Pharmacogenomics Tools for Precision Public Health and Lessons for Low- and Middle-Income Countries: A Scoping Review.

IF 1.8 4区 医学 Q3 PHARMACOLOGY & PHARMACY Pharmacogenomics & Personalized Medicine Pub Date : 2025-01-30 eCollection Date: 2025-01-01 DOI:10.2147/PGPM.S490135
Angélica Borbón, Juan Carlos Briceño, Augusto Valderrama-Aguirre
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Abstract

Pharmacogenomics is the integration of genomics and pharmacology to optimize drug response and reduce side effects. In terms of personalized or individualized medicine, PGx is defined as the identification and analysis of specific genetic variants associated with particular drug treatments for each patient. Under a precision public health (PPH) approach, population-level data are analyzed to generate public health strategies. The objective of this study was to conduct a scoping review of technological tools, examining their evolution, the predominance of high-income countries in their development, and the gaps and needs for genomic data and advances in low- and middle-income countries (LMICs). This review was conducted in accordance with the ScPRISMA guidelines. A search was conducted in PubMed, Web of Science and Embase until January 2024. A total of 40 documents were selected, which revealed the continuous evolution and progressive development of pharmacogenomic tools. The technological tools developed come from high-income countries, particularly the United States, Canada, China, and several European nations, where international collaboration has been essential to maintain and expand these tools, which have evolved to keep pace with the rapid generation of genomic data. This trend shows a scarce development of technological tools for public health precision in LMICs, which evidences the need to increase investment in genomic research infrastructure in this aspect and in the development of capacities to guarantee global accessibility and boost PPH for all populations.

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精准公共卫生的药物基因组学工具及中低收入国家的经验教训:范围审查。
药物基因组学是基因组学和药理学的结合,旨在优化药物反应和减少副作用。在个性化或个体化医疗方面,PGx被定义为识别和分析与每个患者的特定药物治疗相关的特定遗传变异。在精确公共卫生(PPH)方法下,分析人口水平的数据以制定公共卫生战略。本研究的目的是对技术工具进行范围审查,检查其演变,高收入国家在其发展中的主导地位,以及低收入和中等收入国家(LMICs)在基因组数据和进展方面的差距和需求。本次审查是按照ScPRISMA指南进行的。在PubMed, Web of Science和Embase进行了搜索,直到2024年1月。共选择了40篇文献,揭示了药物基因组学工具的不断演变和逐步发展。开发的技术工具来自高收入国家,特别是美国、加拿大、中国和几个欧洲国家,在这些国家,国际合作对于维护和扩展这些工具至关重要,这些工具已经发展到与基因组数据的快速生成保持同步。这一趋势表明,中低收入国家在公共卫生精准度方面的技术工具开发很少,这证明有必要增加对这方面的基因组研究基础设施的投资,并加强能力建设,以保证全球可及性和促进所有人口的PPH。
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来源期刊
Pharmacogenomics & Personalized Medicine
Pharmacogenomics & Personalized Medicine Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
3.30
自引率
5.30%
发文量
110
审稿时长
16 weeks
期刊介绍: Pharmacogenomics and Personalized Medicine is an international, peer-reviewed, open-access journal characterizing the influence of genotype on pharmacology leading to the development of personalized treatment programs and individualized drug selection for improved safety, efficacy and sustainability. In particular, emphasis will be given to: Genomic and proteomic profiling Genetics and drug metabolism Targeted drug identification and discovery Optimizing drug selection & dosage based on patient''s genetic profile Drug related morbidity & mortality intervention Advanced disease screening and targeted therapeutic intervention Genetic based vaccine development Patient satisfaction and preference Health economic evaluations Practical and organizational issues in the development and implementation of personalized medicine programs.
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