AIDS National Reference Laboratory, LNRS, General Hospital of Kinshasa, Kinshasa, Democratic Republic of Congo.
J Acquir Immune Defic Syndr. 2011 Jul 1;57 Suppl 1:S27-33. doi: 10.1097/QAI.0b013e31821f596c.
We studied virological outcome and drug resistance in patients on antiretroviral therapy (ART) in health care centers in the Democratic Republic of Congo and looked for the presence of drug resistance in antiretroviral-naive patients attending the same clinics.
In 2008, we conducted a cross-sectional survey among patients on ART for ≥ 12 months in 4 major cities [Kinshasa (n = 289), Matadi (n = 198), Lubumbashi (n = 77), and Mbuji-Mayi (n = 103)]. Genotypic drug resistance tests were done with an in-house assay on samples with viral load >1000 copies/mL. ART-naive patients (n = 283) were also consecutively enrolled in the same clinics.
Of the 667 patients on ART, >98% received Lamivudine + Stavudine/azidothymidine + Nevirapine/Efavirenz as first-line regimen and 74.4% were women. Median time on ART was 25 months [interquartile ratio (IQR), 19-32] in Kinshasa, 26 months (IQR, 19-32) in Matadi, 27 months (IQR, 19-44) in Lubumbashi, and 19 months (IQR, 16-24) in Mbuji-Mayi. A total of 97 patients (14.6%) had viral load >1000 copies/mL, and among the 93 successfully sequenced samples, 78 (83.9%) were resistant to at least 1 drug of their ART regimen: 68 harbored resistance mutations to nucleoside reverse transcriptase inhibitor (NRTI) and nonnucleoside reverse transcriptase inhibitor (NNRTI), 2 to NRTI only, 7 to NNRTI only, and 1 to NRTI + NNRTI + protease inhibitor. The majority of patients, 70/78 (89.7%), were resistant to at least 2 of the 3 drugs from their treatment. The use of next-generation NNRTI, etravirine was already compromised for 19.2% (15/78) of the patients and 7 patients had the K65R mutation compromising the use of tenofovir in second-line regimens. The proportion of antiretroviral-resistant patients increased over time from 8.4% to 18.6% for patients on ART for 12-23 months or >35 months (P = 0.013), respectively. Virological failure and rates of drug resistance were significantly higher among men than women, 19.9% versus 8.8%, respectively (P = 0.0001). Among the 253 recently diagnosed patients, 20 (7.9%) harbored resistance mutations.
The accumulation of drug resistance mutations with time on ART needs further attention, and surveillance should be reinforced in ART programs in sub-Saharan Africa.
我们研究了在刚果民主共和国医疗机构中接受抗逆转录病毒治疗(ART)的患者的病毒学结果和耐药情况,并寻找在接受相同治疗的无耐药史患者中是否存在耐药性。
2008 年,我们在 4 个主要城市(金沙萨[289 例]、马塔迪[198 例]、卢本巴希[77 例]和姆布吉-马伊[103 例])对接受 ART 治疗≥12 个月的患者进行了一项横断面调查。对病毒载量>1000 拷贝/ml 的样本进行了基于实验室检测的基因型耐药性检测。同时还连续招募了 283 名无耐药史的 ART 初治患者。
在 667 例接受 ART 的患者中,>98%接受了拉米夫定+司他夫定/齐多夫定+奈韦拉平/依非韦伦作为一线治疗方案,且 74.4%为女性。在金沙萨、马塔迪、卢本巴希和姆布吉-马伊,ART 开始后中位时间分别为 25 个月(IQR,19-32)、26 个月(IQR,19-32)、27 个月(IQR,19-44)和 19 个月(IQR,16-24)。共有 97 例(14.6%)患者病毒载量>1000 拷贝/ml,在 93 例成功测序的样本中,78 例(83.9%)对至少 1 种 ART 方案药物耐药:68 例对核苷类逆转录酶抑制剂(NRTI)和非核苷类逆转录酶抑制剂(NNRTI)耐药,2 例仅对 NRTI 耐药,7 例仅对 NNRTI 耐药,1 例对 NRTI+NNRTI+蛋白酶抑制剂耐药。大多数患者(70/78,89.7%)对其治疗方案中的至少 2 种药物耐药。下一代 NNRTI,依曲韦林已对 19.2%(15/78)的患者产生耐药,且 7 例患者的 K65R 突变使替诺福韦在二线方案中受到限制。在接受 ART 治疗 12-23 个月或>35 个月的患者中,耐药患者的比例分别从 8.4%增加到 18.6%(P=0.013)。与女性相比,男性的病毒学失败和耐药率分别显著更高,分别为 19.9%和 8.8%(P=0.0001)。在 253 例新诊断的患者中,有 20 例(7.9%)存在耐药突变。
ART 治疗时间越长,耐药突变的积累就越需要引起重视,应加强撒哈拉以南非洲的 ART 项目的监测。