Wang Xiao-Yu, Wang Li-Li, Xu Lin, Liang Shu-Zhen, Yu Meng-Chao, Zhang Qiu-Yue, Dong Quan-Jiang
Central Laboratories and Department of Gastroenterology, Qingdao Municipal Hospital, Qingdao University, Qingdao 266071, Shandong Province, China.
Department of Clinical Laboratory, the Eighth Medical Center of the General Hospital of the People's Liberation Army, Beijing 100000, China.
World J Gastrointest Oncol. 2023 Feb 15;15(2):276-285. doi: 10.4251/wjgo.v15.i2.276.
Genetic variations are associated with individual susceptibility to gastric cancer. Recently, polygenic risk score (PRS) models have been established based on genetic variants to predict the risk of gastric cancer. To assess the accuracy of current PRS models in the risk prediction, a systematic review was conducted. A total of eight eligible studies consisted of 544842 participants were included for evaluation of the performance of PRS models. The overall accuracy was moderate with Area under the curve values ranging from 0.5600 to 0.7823. Incorporation of epidemiological factors or () status increased the accuracy for risk prediction, while selection of single nucleotide polymorphism (SNP) and number of SNPs appeared to have little impact on the model performance. To further improve the accuracy of PRS models for risk prediction of gastric cancer, we summarized the association between gastric cancer risk and genomic variations, cancer associated bacteria members in the gastric microbiome, discussed the potentials for performance improvement of PRS models with these microbial factors. Future studies on comprehensive PRS models established with human SNPs, epidemiological factors and microbial factors are indicated.
基因变异与个体患胃癌的易感性相关。最近,基于基因变异建立了多基因风险评分(PRS)模型来预测胃癌风险。为了评估当前PRS模型在风险预测中的准确性,进行了一项系统综述。总共纳入了八项符合条件的研究,包括544842名参与者,以评估PRS模型的性能。总体准确性中等,曲线下面积值范围为0.5600至0.7823。纳入流行病学因素或()状态提高了风险预测的准确性,而单核苷酸多态性(SNP)的选择和SNP的数量似乎对模型性能影响不大。为了进一步提高PRS模型对胃癌风险预测的准确性,我们总结了胃癌风险与基因组变异、胃微生物群中与癌症相关的细菌成员之间的关联,并讨论了这些微生物因素改善PRS模型性能的潜力。指出了未来关于用人单核苷酸多态性、流行病学因素和微生物因素建立综合PRS模型的研究方向。