Schmidt Daniel, Kollan Christian, Fätkenheuer Gerd, Schülter Eugen, Stellbrink Hans-Jürgen, Noah Christian, Jensen Björn-Erik Ole, Stoll Matthias, Bogner Johannes R, Eberle Josef, Meixenberger Karolin, Kücherer Claudia, Hamouda Osamah, Bartmeyer Barbara
Department of Infectious Disease Epidemiology, HIV/AIDS, STI and Blood Born Infections, Robert Koch-Institute, Berlin, Germany.
Clinic of Internal Medicine, University Köln, Köln, Germany.
PLoS One. 2014 Aug 22;9(8):e104474. doi: 10.1371/journal.pone.0104474. eCollection 2014.
We assessed trends in the proportion of transmitted (TDR) and acquired (ADR) HIV drug resistance and associated mutations between 2001 and 2011 in the German ClinSurv-HIV Drug Resistance Study.
The German ClinSurv-HIV Drug Resistance Study is a subset of the German ClinSurv-HIV Cohort. For the ClinSurv-HIV Drug Resistance Study all available sequences isolated from patients in five study centres of the long term observational ClinSurv-HIV Cohort were included. TDR was estimated using the first viral sequence of antiretroviral treatment (ART) naïve patients. One HIV sequence/patient/year of ART experienced patients was considered to estimate the proportion of ADR. Trends in the proportion of HIV drug resistance were calculated by logistic regression.
9,528 patients were included into the analysis. HIV-sequences of antiretroviral naïve and treatment experienced patients were available from 34% (3,267/9,528) of patients. The proportion of TDR over time was stable at 10.4% (95% CI 9.1-11.8; p for trend = 0.6; 2001-2011). The proportion of ADR among all treated patients was 16%, whereas it was high among those with available HIV genotypic resistance test (64%; 1,310/2,049 sequences; 95% CI 62-66) but declined significantly over time (OR 0.8; 95% CI 0.77-0.83; p for trend<0.001; 2001-2011). Viral load monitoring subsequent to resistance testing was performed in the majority of treated patients (96%) and most of them (67%) were treated successfully.
The proportion of TDR was stable in this study population. ADR declined significantly over time. This decline might have been influenced by broader resistance testing, resistance test guided therapy and the availability of more therapeutic options and not by a decline in the proportion of TDR within the study population.
在德国临床监测-艾滋病毒耐药性研究中,我们评估了2001年至2011年期间传播性(TDR)和获得性(ADR)艾滋病毒耐药性及相关突变比例的趋势。
德国临床监测-艾滋病毒耐药性研究是德国临床监测-艾滋病毒队列的一个子集。对于临床监测-艾滋病毒耐药性研究,纳入了从长期观察性临床监测-艾滋病毒队列的五个研究中心的患者中分离出的所有可用序列。使用初治抗逆转录病毒治疗(ART)患者的首个病毒序列来估计TDR。对于接受过ART治疗的患者,考虑每年每位患者的一个艾滋病毒序列来估计ADR的比例。通过逻辑回归计算艾滋病毒耐药性比例的趋势。
9528名患者纳入分析。34%(3267/9528)的患者有初治和接受过治疗患者可用的艾滋病毒序列。TDR比例随时间稳定在10.4%(95%可信区间9.1 - 11.8;趋势p值 = 0.6;2001 - 2011年)。所有接受治疗患者中ADR的比例为16%,而在进行了艾滋病毒基因型耐药性检测的患者中比例较高(64%;1310/2049个序列;95%可信区间62 - 66),但随时间显著下降(比值比0.8;95%可信区间0.77 - 0.83;趋势p值<0.001;2001 - 2011年)。在大多数接受治疗的患者(96%)中进行了耐药性检测后的病毒载量监测,其中大多数(67%)治疗成功。
在该研究人群中TDR比例稳定。ADR随时间显著下降。这种下降可能受到更广泛的耐药性检测、耐药性检测指导的治疗以及更多治疗选择的可用性的影响,而不是受研究人群中TDR比例下降的影响。