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dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP
dc.contributor.authorLEBKUCHEN, Adriana
dc.contributor.authorFREITAS, Lunara S.
dc.contributor.authorCARDOZO, Karina H. M.
dc.contributor.authorDRAGER, Luciano F.
dc.date.accessioned2021-06-17T13:50:27Z-
dc.date.available2021-06-17T13:50:27Z-
dc.date.issued2021
dc.identifier.citationTRENDS IN CARDIOVASCULAR MEDICINE, v.31, n.4, p.242-249, 2021
dc.identifier.issn1050-1738
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/40526-
dc.description.abstractSeveral challenges have been noted in the pursuit of a comprehensive knowledge base about the impact of OSA including: 1) the precise mechanisms by which OSA causes metabolic and cardiovascular consequences are not clear, which limits our current ability to address potential targets in OSA; 2) several patients with OSA, even with severe forms, present with no or mild daytime symptoms. Beyond the obvious challenges for obtaining good adherence for conventional OSA treatments, there is evidence that symptomatic vs. asymptomatic patients with OSA do not necessarily have the same metabolic and cardiovascular outcomes; and 3) the cardiovascular response to OSA treatment may vary even in those patients with good adherence. In this scenario, there is an obvious need to develop biomarkers in the OSA research area. This review focuses on describing the advances that have occurred so far in exploring potential OSA biomarkers with clear emphasis for the cardiovascular risk. Particular attention will be devoted to discuss molecular biomarkers including the potential role of microRNAs, proteomics and metabolomics. We also discuss the major challenges and perspectives in this growing research field. Obstructive sleep apnea (OSA) is a common clinical condition associated with increased cardiovascular morbidity and mortality. Recent evidence from clinical studies and animal models suggest that OSA can promote cardiovascular disease by inducing autonomic, hemodynamic, inflammatory and metabolic dysregulation. However, most of the evidence addressing hard endpoints in humans is derived from observational studies. Several challenges have been noted in the pursuit of a comprehensive knowledge base about the impact of OSA including: 1) the precise mechanisms by which OSA causes metabolic and cardiovascular consequences are not clear, which limits our current ability to address potential targets in OSA; 2) several patients with OSA, even with severe forms, present with no or mild daytime symptoms. Beyond the obvious challenges for obtaining good adherence for conventional OSA treatments, there is evidence that symptomatic vs. asymptomatic patients with OSA do not necessarily have the same metabolic and cardiovascular outcomes; and 3) the cardiovascular response to OSA treatment may vary even in those patients with good adherence. In this scenario, there is an obvious need to develop biomarkers in the OSA research area. This review focuses on describing the advances that have occurred so far in exploring potential OSA biomarkers with clear emphasis for the cardiovascular risk. Particular attention will be devoted to discuss molecular biomarkers including the potential role of microRNAs, proteomics and metabolomics. We also discuss the major challenges and perspectives in this growing research field.eng
dc.language.isoeng
dc.publisherELSEVIER SCIENCE LONDONeng
dc.relation.ispartofTrends in Cardiovascular Medicine
dc.rightsrestrictedAccesseng
dc.subjectBiomarkerseng
dc.subjectCardiovascular diseaseeng
dc.subjectPrognosiseng
dc.subjectSleep apneaeng
dc.titleAdvances and challenges in pursuing biomarkers for obstructive sleep apnea: Implications for the cardiovascular risk ?eng
dc.typearticleeng
dc.rights.holderCopyright ELSEVIER SCIENCE LONDONeng
dc.identifier.doi10.1016/j.tcm.2020.04.003
dc.identifier.pmid32413393
dc.subject.wosCardiac & Cardiovascular Systemseng
dc.type.categoryoriginal articleeng
dc.type.versionpublishedVersioneng
hcfmusp.author.externalLEBKUCHEN, Adriana:Fleury Grp, Sao Paulo, Brazil
hcfmusp.author.externalFREITAS, Lunara S.:Univ Sao Paulo, Med Sch, Heart Inst InCor, Hypertens Unit, Ave Dr Eneas de Carvalho Aguiar 44, BR-05403900 Sao Paulo, Brazil
hcfmusp.author.externalCARDOZO, Karina H. M.:Fleury Grp, Sao Paulo, Brazil
hcfmusp.description.beginpage242
hcfmusp.description.endpage249
hcfmusp.description.issue4
hcfmusp.description.volume31
hcfmusp.origemWOS
hcfmusp.origem.idWOS:000635769900008
hcfmusp.origem.id2-s2.0-85085945128
hcfmusp.publisher.cityLONDONeng
hcfmusp.publisher.countryENGLANDeng
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dc.identifier.eissn1873-2615
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