Please use this identifier to cite or link to this item:
http://hdl.handle.net/10553/120817
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Del Amo J. | en_US |
dc.contributor.author | Polo, R. | en_US |
dc.contributor.author | Moreno S. | en_US |
dc.contributor.author | Martínez E. | en_US |
dc.contributor.author | Cabello A. | en_US |
dc.contributor.author | Iribarren JA. | en_US |
dc.contributor.author | Curran A. | en_US |
dc.contributor.author | Macías J. | en_US |
dc.contributor.author | Montero M. | en_US |
dc.contributor.author | Dueñas C. | en_US |
dc.contributor.author | Mariño A. | en_US |
dc.contributor.author | Pérez de la Cámara S. | en_US |
dc.contributor.author | Díaz A. | en_US |
dc.contributor.author | Arribas JR. | en_US |
dc.contributor.author | Jarrín I. | en_US |
dc.contributor.author | Hernán MA. | en_US |
dc.contributor.author | Pérez Arellano, José Luis | en_US |
dc.date.accessioned | 2023-03-02T15:13:37Z | - |
dc.date.available | 2023-03-02T15:13:37Z | - |
dc.date.issued | 2022 | en_US |
dc.identifier.issn | 1473-5571 | en_US |
dc.identifier.uri | http://hdl.handle.net/10553/120817 | - |
dc.description.abstract | Background: Effective, safe, and affordable antivirals are needed for coronavirus disease 2019 (COVID-19). Several lines of research suggest that tenofovir may be effective against COVID-19, but no large-scale human studies with appropriate adjustment for comorbidities have been conducted. Methods: We studied HIV-positive individuals on antiretroviral therapy (ART) in 2020 at 69 HIV clinics in Spain. We collected data on sociodemographics, ART, CD4+ cell count, HIV-RNA viral-load, comorbidities and the following outcomes: laboratory-confirmed severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection, COVID-19 hospitalization, intensive care unit (ICU) admission and death. We compared the 48-week risks for individuals receiving tenofovir disoproxil fumarate (TDF)/emtricitabine (FTC), tenofovir alafenamide (TAF)/FTC, abacavir (ABC)/lamivudine (3TC), and other regimes. All estimates were adjusted for clinical and sociodemographic characteristics via inverse probability weighting. Results: Of 51 558 eligible individuals, 39.6% were on TAF/FTC, 11.9% on TDF/FTC, 26.6% on ABC/3TC, 21.8% on other regimes. There were 2402 documented SARS-CoV-2 infections (425 hospitalizations, 45 ICU admissions, 37 deaths). Compared with TAF/FTC, the estimated risk ratios (RR) (95% confidence interval) of hospitalization were 0.66 (0.43, 0.91) for TDF/FTC and 1.29 (1.02, 1.58) for ABC/3TC, the RRs of ICU admission were 0.28 (0.11, 0.90) for TDF/FTC and 1.39 (0.70, 2.80) for ABC/3TC, and the RRs of death were 0.37 (0.23, 1.90) for TDF/FTC and 2.02 (0.88-6.12) for ABC/3TC. The corresponding RRs of hospitalization for TDF/FTC were 0.49 (0.24, 0.81) in individuals ≥50 years and 1.15 (0.59, 1.93) in younger individuals. Discussion: Compared with other antiretrovirals, TDF/FTC lowers COVID-19 severity among HIV-positive individuals with virological control. This protective effect may be restricted to individuals aged 50 years and older. | en_US |
dc.language | eng | en_US |
dc.relation.ispartof | AIDS | en_US |
dc.source | AIDS [ISSN 1473-5571], v. 36 (15), p. 2171-2179, (Diciembre 2022) | en_US |
dc.subject | 32 Ciencias médicas | en_US |
dc.subject | 320505 Enfermedades infecciosas | en_US |
dc.subject | 3209 Farmacología | en_US |
dc.subject.other | Coronavirus disease 2019 | en_US |
dc.subject.other | Repositioning of drug | en_US |
dc.subject.other | Severe acute respiratory syndrome coronavirus 2 | en_US |
dc.title | Tenofovir disoproxil fumarate/emtricitabine and severity of coronavirus disease 2019 in people with HIV infection. | en_US |
dc.type | info:eu-repo/semantics/article | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1097/QAD.0000000000003372 | en_US |
dc.description.lastpage | 2179 | en_US |
dc.identifier.issue | 15 | - |
dc.description.firstpage | 2171 | en_US |
dc.relation.volume | 36 | en_US |
dc.investigacion | Ciencias de la Salud | en_US |
dc.type2 | Artículo | en_US |
dc.description.notas | Con la participación de CoVIHd Collaboration in Spain | en_US |
dc.description.numberofpages | 9 | en_US |
dc.utils.revision | Sí | en_US |
dc.date.coverdate | Diciembre 2022 | en_US |
dc.identifier.ulpgc | Sí | en_US |
dc.contributor.buulpgc | BU-MED | en_US |
dc.description.sjr | 1,26 | |
dc.description.jcr | 3,8 | |
dc.description.sjrq | Q1 | |
dc.description.jcrq | Q3 | |
dc.description.scie | SCIE | |
dc.description.miaricds | 11,0 | |
item.grantfulltext | open | - |
item.fulltext | Con texto completo | - |
crisitem.author.dept | GIR IUIBS: Trypanosomosis, Resistencia a Antibióticos y Medicina Animal | - |
crisitem.author.dept | IU de Investigaciones Biomédicas y Sanitarias | - |
crisitem.author.dept | Departamento de Ciencias Médicas y Quirúrgicas | - |
crisitem.author.orcid | 0000-0002-2936-8242 | - |
crisitem.author.parentorg | IU de Investigaciones Biomédicas y Sanitarias | - |
crisitem.author.fullName | Pérez Arellano, José Luis | - |
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