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Top Three Pharmacogenomics and Personalized Medicine Applications at the Nexus of Renal Pathophysiology and Cardiovascular Medicine.

机译:肾脏病理生理学与心血管医学研究的三大药物基因组学和个性化医学应用。

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摘要

Pharmacogenomics is a field with origins in the study of monogenic variations in drug metabolism in the 1950s. Perhaps because of these historical underpinnings, there has been an intensive investigation of 'hepatic pharmacogenes' such as CYP450s and liver drug metabolism using pharmacogenomics approaches over the past five decades. Surprisingly, kidney pathophysiology, attendant diseases and treatment outcomes have been vastly under-studied and under-theorized despite their central importance in maintenance of health, susceptibility to disease and rational personalized therapeutics. Indeed, chronic kidney disease (CKD) represents an increasing public health burden worldwide, both in developed and developing countries. Patients with CKD suffer from high cardiovascular morbidity and mortality, which is mainly attributable to cardiovascular events before reaching end-stage renal disease. In this paper, we focus our analyses on renal function before end-stage renal disease, as seen through the lens of pharmacogenomics and human genomic variation. We herein synthesize the recent evidence linking selected Very Important Pharmacogenes (VIP) to renal function, blood pressure and salt-sensitivity in humans, and ways in which these insights might inform rational personalized therapeutics. Notably, we highlight and present the rationale for three applications that we consider as important and actionable therapeutic and preventive focus areas in renal pharmacogenomics: 1) ACE inhibitors, as a confirmed application, 2) VDR agonists, as a promising application, and 3) moderate dietary salt intake, as a suggested novel application. Additionally, we emphasize the putative contributions of gene-environment interactions, discuss the implications of these findings to treat and prevent hypertension and CKD. Finally, we conclude with a strategic agenda and vision required to accelerate advances in this under-studied field of renal pharmacogenomics with vast significance for global public health.
机译:药物基因组学是一个研究1950年代药物代谢的单基因变异的领域。也许由于这些历史基础,在过去的五十年中,已经使用药物基因组学方法对CYP450等“肝药基因”和肝脏药物代谢进行了深入研究。出乎意料的是,尽管肾脏病理生理学,伴随疾病和治疗结果在维护健康,疾病易感性和合理的个性化治疗中具有重要意义,但它们仍被大量研究和理论不足。确实,无论是在发达国家还是在发展中国家,慢性肾脏病(CKD)代表着全球范围内日益增加的公共卫生负担。 CKD患者患有较高的心血管疾病发病率和死亡率,这主要归因于达到终末期肾脏疾病之前的心血管事件。在本文中,我们将重点放在终末期肾脏疾病之前的肾功能上,从药物基因组学和人类基因组变异的角度来看。我们在此综合了最近的证据,这些证据将选定的非常重要的药物原(VIP)与人的肾功能,血压和盐敏感性相关联,以及这些见识可为合理的个性化疗法提供信息的方式。值得注意的是,我们重点介绍了三种应用,我们认为它们是肾脏药物基因组学中重要且可操作的治疗和预防重点领域的原理:1)ACE抑制剂(已确认的应用),2)VDR激动剂(有希望的应用)和3)作为建议的新应用,适度的饮食盐摄入量。此外,我们强调基因与环境相互作用的假定作用,讨论这些发现对治疗和预防高血压和CKD的意义。最后,我们以战略议程和远见作为结局,以加快在这个尚未充分研究的肾脏药物基因组学领域的进展,这对全球公共卫生具有重大意义。

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