PharmAccess Foundation, Department of Global Health, Amsterdam Institute for Global Health and Development, Academic Medical Centre, University of Amsterdam, Amsterdam, Netherlands.
Lancet Infect Dis. 2012 Apr;12(4):307-17. doi: 10.1016/S1473-3099(11)70255-9. Epub 2011 Oct 27.
The effect of pretreatment HIV-1 drug resistance on the response to first-line combination antiretroviral therapy (ART) in sub-Saharan Africa has not been assessed. We studied pretreatment drug resistance and virological, immunological, and drug-resistance treatment outcomes in a large prospective cohort.
HIV-1 infected patients in the PharmAccess African Studies to Evaluate Resistance Monitoring (PASER-M) cohort started non-nucleoside reverse transcriptase inhibitor-based ART at 13 clinical sites in six countries, from 2007 to 2009. We used the International Antiviral Society-USA drug resistance mutation list and the Stanford algorithm to classify participants into three pretreatment drug resistance categories: no pretreatment drug resistance, pretreatment drug resistance with fully active ART prescribed, or pretreatment drug resistance with reduced susceptibility to at least one prescribed drug. We assessed risk factors of virological failure (≥400 copies per mL) and acquired drug resistance after 12 months of ART by use of multilevel logistic regression with multiple imputations for missing data. CD4 cell count increase was estimated with linear mixed models.
Pretreatment drug resistance results were available for 2579 (94%) of 2733 participants; 2404 (93%) had no pretreatment drug resistance, 123 (5%) had pretreatment drug resistance to at least one prescribed drug, and 52 (2%) had pretreatment drug resistance and received fully active ART. Compared with participants without pretreatment drug resistance, the odds ratio (OR) for virological failure (OR 2·13, 95% CI 1·44-3·14; p<0·0001) and acquired drug-resistance (2·30, 1·55-3·40; p<0·0001) was increased in participants with pretreatment drug resistance to at least one prescribed drug, but not in those with pretreatment drug resistance and fully active ART. CD4 count increased less in participants with pretreatment drug resistance than in those without (35 cells per μL difference after 12 months; 95% CI 13-58; p=0·002).
At least three fully active antiretroviral drugs are needed to ensure an optimum response to first-line regimens and to prevent acquisition of drug resistance. Improved access to alternative combinations of antiretroviral drugs in sub-Saharan Africa is warranted.
The Netherlands Ministry of Foreign Affairs.
在撒哈拉以南非洲,尚未评估治疗前 HIV-1 耐药性对一线联合抗逆转录病毒治疗(ART)反应的影响。我们在一个大型前瞻性队列中研究了治疗前耐药性以及病毒学、免疫学和耐药性治疗结局。
2007 年至 2009 年,PharmAccess 非洲研究评估耐药监测(PASER-M)队列中的 HIV-1 感染患者在六个国家的 13 个临床点开始使用非核苷类逆转录酶抑制剂为基础的 ART。我们使用国际抗病毒学会-美国耐药突变列表和斯坦福算法将参与者分为三种治疗前耐药类别:无治疗前耐药、有完全活性 ART 处方的治疗前耐药,或对至少一种处方药物敏感性降低的治疗前耐药。我们使用具有多重插补的多级逻辑回归评估了治疗 12 个月后的病毒学失败(≥400 拷贝/毫升)和获得性耐药的风险因素。使用线性混合模型估计 CD4 细胞计数增加。
2733 名参与者中的 2579 名(94%)可获得治疗前耐药结果;2404 名(93%)无治疗前耐药,123 名(5%)至少有一种处方药物耐药,52 名(2%)有治疗前耐药且接受了完全活性的 ART。与无治疗前耐药的参与者相比,至少有一种处方药物耐药的参与者发生病毒学失败的比值比(OR)(2.13,95%CI 1.44-3.14;p<0.0001)和获得性耐药的 OR(2.30,1.55-3.40;p<0.0001)增加,但治疗前耐药且接受了完全活性 ART 的参与者则不然。与无治疗前耐药的参与者相比,有治疗前耐药的参与者的 CD4 计数增加较少(12 个月后相差 35 个细胞/μL;95%CI 13-58;p=0.002)。
需要至少三种完全活性的抗逆转录病毒药物来确保一线方案的最佳反应并预防耐药性的产生。撒哈拉以南非洲需要更好地获得替代的抗逆转录病毒药物组合。
荷兰外交部。