Advancing stroke genetics in Hawai‘i and the Pacific Islands

Stacy C. Brown, Christine Anne T. Galang, Mālialani Kana'iaupuni, Leah Dowsett, Keolu Fox, Kazuma Nakagawa
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Abstract

Stroke, the second leading cause of death worldwide, has partially heritable risk. Genome-wide association studies (GWAS) of stroke continue to identify increasing genetic risk loci. These discoveries point to novel disease mechanisms and causal risk factors, and herald genetics-based precision medicine strategies. In Hawai‘i, people of Indigenous communities who identify as Native Hawaiian or Pacific Islanders present with stroke at younger ages and suffer dramatically higher stroke mortality rates compared with other regional populations. This disparity is compounded by relative ancestral underrepresentation in stroke genetics research and, by extension, exclusion from cutting-edge medical opportunities based on genetic discovery. In this article, we discuss the issues contributing to the scientific biases experienced by Indigenous populations in the Pacific Islands, as well as community-based efforts now underway to address them.
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在夏威夷和太平洋岛屿推进中风遗传学研究
中风是全球第二大死亡原因,有部分遗传风险。卒中的全基因组关联研究(GWAS)继续确定增加的遗传风险位点。这些发现指出了新的疾病机制和因果风险因素,并预示着基于遗传学的精准医学策略。在夏威夷,认为自己是夏威夷原住民或太平洋岛民的土著社区居民在较年轻的时候就出现中风,与其他地区的人口相比,中风死亡率要高得多。在中风遗传学研究中,祖先的代表性相对不足,以及基于基因发现的尖端医疗机会被排除在外,加剧了这种差距。在这篇文章中,我们讨论了导致太平洋岛屿土著居民所经历的科学偏见的问题,以及目前正在进行的以社区为基础的解决这些问题的努力。
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