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 inThe Journal of infectious diseases Vol. 216; no. 12; pp. 1569 - 1578
Main Authors 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.
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LanguageEnglish
Published US 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.
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
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ContentType Journal Article
Copyright The Author 2017
The Author 2017. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com. 2017
The Author 2017. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.
Copyright_xml – notice: The Author 2017
– notice: The Author 2017. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com. 2017
– notice: The Author 2017. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.
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Issue 12
Keywords HIV
transmitted drug resistance
oligonucleotide ligation assay
antiretroviral therapy
Pretreatment drug resistance
Language English
License The Author 2017. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.
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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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