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dc.contributor.author | Blanco Vázquez, Marta | |
dc.contributor.author | Vázquez Hernández, Amanda | |
dc.contributor.author | Fernández Martínez, Itziar | |
dc.contributor.author | Novo Díez, Andrea | |
dc.contributor.author | Martínez Plaza, Elena | |
dc.contributor.author | García Vázquez, Carmen | |
dc.contributor.author | González García, María Jesús | |
dc.contributor.author | Sobas Abad, Eva María | |
dc.contributor.author | Calonge, Margarita | |
dc.contributor.author | Enriquez De Salamanca Aladro, Amalia | |
dc.date.accessioned | 2022-09-27T11:02:39Z | |
dc.date.available | 2022-09-27T11:02:39Z | |
dc.date.issued | 2022 | |
dc.identifier.citation | Experimental Eye Research, Volume 219, 2022, 109057 | es |
dc.identifier.issn | 0014-4835 | es |
dc.identifier.uri | https://uvadoc.uva.es/handle/10324/55665 | |
dc.description | Producción Científica | es |
dc.description.abstract | The 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.mimetype | application/pdf | es |
dc.language.iso | eng | es |
dc.publisher | Elsevier | es |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | es |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
dc.title | Inflammation-related molecules in tears of patients with chronic ocular pain and dry eye disease | es |
dc.type | info:eu-repo/semantics/article | es |
dc.identifier.doi | 10.1016/j.exer.2022.109057 | es |
dc.relation.publisherversion | https://www.sciencedirect.com/science/article/pii/S0014483522001373?via%3Dihub | es |
dc.identifier.publicationfirstpage | 109057 | es |
dc.identifier.publicationtitle | Experimental Eye Research | es |
dc.identifier.publicationvolume | 219 | es |
dc.peerreviewed | SI | es |
dc.description.project | This work was supported by the Ministry of Science, Innovation and Universities, Spain [grant references SAF-2016-77080-P (AEI/FEDER, UE), FPU17/02715 and FPU15/01443]. | es |
dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 Internacional | * |
dc.type.hasVersion | info:eu-repo/semantics/publishedVersion | es |
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