Abstract
While pharmacogenomic studies have facilitated the rapid expansion of personalized medicine, the benefits of these findings have not been evenly distributed. Genomic datasets pertaining to Indigenous populations are sorely lacking, leaving members of these communities at a higher risk of adverse drug reactions (ADRs), and associated negative outcomes. Australia has one of the largest Indigenous populations in the world. Pharmacogenomic studies of these diverse Indigenous Australian populations have been hampered by a paucity of data. In this article, we discuss the history of pharmacogenomics and highlight the inequalities that must be addressed to ensure equal access to pharmacogenomic-based healthcare. We also review efforts to conduct the pharmacogenomic profiling of chronic diseases among Australian Indigenous populations and survey the impact of the lack of drug safety-related information on potential ADRs among individuals in these communities.
Original language | English |
---|---|
Article number | 687116 |
Pages (from-to) | 1-6 |
Number of pages | 6 |
Journal | Frontiers in Genetics |
Volume | 12 |
DOIs | |
Publication status | Published - 20 Sept 2021 |
Externally published | Yes |
Bibliographical note
Funding Information:Funding for this research was supported by the MRFF Genomics Health Futures Mission grant (76757).
Publisher Copyright:
© Copyright © 2021 Nagaraj and Toombs.