Greenfield Andy
Nuffield Department of Women's & Reproductive Health, Institute of Reproductive Sciences, University of Oxford, Alec Issigonis Way, Building 8000, OX4 2HW, Oxford, UK.
Mamm Genome. 2024 Oct 26. doi: 10.1007/s00335-024-10080-1.
There is a thriving, worldwide, biomedical research community working to understand the molecular bases of diseases of all types, continuously driving improved diagnostics and therapies. Developments in genetics and experimental medicine are yielding novel genetic therapies that were hardly dreamt of 40 years ago. But along with these scientific achievements, there exist challenges in ensuring that 21st century medical interventions are accessible to all who need them. This perspective will discuss how preclinical research, with a focus on rare diseases, can better contribute to healthcare ecosystems that are oriented towards greater health equity. This contribution may require changes to the prevailing scientific research culture that will need support from relevant institutions and the wider community.
全球有一个蓬勃发展的生物医学研究群体,致力于了解各类疾病的分子基础,不断推动诊断和治疗方法的改进。遗传学和实验医学的发展正在产生40年前几乎无法想象的新型基因疗法。但伴随着这些科学成就,在确保21世纪的医疗干预措施能为所有有需要的人所用方面也存在挑战。本文将探讨以罕见病为重点的临床前研究如何能更好地为以实现更大健康公平为导向的医疗生态系统做出贡献。这种贡献可能需要改变当前的科研文化,而这需要相关机构和更广泛社区的支持。