Tsuchiya Naho, Pathipvanich Panita, Wichukchinda Nuanjun, Rojanawiwat Archawin, Auwanit Wattana, Ariyoshi Koya, Sawanpanyalert Pathom
Department of Clinical Medicine, Institute of Tropical Medicine, Nagasaki University, 1-12-4, Sakamoto, Nagasaki, 852-8523, Japan.
Global COE program, Nagasaki University, 1-12-4, Sakamoto, Nagasaki, 852-8523, Japan.
BMC Infect Dis. 2014 Oct 30;14:565. doi: 10.1186/s12879-014-0565-5.
Antiretroviral therapy markedly reduced mortality in HIV-infected individuals. However, in the previous studies, up to 50% of patients are compelled to modify their regimen in middle and low-income countries where salvage drug is still limited. This cohort study aimed to investigate the incidence and predictors of regimen modification from the first-line antiretroviral regimen in northern Thailand.
All HIV-infected patients starting antiretroviral therapy (ART) with generic drug (GPOvir®; stavudine, lamivudine and nevirapine) at a governmental hospital in northern Thailand from 2002 to 2007 were recruited. Baseline characteristics and detailed information of regimen modification until the end of 2010 were ascertained from cohort database and medical charts. As a potential genetic predictor of regimen modification, HLA B allele was determined by bead-based array hybridization (WAKFlow® HLA typing kit). We investigated predictors of the regimen modification using Cox's proportional hazard models.
Of 979 patients, 914 were eligible for the analysis. The observed events of regimen modification was 377, corresponding to an incidence 13.8/100 person-year-observation (95% CI:12.5-15.3) over 2,728 person years (PY) follow up. The main reasons for regimen modification were adverse effects (73.5%), especially lipodystrophy (63.2%) followed by rash (17.7%). Sixty three patients (17.1%) changed the regimen due to treatment failure. 2% and 19% of patients had HLA-B35:05 and B4001, respectively. HLA-B35:05 was independently associated with rash-related regimen modification (aHR 7.73, 95% CI:3.16-18.9) while female gender was associated with lipodystrophy (aHR 2.11, 95% CI:1.51-2.95). Female gender (aHR 0.54, 95% CI: 0.30-0.96), elder age (aHR 0.56, 95% CI: 0.32-0.99) and having HLA-B40:01 (aHR 0.29, 95% CI: 0.10-0.82) were protective for treatment failure related modification.
HLA-B35:05 and female gender were strong predictors of regimen modification due to rash and lipodystrophy, respectively. Female gender, elder age, and having HLA-B40:01 had protective effects on treatment failure-related regimen modification. This study provides further information of regimen modification for future tailored ART in Asia.
抗逆转录病毒疗法显著降低了艾滋病毒感染者的死亡率。然而,在之前的研究中,在挽救药物仍然有限的中低收入国家,高达50%的患者被迫调整他们的治疗方案。这项队列研究旨在调查泰国北部一线抗逆转录病毒治疗方案调整的发生率及预测因素。
招募了2002年至2007年期间在泰国北部一家政府医院开始使用仿制药(GPOvir®;司他夫定、拉米夫定和奈韦拉平)进行抗逆转录病毒治疗(ART)的所有艾滋病毒感染患者。从队列数据库和病历中确定了截至2010年底的基线特征和治疗方案调整的详细信息。作为治疗方案调整的潜在基因预测因素,通过基于微珠的阵列杂交(WAKFlow® HLA分型试剂盒)确定HLA B等位基因。我们使用Cox比例风险模型研究治疗方案调整的预测因素。
979名患者中,914名符合分析条件。观察到的治疗方案调整事件为377例,在2728人年(PY)的随访期间,发病率为13.8/100人年观察期(95%CI:12.5-15.3)。治疗方案调整的主要原因是不良反应(73.5%),尤其是脂肪代谢障碍(63.2%),其次是皮疹(17.7%)。63名患者(17.1%)因治疗失败而改变治疗方案。分别有2%和19%的患者携带HLA-B35:05和B40:01。HLA-B35:05与皮疹相关的治疗方案调整独立相关(调整后风险比7.73,95%CI:3.16-18.9),而女性与脂肪代谢障碍相关(调整后风险比2.11,95%CI:1.51-2.95)。女性(调整后风险比0.54,95%CI:0.30-0.96)、年龄较大(调整后风险比0.56,95%CI:0.32-0.99)和携带HLA-B40:01(调整后风险比0.29,95%CI:0.10-0.82)对治疗失败相关的调整有保护作用。
HLA-B35:05和女性分别是皮疹和脂肪代谢障碍导致治疗方案调整的强预测因素。女性、年龄较大和携带HLA-B40:01对治疗失败相关的治疗方案调整有保护作用。本研究为亚洲未来量身定制抗逆转录病毒治疗提供了治疗方案调整的进一步信息。