PMID- 28745207 OWN - NLM STAT- MEDLINE DCOM- 20180515 LR - 20180515 IS - 1873-4251 (Electronic) IS - 1570-162X (Linking) VI - 15 IP - 4 DP - 2017 TI - HIV Drug Resistance Testing in a Resource Limited Setting with High Viral Diversity: The First Twenty Eight Months Experience. PG - 297-305 LID - 10.2174/1570162X15666170725143835 [doi] AB - BACKGROUND: First line antiretroviral therapy in a resource-limited setting consists of nucleotide and non-nucleotide reverse transcriptase inhibitors. Protease inhibitors are the hub of second line therapy. The decision to change antiretroviral therapy for a patient is frequently presumptive because of the lack of genotypic resistance tests in routine follow-up. We describe here the resistance profiles observed in patients with varying terms of antiretroviral therapy in Cameroon after implementation of HIV genotypic resistance testing in routine practice. METHODS: HIV genotypic resistance testing was carried out on consecutive samples received between August 2013 and November 2015. Protease (Prot) and reverse transcriptase (Rt) genes of the HIV genome were amplified, sequenced and analyzed for drug resistance mutations following the algorithm set up by the French National Agency for research on HIV/AIDS and viral hepatitis. RESULTS: Specimens from a total of 167 patients infected with non-B HIV subtypes were received during the study period. Overall 61.7% patients had viral loads of more than 3log copies/ml, suggesting treatment failure. Among the 72 patients on first line, 56 (77.8%) were resistant to Lamivudine, 57 (79.1%) to Efavirenz and 58 (80.6%) to Nevirapine. Overall, more patients (75.0%) on first line antiretroviral therapy harbored multi-drug resistance compared to their counterparts on second line (25.8%). CONCLUSION: This study revealed that a group of patients with antiretroviral therapy failure harbored multi-drug resistance mutations related to the majority of drugs in the first line regimen. Therefore, HIV resistance testing could be a useful tool to improve HIV care in resource limited settings like Cameroon where treatment options are limited. CI - Copyright(c) Bentham Science Publishers; For any queries, please email at epub@benthamscience.org. FAU - Ngo-Malabo, Elodie Teclaire AU - Ngo-Malabo ET AD - Virology department, Centre Pasteur of Cameroon, Yaounde. Cameroon. FAU - Ngoupo, Paul Alain AU - Ngoupo PA AD - Virology department, Centre Pasteur of Cameroon, Yaounde. Cameroon. FAU - Sadeuh-Mba, Serge Alain AU - Sadeuh-Mba SA AD - Virology department, Centre Pasteur of Cameroon, Yaounde. Cameroon. FAU - Akongnwi, Emmanuel AU - Akongnwi E AD - Virology department, Centre Pasteur of Cameroon, Yaounde. Cameroon. FAU - Banai, Robert AU - Banai R AD - Virology department, Centre Pasteur of Cameroon, Yaounde. Cameroon. FAU - Ngono, Laure AU - Ngono L AD - Virology department, Centre Pasteur of Cameroon, Yaounde. Cameroon. FAU - Bilong-Bilong, Charles Felix AU - Bilong-Bilong CF AD - Laboratory of Parasitology and Ecology, University of Yaounde I Faculty of Science, Yaounde. Cameroon. FAU - Kfutwah, Anfumbom AU - Kfutwah A AD - Virology department, Centre Pasteur of Cameroon, Yaounde. Cameroon. FAU - Njouom, Richard AU - Njouom R AD - Virology department, Centre Pasteur of Cameroon, Yaounde. Cameroon. LA - eng PT - Journal Article PL - Netherlands TA - Curr HIV Res JT - Current HIV research JID - 101156990 RN - 0 (Anti-HIV Agents) RN - 0 (Human Immunodeficiency Virus Proteins) SB - IM MH - Adolescent MH - Adult MH - Anti-HIV Agents/*therapeutic use MH - Cameroon MH - *Drug Resistance, Viral MH - Female MH - Genotyping Techniques/*methods MH - HIV/*drug effects MH - HIV Infections/*drug therapy MH - Human Immunodeficiency Virus Proteins/genetics MH - Humans MH - Male MH - Microbial Sensitivity Tests/*methods MH - Middle Aged MH - Mutation, Missense MH - Sequence Analysis, DNA MH - Treatment Failure MH - Young Adult OTO - NOTNLM OT - Cameroon OT - HIV OT - Treatment failure OT - Viral Diversity OT - drug resistance OT - genotyping resistance test OT - mutation OT - resource limited setting EDAT- 2017/07/27 06:00 MHDA- 2018/05/16 06:00 CRDT- 2017/07/27 06:00 PHST- 2017/04/05 00:00 [received] PHST- 2017/06/07 00:00 [revised] PHST- 2017/07/21 00:00 [accepted] PHST- 2017/07/27 06:00 [pubmed] PHST- 2018/05/16 06:00 [medline] PHST- 2017/07/27 06:00 [entrez] AID - CHR-EPUB-84985 [pii] AID - 10.2174/1570162X15666170725143835 [doi] PST - ppublish SO - Curr HIV Res. 2017;15(4):297-305. doi: 10.2174/1570162X15666170725143835.