Jevtović Djordje, Salemović Dubravka, Ranin Jovan, Brmbolić Branko, Pesić-Pavlović Ivana, Zerjav Sonja, Djurković-Djaković Olgica
Institute for Infectious & Tropical Diseases, University of Belgrade School of Medicine, Belgrade, Serbia.
Open Virol J. 2009 Oct 23;3:84-8. doi: 10.2174/1874357900903010084.
To examine the prognosis of patients who present with very advanced HIV-induced immunodeficiency, and their response to highly active antiretroviral therapy (HAART), a series of 101 treatment naïve patients from the Serbian cohort of HIV infected patients, who presented with a CD4 count of </= 50/microL before commencing HAART, was retrospectively analyzed and factors influencing response to HAART and survival investigated. After a mean of three years (range 1-9) of treatment with PI-based and/or NNRTI-based regimens, a favorable response was achieved in 54.5% of the patients, treatment failure occurred in 13.9%, while 31.7% had a dissociative immunological/virological response. The overall estimated survival was eight years. Achievement of undetectable viremia during treatment appeared life saving (OR = 42.5, 95% CI 7.1 - 251.9, P = 0.000, as was a rise in CD4 cell count to over 200/muL (OR = 6.4, 95% CI 1.2-31.8, P = 0.023). However, undetectable viremia was the single predictor of longer survival (OR = 42.5, 95% CI 7.1 - 251.9, P = 0.000), regardless of the level of immune reconstitution (log rank, P = 0.31). Late presenters had a high probability of developing the metabolic syndrome while on HAART, with a median time to hyperlipidemia and lypodystrophy of 5 and 6 years, respectively. We conclude that late presenters on HAART may have a good prognosis, a prerequisite for which is sustained undetectable viremia regardless of the immune recovery.
为了研究出现非常严重的HIV诱导免疫缺陷的患者的预后情况,以及他们对高效抗逆转录病毒疗法(HAART)的反应,我们对塞尔维亚HIV感染患者队列中的101例初治患者进行了回顾性分析,这些患者在开始HAART前CD4细胞计数≤50/μL,并调查了影响HAART反应和生存的因素。在用基于蛋白酶抑制剂(PI)和/或非核苷类逆转录酶抑制剂(NNRTI)的方案平均治疗三年(范围1 - 9年)后,54.5%的患者获得了良好反应,13.9%出现治疗失败,而31.7%有免疫/病毒学分离反应。总体估计生存期为八年。治疗期间实现病毒血症检测不到似乎可挽救生命(比值比[OR]=42.5,95%置信区间[CI] 7.1 - 251.9,P = 0.000),CD4细胞计数升至超过200/μL时也是如此(OR = 6.4,95% CI 1.2 - 31.8,P = 0.023)。然而,无论免疫重建水平如何,病毒血症检测不到是生存期延长的唯一预测因素(OR = 42.5,95% CI 7.1 - 251.9,P = 0.000)(对数秩检验,P = 0.31)。晚期就诊者在接受HAART时发生代谢综合征的可能性很高,高脂血症和脂肪代谢障碍的中位时间分别为5年和6年。我们得出结论,接受HAART的晚期就诊者可能有良好的预后,其前提是无论免疫恢复情况如何,病毒血症持续检测不到。