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Genotype and Phenotype at Baseline and at Failure in Human Immunodeficiency Virus–Infected Antiretroviral‐Naive Patients in a Randomized Trial Comparing Zidovudine and Lamivudine plus Nelfinavir or Nevirapine
Author(s) -
Elena Ferrer,
Daniel Podzamczer,
Mireia Arnedo,
Emilio Fumero,
Paula McKenna,
Alex R. Rinehart,
José L. Pérez,
María Jesús Barberà,
Tomàs Pumarola,
José M. Gatell,
Francisco Gudiol
Publication year - 2003
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/367987
Subject(s) - nevirapine , nelfinavir , zidovudine , lamivudine , reverse transcriptase , virology , genotype , reverse transcriptase inhibitor , medicine , protease inhibitor (pharmacology) , biology , sida , human immunodeficiency virus (hiv) , virus , viral disease , viral load , polymerase chain reaction , antiretroviral therapy , genetics , gene , hepatitis b virus
For the 127 Spanish patients enrolled in the Combine Study, a resistance substudy was performed with 100 (79%) plasma samples obtained at baseline and with 18 samples obtained from 19 patients at the time they experienced treatment failure. At baseline, primary mutations to nonnucleoside reverse-transcriptase inhibitors and protease inhibitors were not detected, whereas mutations to nucleoside reverse-transcriptase inhibitors were observed in 10% of patients. At failure, mutations were detected in 7 of 16 patients. An agreement in the results of virtual and real phenotypes was observed in the 93 samples in which both tests were performed.

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