利用基因组学的力量治疗高血压:冰山一角?

Cambridge prisms, Precision medicine Pub Date : 2025-02-04 eCollection Date: 2025-01-01 DOI:10.1017/pcm.2025.1
Hafiz Naderi, Helen R Warren, Patricia B Munroe
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引用次数: 0

摘要

尽管对其复杂的遗传结构有了深入的了解,但高血压仍然是一种难以捉摸的疾病。到目前为止,对血压的遗传研究已经取得了苦乐参半的结果,发现了2000多个基因位点,尽管候选的致病基因和生物学途径在很大程度上仍然未知。大数据和复杂统计工具的时代推动了对病理生理学和因果推理的深入研究。然而,新的高血压遗传风险工具只是冰山一角,基因组技术的应用可能会激增。我们回顾了高血压的基因组学,探索了我们目前对这种情况的理解的重要里程碑,以及高血压个性化治疗和管理的进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Harnessing the power of genomics in hypertension: tip of the iceberg?

Despite the blaze of advancing knowledge on its complex genetic architecture, hypertension remains an elusive condition. Genetic studies of blood pressure have yielded bitter-sweet results thus far with the identification of more than 2,000 genetic loci, though the candidate causal genes and biological pathways remain largely unknown. The era of big data and sophisticated statistical tools has propelled insights into pathophysiology and causal inferences. However, new genetic risk tools for hypertension are the tip of the iceberg, and applications of genomic technology are likely to proliferate. We review the genomics of hypertension, exploring the significant milestones in our current understanding of this condition and the progress towards personalised treatment and management for hypertension.

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