动脉粥样硬化潜在药物靶点:现状和未来展望。

Omar Mohammed Ali Saleh Al Qarawani, Palwinder Kaur, Manish Vyas, Sandeep Sharma
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引用次数: 0

摘要

背景:动脉粥样硬化的全球负担及其对冠心病和缺血性心脏问题的影响是发病率和住院率最高的原因。在美国,在过去十年中,心脏问题患者的数量有所增加,并且仍然是欧洲和美国的主要死亡原因。目的:尽管治疗干预和早期诊断脂肪病变的形成及其后续步骤是可能的,当观察到临床数据时,该疾病的治疗管理仍然值得怀疑。适当的靶点识别和生物标志物识别仍有空间,这可以作为开发有效药物和递送系统的基线,从而控制疾病的发生率和流行率。本文重点介绍了该疾病目前的病理生理状态以及用于治疗该疾病的新策略。研究结果:本文深入了解了各种常规治疗药物在疾病治疗中的局限性。新出现的策略可能被证明对疾病治疗有效。这篇文章还深入了解了细胞和分子生物学领域的最新发现,如引起血脂异常的遗传作用、免疫细胞的作用和非编码小RNA的作用,这可以为开发动脉粥样硬化的治疗干预措施奠定未来的方向。
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Atherosclerosis Potential Drug Targets: Current Scenario and Future Perspectives.

Background: The global burden of atherosclerosis and its implication to cause coronary heart disease and ischemic cardiac problems is the most prevalent cause of morbidity and hospitalization. In the US, there has been an increase in the number of patients with cardiac problems in the last decade, and still remains the primary cause of death in Europe as well as in the US.

Objectives: Even though therapeutic interventions and early diagnosis the formation of the fatty lesion and its subsequent steps are possible, the therapeutic management of the disease remains questionable when clinical data is observed. There is still scope for proper target identification and biomarker recognition, which can serve as a baseline to develop efficient pharmacological agent and delivery systems so that the disease incidence and prevalence can be controlled. The present article highlights the current pathophysiological state of the disease and emerging strategies that are applied to manage the disease.

Findings: This article gives an insight into the limitations of various conventionally used therapeutic agents for disease treatment. The emerging strategies that could prove efficacious in disease treatment. This article also gives an insight into current discoveries in the field of cellular and molecular biology, such as the genetic role in causing dyslipidemia and the role of immune cells and the role of non-coding small RNA, which can set the future direction to develop therapeutics interventions for atherosclerosis.

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