 EOPC 特异性相关的新遗传变异,并且我们发现已确定的 PDAC 风险变异没有很强的年龄依赖性。此外,我们增加了吸烟和糖尿病在 EOPC 中作用的证据。

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