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dc.contributor.authorBlanco Vázquez, Marta 
dc.contributor.authorVázquez Hernández, Amanda 
dc.contributor.authorFernández Martínez, Itziar 
dc.contributor.authorNovo Díez, Andrea 
dc.contributor.authorMartínez Plaza, Elena 
dc.contributor.authorGarcía Vázquez, Carmen
dc.contributor.authorGonzález García, María Jesús 
dc.contributor.authorSobas Abad, Eva María 
dc.contributor.authorCalonge, Margarita 
dc.contributor.authorEnriquez De Salamanca Aladro, Amalia 
dc.date.accessioned2022-03-30T11:16:08Z
dc.date.available2022-03-30T11:16:08Z
dc.date.issued2022
dc.identifier.citationExperimental Eye Research, 2022, vol. 19, 109057es
dc.identifier.issn0014-4835es
dc.identifier.urihttps://uvadoc.uva.es/handle/10324/52737
dc.descriptionProducción Científicaes
dc.description.abstractThe purpose of this study was to analyze inflammation- and pain-related molecules in tears of patients suffering from chronic ocular pain associated with dry eye (DE) and/or a previous corneal refractive surgery (RS). Based on history, symptomatology, and clinical signs, the subjects (n = 180, 51.0 ± 14.7 years, 118 females, 62 males) in this cross-sectional study were assigned to one of five groups: DE and chronic ocular pain after RS (P/DE-RS, n = 52); asymptomatic subjects, i.e., without DE and chronic ocular pain, after RS (A-RS, n = 30); DE and chronic ocular pain without previous RS (P/DE-nonRS, n = 31); DE, no pain, and no previous RS (DE-nonRS, n = 35); and asymptomatic subjects with no previous RS (controls, n = 32). The tear concentrations of 20 cytokines and substance P (SP) were analyzed by immunobead-based assay and enzyme-linked immunosorbent assay, respectively. We found that tear levels of interleukin (IL)-10 and SP were increased in the RS groups. There were significant differences in IL-8/CXCL8 among the five groups. Nerve growth factor (NGF) tear levels were significantly higher in P/DE-RS than in DE-nonRS and controls. IL-9 had the highest percentage of detection in the P/DE-RS and P/DE-nonRS groups, while macrophage inflammatory protein (MIP)-1α, IL-2, and interferon (IFN)-γ were higher in the P/DE-RS, A-RS, and P/DE-nonRS groups. IL-17A was detected only in the A-RS group. Moderate correlations were observed in the A-RS, P/DE-nonRS, DE-nonRS and controls groups. A positive correlation was obtained between growth related oncogene concentration and tear break-up time (rho = 0.550; p = 0.012), while negative correlation was found between monocyte chemoattractant protein-3/CCL7 and conjunctival staining (rho = −0.560; p = 0.001), both in the A-RS group. IL-10 correlated positively with ocular pain intensity (rho = 0.513; p = 0.003) in the P/DE-nonRS group. Regulated on Activation Normal T Cell Expressed and Secreted/CCL5 correlated negatively with conjunctival staining (rho = −0.545; p = 0.001) in the DE-nonRS group. SP correlated negatively with corneal staining (rho = −0.559; p = 0.001) in the controls. In conclusion, chronic ocular pain was associated with higher IL-9 tear levels. IL-10, SP, MIP-1α/CCL3, IL-2, and IFN-γ were associated with previous RS. Higher levels of IL-8/CXCL8, MIP-1α/CCL3, IL-2, and IFN-γ were associated with DE-related inflammation, while NGF levels were related to chronic ocular pain and DE in RS patients. These findings suggest that improved knowledge of tear cytokines and neuromodulators will lead to a more nuanced understanding of how these molecules can serve as biomarkers of chronic ocular pain, leading to better therapeutic and disease management decisions.es
dc.format.mimetypeapplication/pdfes
dc.language.isoenges
dc.publisherElsevieres
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.classificationChronic ocular paines
dc.subject.classificationDolor ocular crónicoes
dc.subject.classificationDry eyees
dc.subject.classificationOjo secoes
dc.subject.classificationNeuromodulatorses
dc.subject.classificationNeuromoduladoreses
dc.subject.classificationRefractive surgeryes
dc.subject.classificationCirugía refractivaes
dc.titleInflammation-related molecules in tears of patients with chronic ocular pain and dry eye diseasees
dc.typeinfo:eu-repo/semantics/articlees
dc.rights.holder© 2022 Elsevieres
dc.identifier.doi10.1016/j.exer.2022.109057es
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S0014483522001373?via%3Dihubes
dc.peerreviewedSIes
dc.description.projectMinisterio de Ciencia, Innovación y Universidades (grants SAF-2016-77080-P, FPU17/02715 and FPU15/01443)es
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones


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