首页> 美国卫生研究院文献>International Journal of Biomedical Science : IJBS >Dyslipidaemia and Intima-Media Thickness of Carotid Arteries in Thirty-Five HIV/AIDS Patients Receiving Highly Active Antiretroviral Therapy
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Dyslipidaemia and Intima-Media Thickness of Carotid Arteries in Thirty-Five HIV/AIDS Patients Receiving Highly Active Antiretroviral Therapy

机译:35名接受高效抗逆转录病毒疗法的HIV / AIDS患者的血脂异常和颈动脉内膜中层厚度

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摘要

Objectives:Highly active antiretroviral therapy (HAART) has being impacted significantly therapies for natural human immunodeficiency virus (HIV) infection, which leads to a remarkable decrease in its morbidity and mortality but it is frequently associated with metabolic complications such as dyslipidaemia and cardiovascular complications. HIV reverse transcriptase (RT) inhibitors can be classified into nucleoside and non-nucleoside types. Mitochondrial dysfunction due to the depletion of mt-DNA is partly responsible for various nucleoside RT inhibitors-associated adverse effects including dyslipidaemia. Efavirenz (EFV) is metabolized primarily by cytochrome P450 2B6 (CYP2B6) and the metabolic effects of EFV have been described previously. All patients in this study received the same HAART treatment regime (Stavudine (d4T) + Lamivudine (3TC) + Efavirenz (EFV)). This study aims to assess incidences for dyslipidaemia and atherosclerosis.
机译:目的:高效抗逆转录病毒疗法(HAART)已显着影响自然人免疫缺陷病毒(HIV)感染的疗法,从而导致其发病率和死亡率显着降低,但通常与代谢并发症如血脂异常和心血管并发症相关。 HIV逆转录酶(RT)抑制剂可分为核苷和非核苷类型。由于mt-DNA的消耗而导致的线粒体功能障碍部分是与各种核苷RT抑制剂相关的不良反应(包括血脂异常)的部分原因。 Efavirenz(EFV)主要通过细胞色素P450 2B6(CYP2B6)代谢,并且EFV的代谢作用已在前面进行了描述。该研究中的所有患者均接受相同的HAART治疗方案(司他夫定(d4T)+拉米夫定(3TC)+依非韦伦(EFV))。这项研究旨在评估血脂异常和动脉粥样硬化的发生率。

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