Figures
Abstract
Objective
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.
Method
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.
Results
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.
Conclusions
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.
Citation: Schmidt D, Kollan C, Fätkenheuer G, Schülter E, Stellbrink H-J, Noah C, et al. (2014) Estimating Trends in the Proportion of Transmitted and Acquired HIV Drug Resistance in a Long Term Observational Cohort in Germany. PLoS ONE 9(8): e104474. https://doi.org/10.1371/journal.pone.0104474
Editor: Paul Richard Harrigan, University of British Columbia, Canada
Received: December 13, 2013; Accepted: July 14, 2014; Published: August 22, 2014
Copyright: © 2014 Schmidt et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: The study received grants from the Collaborative HIV and Anti-HIV Drug Resistance Network CHAIN, 7th Framework of the European Commission, http://www.chain-hiv.eu/. Laboratory Lademannbogen provided support in the form of a salary for author CN, but did not have any additional role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of these authors are articulated in the ‘author contributions’ section.
Competing interests: The authors do not have any potential conflicts of interest. CN is an employee of Laboratory Lademannbogen. There are no patents, products in development or marketed products to declare. This does not alter the authors' adherence to all the PLOS ONE policies on sharing data and materials.
Introduction
Since the introduction of combination antiretroviral therapy the morbidity and mortality among people infected with HIV has been reduced dramatically [1]. However, antiretroviral treatment (ART) of HIV is still life-long, and the prolonged duration of therapy with emerging HIV drug resistance might leave many patients without treatment options. In recent years treatment options improved due to the approval of second generation drugs and new antiretroviral drug classes [2]. Moreover, fixed dose combinations were approved, increasing the level of adherence among patients [3], which also affects resistance development [4]. HIV drug resistance may be transmitted among recently infected patients within transmission chains but may also be acquired during non-suppressive antiretroviral treatment from ART experienced patients [5], [6]. In Germany, according to current treatment guidelines all patients should be genotyped routinely prior to ART initiation [7].
HIV drug resistance surveillance has been performed in many Western European countries within different study populations and settings. Most studies were performed in patients during primary HIV infection or in patients chronically infected with HIV prior to ART initiation [8]–[12]. Currently no epidemiological resistance data base exists, and no central repository for viral sequences is established in Germany. Studies on population level including all HIV sequences produced in routine clinical settings for estimating the proportion of TDR or ADR are not available. Therefore the aim of this study was to estimate trends in the proportion of overall TDR and ADR and within different drug classes between 2001 and 2011, as well as single mutations within the German ClinSurv-HIV Drug Resistance Study. This is the first time that viral sequence data is linked with epidemiological and antiretroviral treatment data in a large resistance study in Germany including ART naïve as well as treated patients in order to estimate the proportion of transmitted and acquired HIV drug resistance.
Materials and Methods
The ClinSurv-HIV Cohort, study design
The ClinSurv-HIV project protocol was approved by the German Federal Commissioner for Data Protection. ClinSurv-HIV is an ongoing, prospective, long-term observational cohort study. The study design has been described in detail elsewhere [13]. In brief, 15 clinical centres in different, predominantly urban areas in Germany are involved in the study and consecutively monitored subjects since January 1st 1999. The cohort comprises all individuals infected with HIV in the participating clinical centres. Only basic data are reported every six months. The data set is anonymized and comprises demographic data, time-related variables on clinical events, AIDS-defining diagnoses, and detailed data on antiretroviral treatment. Patients with available sequences were identified at the five ClinSurv-HIV Drug Resistance Study centres participating in this analysis. Any identifying information was removed at the local study centres, the sequences were labelled with a new identifier allowing linkage with anonymized patient data in the ClinSurv data base. All data analyses were performed on the anonymized data set.
The Robert Koch Institute (RKI) is the German national public health institute, therefore the Federal Commissioner for Data Protection is the responsible entity for studies which are conducted by the Robert Koch Institute. Information on HIV infection collected in ClinSurv corresponds to the data reported to the RKI according to legal requirements implemented by the national Protection against Infection act (IfSG) of 2001. All patient data collected in ClinSurv are generated during routine care. The German Federal Commissioner for Data Protection therefore waived the need for ethical approval for the ClinSurv study. No written informed consent is required from patients.
ClinSurv-HIV Drug Resistance Study
For the ClinSurv-HIV Drug Resistance substudy, all patients infected with HIV under care in five study sites (University of Cologne, University of Düsseldorf, University of Hanover, University of Munich, ICH Study Centre Hamburg) of the ClinSurv-HIV Cohort study group with at least one HIV genotypic resistance analysis result were identified. The nucleotide sequences were processed through the Stanford University Genotypic Resistance Interpretation Algorithm (www.hivdb.stanford.edu; HIVdb version 6.2.0; 2012) in order to identify amino acid substitutions and to determine drug susceptibility. For epidemiological analysis, HIV sequences isolated from ART naïve patients were analysed using the surveillance HIV drug resistance mutation list, SDRM [14]. Only the first HIV genotypic resistance test per patient while treatment naïve was considered for the estimation of the prevalence of TDR. HIV sequences isolated from ART experienced patients were analysed using the mutation list of the International Antiviral Society-USA, IAS, 2011 [15]. Overall ADR was estimated by including one HIV sequence/patient/year from antiretroviral treatment experienced patients. For the estimation of ADR within different drug classes only viral sequences of patients treated with the respective drug class were considered. HIV subtype on patient level was assigned based on the first available viral sequence of a patient centrally using the REGA HIV-1 Subtyping Tool - Version 2.0 [16].
Statistical analysis
Viral sequences available between 1998 and 2011 were collected and analysed. For the estimation of trends in the proportion of HIV drug resistance over time viral sequences sampled between 2001 and 2011 were included into the analyses. The characteristics of patients with available sequences compared to those who were not genotyped were compared with simple logistic regression. Patients and viral sequences were categorised into ART naïve and treatment experienced. Viral sequences were considered to originate from treatment naïve patients in case of ART start ≤15 days prior to the date of resistance testing, to account for delays in the documentation of the date of resistance testing results and the actual date of blood sampling. The time between resistance testing and antiretroviral treatment start and the proportion of patients with resistance test before ART start were analysed by using data from patients with documented first-line treatment start. The proportion of patients with antiretroviral treatment failure undergoing resistance testing was calculated for patients with first line treatment start in one of the resistance study centres who had >180 days of treatment experience and a resistance test within 90 days after virologic failure. Virologic failure was defined as two consecutive viral load measurements with >50 copies/ml within 180 days or one viral load measurement with >1000 copies/ml. For different drug classes the proportion of cumulative ART exposure per year, the median days of previous ART exposure and the proportion of patients showing history of exposure to the respective drug class were calculated, excluding treatment interruption time. A simple linear regression was performed on the duration of antiretroviral treatment exposure in days prior to resistance testing with increasing year of genotyping for different drug classes and on the total treatment exposure. In a univariate analysis of factors associated with HIV drug resistance the following covariates were separately included: age, gender, transmission group category, HIV subtype, ART interruption, duration of previous ART exposure, CD4 cell count, and plasma viral load at the time point of testing or 30 days prior to or 15 days after testing, year of resistance test at documented ART start. Factors significantly associated with acquired HIV drug resistance in a univariate analysis were included into multiple logistic regression. For the analysis of factors associated with acquired HIV drug resistance only the last sequence of ART experienced patients was included. The proportion of patients showing a history of exposure to a drug class, trends in the proportion of patients with ART interruption, gender, transmission group category, HIV subtype were calculated by simple logistic regression. Median plasma viral loads and CD4 cell counts were calculated for ART naïve and treated patients. The Mann-Whitney-U-test (MWT) was used to compare viral loads, CD4 cell counts and the age at ART start for patients with resistant and susceptible HIV. Confidence intervals were calculated using a Wilson score confidence interval. Trends in the prevalence of HIV drug resistance mutations, DRMs, (pfor trend) were calculated by logistic regression. All p-values were two sided, and a p-value of <0.05 was considered significant. Data were analysed using SPSS 18.0.3 and R 2.12.1.
Results
A total of 9,528 ClinSurv patients were enrolled in the five study centers participating in the resistance study. 4,989 viral sequences were collected from 34% (3,267/9,528) of these patients. Nearly half of these HIV sequences (47%; 2,365/4,989) were generated while patients were ART naïve, the other half of viral sequences (50%; 2,495/4,989) were produced while patients were treated with antiretroviral drugs. The ART status of the patients could not be clarified for 3% (129/4,989) of the HIV sequence data. Of the patients who have not been genotyped (n = 6,261), 4,895 patients were seen in the resistance study centres while ART naïve, and of 5,262 patients data were collected while treated with antiretroviral drugs (Table 1). In total 86% (8,165/9,528) of the patients in the five Resistance Study centres were ART experienced. Among all patients who have been treated, HIV drug resistance was identified in 16% (1,347/8,165) of patients.
Characteristics of patients with available sequences
Patients were predominantly male (82%; 2,683/3,267); 18% (584/3,267) were female. Median age at the time point of HIV genotypic resistance testing was 40 years (33.0–47.0). Median CD4 cell count at first visit was 310 cells/µl (IQR: 147–490). The main transmission group category was sex between men (58%; 1,904/3,267), followed by heterosexual contacts (14%; 445/3,267) and by patients originating from high-prevalence countries (12%; 405/3,267). Median time between first HIV genotypic resistance test and ART start was 33 days (IQR: 13–169). The proportion of patients with resistance test before ART start in the five study centres increased from 0.4% in 2000 to 69% in 2009 and declined thereafter to 46% in 2010 and 21% in 2011. The duration between HIV diagnosis and first resistance test was in median 45 days (IQR: 16–481) for ART naïve patients.
The characteristics of patients with resistance test and those without differed as follows: within the category risk of transmission in the Resistance study group we observed more patients with heterosexual contacts (with resistance test: 13.6% vs. 11.6% without test, p = 0.04), more patients from high prevalence countries (with resistance test: 12.4% vs. 10.5% without test, p = 0.03) and fewer patients with intravenous drug use (with resistance test: 5.5% vs. 8.8% without test, p<0.001); within the category region of origin in the Resistance study group we observed more patients being from Africa, Near East (with resistance test: 11.6% vs. 9.1% without test) (Table 1). Patients were predominantly infected with HIV-1 subtype B strains (69%; 2,240/3,267), but 18% (604/3,267) of patients harbored a non-B subtype infection. For 13% (423/3,267) of patients the HIV-1 subtype could not be determined by REGA HIV-1 Subtyping Tool. HIV-1 subtype A was most prevalent among the non-B subtypes (9%), followed by circulating recombinant forms (4%) (Table 1). The majority of women were infected with HIV-1 non-B subtypes (non-B subtypes: 53%; 312/584 vs. subtype-B: 33%; 192/584), predominantly subtype A (24%; 140/584). Nearly half of the female study population originated from high-prevalence countries: 46% (270/584). At time point of HIV genotypic resistance testing, the median viral load (VL) for ART naïve patients was 4.73 log10 copies/ml (IQR: 4.1–5.3), median CD4 cell count was 285 cells/µl (IQR: 151–437). Both VL and CD4 cell counts did not differ significantly between patients infected with susceptible or resistant viruses (VL susceptible: 4.74, IQR: 4.1–5.3 vs. VL resistant: 4.69, IQR: 4.2–5.3, p = 0.93; CD4 susceptible: 286, IQR: 150–437 vs. CD4 resistant: 274, IQR: 169–443, p = 0.90). The median VL of treated patients with detectable plasma virus was 4.02 log10 copies/ml (IQR: 3.1–4.8), median CD4 cell count of treated patients was 271 cells/µl (IQR: 150–423). VL and CD4 cell count did not differ significantly between patients infected with susceptible or resistant viruses (VL susceptible: 4.13, IQR: 2.8–4.9 vs. VL resistant: 3.96, IQR: 3.2–4.7, p = 0.50; CD4 susceptible: 280, IQR: 160–430 vs. CD4 resistant: 266, IQR: 145–420, p = 0.29).
Transmitted HIV drug resistance, TDR
Overall TDR according to SDRM list was identified among the first HIV sequences available before ART initiation in 10.4% (203/1,950; 95% CI 9.1–11.8) and remained stable over time (OR: 0.98; p for trend = 0.6; 2001–2011) (Figure 1A). Nucleoside reverse transcriptase inhibitor (NRTI) resistance was detected in 7% (128/1,950; 95% CI 6–8), followed by 3% (61/1,950; 95% CI 2–4) non-nucleoside reverse transcriptase inhibitor (NNRTI) resistance and 3% (56/1,950; 95% CI 2–4) protease inhibitor (PI) resistance. The prevalence of thymidine analogue mutations (TAMs) was 5% (89/1,950; 95% CI 4–6), and revertant mutations at position 215 of the reverse transcriptase (RT) were found in 3% (56/1,950; 95% CI 2–4) of first viral strains analysed from ART naïve patients (Table 2).
A Proportion of HIV drug resistance was determined using the first Prot/RT sequences from treatment naïve patients (n = 1950) by year according to the SDRM mutation list (Bennett et al. 2009). The proportion of TDR over time was stable at 10.4% (95% CI 9.1–11.8; p for trend = 0.6; 2001–2011). B Proportion of overall ADR (64%; 1,310/2,049 sequences; 95% CI 62–66) declined significantly over time (OR 0.8; 95% CI 0.77–0.83; p for trend<0.001; 2001–2011) in sequences from treated patients (n = 2,049) according to IAS mutation list 2011. C Proportion of ADR within different antiretroviral drug classes declined for all classes (NNRTI 55%, NRTI 51%, PI 30%; p for trend<0.001; 2001–2011) in sequences from patients treated with the respective drug class according to IAS mutation list 2011.
Acquired HIV drug resistance, ADR
ADR was calculated using maximal one HIV sequence per year of antiretroviral treatment experienced patients. Overall ADR was high (64%; 1,310/2,049 sequences; 95% CI 62–66) but declined significantly over time (OR 0.8; 95% CI 0.77–0.83; pfor trend<0.001; 2001–2011) (Figure 1B). To estimate HIV drug resistance in different drug classes, only viral sequences isolated from those patients who received the respective drug class were included into the analysis. Predominantly NNRTI resistance was identified (55%; 730/1333; 95% CI 52–57), followed by NRTI resistance in 51% (1,007/1,958; 95% CI 49–54) and PI resistance in 30% (473/1586; 95% CI 28–32). The proportion of ADR declined significantly over time for all three drug classes (pfor trend<0.001; 2001–2011) (Figure 1C). INI resistance was detected in 30% (10/33; 95% CI 17–47) of INI treated patients corresponding to 7% (10/150; 95% CI 4–12) among all HIV integrase sequences of ART experienced patients (Table 2). The most prevalent NRTI associated mutation identified among ART experienced patients was M184IV (34%). The most common TAMs were T215FY (25%), M41L (21%) and D67N (18%). The prevalence of PI mutations I84V and I54LM associated with darunavir and atazanavir resistance were 8% and 5%, respectively. The PI associated resistance mutations M46L and L90M were most prevalent with 14% (Figure 2).
A Proportion of resistance mutations in first Prot/RT sequence from treatment naïve patients (n = 1950; mutations with ≥0.3% shown) according to SDRM mutation list (Bennett 2009 et al.). B Proportion of resistance mutations in sequences from treated patients (Prot/RT n = 2,049; Int n = 150) according to IAS mutation list 2011. Bars in black: NRTI mutations, grey bars: TAMS, white bars: NNRTI mutations, bars in light grey: PI mutations, dark grey bars: INI mutations.
Factors associated with acquired HIV drug resistance
Factors significantly associated with a lower risk of ADR by using a univariate model were being female compared to male, transmission group category IDU compared to MSM, being infected with non-B subtype compared to subtype B, reported ART interruption at genotyping compared to reported continuous antiretroviral treatment at the time of genotyping and the cumulative duration of ART interruption (Table 3). In a multiple logistic regression significant factors from the univariate analysis were included into the model. Factors significantly associated with a lower risk of ADR were being female compared to male, reported ART interruption compared to reported continuous antiretroviral treatment at the time of genotyping, increasing calendar year of genotyping and the cumulative duration of ART interruption (Table 4). The duration of antiretroviral treatment was associated with a higher risk of ADR in both the univariate and multiple logistic regression.
To investigate the reduced risk for women to carry resistant viral strains, the duration of previous ART exposure was analysed. Results showed, that women had a significantly lower ART exposure time than men (women median 3.9 years, IQR 0.8–7.1 to men median 5.0, IQR 1.3–9.1, respectively; OR 0.95, 95%CI 0.92–0.98, p<0.001).
Treatment exposure
The majority of antiretroviral treated patients (98%; 1,956/1,987) showed a history of exposure to NRTIs, 67% (1,333/1,987) to NNRTIs, 80% (1,584/1,987) to PIs and 5% (103/1,987) to INIs.
Over time there was a small but significant decrease in the proportion of patients with exposure to NRTI (from 100% in 2001 to 98% in 2011; OR 0.78; 95% CI 0.67–0.91; p = 0.002), NNRTI use remained stable during the period of observation (from 65% in 2001, peaking in 2007 at 76% and leveling off thereafter with 63% in 2011; OR 1.0; 95% CI 0.96–1.0; p = 0.92). PI exposure increased significantly over time (from 80% in 2001 to 90% in 2011; OR 1.1; 95% CI 1.0–1.1; p = 0.009). INI use increased significantly over time (from 3% in 2007 to 25% in 2011; OR 2.0; 95% CI 1.7–2.3; p<0.001).
The simple linear regression showed a non-significant slight increase in the duration of ART exposure in days prior to resistance testing with increasing year of genotyping for NRTI (R2: 0.00; coefficient B: 6.6; 95% CI −19–32; p = 0.62), a significant increase for NNRTI (R2: 0.007; coefficient B: 26.6; 95% CI 13–40; p<0.001), for PI (R2: 0.006; coefficient B: 35.8; 95% CI 16–55; p<0.001) and for INI (R2: 0.045; coefficient B: 8.6; 95% CI 7–10; p<0.001). The duration of total ART exposure prior to resistance testing increased but not significantly over time (R2: 0.001; coefficient B: 22.8; 95% CI −3.3–49; p = 0.087).
Considering the regimen at resistance testing there was an increase in boosted PI containing regimens, especially for ritonavir boosted NRTI/PI combinations (from 10% in 2001 to 46% in 2011, NRTI+PI, overall 35%). PI regimens without booster almost disappeared over time. Triple class combinations like NRTI/NNRTI/PI declined over time whereas newer drug class containing regimens increased (from 0.6% in 2002 to 21% in 2011, overall 7%). Combination of NRTI/NNRTI showed a decline over time (from 29% in 2001 to 20% in 2010 and only 10% in 2011, overall 20%). Treatment interruption at the time of resistance testing was highly frequent in this study population but remained stable over time (17% in 2002 to 17% in 2011, overall 20%; OR 1.04; 95% CI 1.0–1.1; p for trend = 0.073; 2002–2011).
The proportion of patients undergoing resistance testing within 90 days after failing ART in the five study centres increased from 2.2% in 2001 to 21% in 2010 and amounted to 13% in 2011.
Treatment success post resistance testing was observed for 67% (928/1,386) of ART experienced patients. HIV drug resistance was observed in 60% (828/1,386) of this study population whereas 40% (558/1,386) showed no resistance associated mutations. However, the proportion of patients with successful viral suppression after resistance testing did not differ between those patients with susceptible and resistant HIV strains (67%; 553/828 resistant HIV vs. 67%; 375/558 susceptible HIV). A switch of therapy between different drug classes was observed significantly more frequent for patients harbouring resistant strains (64%; 530/828) than for patients with susceptible viruses (50%; 279/558).
Discussion
Results of this study showed that the estimated prevalence of TDR over time among ART naïve patients remained stable at a high level, whereas overall prevalence of ADR as well as drug resistance within different drug classes in patients under antiretroviral treatment declined significantly over time. The decline of ADR could be influenced by several factors. Presumably antiretroviral drug related effects like enhanced treatment optimization and resistance test guided therapy as well as broader resistance testing in the study population are considered to be reasonable factors influencing this decline.
The high but stable level of TDR is comparable to other prevalence estimates in long term observational cohorts in Germany as well as in other European countries [8], [17], [18] and to cohorts with patients chronically infected with HIV in other Western European countries [17]–[19]. Since the date of HIV infection is not known in this study population, the estimates of TDR might be underestimates as in many cases reversion to wild type virus might have occurred. However, the proportion of TDR observed in antiretroviral treatment naïve patients (10.4%) was comparable to those observed in German HIV-1 seroconverters (12%) [8], [12]. The proportion of TDR in previously untreated patients reflects transmission of resistant strains at the time-point of infection mostly some years ago with the risk that primary transmitted mutations at the time of resistance testing are not visible anymore. This requires regular monitoring and evaluation of TDR. The most frequent mutations observed in ART naïve patients were T215 revertants which were transmitted as revertant or evolved from viruses harbouring a T215F or T215Y mutation. As also reported by studies from other countries [20] TAMs were the predominant single mutations determined in this study population despite changing prescription policies regarding stavudine and zidovudine, which select for these mutations. One possible explanation for this phenomenon might be that frequently used drugs like abacavir and tenofovir maintain the prevalence of such mutations in patients receiving antiretroviral therapy, and mutations may be transmitted in case of insufficient virus suppression [21], [22]. In contrast, the proportion of ADR in antiretroviral treatment experienced patients at the time point of resistance testing declined significantly over the period of observation in this study population, as also observed in other Western European study populations [23]. This decline was not related to a lower proportion of TDR in treatment naïve patients. The proportion of ADR among the treated population could be influenced by the time of drug exposure to different drug classes, the number of substances ever used, and the time of ART interruption. The risk of ADR was significantly lower in patients with documented ART interruption at the time of genotyping than in those patients with continuous treatment as showed by the univariate and multivariate analysis of factors associated with the risk of ADR. The reason might be that in the absence of selective drug pressure, secondary resistant mutations are rapidly overgrown by wild type virus [24]. Although studies of ART interruption have demonstrated the potential for negative clinical consequences like increased risk of death and serious AIDS defining events [25], non-structured ART interruptions are common in daily clinical routine and the proportion of patients who interrupted therapy remained stable over time at a high level (21%) as shown in this study.
As expected the time a patient was exposed to ART prior to resistance testing was significantly associated with a higher risk of ADR in the univariate and multivariate analysis. The significantly lower risk of ADR for women was most likely caused by their significantly shorter duration of ART exposure prior genotyping.
Regarding the duration of ART exposure prior to resistance testing there was a significant increase in treatment exposure for NNRTIs, PIs and INIs whereas NRTI exposure and the complete duration of treatment exposure increased without a level of significance. Therefore the highly significant decline in ADR observed among treated patients with available resistance test was not influenced by a declining duration of previous ART exposure or by increasing ART interruptions over time in the study population. In this study population PI exposure increased significantly over time. In contrast, PI associated HIV drug resistance in treated patients declined significantly. The enhanced use of PI containing regimens and the increasing variety of second generation PIs with higher resistance barriers might influence this phenomenon [26]. Although the proportion of ADR was high in treated patients, the majority of patients showed viral load measurements under the detection limit subsequent to the last resistance test. In view of the preventive effect of ART, these subjects are unlikely to contribute substantially to onward transmission of resistant HIV strains. The proportion of patients who were successfully treated did not differ between those with resistant HIV and those with susceptible viral strains, reflecting a sufficient number of antiretroviral treatment options and a high expertise in tailored individual treatment of HIV and careful monitoring of antiretroviral treatment for the majority of patients with ADR in this study. Since the introduction of the remuneration of HIV resistance testing by statutory health insurances in Germany in 2005, more and more patients were tested in clinical routine assuming that this have influenced the decline of ADR in the treated study population [7]. A significant increase in the proportion of patients who were resistance tested before ART initiation as well as in case of treatment failure was observed in this study population. However, the figures are still lower than expected if all patients are tested before ART start or in case of treatment failure as recommended in the guidelines. The proportion of patients tested before ART over calendar year as well as the proportion of patients failing therapy undergoing resistance testing may influence the proportion of observed HIV drug resistance in a study population. Perhaps the selection among persons before ART start, where we observe a rather consistent trend of TDR, was not as large as among treated patients. It is conceivable that there was a stronger selection bias to test patients with more problematic courses of therapy and thus towards cases with higher probability of HIV drug resistance in the initial years before statutory introduction of resistance testing in 2005.
Currently only HIV resistance data from long term observational studies in different study populations before ART initiation is available in Germany [8], [9], [19]. Therefore the ClinSurv- HIV Drug Resistance Study attempted to link HIV viral sequence data with epidemiological and treatment data to describe daily clinical resistance testing practices and the proportion of HIV drug resistance for both ART naïve patients as well as for treatment experienced patients in a subset of a large cohort study of people infected with HIV in Germany.
Limitations
This study has some limitations. First, it is a convenience sample of data collected from 5 urban sites of Germany. Therefore, the study is only able to describe the situation based on the information that has been provided by those study centers, and did not reflect the overall situation for Germany. Furthermore, the data was collected over time periods where resistance testing became more widely used in routine clinical care. As we see the majority of the tests were performed after statutory introduction of resistance testing in 2005. Since the proportion of patients tested is correlated with the proportion of observed cases this is important to keep in mind in view of the findings. In addition, certain information is not retrieved, such as the reasons why, despite indication, no test was performed or the reasons for resistance testing, e.g. in view of future treatment options after interruption or due to an actual treatment failure. Evidence exists that in the participating centers more HIV drug resistance tests were performed than we observed by recording the data. It might be that resistance tests were carried out in other laboratories that we have not reached.
However, this report is the first description of HIV drug resistance for both ART naïve and treatment experienced persons infected with HIV in Germany. With all constraints, it is nevertheless one of the most comprehensive reports currently available and gives insight into clinical resistance testing practices and prevalence of HIV drug resistance of people infected with HIV in Germany.
Acknowledgments
The authors would like to thank Andrea Kühne, Bernd Reinhardt and all participating ClinSurv-HIV Cohort Study Centers:
Berlin: Vivantes Auguste-Viktoria-Hospital: K. Arasteh, D. Hampf;
Berlin: Charité University Medicine: F. Bergmann, M. Warncke;
Bonn: University Hospital: J. Rockstroh, J. Wasmuth, S. Hass;
Düsseldorf: University Hospital Düsseldorf: S. Reuter, D. Häussinger;
Essen: University Hospital Essen: S. Esser, P. Schenk-Westkamp;
Frankfurt: HIV Center J.W.Goethe-University Frankfurt: A. Haberl, P. Khaykin;
Hamburg: IfI-Institute for Interdisciplinary Medicine: A. Plettenberg, T. Lorenzen, I. Walther;
ICH Studycenter: A. Adam, L. Weitner, K. Schewe, S. Fenske, T. Buhk, C. Hoffmann; University Hospital Hamburg Eppendorf: J. van Lunzen, K. Wassmus;
Hannover: Medical University Hanover: K. Hoeper;
Kiel: University Schleswig Holstein, Campus Kiel: H.A. Horst, S. Trautmann;
Cologne: University Hospital Cologne: T.Kümmerle, D. Gillor;
Munich: University Hospital, Ludwig-Maximilians University: B. Sonntag;
Regensburg: University Hospital Regensburg: B. Salzberger;
Rostock: University Hospital Rostock: C. Fritzsche.
Further we thank the CHAIN HIV Drug Resistance Network.
CHAIN Executive Board:
Deenan Pillay (Chair), contact email address: d.pillay@ucl.ac.uk
Charles Boucher, Francoise Brun-Vezinet, Bonaventura Clotet, Jan Albert, Carlo Federico Perno
CHAIN Workpackages:
WP1 - Novel resistance mechanisms: Leader - Deen Pillay, Manager – Frank Degee; WP2 - Monitoring Tools: Leader - Francoise Brun-Vezinet; WP3 - Clinical magement of HIV resistance: Leader - Bonaventura Clotet, Manager - Anna Tor Font, Scientific Manager - Roger Paredes; WP4 - Bioinformatics & Molecular Epidemiology: Leader - Jan Albert, Manager - Matthias Mild and Lisbeth Lofstrand; WP5 - Monitoring and surveillance of resistance: Leader - Deenan Pillay, Manager - Pinki Amin; WP6 - Evidence based public health: Leader - Deenan Pillay, Manager - Pinki Amin; WP7 - Training and capacity building: Leader - Carlo Perno, Manager - Valentina Svicher; WP8 - Consortium Management: Leader - Deenan Pillay, Manager - Pinki Amin; WP9 - Ethics: Leader - Deenan Pillay, Manager - Pinki Amin.
CHAIN consortium partners: University College London; Erasmus Medical Centre; INFORMA; Association de Recherche en Virologie et Dermatologie, Fundació “irsiCaixa”; Hospital Universitari “Germans Trias i Pujol”; Medical Research Council; Fondazione Penta; University of Copenhagen, Panum Institute; Université Victor Segalen Bordeaux2; ICONA; Laboratoire de Bacterilogie Virologie, Universite Cheikh Anta; The D.I. Ivanovsky Institute of Virology Russian Academy of Medical Sciences; Univerza V Ljubljani; World Health Organisation; Karolinska Institutet; Universitätsspital Zürich, Klinik für Infektionskrankheiten und Spitalhygiene; Katholieke Universiteit Leuven; Robert Koch Institute; Instituto de Higiene e Medicina Tropical/Universidade Nova de Lisboa; Hospital Carlos III, Madrid; Virco; EuResist Network GEIE; Università degli Studi di Roma “Tor Vergata”; Centre International De Référence “Chantal Biya”.
Author Contributions
Conceived and designed the experiments: BB C. Kollan OH DS. Performed the experiments: DS C. Kollan BB. Analyzed the data: DS C. Kollan. Contributed reagents/materials/analysis tools: GF ES HJS CN BJ MS JRB JE KM C. Kücherer. Wrote the paper: BB DS.
References
- 1. Palella FJ Jr, Delaney KM, Moorman AC, Loveless MO, Fuhrer J, et al. (1998) Declining morbidity and mortality among patients with advanced human immunodeficiency virus infection. New Engl J Med 338: 853–860.
- 2. Jones J, Taylor B, Wilkin TJ, Hammer SM (2007) Advances in antiretroviral therapy. Top HIV Med 15: 48–82.
- 3. Kauf TL, Davis KL, Earnshaw SR, Davis EA (2012) Spillover adherence effects of fixed-dose combination HIV therapy. Patient Prefer Adherence 6: 155.
- 4. Llibre JM, Arribas JR, Domingo P, Gatell JM, Lozano F, et al. (2011) Clinical implications of fixed-dose coformulations of antiretrovirals on the outcome of HIV-1 therapy. Aids 25: 1683–1690.
- 5. Brenner BG, Roger M, Moisi DD, Oliveira M, Hardy I, et al. (2008) Transmission networks of drug resistance acquired in primary/early stage HIV infection. Aids 22: 2509–2515.
- 6. de Mendoza C, Garrido C, Corral A, Ramirez-Olivencia G, Jimenez-Nacher I, et al. (2007) Changing rates and patterns of drug resistance mutations in antiretroviral-experienced HIV-infected patients. AIDS Res Hum Retroviruses 23: 879–885.
- 7.
BUB-Richtlinien/Anlage A (2004) Genotypische Resistenztestung. Bundesanzeiger Nr. 57 (S. 5679).
- 8. Bartmeyer B, Kuecherer C, Houareau C, Werning J, Keeren K, et al. (2010) Prevalence of Transmitted Drug Resistance and Impact of Transmitted Resistance on Treatment Success in the German HIV-1 Seroconverter Cohort. PLoS ONE 5: e12718.
- 9. Oette M, Kaiser R, Daumer M, Fatkenheuer G, Rockstroh JK, et al. (2007) Epidemiology of primary drug resistance in chronically HIV-infected patients in Nordrhein-Westfalen, Germany, 2001–2005. Dtsch Med Wochenschr 132: 977–982.
- 10. Descamps D, Chaix ML, Andre P, Brodard V, Cottalorda J, et al. (2005) French national sentinel survey of antiretroviral drug resistance in patients with HIV-1 primary infection and in antiretroviral-naive chronically infected patients in 2001–2002. J Acquir Immune Defic Syndr 38: 545–552.
- 11. Costagliola D, Descamps D, Assoumou L, Morand-Joubert L, Marcelin AG, et al. (2007) Prevalence of HIV-1 drug resistance in treated patients: a French nationwide study. J Acquir Immune Defic Syndr 46: 12–18.
- 12. zu Knyphausen F, Scheufele R, Kücherer C, Jansen K, Somogyi S, et al. (2014) First Line Treatment Response in Patients with Transmitted HIV Drug Resistance and Well Defined Time Point of HIV Infection: Updated Results from the German HIV-1 Seroconverter Study. PLoS ONE 9(5): e95956.
- 13. Bätzing-Feigenbaum J, Kollan C, Kühne A, Matysiak-Klose D, Gunsenheimer-Bartmeyer B, et al. (2011) Cohort Profile: The German ClinSurv HIV project. A multicentre open clinical cohort as supplement of national HIV surveillance. HIV Medicine 12: 269–278.
- 14. Bennett DE, Camacho RJ, Otelea D, Kuritzkes DR, Fleury H, et al. (2009) Drug resistance mutations for surveillance of transmitted HIV-1 drug-resistance: 2009 update. PLoS One 4: e4724.
- 15. Johnson VA, Calvez V, Günthard HF, Paredes R, Pillay D, et al. (2011) 2011 update of the drug resistance mutations in HIV-1. Top Antivir Med 19: 156–164.
- 16. De Oliveira T, Deforche K, Cassol S, Salminen M, Paraskevis D, et al. (2005) An automated genotyping system for analysis of HIV-1 and other microbial sequences. Bioinformatics 21: 3797–3800.
- 17. Bezemer D, Jurriaans S, Prins M, van der Hoek L, Prins JM, et al. (2004) Declining trend in transmission of drug-resistant HIV-1 in Amsterdam. Aids 18: 1571–1577.
- 18. UK Collaborative Group on HIV Drug Resistance (2007) Evidence of a decline in transmitted HIV-1 drug resistance in the United Kingdom. Aids 21: 1035–1039.
- 19. Sagir A, Oette M, Kaiser R, Daumer M, Fatkenheuer G, et al. (2007) Trends of prevalence of primary HIV drug resistance in Germany. J Antimicrob Chemother 60: 843–848.
- 20. Marcelin AG, Delaugerre C, Wirden M, Viegas P, Simon A, et al. (2004) Thymidine analogue reverse transcriptase inhibitors resistance mutations profiles and association to other nucleoside reverse transcriptase inhibitors resistance mutations observed in the context of virological failure. J Med Virol 72: 162–165.
- 21. Dolling D, Sabin C, Delpech V, Smit E, Pozniak A, et al. (2012) Time trends in drug resistant HIV-1 infections in the United Kingdom up to 2009: multicentre observational study. BMJ (Clinical Research ed.) 345: e5253.
- 22. Betancor G, Garriga C, Puertas MC, Nevot M, Anta L, et al. (2012) Clinical, virological and biochemical evidence supporting the association of HIV-1 reverse transcriptase polymorphism R284K and thymidine analogue resistance mutations M41L, L210W and T215Y in patients failing tenofovir/emtricitabine therapy. Retrovirology 9: 68.
- 23. De Luca A, Dunn D, Zazzi M, Camacho R, Torti C, et al. (2013) Declining prevalence of HIV-1 drug resistance in antiretroviral treatment-exposed individuals in Western Europe. J Infect Dis 207: 1216–20.
- 24. Deeks SG, Wrin T, Liegler T, Hoh R, Hayden M, et al. (2001) Virologic and immunologic consequences of discontinuing combination antiretroviral-drug therapy in HIV-infected patients with detectable viremia. New Engl J Med 344: 472–480.
- 25. Lundgren JD, Babiker A, El-Sadr W, Emery S, Grund B, et al. (2008) Inferior clinical outcome of the CD4+ cell count-guided antiretroviral treatment interruption strategy in the SMART study: role of CD4+ Cell counts and HIV RNA levels during follow-up. J Infect Dis 197: 1145–1155.
- 26. Tejerina F, de Quirós JCLB (2011) Protease Inhibitors as Preferred Initial Regimen for Antiretroviral-Naive HIV Patients. AIDS Rev 13: 227–233.