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HIV multidrug class resistance prediction with a time sliding anchor approach

datacite.subject.fosCiências Médicas::Ciências da Saúde
datacite.subject.sdg03:Saúde de Qualidade
dc.contributor.authorArslan, Nurhan
dc.contributor.authorEggeling, Ralf
dc.contributor.authorReuter, Bernhard
dc.contributor.authorLeathem, Kristel Van
dc.contributor.authorPingarilho, Marta
dc.contributor.authorGomes, Perpétua
dc.contributor.authorSönnerborg, Anders
dc.contributor.authorKaiser, Rolf
dc.contributor.authorZazzi, Maurizio
dc.contributor.authorPfeifer, Nico
dc.contributor.authorEuResist Network Study Group
dc.date.accessioned2026-05-11T09:17:02Z
dc.date.available2026-05-11T09:17:02Z
dc.date.issued2025-05
dc.description.abstractMotivation: The emergence of multidrug class resistance (MDR) in Human Immunodeficiency Virus (HIV) is a rare but significant challenge in antiretroviral therapy (ART). MDR, which may arise from prolonged drug exposure, treatment failures, or transmission of resistant strains, accelerates disease progression and poses particular challenges in resource-limited settings with restricted access to resistance testing and advanced therapies. Early prediction of future MDR development is important to inform therapeutic decisions and mitigate its occurrence. Results: In this study, we employ various machine learning classifiers to predict future resistance to all four major antiretroviral drug classes using features extracted from clinical HIV sequence data. We systematically explore several variations of the problem that differ in the pre-existing resistance level and the temporal gap between sample collection and observed MDR occurrence. Our models show the ability to predict multidrug class resistance even in the most challenging variations, albeit at a reduced accuracy. Feature importance analysis reveals that our models primarily utilize known drug resistance mutations for easier classification tasks, but rely on new mutations for the difficult task of distinguishing four class drug resistance from three class drug resistance. Availability and implementation: All analysis was performed using the Euresist Integrated DataBase (EIDB). Researchers wishing to reproduce, validate or extend these findings can request access to the latest EIDB release via the Euresist Network.eng
dc.identifier.citationNurhan Arslan, Ralf Eggeling, Bernhard Reuter, Kristel Van Leathem, Marta Pingarilho, Perpétua Gomes, Anders Sönnerborg, Rolf Kaiser, Maurizio Zazzi, Nico Pfeifer, The EuResist Network Study Group, HIV multidrug class resistance prediction with a time sliding anchor approach, Bioinformatics Advances, Volume 5, Issue 1, 2025, vbaf099, https://doi.org/10.1093/bioadv/vbaf099
dc.identifier.doi10.1093/bioadv/vbaf099
dc.identifier.issn2635-0041
dc.identifier.urihttp://hdl.handle.net/10400.26/63056
dc.language.isoeng
dc.peerreviewedyes
dc.publisherOxford University Press
dc.relation.hasversionhttps://doi.org/10.1093/bioadv/vbaf099
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectHIV
dc.subjectmultidrug class resistance
dc.subjectantiretroviral therapy
dc.titleHIV multidrug class resistance prediction with a time sliding anchor approacheng
dc.typecontribution to journal
dspace.entity.typePublication
oaire.citation.issue1
oaire.citation.startPagevbaf099
oaire.citation.titleBioinformatics Advances
oaire.citation.volume5
oaire.versionhttp://purl.org/coar/version/c_970fb48d4fbd8a85

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