Prevalence of Pre-antiretroviral-Treatment Drug Resistance by Gender, Age, and Other Factors in HIV-Infected Individuals Initiating Therapy in Kenya, 2013–2014
HIV-infected participants initiating first-line antiretroviral therapy in Kenya were tested for pretreatment drug resistance (PDR) using an oligonucleotide ligation assay. PDR was detected in 9.6% (95% CI, 7.9%–11.6%), including 19.5% (95% CI, 8.8%–34.9%) of all 18–24-year-old women. Abstract Backgr...
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Published in | The Journal of infectious diseases Vol. 216; no. 12; pp. 1569 - 1578 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
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Oxford University Press
19.12.2017
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Abstract | HIV-infected participants initiating first-line antiretroviral therapy in Kenya were tested for pretreatment drug resistance (PDR) using an oligonucleotide ligation assay. PDR was detected in 9.6% (95% CI, 7.9%–11.6%), including 19.5% (95% CI, 8.8%–34.9%) of all 18–24-year-old women.
Abstract
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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AbstractList | BackgroundPre-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.MethodsWe 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.ResultsPDR 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).ConclusionsThe 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 RegistrationNCT01898754. HIV-infected participants initiating first-line antiretroviral therapy in Kenya were tested for pretreatment drug resistance (PDR) using an oligonucleotide ligation assay. PDR was detected in 9.6% (95% CI, 7.9%–11.6%), including 19.5% (95% CI, 8.8%–34.9%) of all 18–24-year-old women. 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. 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. 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). 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. NCT01898754. HIV-infected participants initiating first-line antiretroviral therapy in Kenya were tested for pretreatment drug resistance (PDR) using an oligonucleotide ligation assay. PDR was detected in 9.6% (95% CI, 7.9%–11.6%), including 19.5% (95% CI, 8.8%–34.9%) of all 18–24-year-old women. Abstract 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. |
Author | Levine, Molly Kiarie, James N. Milne, Ross Kiptinness, Catherine Silverman, Rachel A. Sakr, Samah R. Bii, Steve Frenkel, Lisa M. McGrath, Christine J. Chung, Michael H. John-Stewart, Grace Beck, Ingrid A. Richardson, Barbra A. Chohan, Bhavna |
AuthorAffiliation | 8 Department of Obstetrics and Gynaecology, University of Nairobi, Kenya 3 Seattle Children’s Research Institute, Washington 2 Department of Global Health, University of Washington, Seattle 5 Department of Medicine, University of Washington, Seattle 7 Coptic Hospital, Nairobi 4 Department of Biostatistics, University of Washington, Seattle 6 Department of Pediatrics, University of Washington, Seattle 9 Department of Laboratory Medicine, University of Washington, Seattle 1 Department of Epidemiology, University of Washington, Seattle |
AuthorAffiliation_xml | – name: 8 Department of Obstetrics and Gynaecology, University of Nairobi, Kenya – name: 6 Department of Pediatrics, University of Washington, Seattle – name: 1 Department of Epidemiology, University of Washington, Seattle – name: 4 Department of Biostatistics, University of Washington, Seattle – name: 9 Department of Laboratory Medicine, University of Washington, Seattle – name: 2 Department of Global Health, University of Washington, Seattle – name: 7 Coptic Hospital, Nairobi – name: 3 Seattle Children’s Research Institute, Washington – name: 5 Department of Medicine, University of Washington, Seattle |
Author_xml | – sequence: 1 givenname: Rachel A. surname: Silverman fullname: Silverman, Rachel A. organization: Department of Global Health, University of Washington, Seattle – sequence: 2 givenname: Ingrid A. surname: Beck fullname: Beck, Ingrid A. organization: Seattle Children’s Research Institute, Washington – sequence: 3 givenname: Catherine surname: Kiptinness fullname: Kiptinness, Catherine organization: Department of Global Health, University of Washington, Seattle – sequence: 4 givenname: Molly surname: Levine fullname: Levine, Molly organization: Seattle Children’s Research Institute, Washington – sequence: 5 givenname: Ross surname: Milne fullname: Milne, Ross organization: Seattle Children’s Research Institute, Washington – sequence: 6 givenname: Christine J. surname: McGrath fullname: McGrath, Christine J. organization: Department of Global Health, University of Washington, Seattle – sequence: 7 givenname: Steve surname: Bii fullname: Bii, Steve organization: Seattle Children’s Research Institute, Washington – sequence: 8 givenname: Barbra A. surname: Richardson fullname: Richardson, Barbra A. organization: Department of Global Health, University of Washington, Seattle – sequence: 9 givenname: Grace surname: John-Stewart fullname: John-Stewart, Grace organization: Department of Pediatrics, University of Washington, Seattle – sequence: 10 givenname: Bhavna surname: Chohan fullname: Chohan, Bhavna organization: Department of Global Health, University of Washington, Seattle – sequence: 11 givenname: Samah R. surname: Sakr fullname: Sakr, Samah R. organization: Coptic Hospital, Nairobi – sequence: 12 givenname: James N. surname: Kiarie fullname: Kiarie, James N. organization: Department of Obstetrics and Gynaecology, University of Nairobi, Kenya – sequence: 13 givenname: Lisa M. surname: Frenkel fullname: Frenkel, Lisa M. organization: Seattle Children’s Research Institute, Washington – sequence: 14 givenname: Michael H. surname: Chung fullname: Chung, Michael H. organization: Department of Medicine |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29040633$$D View this record in MEDLINE/PubMed |
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Keywords | HIV transmitted drug resistance oligonucleotide ligation assay antiretroviral therapy Pretreatment drug resistance |
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Snippet | HIV-infected participants initiating first-line antiretroviral therapy in Kenya were tested for pretreatment drug resistance (PDR) using an oligonucleotide... Pre-antiretroviral-treatment drug resistance (PDR) is a predictor of human immunodeficiency virus (HIV) treatment failure. We determined PDR prevalence and... BackgroundPre-antiretroviral-treatment drug resistance (PDR) is a predictor of human immunodeficiency virus (HIV) treatment failure. We determined PDR... |
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SubjectTerms | HIV/AIDS Major and Brief Reports |
Title | Prevalence of Pre-antiretroviral-Treatment Drug Resistance by Gender, Age, and Other Factors in HIV-Infected Individuals Initiating Therapy in Kenya, 2013–2014 |
URI | https://www.jstor.org/stable/26491736 https://www.ncbi.nlm.nih.gov/pubmed/29040633 https://search.proquest.com/docview/1952525860 https://pubmed.ncbi.nlm.nih.gov/PMC5853791 |
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