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    Por favor, use este identificador para citar o enlazar este ítem:https://uvadoc.uva.es/handle/10324/52737

    Título
    Inflammation-related molecules in tears of patients with chronic ocular pain and dry eye disease
    Autor
    Blanco Vázquez, MartaAutoridad UVA
    Vázquez Hernández, AmandaAutoridad UVA
    Fernández Martínez, ItziarAutoridad UVA Orcid
    Novo Díez, AndreaAutoridad UVA
    Martínez Plaza, ElenaAutoridad UVA
    García Vázquez, Carmen
    González García, María JesúsAutoridad UVA Orcid
    Sobas Abad, Eva MaríaAutoridad UVA
    Calonge, MargaritaAutoridad UVA Orcid
    Enriquez De Salamanca Aladro, AmaliaAutoridad UVA Orcid
    Año del Documento
    2022
    Editorial
    Elsevier
    Descripción
    Producción Científica
    Documento Fuente
    Experimental Eye Research, 2022, vol. 19, 109057
    Zusammenfassung
    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.
    Palabras Clave
    Chronic ocular pain
    Dolor ocular crónico
    Dry eye
    Ojo seco
    Neuromodulators
    Neuromoduladores
    Refractive surgery
    Cirugía refractiva
    ISSN
    0014-4835
    Revisión por pares
    SI
    DOI
    10.1016/j.exer.2022.109057
    Patrocinador
    Ministerio de Ciencia, Innovación y Universidades (grants SAF-2016-77080-P, FPU17/02715 and FPU15/01443)
    Version del Editor
    https://www.sciencedirect.com/science/article/pii/S0014483522001373?via%3Dihub
    Propietario de los Derechos
    © 2022 Elsevier
    Idioma
    eng
    URI
    https://uvadoc.uva.es/handle/10324/52737
    Tipo de versión
    info:eu-repo/semantics/publishedVersion
    Derechos
    openAccess
    Aparece en las colecciones
    • IOBA - Artículos de revista [80]
    • DEP11 - Artículos de revista [241]
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    Nombre:
    Inflammation-related-molecules.pdf
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    974.2Kb
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