Prevalence of Drug‐Resistant HIV‐1 Variants in Untreated Individuals in Europe: Implications for Clinical Management

Annemarie M. J. Wensing(Utrecht University), David van de Vijver(Eijkman Institute for Molecular Biology), Gioacchino Angarano(University of Foggia), Birgitta Åsjö(University of Bergen), Claudia Balotta(University of Milan), Enzo Boeri, Ricardo Camacho(Hospital de Egas Moniz), Maire‐Laure Chaix, Dominique Costagliola(Inserm), Andrea De Luca(Catholic University of America), Inge Derdelinckx(Rega Institute for Medical Research), Zehava Grossman(Sheba Medical Center), Osamah Hamouda(Robert Koch Institute), Angelos Hatzakis(Athens Medical Center), R Hemmer(Centre Hospitalier de Luxembourg), Andy I. M. Hoepelman(University Medical Center Utrecht), Andrzej Horban, Klaus Korn(Friedrich-Alexander-Universität Erlangen-Nürnberg), Claudia Kücherer(Robert Koch Institute), Thomas Leitner(Los Alamos National Laboratory), Clive Loveday, E MacRae, Irina Maljkovic(Swedish Institute), Carmen de Mendoza(Hospital Clínico San Carlos), Laurence Meyer(Inserm), Claus Nielsen(Statens Serum Institut), Eline LM Op de Coul(National Institute for Public Health and the Environment), Vidar Ormaasen(Oslo University Hospital), Dimitris Paraskevis(Athens Medical Center), Luc Perrin(University Hospital of Geneva), Elisabeth Puchhammer‐Stöckl(University of Vienna), Lı́dia Ruiz(IrsiCaixa), Mika Salminen(Institute for Molecular Medicine Finland), Jean‐Claude Schmit(Centre Hospitalier de Luxembourg), F Schneider(Centre Hospitalier de Luxembourg), Rob Schuurman(Eijkman Institute for Molecular Biology), Vincent Soriano(Hospital Clínico San Carlos), G Stanczak, Maja Stanojević(University of Belgrade), Anne‐Mieke Vandamme(Rega Institute for Medical Research), Kristel Van Laethem(Rega Institute for Medical Research), Michela Violin(University of Milan), Karin Wilbe(Swedish Institute), Sabine Yerly(University Hospital of Geneva), Maurizio Zazzi(University of Siena), Charles A. Boucher(Eijkman Institute for Molecular Biology), SPREAD Programme
The Journal of Infectious Diseases
August 19, 2005
Cited by 420Open Access
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Abstract

BACKGROUND: Infection with drug-resistant human immunodeficiency virus type 1 (HIV-1) can impair the response to combination therapy. Widespread transmission of drug-resistant variants has the disturbing potential of limiting future therapy options and affecting the efficacy of postexposure prophylaxis. METHODS: We determined the baseline rate of drug resistance in 2208 therapy-naive patients recently and chronically infected with HIV-1 from 19 European countries during 1996-2002. RESULTS: In Europe, 1 of 10 antiretroviral-naive patients carried viruses with > or = 1 drug-resistance mutation. Recently infected patients harbored resistant variants more often than did chronically infected patients (13.5% vs. 8.7%; P=.006). Non-B viruses (30%) less frequently carried resistance mutations than did subtype B viruses (4.8% vs. 12.9%; P<.01). Baseline resistance increased over time in newly diagnosed cases of non-B infection: from 2.0% (1/49) in 1996-1998 to 8.2% (16/194) in 2000-2001. CONCLUSIONS: Drug-resistant variants are frequently present in both recently and chronically infected therapy-naive patients. Drug-resistant variants are most commonly seen in patients infected with subtype B virus, probably because of longer exposure of these viruses to drugs. However, an increase in baseline resistance in non-B viruses is observed. These data argue for testing all drug-naive patients and are of relevance when guidelines for management of postexposure prophylaxis and first-line therapy are updated.


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