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dc.contributor.authorMartín-Iguacel, R.*
dc.contributor.authorVázquez Friol, María del Carmen*
dc.contributor.authorBurgos, J.*
dc.contributor.authorBruguera, A.*
dc.contributor.authorReyes-Urueña, J.*
dc.contributor.authorMoreno-Fornés, S.*
dc.contributor.authorAceitón, J.*
dc.contributor.authorDíaz, Y.*
dc.contributor.authorDomingo, P.*
dc.contributor.authorSaumoy, M.*
dc.contributor.authorKnobel, H.*
dc.contributor.authorDalmau, D.*
dc.contributor.authorBorjabad, B.*
dc.contributor.authorJohansen, I.S.*
dc.contributor.authorMiro, J.M.*
dc.contributor.authorCasabona, J.*
dc.contributor.authorLlibre, J.M.*
dc.date.accessioned2025-09-08T11:49:17Z
dc.date.available2025-09-08T11:49:17Z
dc.date.issued2023
dc.identifier.citationMartín-Iguacel R, Vazquez-Friol MC, Burgos J, Bruguera A, Reyes-Urueña J, Moreno-Fornés S, et al. Cardiovascular events in delayed presentation of HIV: the prospective PISCIS cohort study. Frontiers in Medicine. 2023;10.
dc.identifier.issn2296-858X
dc.identifier.otherhttps://portalcientifico.sergas.gal//documentos/64be330d3bbfc602eae59382
dc.identifier.urihttp://hdl.handle.net/20.500.11940/21184
dc.description.abstractObjectives: People with HIV (PWH) have a higher cardiovascular risk than the general population. It remains unclear, however, whether the risk of cardiovascular disease (CVD) is higher in late HIV presenters (LP; CD4 ? 350 cells/?L at HIV diagnosis) compared to PWH diagnosed early. We aimed to assess the rates of incident cardiovascular events (CVEs) following ART initiation among LP compared to non-LP. Methods: From the prospective, multicentre PISCIS cohort, we included all adult people with HIV (PWH) initiating antiretroviral therapy (ART) between 2005 and 2019 without prior CVE. Additional data were extracted from public health registries. The primary outcome was the incidence of first CVE (ischemic heart disease, congestive heart failure, cerebrovascular, or peripheral vascular disease). The secondary outcome was all-cause mortality after the first CVE. We used Poisson regression. Results: We included 3,317 PWH [26 589.1 person/years (PY)]: 1761 LP and 1556 non-LP. Overall, 163 (4.9%) experienced a CVE [IR 6.1/1000PY (95%CI: 5.3-7.1)]: 105 (6.0%) LP vs. 58 (3.7%) non-LP. No differences were observed in the multivariate analysis adjusting for age, transmission mode, comorbidities, and calendar time, regardless of CD4 at ART initiation [aIRR 0.92 (0.62-1.36) and 0.84 (0.56-1.26) in LP with CD4 count <200 and 200- ? 350 cells/?L, respectively, compared to non-LP]. Overall mortality was 8.5% in LP versus 2.3% in non-LP (p < 0.001). Mortality after the CVE was 31/163 (19.0%), with no differences between groups [aMRR 1.24 (0.45-3.44)]. Women vs. MSM and individuals with chronic lung and liver disease experienced particularly high mortality after the CVE [aMRR 5.89 (1.35-25.60), 5.06 (1.61-15.91), and 3.49 (1.08-11.26), respectively]. Sensitivity analyses including only PWH surviving the first 2 years yielded similar results. Conclusion: CVD remains a common cause of morbidity and mortality among PWH. LP without prior CVD did not exhibit an increased long-term risk of CVE compared with non-LP. Identifying traditional cardiovascular risk factors is essential for CVD risk reduction in this population.
dc.description.sponsorshipThis work was supported by scholarships from the University of Southern Denmark, the Danish AIDS-foundation, and Public Regional Funds. JM received a personal 80:20 research grant from Institut d'Investigacions Biomediques August Pi i Sunyer (IDIBAPS), Barcelona, Spain, during 2017-23. The study was investigator-driven and thus independent of any pharmaceutical company. The funding sources were not involved in study design, data collection, analyses, report writing, or the decision to submit the paper.
dc.languageeng
dc.rightsAttribution 4.0 International (CC BY 4.0)*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.titleCardiovascular events in delayed presentation of HIV: the prospective PISCIS cohort study
dc.typeArtigo
dc.authorsophosMartín-Iguacel, R.; Vazquez-Friol, M.C.; Burgos, J.; Bruguera, A.; Reyes-Urueña, J.; Moreno-Fornés, S.; Aceitón, J.; Díaz, Y.; Domingo, P.; Saumoy, M.; Knobel, H.; Dalmau, D.; Borjabad, B.; Johansen, I.S.; Miro, J.M.; Casabona, J.; Llibre, J.M.
dc.identifier.doi10.3389/fmed.2023.1182359
dc.identifier.sophos64be330d3bbfc602eae59382
dc.journal.titleFrontiers in Medicine*
dc.organizationServizo Galego de Saúde::Áreas Sanitarias (A.S.) - Complexo Hospitalario Universitario de Ferrol::Medicina interna
dc.relation.projectIDUniversity of Southern Denmark
dc.relation.projectIDDanish AIDS-foundation
dc.relation.projectIDPublic Regional Funds
dc.relation.projectIDInstitut d'Investigacions Biomediques August Pi i Sunyer (IDIBAPS), Barcelona, Spain
dc.relation.publisherversionhttps://doi.org/10.3389/fmed.2023.1182359
dc.rights.accessRightsopenAccess*
dc.subject.keywordAS Ferrol
dc.subject.keywordCHUF
dc.typefidesArtículo Científico (incluye Original, Original breve, Revisión Sistemática y Meta-análisis)
dc.typesophosArtículo Original
dc.volume.number10


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Attribution 4.0 International (CC BY 4.0)
Excepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International (CC BY 4.0)