One Step Ahead in Realizing Pharmacogenetics in Low- and Middle-Income Countries: What Should We Do?

IF 2.7 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Journal of Multidisciplinary Healthcare Pub Date : 2024-10-23 eCollection Date: 2024-01-01 DOI:10.2147/JMDH.S458564
Yudisia Ausi, Melisa Intan Barliana, Maarten J Postma, Auliya A Suwantika
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引用次数: 0

Abstract

Pharmacogenetics is a promising approach in future personalized medicine. This field holds excellent prospects for healthcare quality acceleration. It promotes the transition to the precision medicine era, whereby a health treatment is driven by a deeper understanding of individual characteristics by interpreting the underlying genomic variation. Pharmacogenetics has been developing rapidly since the human genome project. Many pharmacogenetics studies have shown the association between genetic variants and therapy outcomes. Several pharmacogenetics working groups have recommended guidelines for the clinical application of pharmacogenetics. However, the development of pharmacogenetics in low- and middle-income countries (LMICs) is still retarded behind. The problems mainly include clinical evidence, technology, policy and regulation, and human resources. Currently, available genome and drug effect data in LMICs are scarce. Pharmacogenetics development should be escalated with evidence proof through research collaboration across countries. The challenges of pharmacogenetics implementation are discussed comprehensively in this article, along with the prospect of pharmacogenetics-guided personalized medicine in developed countries. Stepwise is expected to help the researchers and stakeholders define the problem that hindered the pharmacogenetics application.

中低收入国家在实现药物基因学方面先行一步:我们应该做些什么?
药物遗传学是未来个性化医疗的一种前景广阔的方法。这一领域在提高医疗质量方面前景广阔。它促进了向精准医疗时代的过渡,即通过解读潜在的基因组变异来深入了解个体特征,从而推动健康治疗。自人类基因组计划以来,药物遗传学发展迅速。许多药物遗传学研究表明,基因变异与治疗效果之间存在关联。一些药物遗传学工作小组推荐了药物遗传学临床应用指南。然而,药物基因学在中低收入国家(LMICs)的发展仍然滞后。问题主要包括临床证据、技术、政策法规和人力资源。目前,中低收入国家可用的基因组和药物效应数据很少。药物基因学的发展应通过各国间的研究合作,在证据证明的基础上不断升级。本文全面探讨了药物遗传学实施过程中面临的挑战,以及发达国家以药物遗传学为指导的个性化医疗的前景。希望 Stepwise 能帮助研究人员和利益相关者明确阻碍药物基因学应用的问题所在。
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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来源期刊
Journal of Multidisciplinary Healthcare
Journal of Multidisciplinary Healthcare Nursing-General Nursing
CiteScore
4.60
自引率
3.00%
发文量
287
审稿时长
16 weeks
期刊介绍: The Journal of Multidisciplinary Healthcare (JMDH) aims to represent and publish research in healthcare areas delivered by practitioners of different disciplines. This includes studies and reviews conducted by multidisciplinary teams as well as research which evaluates or reports the results or conduct of such teams or healthcare processes in general. The journal covers a very wide range of areas and we welcome submissions from practitioners at all levels and from all over the world. Good healthcare is not bounded by person, place or time and the journal aims to reflect this. The JMDH is published as an open-access journal to allow this wide range of practical, patient relevant research to be immediately available to practitioners who can access and use it immediately upon publication.
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