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Analytical validity of a genotyping assay for use with personalized antihypertensive and chronic kidney disease therapy

机译:用于个性化抗高血压和慢性肾病治疗的基因分型测定的分析有效性

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摘要

Hypertension and chronic kidney disease are inextricably linked. Hypertension is a well-recognized contributor to chronic kidney disease progression and, in turn, renal disease potentiates hypertension. A generalized approach to drug selection and dosage has not proven effective in managing these conditions, in part, because patients with heterogeneous kidney disease and hypertension etiologies are frequently grouped according to functional or severity classifications. Genetic testing may serve as an important tool in the armamentarium of clinicians who embrace precision medicine. Increasing scientific evidence has supported the utilization of genomic information to select efficacious antihypertensive therapy and understand hereditary contributors to chronic kidney disease progression. Given the wide array of antihypertensive agents available and diversity of genetic renal disease predictors, a panel-based approach to genotyping may be an efficient and economic means of establishing an individualized blood pressure response profile for patients with various forms of chronic kidney disease and hypertension. In this manuscript, we discuss the validation process of a Clinical Laboratory Improvement Amendments-approved genetic test to relay information on 72 genetic variants associated with kidney disease progression and hypertension therapy. These genomic-based interventions, in addition to routine clinical data, may help inform physicians to provide personalized therapy. Copyright (c) 2018 Wolters Kluwer Health, Inc. All rights reserved.
机译:高血压和慢性肾疾病是密不可分的。高血压是一种公认​​的慢性肾病进展的贡献者,又转,肾病调高高血压。药物选择和剂量的广义方法没有被证明有效地管理这些条件,因为患有异质肾病和高血压病因的患者经常根据功能或严重程度进行分组。基因检测可以作为拥抱精密药物的临床医生的武器中的重要工具。增加科学证据支持利用基因组信息,以选择有效的抗高血压治疗,了解患有慢性肾病进展的遗传源。鉴于各种抗高血压药物可用和遗传肾病预测因子的多样性,基于基于面板的基因分型方法可能是建立各种形式的慢性肾病和高血压患者的个性化血压反应概况的有效和经济手段。在本手稿中,我们讨论了临床实验室改进修正案的验证过程 - 批准的遗传测试,以便在与肾病进展和高血压治疗相关的72种遗传变异中继信息。除常规临床数据外,这些基因组的干预措施还可以帮助医生提供个性化治疗。版权所有(c)2018 Wolters Kluwer Health,Inc。保留所有权利。

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