权衡临床实践中基于多基因风险的方法的成本和收益的证据:对经济评估的系统回顾

IF 8.1 1区 生物学 Q1 GENETICS & HEREDITY
Leonardo Maria Siena, Valentina Baccolini, Marianna Riccio, Annalisa Rosso, Giuseppe Migliara, Antonio Sciurti, Claudia Isonne, Jessica Iera, Francesco Pierri, Carolina Marzuillo, Corrado De Vito, Giuseppe La Torre, Paolo Villari
{"title":"权衡临床实践中基于多基因风险的方法的成本和收益的证据:对经济评估的系统回顾","authors":"Leonardo Maria Siena, Valentina Baccolini, Marianna Riccio, Annalisa Rosso, Giuseppe Migliara, Antonio Sciurti, Claudia Isonne, Jessica Iera, Francesco Pierri, Carolina Marzuillo, Corrado De Vito, Giuseppe La Torre, Paolo Villari","doi":"10.1016/j.ajhg.2025.05.012","DOIUrl":null,"url":null,"abstract":"Polygenic risk scores (PRSs) represent a promising innovation in the context of precision health, but their benefits for patients and healthcare systems remain unclear. This systematic review examined the methods used to quantify the costs and benefits of PRS-based approaches across different healthcare contexts, summarizing current evidence and identifying challenges. A systematic search of three databases was conducted, and full economic evaluations related to any intervention based on polygenic risk stratification strategies were included (PROSPERO CRD42023442780). Quality was assessed using the Quality of Health Economic Studies instrument. Studies were grouped into three categories (cancer, cardiovascular disease, and other diseases), and key methodological features and characteristics were extracted. A total of 24 cost-utility analyses of generally high quality were included: 16 studies focused on cancer, five on cardiovascular disease, and three on other diseases. Studies on cancer mainly aimed to optimize screening programs, while in the other fields, PRSs were mostly used to refine eligibility for preventive therapies. Analyses were robust, but they mostly relied on hypothetical cohorts, had limited generalizability, paid insufficient attention to implementation aspects—including the delivery model—and considered only clinical benefits. Despite a positive trend toward cost effectiveness following PRS implementation, several challenges remain. These include the limited use of real-world data, issues of representativeness, and gaps in accounting for implementation costs, as well as long-term health and non-health benefits. Further research and pilot studies are needed to evaluate both the costs and benefits of PRS applications across diverse populations for multiple health outcomes simultaneously.","PeriodicalId":7659,"journal":{"name":"American journal of human genetics","volume":"20 1","pages":""},"PeriodicalIF":8.1000,"publicationDate":"2025-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Weighing the evidence on costs and benefits of polygenic risk-based approaches in clinical practice: A systematic review of economic evaluations\",\"authors\":\"Leonardo Maria Siena, Valentina Baccolini, Marianna Riccio, Annalisa Rosso, Giuseppe Migliara, Antonio Sciurti, Claudia Isonne, Jessica Iera, Francesco Pierri, Carolina Marzuillo, Corrado De Vito, Giuseppe La Torre, Paolo Villari\",\"doi\":\"10.1016/j.ajhg.2025.05.012\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Polygenic risk scores (PRSs) represent a promising innovation in the context of precision health, but their benefits for patients and healthcare systems remain unclear. This systematic review examined the methods used to quantify the costs and benefits of PRS-based approaches across different healthcare contexts, summarizing current evidence and identifying challenges. A systematic search of three databases was conducted, and full economic evaluations related to any intervention based on polygenic risk stratification strategies were included (PROSPERO CRD42023442780). Quality was assessed using the Quality of Health Economic Studies instrument. Studies were grouped into three categories (cancer, cardiovascular disease, and other diseases), and key methodological features and characteristics were extracted. A total of 24 cost-utility analyses of generally high quality were included: 16 studies focused on cancer, five on cardiovascular disease, and three on other diseases. Studies on cancer mainly aimed to optimize screening programs, while in the other fields, PRSs were mostly used to refine eligibility for preventive therapies. Analyses were robust, but they mostly relied on hypothetical cohorts, had limited generalizability, paid insufficient attention to implementation aspects—including the delivery model—and considered only clinical benefits. Despite a positive trend toward cost effectiveness following PRS implementation, several challenges remain. These include the limited use of real-world data, issues of representativeness, and gaps in accounting for implementation costs, as well as long-term health and non-health benefits. Further research and pilot studies are needed to evaluate both the costs and benefits of PRS applications across diverse populations for multiple health outcomes simultaneously.\",\"PeriodicalId\":7659,\"journal\":{\"name\":\"American journal of human genetics\",\"volume\":\"20 1\",\"pages\":\"\"},\"PeriodicalIF\":8.1000,\"publicationDate\":\"2025-06-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"American journal of human genetics\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1016/j.ajhg.2025.05.012\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"American journal of human genetics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.ajhg.2025.05.012","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

摘要

多基因风险评分(PRSs)在精准医疗领域是一项很有前途的创新,但其对患者和医疗系统的益处尚不清楚。本系统综述研究了用于在不同医疗环境中量化基于prs的方法的成本和收益的方法,总结了当前的证据并确定了挑战。系统检索了三个数据库,并纳入了与任何基于多基因风险分层策略的干预相关的全面经济评估(PROSPERO CRD42023442780)。使用卫生经济研究质量工具评估质量。研究分为三类(癌症、心血管疾病和其他疾病),提取关键的方法学特征和特征。总共纳入了24项总体质量较高的成本效用分析:16项研究重点是癌症,5项研究重点是心血管疾病,3项研究重点是其他疾病。在癌症领域的研究主要是为了优化筛查方案,而在其他领域,PRSs主要用于完善预防治疗的资格。分析是可靠的,但它们大多依赖于假设的队列,泛化性有限,对实施方面(包括交付模式)关注不足,只考虑临床效益。尽管实施PRS后成本效益有积极的趋势,但仍存在一些挑战。这些问题包括实际数据的使用有限、代表性问题、执行成本核算方面的差距以及长期健康和非健康效益。需要进行进一步的研究和试点研究,以评估在不同人群中同时实现多种健康结果的减贫计划应用的成本和收益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Weighing the evidence on costs and benefits of polygenic risk-based approaches in clinical practice: A systematic review of economic evaluations
Polygenic risk scores (PRSs) represent a promising innovation in the context of precision health, but their benefits for patients and healthcare systems remain unclear. This systematic review examined the methods used to quantify the costs and benefits of PRS-based approaches across different healthcare contexts, summarizing current evidence and identifying challenges. A systematic search of three databases was conducted, and full economic evaluations related to any intervention based on polygenic risk stratification strategies were included (PROSPERO CRD42023442780). Quality was assessed using the Quality of Health Economic Studies instrument. Studies were grouped into three categories (cancer, cardiovascular disease, and other diseases), and key methodological features and characteristics were extracted. A total of 24 cost-utility analyses of generally high quality were included: 16 studies focused on cancer, five on cardiovascular disease, and three on other diseases. Studies on cancer mainly aimed to optimize screening programs, while in the other fields, PRSs were mostly used to refine eligibility for preventive therapies. Analyses were robust, but they mostly relied on hypothetical cohorts, had limited generalizability, paid insufficient attention to implementation aspects—including the delivery model—and considered only clinical benefits. Despite a positive trend toward cost effectiveness following PRS implementation, several challenges remain. These include the limited use of real-world data, issues of representativeness, and gaps in accounting for implementation costs, as well as long-term health and non-health benefits. Further research and pilot studies are needed to evaluate both the costs and benefits of PRS applications across diverse populations for multiple health outcomes simultaneously.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
14.70
自引率
4.10%
发文量
185
审稿时长
1 months
期刊介绍: The American Journal of Human Genetics (AJHG) is a monthly journal published by Cell Press, chosen by The American Society of Human Genetics (ASHG) as its premier publication starting from January 2008. AJHG represents Cell Press's first society-owned journal, and both ASHG and Cell Press anticipate significant synergies between AJHG content and that of other Cell Press titles.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信