Academic Journal

Aspiring toward equitable benefits from genomic advances to individuals of ancestrally diverse backgrounds.

التفاصيل البيبلوغرافية
العنوان: Aspiring toward equitable benefits from genomic advances to individuals of ancestrally diverse backgrounds.
المؤلفون: Wang, Ying, He, Yixuan, Shi, Yue, Qian, David C, Gray, Kathryn J, Winn, Robert, Martin, Alicia R
المصدر: Am J Hum Genet ; ISSN:1537-6605 ; Volume:111 ; Issue:5
بيانات النشر: Elsevier Science
سنة النشر: 2024
المجموعة: PubMed Central (PMC)
مصطلحات موضوعية: SDOH, carrier screening, cell-free DNA screening, cfDNA screening, diversity, genetic testing, health disparities, health equity, precision oncology, reproductive medicine, social determinants of health
الوصف: Advancements in genomic technologies have shown remarkable promise for improving health trajectories. The Human Genome Project has catalyzed the integration of genomic tools into clinical practice, such as disease risk assessment, prenatal testing and reproductive genomics, cancer diagnostics and prognostication, and therapeutic decision making. Despite the promise of genomic technologies, their full potential remains untapped without including individuals of diverse ancestries and integrating social determinants of health (SDOHs). The NHGRI launched the 2020 Strategic Vision with ten bold predictions by 2030, including "individuals from ancestrally diverse backgrounds will benefit equitably from advances in human genomics." Meeting this goal requires a holistic approach that brings together genomic advancements with careful consideration to healthcare access as well as SDOHs to ensure that translation of genetics research is inclusive, affordable, and accessible and ultimately narrows rather than widens health disparities. With this prediction in mind, this review delves into the two paramount applications of genetic testing-reproductive genomics and precision oncology. When discussing these applications of genomic advancements, we evaluate current accessibility limitations, highlight challenges in achieving representativeness, and propose paths forward to realize the ultimate goal of their equitable applications.
نوع الوثيقة: article in journal/newspaper
review
other non-article part of journal/newspaper
اللغة: English
Relation: https://doi.org/10.1016/j.ajhg.2024.04.002; https://pubmed.ncbi.nlm.nih.gov/38642557; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11080611/
DOI: 10.1016/j.ajhg.2024.04.002
الاتاحة: https://doi.org/10.1016/j.ajhg.2024.04.002
https://pubmed.ncbi.nlm.nih.gov/38642557
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11080611/
Rights: Copyright © 2024 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved.
رقم الانضمام: edsbas.90790ADB
قاعدة البيانات: BASE
الوصف
DOI:10.1016/j.ajhg.2024.04.002