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Prevalence of Pre-antiretroviral-Treatment Drug Resistance by Gender, Age, and Other Factors in HIV-Infected Individuals Initiating Therapy in Kenya, 2013-2014.
Silverman, Rachel A; Beck, Ingrid A; Kiptinness, Catherine; Levine, Molly; Milne, Ross; McGrath, Christine J; Bii, Steve; Richardson, Barbra A; John-Stewart, Grace; Chohan, Bhavna; Sakr, Samah R; Kiarie, James N; Frenkel, Lisa M; Chung, Michael H.
Afiliación
  • Silverman RA; Department of Epidemiology, University of Washington, Seattle.
  • Beck IA; Department of Global Health, University of Washington, Seattle.
  • Kiptinness C; Seattle Children's Research Institute, Washington.
  • Levine M; Department of Global Health, University of Washington, Seattle.
  • Milne R; Seattle Children's Research Institute, Washington.
  • McGrath CJ; Seattle Children's Research Institute, Washington.
  • Bii S; Department of Global Health, University of Washington, Seattle.
  • Richardson BA; Seattle Children's Research Institute, Washington.
  • John-Stewart G; Department of Global Health, University of Washington, Seattle.
  • Chohan B; Department of Biostatistics, University of Washington, Seattle.
  • Sakr SR; Department of Epidemiology, University of Washington, Seattle.
  • Kiarie JN; Department of Global Health, University of Washington, Seattle.
  • Frenkel LM; Department of Medicine, University of Washington, Seattle.
  • Chung MH; Department of Pediatrics, University of Washington, Seattle.
J Infect Dis ; 216(12): 1569-1578, 2017 12 19.
Article en En | MEDLINE | ID: mdl-29040633
Background: Pre-antiretroviral-treatment drug resistance (PDR) is a predictor of human immunodeficiency virus (HIV) treatment failure. We determined PDR prevalence and correlates in a Kenyan cohort. Methods: We conducted a cross-sectional analysis of antiretroviral (ARV) treatment-eligible HIV-infected participants. PDR was defined as ≥2% mutant frequency in a participant's HIV quasispecies at pol codons K103N, Y181C, G190A, M184 V, or K65R by oligonucleotide ligation assay and Illumina sequencing. PDR prevalence was calculated by demographics and codon, stratifying by prior ARV experience. Poisson regression was used to estimate prevalence ratios. Results: PDR prevalences (95% confidence interval [CI]) in 815 ARV-naive adults, 136 ARV-experienced adults, and 36 predominantly ARV-naive children were 9.4% (7.5%-11.7%), 12.5% (7.5%-19.3%), and 2.8% (0.1%-14.5%), respectively. Median mutant frequency within an individual's HIV quasispecies was 67%. PDR prevalence in ARV-naive women 18-24 years old was 21.9% (9.3%-40.0%). Only age in females associated with PDR: A 5-year age decrease was associated with adjusted PDR prevalence ratio 1.20 (95% CI, 1.06-1.36; P = .004). Conclusions: The high PDR prevalence may warrant resistance testing and/or alternative ARVs in high HIV prevalence settings, with attention to young women, likely to have recent infection and higher rates of resistance. Clinical Trials Registration: NCT01898754.
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Texto completo: 1 Colección: 01-internacional Asunto principal: Infecciones por VIH / VIH / Farmacorresistencia Viral Tipo de estudio: Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged País/Región como asunto: Africa Idioma: En Revista: J infect dis Año: 2017 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Asunto principal: Infecciones por VIH / VIH / Farmacorresistencia Viral Tipo de estudio: Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged País/Región como asunto: Africa Idioma: En Revista: J infect dis Año: 2017 Tipo del documento: Article