Realising the potential impact of artificial intelligence for rare diseases – A framework

Rare Pub Date : 2025-01-01 DOI:10.1016/j.rare.2024.100057
Tudor Groza , Chun-Hung Chan , David A. Pearce , Gareth Baynam
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Abstract

Rare diseases (RD) are conditions affecting fewer than 1 in 2000 persons, with over 7000 largely genetic RDs affecting 3.5 %-5.9 % of the global population, or approximately 262.9–446.2 million people. The substantial healthcare burden and costs, such as the $1 trillion annual expense in the USA, highlight the urgent need for improved RD management. The International Rare Diseases Research Consortium (IRDiRC) addresses this need through global collaboration, aiming for timely and accurate diagnosis, development of 1000 new therapies, and methodologies to measure impact by 2027.
IRDiRC's initiatives include biannual meetings and workshops, like the AI-focused workshop in October 2023. This identified AI as crucial for advancing RD research and proposed a Framework for AI to enhance the RD patient journey by addressing efficiency and quality of life through modular solutions mapped to critical stages. The Framework integrates diverse data sources to improve diagnosis, treatment, and impact assessment, reflecting a holistic, cross-sector approach. By guiding multi-stakeholder efforts, the Framework aims to harness AI’s potential to significantly improve rare disease care.
实现人工智能对罕见疾病的潜在影响——一个框架
罕见病是每2000人中影响不到1人的疾病,其中7000多种主要是遗传性罕见病,影响全球人口的3.5% %- 5.9% %,即约2.629亿- 4.462亿人。巨大的医疗保健负担和成本,如美国每年1万亿美元的费用,突出了改进研发管理的迫切需要。国际罕见病研究联盟(IRDiRC)通过全球合作来解决这一需求,目标是到2027年实现及时准确的诊断,开发1000种新疗法,以及衡量影响的方法。IRDiRC的计划包括两年一次的会议和研讨会,比如2023年10月举行的以人工智能为重点的研讨会。该报告确定人工智能对于推进研发研究至关重要,并提出了一个人工智能框架,通过映射到关键阶段的模块化解决方案来解决效率和生活质量问题,从而改善研发患者的旅程。该框架整合了多种数据来源,以改进诊断、治疗和影响评估,反映了一种全面的跨部门方法。通过指导多方利益攸关方的努力,该框架旨在利用人工智能的潜力,显著改善罕见病的治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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