Gut epithelial barrier markers in patients with obstructive sleep apnea

dc.contributor.authorBarceló, Antonia
dc.contributor.authorEsquinas López, Cristina
dc.contributor.authorRobles, Juan
dc.contributor.authorPiérola, Javier
dc.contributor.authorPeña, Mónica de la
dc.contributor.authorAguilar, Irene
dc.contributor.authorMorell-Garcia, Daniel
dc.contributor.authorAlonso, Alberto
dc.contributor.authorToledo Pons, Nuria
dc.contributor.authorSánchez de la Torre, Manuel
dc.contributor.authorBarbé, Ferran
dc.date.accessioned2018-03-26T12:10:14Z
dc.date.available2018-03-26T12:10:14Z
dc.date.issued2016-10-01
dc.date.updated2018-03-26T12:10:14Z
dc.description.abstractBackground: obstructive sleep apnea (OSA) is now being recognized as an additional contributing factor to the pathogenesis of obesity-related comorbidities. At the same time, there is now increasing evidence to suggest that intestinal wall permeability plays a role in the development of metabolic syndrome. In the present study, circulating zonulin and fatty acid binding protein (I-FABP) were measured in association with metabolic, hepatic, and inflammatory parameters. Results: compared with controls, plasma I-FABP levels were significantly higher in patients with OSA (571 pg/mL [IQR 290-950] vs 396 pg/mL [IQR 234-559], p = 0.04). Zonulin levels were similar between groups. Significant relationships were observed between zonulin levels and waist circumference (p < 0.05), glucose (p < 0.05), and insulin (p < 0.05). In addition, in the OSA group, zonulin levels correlated negatively with the mean nocturnal oxygenation saturation (p < 0.05) and positively with total cholesterol (p < 0.05), alanine aminotransferase (ALT) (p < 0.005), aminotransferase (AST) (p < 0.01), gamma glutamyltransferase (GGT) (p < 0.005), and high-sensitivity C-reactive protein (hs-CRP) (p < 0.05). Multivariate analysis showed that associations between zonulin and ALT, AST, and hs-CRP were attenuated, but not eliminated, after adjustment for other variables. Conclusions: the results of this study suggest that OSA is a risk factor for intestinal damage, regardless of metabolic profile, and that intestinal permeability might be a possible contributor to nonalcoholic fatty liver disease in patients with OSA.
dc.format.extent4 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec678838
dc.identifier.issn1389-9457
dc.identifier.pmid28007354
dc.identifier.urihttps://hdl.handle.net/2445/121109
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1016/j.sleep.2016.01.019
dc.relation.ispartofSleep Medicine, 2016, vol. 26, p. 12-15
dc.relation.urihttps://doi.org/10.1016/j.sleep.2016.01.019
dc.rightscc-by-nc-nd (c) Elsevier B.V., 2016
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es
dc.sourceArticles publicats en revistes (Infermeria de Salut Pública, Salut mental i Maternoinfantil)
dc.subject.classificationProteïnes portadores
dc.subject.classificationFixació de proteïnes
dc.subject.classificationSíndrome metabòlica
dc.subject.classificationAbsorció intestinal
dc.subject.classificationSíndromes d'apnea del son
dc.subject.classificationObesitat
dc.subject.otherCarrier proteins
dc.subject.otherProtein binding
dc.subject.otherMetabolic syndrome
dc.subject.otherIntestinal absorption
dc.subject.otherSleep apnea syndromes
dc.subject.otherObesity
dc.titleGut epithelial barrier markers in patients with obstructive sleep apnea
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/acceptedVersion

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