Harnessing Pharmacogenomics for Personalized Medicine: Tailoring Drug Therapy to Genetic Profiles.

Q4 Medicine
Pushpendra Kumar, Ankit Goel, Pooja Malik, Surbhi Sirswal, Poonam Rishishwar, Sanjay Rishishwar
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引用次数: 0

Abstract

This study means to investigate the capability of pharmacogenetics which can customize drug treatment through altered treatment of male genetic profiles. We finished hereditary profiling utilizing cutting edge sequencing (NGS) to figure out the key hereditary varieties that impact the medications metabolic adequacy and security. Patients were checked for a very long time to evaluate clinical results including ADRs and general wellness. Hereditary assessment uncovered variations in enormous qualities, for example, CYP2C9 CYP2D6 ABCB1 VKORC1 and SLCO1B1 which assume significant parts in drug digestion and transport. These hereditary markers are related with clinical realities to evaluate their effect on drug reactions and unfriendly impacts. The outcomes recommend that customized treatment dependent exclusively upon hereditary profiles could prompt better treatment results. For instance, patients with VKORC1 changes answer better to anticoagulants and drain less while patients with SLCO1B1 transformations have statin-incited myopathy which is more expensive and requires portion changes. This mirrors the useful effect of altered treatment on wellness results. Pharmacogenomics gives a useful asset to customized medication to tailor drug medicines dependent exclusively upon a person's genetic profile.

利用药物基因组学进行个性化医疗:根据基因谱定制药物治疗。
本研究旨在探讨药物遗传学的能力,通过改变男性基因谱的治疗来定制药物治疗。我们利用尖端测序(NGS)完成遗传分析,找出影响药物代谢充分性和安全性的关键遗传变异。对患者进行很长时间的检查,以评估临床结果,包括不良反应和总体健康状况。遗传评估揭示了许多性状的变异,例如CYP2C9 CYP2D6 ABCB1 VKORC1和SLCO1B1,它们在药物消化和运输中起着重要作用。这些遗传标记结合临床实际,评价其对药物反应和不良反应的影响。结果表明,完全依赖于遗传谱的定制治疗可以促进更好的治疗效果。例如,VKORC1改变的患者抗凝反应更好,排血更少,而SLCO1B1改变的患者有他汀类药物诱发的肌病,这更昂贵,需要改变部分。这反映了改变治疗对健康结果的有益影响。药物基因组学为定制药物提供了有用的资产,可以完全依赖于一个人的基因图谱来定制药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
53
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