TY - JOUR
T1 - Pretreatment and Acquired Antiretroviral Drug Resistance Among Persons Living With HIV in Four African Countries
AU - for the AFRICOS Study Group
AU - Crowell, Trevor A.
AU - Danboise, Brook
AU - Parikh, Ajay
AU - Esber, Allahna
AU - Dear, Nicole
AU - Coakley, Peter
AU - Kasembeli, Alex
AU - Maswai, Jonah
AU - Khamadi, Samoel
AU - Bahemana, Emmanuel
AU - Iroezindu, Michael
AU - Kiweewa, Francis
AU - Owuoth, John
AU - Freeman, Joanna
AU - Jagodzinski, Linda L.
AU - Malia, Jennifer A.
AU - Eller, Leigh Ann
AU - Tovanabutra, Sodsai
AU - Peel, Sheila A.
AU - Ake, Julie A.
AU - Polyak, Christina S.
N1 - Publisher Copyright:
© The Author(s) 2020.
PY - 2021/10/1
Y1 - 2021/10/1
N2 - Background. Emerging HIV drug resistance (HIVDR) could jeopardize the success of standardized HIV management protocols in resource-limited settings. We characterized HIVDR among antiretroviral therapy (ART)-naive and experienced participants in the African Cohort Study (AFRICOS). Methods. From January 2013 to April 2019, adults with HIV-1 RNA >1000 copies/mL underwent ART history review and HIVDR testing upon enrollment at 12 clinics in Uganda, Kenya, Tanzania, and Nigeria. We calculated resistance scores for specific drugs and tallied major mutations to non-nucleoside reverse transcriptase inhibitors (NNRTIs), nucleoside reverse transcriptase inhibitors (NRTIs), and protease inhibitors (PIs) using Stanford HIVDB 8.8 and SmartGene IDNS software. For ART-naive participants, World Health Organization surveillance drug resistance mutations (SDRMs) were noted. Results. HIVDR testing was performed on 972 participants with median age 35.7 (interquartile range [IQR] 29.7–42.7) years and median CD4 295 (IQR 148–478) cells/mm3. Among 801 ART-naive participants, the prevalence of SDRMs was 11.0%, NNRTI mutations 8.2%, NRTI mutations 4.7%, and PI mutations 0.4%. Among 171 viremic ART-experienced participants, NNRTI mutation prevalence was 83.6%, NRTI 67.8%, and PI 1.8%. There were 90 ART-experienced participants with resistance to both efavirenz and lamivudine, 33 (36.7%) of whom were still prescribed these drugs. There were 10 with resistance to both tenofovir and lamivudine, 8 (80.0%) of whom were prescribed these drugs. Conclusions. Participants on failing ART regimens had a high burden of HIVDR that potentially limited the efficacy of standardized first- and second-line regimens. Management strategies that emphasize adherence counseling while delaying ART switch may promote drug resistance and should be reconsidered.
AB - Background. Emerging HIV drug resistance (HIVDR) could jeopardize the success of standardized HIV management protocols in resource-limited settings. We characterized HIVDR among antiretroviral therapy (ART)-naive and experienced participants in the African Cohort Study (AFRICOS). Methods. From January 2013 to April 2019, adults with HIV-1 RNA >1000 copies/mL underwent ART history review and HIVDR testing upon enrollment at 12 clinics in Uganda, Kenya, Tanzania, and Nigeria. We calculated resistance scores for specific drugs and tallied major mutations to non-nucleoside reverse transcriptase inhibitors (NNRTIs), nucleoside reverse transcriptase inhibitors (NRTIs), and protease inhibitors (PIs) using Stanford HIVDB 8.8 and SmartGene IDNS software. For ART-naive participants, World Health Organization surveillance drug resistance mutations (SDRMs) were noted. Results. HIVDR testing was performed on 972 participants with median age 35.7 (interquartile range [IQR] 29.7–42.7) years and median CD4 295 (IQR 148–478) cells/mm3. Among 801 ART-naive participants, the prevalence of SDRMs was 11.0%, NNRTI mutations 8.2%, NRTI mutations 4.7%, and PI mutations 0.4%. Among 171 viremic ART-experienced participants, NNRTI mutation prevalence was 83.6%, NRTI 67.8%, and PI 1.8%. There were 90 ART-experienced participants with resistance to both efavirenz and lamivudine, 33 (36.7%) of whom were still prescribed these drugs. There were 10 with resistance to both tenofovir and lamivudine, 8 (80.0%) of whom were prescribed these drugs. Conclusions. Participants on failing ART regimens had a high burden of HIVDR that potentially limited the efficacy of standardized first- and second-line regimens. Management strategies that emphasize adherence counseling while delaying ART switch may promote drug resistance and should be reconsidered.
KW - Africa South of the Sahara
KW - acquired immunodeficiency syndrome
KW - drug resistance
KW - public health surveillance
UR - http://www.scopus.com/inward/record.url?scp=85099767988&partnerID=8YFLogxK
U2 - 10.1093/cid/ciaa1161
DO - 10.1093/cid/ciaa1161
M3 - Article
C2 - 32785695
AN - SCOPUS:85099767988
SN - 1058-4838
VL - 73
SP - E2311-E2322
JO - Clinical Infectious Diseases
JF - Clinical Infectious Diseases
IS - 7
ER -