Bottaro Edgardo Gabriel, Caravello Oscar, Scapellato Pablo Gustavo, Stambulian Marcela, Vidal Gabriela Inés, Loggia Verónica, Scapellato José Luis, Thompson Flavia, Cassetti Isabel
Helios Salud, Ciudad Autónoma de Buenos Aires, Buenos Aires, Argentina. Argentina.
Enferm Infecc Microbiol Clin. 2008 Jun-Jul;26(6):325-9. doi: 10.1157/13123836.
Highly active antiviral therapy (HAART) results in a sharp decrease in HIV-related morbidity and mortality, but also induces adverse effects such as dyslipidemia, which is difficult treat because of drug interactions. Guidelines recommend lipid-lowering therapy with pravastatin or atorvastatin to reduce LDL cholesterol in these patients, and gemfibrozil or fenofibrate for treating hypertriglyceridemia. The use of statins in the management of dyslipidemia is complicated by drug interactions with some of the components of HAART. Rosuvastatin, a statin with minimal cytochrome P-450-mediated metabolism, could be an alternative option for this population.
Retrospective study to evaluate the efficacy and safety of rosuvastatin (10 mg/day) for 16 weeks in HAART-treated HIV-infected patients with dyslipidemia, and moderate to high cardiovascular risk. Results were analyzed with the Shapiro-Wilks, K-S Lilliefors, and sign tests. Percentages were analyzed with the chi-square test.
Seventy-eight patients were started on rosuvastatin for dyslipidemia, 60 as single therapy. After 16 weeks of treatment, a significant median decrease was seen in both LDL-cholesterol and non-HDL cholesterol (31.3% reduction in LDL and 29.9% in non-HDL). The therapeutic goal for non-HDL was achieved in 65.8% of patients. The decrease in triglyceride levels was also significant (34.1%); 35% of subjects achieved the therapeutic goal. The drug was withdrawn in 2 patients because of myositis, and in 1 because of gastrointestinal intolerance. There were no differences in efficacy or toxicity between patients receiving protease inhibitors, non-nucleoside reverse transcriptase inhibitors, or fibrates.
Rosuvastatin was safe and effective for treating dyslipidemia in HAART-treated HIV-infected patients. Results were similar to those observed in the HIV-uninfected population.
高效抗逆转录病毒疗法(HAART)使与HIV相关的发病率和死亡率大幅下降,但也会引发如血脂异常等不良反应,由于药物相互作用,这种不良反应难以治疗。指南推荐使用普伐他汀或阿托伐他汀进行降脂治疗,以降低这些患者的低密度脂蛋白胆固醇,使用吉非贝齐或非诺贝特治疗高甘油三酯血症。他汀类药物在血脂异常管理中的应用因与HAART的某些成分存在药物相互作用而变得复杂。瑞舒伐他汀是一种细胞色素P - 450介导的代谢作用极小的他汀类药物,可能是这类人群的替代选择。
一项回顾性研究,评估瑞舒伐他汀(10毫克/天)对接受HAART治疗且患有血脂异常、具有中度至高度心血管风险的HIV感染患者进行为期16周治疗的疗效和安全性。结果采用夏皮罗 - 威尔克检验、K - S 利列福斯检验和符号检验进行分析。百分比采用卡方检验进行分析。
78例患者开始使用瑞舒伐他汀治疗血脂异常,其中60例采用单一疗法。治疗16周后,低密度脂蛋白胆固醇和非高密度脂蛋白胆固醇均出现显著的中位数下降(低密度脂蛋白降低31.3%,非高密度脂蛋白降低29.9%)。65.8%的患者实现了非高密度脂蛋白的治疗目标。甘油三酯水平的下降也很显著(34.1%);35%的受试者实现了治疗目标。2例患者因肌炎停药,1例因胃肠道不耐受停药。接受蛋白酶抑制剂、非核苷类逆转录酶抑制剂或贝特类药物治疗的患者在疗效或毒性方面没有差异。
瑞舒伐他汀治疗接受HAART治疗的HIV感染患者的血脂异常安全有效。结果与未感染HIV人群中观察到的结果相似。