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Molecular Epidemiology of HIV-1 Infected Migrants Followed Up in Portugal: Trends between 2001–2017

Migration is associated with HIV-1 vulnerability. Objectives: To identify long-term trends in HIV-1 molecular epidemiology and antiretroviral drug resistance (ARV) among migrants followed up in Portugal Methods: 5177 patients were included between 2001 and 2017. Rega, Scuel, Comet, and jPHMM algorit...

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Autores principales: Pimentel, Victor, Pingarilho, Marta, Alves, Daniela, Diogo, Isabel, Fernandes, Sandra, Miranda, Mafalda, Pineda-Peña, Andrea-Clemencia, Libin, Pieter, Martins, M. Rosário O., Vandamme, Anne-Mieke, Camacho, Ricardo, Gomes, Perpétua, Abecasis, Ana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7150888/
https://www.ncbi.nlm.nih.gov/pubmed/32121161
http://dx.doi.org/10.3390/v12030268
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author Pimentel, Victor
Pingarilho, Marta
Alves, Daniela
Diogo, Isabel
Fernandes, Sandra
Miranda, Mafalda
Pineda-Peña, Andrea-Clemencia
Libin, Pieter
Martins, M. Rosário O.
Vandamme, Anne-Mieke
Camacho, Ricardo
Gomes, Perpétua
Abecasis, Ana
author_facet Pimentel, Victor
Pingarilho, Marta
Alves, Daniela
Diogo, Isabel
Fernandes, Sandra
Miranda, Mafalda
Pineda-Peña, Andrea-Clemencia
Libin, Pieter
Martins, M. Rosário O.
Vandamme, Anne-Mieke
Camacho, Ricardo
Gomes, Perpétua
Abecasis, Ana
author_sort Pimentel, Victor
collection PubMed
description Migration is associated with HIV-1 vulnerability. Objectives: To identify long-term trends in HIV-1 molecular epidemiology and antiretroviral drug resistance (ARV) among migrants followed up in Portugal Methods: 5177 patients were included between 2001 and 2017. Rega, Scuel, Comet, and jPHMM algorithms were used for subtyping. Transmitted drug resistance (TDR) and Acquired drug resistance (ADR) were defined as the presence of surveillance drug resistance mutations (SDRMs) and as mutations of the IAS-USA 2015 algorithm, respectively. Statistical analyses were performed. Results: HIV-1 subtypes infecting migrants were consistent with the ones prevailing in their countries of origin. Over time, overall TDR significantly increased and specifically for Non-nucleoside reverse transcriptase inhibitor (NNRTIs) and Nucleoside reverse transcriptase inhibitor (NRTIs). TDR was higher in patients from Mozambique. Country of origin Mozambique and subtype B were independently associated with TDR. Overall, ADR significantly decreased over time and specifically for NRTIs and Protease Inhibitors (PIs). Age, subtype B, and viral load were independently associated with ADR. Conclusions: HIV-1 molecular epidemiology in migrants suggests high levels of connectivity with their country of origin. The increasing levels of TDR in migrants could indicate an increase also in their countries of origin, where more efficient surveillance should occur.
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spelling pubmed-71508882020-04-20 Molecular Epidemiology of HIV-1 Infected Migrants Followed Up in Portugal: Trends between 2001–2017 Pimentel, Victor Pingarilho, Marta Alves, Daniela Diogo, Isabel Fernandes, Sandra Miranda, Mafalda Pineda-Peña, Andrea-Clemencia Libin, Pieter Martins, M. Rosário O. Vandamme, Anne-Mieke Camacho, Ricardo Gomes, Perpétua Abecasis, Ana Viruses Article Migration is associated with HIV-1 vulnerability. Objectives: To identify long-term trends in HIV-1 molecular epidemiology and antiretroviral drug resistance (ARV) among migrants followed up in Portugal Methods: 5177 patients were included between 2001 and 2017. Rega, Scuel, Comet, and jPHMM algorithms were used for subtyping. Transmitted drug resistance (TDR) and Acquired drug resistance (ADR) were defined as the presence of surveillance drug resistance mutations (SDRMs) and as mutations of the IAS-USA 2015 algorithm, respectively. Statistical analyses were performed. Results: HIV-1 subtypes infecting migrants were consistent with the ones prevailing in their countries of origin. Over time, overall TDR significantly increased and specifically for Non-nucleoside reverse transcriptase inhibitor (NNRTIs) and Nucleoside reverse transcriptase inhibitor (NRTIs). TDR was higher in patients from Mozambique. Country of origin Mozambique and subtype B were independently associated with TDR. Overall, ADR significantly decreased over time and specifically for NRTIs and Protease Inhibitors (PIs). Age, subtype B, and viral load were independently associated with ADR. Conclusions: HIV-1 molecular epidemiology in migrants suggests high levels of connectivity with their country of origin. The increasing levels of TDR in migrants could indicate an increase also in their countries of origin, where more efficient surveillance should occur. MDPI 2020-02-28 /pmc/articles/PMC7150888/ /pubmed/32121161 http://dx.doi.org/10.3390/v12030268 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Pimentel, Victor
Pingarilho, Marta
Alves, Daniela
Diogo, Isabel
Fernandes, Sandra
Miranda, Mafalda
Pineda-Peña, Andrea-Clemencia
Libin, Pieter
Martins, M. Rosário O.
Vandamme, Anne-Mieke
Camacho, Ricardo
Gomes, Perpétua
Abecasis, Ana
Molecular Epidemiology of HIV-1 Infected Migrants Followed Up in Portugal: Trends between 2001–2017
title Molecular Epidemiology of HIV-1 Infected Migrants Followed Up in Portugal: Trends between 2001–2017
title_full Molecular Epidemiology of HIV-1 Infected Migrants Followed Up in Portugal: Trends between 2001–2017
title_fullStr Molecular Epidemiology of HIV-1 Infected Migrants Followed Up in Portugal: Trends between 2001–2017
title_full_unstemmed Molecular Epidemiology of HIV-1 Infected Migrants Followed Up in Portugal: Trends between 2001–2017
title_short Molecular Epidemiology of HIV-1 Infected Migrants Followed Up in Portugal: Trends between 2001–2017
title_sort molecular epidemiology of hiv-1 infected migrants followed up in portugal: trends between 2001–2017
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7150888/
https://www.ncbi.nlm.nih.gov/pubmed/32121161
http://dx.doi.org/10.3390/v12030268
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