Tear Film Mediators After Corneal Cross-Linking: Methodology Validation

Detalhes bibliográficos
Autor(a) principal: Costa, Celso
Data de Publicação: 2023
Outros Autores: Araújo, Mariana, Rosa, Andreia, Gil, João, Quadrado, Maria João, Tavares, Cristina, Costa, Esmeralda, Fernandes, Rosa, Costa, Lígia, Melo, Pedro, Murta, Joaquim
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://doi.org/10.48560/rspo.25967
Resumo: Introduction: Currently, the gold-standard treatment of progressive keratoconus (KC) is corneal collagen cross-linking (CXL), in which riboflavin and ultraviolet-A radiation increase the corneal biomechanical rigidity, arresting progression. However, post-operatory results vary significantly among patients. Although it has been suggested that corneal thickness, cone location and patient’s age are important factors, their contribution is controversial. The reason for this variability remains obscure. This project aims to find biomarkers that could explain the variability within surgical results after corneal CXL by investigating the correlation between the local corneal inflammatory environment and these results. We hypothesize that better post-operatory results are related to a reduction in the inflammatory cytokine levels in the patients’ tear film. Ultimately, we aim to optimize the patients’ surgical outcomes according to their corneal inflammatory environment. Methodology: The research protocol was established after testing different sample collection methods. Patients are interviewed to assess their medical history and relevant habits. Their corneal tomographic and best corrected visual acuity data are registered before and 6 months after surgery. The patient´s tear film is sampled twice 6 months apart using Schirmer strips, as the volume yield is larger compared to direct methods (microcapillary tubes or micropipettes), which are more difficult to perform and require stimulation or the instillation of saline into the cul-de-sac, originating reflex tearing. The samples are analyzed for their total protein content (BCA Protein Assay Kit) and cytokine concentration using Multiplex technology (Th1/Th2/Th9/Th17 Cytokine 18-Plex Human Procarta-Plex™ Panel) and not ELISA, as we tried before. Statistical analysis to assess sample differences and the correlation between cytokine concentration and tomographic indexes and visual acuity values for each group and subgroup is performed at 6 months. Results: Twenty patients and eight control subjects have been enrolled in the study and the first collection of tears has been carried out. CXL surgeries for the twenty patients were per-formed from October 2020 to September 2021. Two samples were lost due to excessively length of dry Schirmer strip, which we improved by cutting the dry portion. Additionally, the tear fluid from the first eight samples from patients and from control participants was successfully processed for their total protein content. Conclusion: Tear film analysis poses several challenges concerning the small amount of material available without reflex production. This fact precludes the use of conventional ELISA, requiring multiplex modified technology. When dealing with tears it is also important to avoid contamination by using sterilized material, to avoid dilution and to establish an efficient flow of samples from the clinic to the laboratory. This pilot study enabled to identify several methodological frailties and to establish a solid research protocol that can be replicated by other researchers. Understanding the correlation between inflammatory cytokines and surgical outcomes of CXL may allow for the optimization and personalization of CXL. In addition, the results of this research protocol are expected to establish prognostic factors for CXL-related surgical outcomes, ultimately improving the quality of life of KC patients.
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spelling Tear Film Mediators After Corneal Cross-Linking: Methodology ValidationMediadores do Filme Lacrimal Após Cross-Linking Corneano: Validação de MetodologiaArtigos OriginaisIntroduction: Currently, the gold-standard treatment of progressive keratoconus (KC) is corneal collagen cross-linking (CXL), in which riboflavin and ultraviolet-A radiation increase the corneal biomechanical rigidity, arresting progression. However, post-operatory results vary significantly among patients. Although it has been suggested that corneal thickness, cone location and patient’s age are important factors, their contribution is controversial. The reason for this variability remains obscure. This project aims to find biomarkers that could explain the variability within surgical results after corneal CXL by investigating the correlation between the local corneal inflammatory environment and these results. We hypothesize that better post-operatory results are related to a reduction in the inflammatory cytokine levels in the patients’ tear film. Ultimately, we aim to optimize the patients’ surgical outcomes according to their corneal inflammatory environment. Methodology: The research protocol was established after testing different sample collection methods. Patients are interviewed to assess their medical history and relevant habits. Their corneal tomographic and best corrected visual acuity data are registered before and 6 months after surgery. The patient´s tear film is sampled twice 6 months apart using Schirmer strips, as the volume yield is larger compared to direct methods (microcapillary tubes or micropipettes), which are more difficult to perform and require stimulation or the instillation of saline into the cul-de-sac, originating reflex tearing. The samples are analyzed for their total protein content (BCA Protein Assay Kit) and cytokine concentration using Multiplex technology (Th1/Th2/Th9/Th17 Cytokine 18-Plex Human Procarta-Plex™ Panel) and not ELISA, as we tried before. Statistical analysis to assess sample differences and the correlation between cytokine concentration and tomographic indexes and visual acuity values for each group and subgroup is performed at 6 months. Results: Twenty patients and eight control subjects have been enrolled in the study and the first collection of tears has been carried out. CXL surgeries for the twenty patients were per-formed from October 2020 to September 2021. Two samples were lost due to excessively length of dry Schirmer strip, which we improved by cutting the dry portion. Additionally, the tear fluid from the first eight samples from patients and from control participants was successfully processed for their total protein content. Conclusion: Tear film analysis poses several challenges concerning the small amount of material available without reflex production. This fact precludes the use of conventional ELISA, requiring multiplex modified technology. When dealing with tears it is also important to avoid contamination by using sterilized material, to avoid dilution and to establish an efficient flow of samples from the clinic to the laboratory. This pilot study enabled to identify several methodological frailties and to establish a solid research protocol that can be replicated by other researchers. Understanding the correlation between inflammatory cytokines and surgical outcomes of CXL may allow for the optimization and personalization of CXL. In addition, the results of this research protocol are expected to establish prognostic factors for CXL-related surgical outcomes, ultimately improving the quality of life of KC patients.Introdução: Atualmente, o tratamento gold-standard do queratocone (QC) progressivo é o cross-linking do colagénio corneano (CXL), no qual a riboflavina e a radiação ultravioleta-A aumentam a rigidez biomecânica da córnea, parando a progressão. No entanto, os resultados pós-operatórios variam significativamente entre os doentes. Embora se tenha sugerido na literatura que a espessura da córnea, a localização do cone e a idade do doente são fatores importantes, a contribuição destes fatores é controversa. A razão para esta variabilidade permanece incógnita. Este projeto visa descobrir biomarcadores que possam explicar a variabilidade dos resultados cirúrgicos após CXL corneano, investigando a correlação entre o ambiente inflamatório local da córnea e estes resultados. A nossa hipótese é que melhores resultados pós-operatórios estão relacionados com uma redução nos níveis de citocinas inflamatórias no filme lacrimal dos doentes. Em última instância, pretendemos otimizar os resultados cirúrgicos dos pacientes de acordo com o seu ambiente inflamatório corneano. Métodos: O nosso protocolo de pesquisa foi estabelecido após testagem de diferentes métodos de colheita de amostras. Os doentes são entrevistados para avaliar os seus antecedentes pessoais e hábitos relevantes. Os dados tomográficos da córnea e a melhor acuidade visual corrigida são registados antes e 6 meses após a cirurgia. Amostras de filme lacrimal dos doentes são colhidas duas vezes, com 6 meses de intervalo, usando tiras de Schirmer, pois o volume conseguido é maior em comparação com os métodos diretos (tubos microcapilares ou micropipetas), que são mais difíceis de realizar e requerem estimulação ou instilação de solução salina no fundo de saco conjuntival, originando lacrimejo reflexo. As amostras são analisadas quanto ao seu conteúdo de proteína total (BCA Protein Assay Kit) e concentração de citocinas através de tecnologia Multiplex (Th1/Th2/Th9/Th17 Cytokine 18-Plex Human ProcartaPlex™ Panel) e não ELISA, como previamente tentado. A análise estatística para avaliar as diferenças entre as amostras e a correlação entre a concentração de citocinas e índices tomográficos e valores de acuidade visual para cada grupo e subgrupo é realizada aos 6 meses. Resultados: Vinte doentes e oito controlos foram incluídos no estudo e a primeira colheita de lágrimas foi realizada. As cirurgias de CXL dos vinte doentes foram realizadas de outubro de 2020 a setembro de 2021. Duas amostras foram perdidas devido ao comprimento excessivo da tira de Schirmer, facto que melhorámos cortando a parte seca da tira. Além disso, as amostras de filme lacrimal dos primeiros oito doentes e dos 8 controlos foram processadas com sucesso para obtenção do conteúdo de proteína total. Conclusão: A análise do filme lacrimal apresenta vários desafios, tendo em conta a pe-quena quantidade de material disponível sem estimulação da produção de lágrimas reflexa. Este facto impossibilita o uso de ELISA convencional, exigindo assim tecnologia multiplex modificada. Ao lidar com lágrimas, também é crucial evitar a contaminação, através do uso de material esterilizado, evitar a diluição e estabelecer um eficiente fluxo de amostras do hospital para o laboratório. Este estudo piloto permitiu identificar várias fragilidades metodológicas e estabelecer um protocolo de investigação sólido que pode ser replicado por outros investigadores. Compreender a correlação entre citocinas inflamatórias e resultados cirúrgicos do CXL pode permitir a otimização e personalização do CXL. Além disso, é expectável que os resultados deste protocolo estabeleçam fatores prognósticos para os resultados cirúrgicos do CXL, melhorando, em última análise, a qualidade de vida dos doentes com QC.Ajnet2023-03-28info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://doi.org/10.48560/rspo.25967eng1646-69501646-6950Costa, CelsoAraújo, MarianaRosa, AndreiaGil, JoãoQuadrado, Maria JoãoTavares, CristinaCosta, EsmeraldaFernandes, RosaCosta, LígiaMelo, PedroMurta, Joaquiminfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-03-30T20:30:12Zoai:ojs.revistas.rcaap.pt:article/25967Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T17:48:08.845208Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Tear Film Mediators After Corneal Cross-Linking: Methodology Validation
Mediadores do Filme Lacrimal Após Cross-Linking Corneano: Validação de Metodologia
title Tear Film Mediators After Corneal Cross-Linking: Methodology Validation
spellingShingle Tear Film Mediators After Corneal Cross-Linking: Methodology Validation
Costa, Celso
Artigos Originais
title_short Tear Film Mediators After Corneal Cross-Linking: Methodology Validation
title_full Tear Film Mediators After Corneal Cross-Linking: Methodology Validation
title_fullStr Tear Film Mediators After Corneal Cross-Linking: Methodology Validation
title_full_unstemmed Tear Film Mediators After Corneal Cross-Linking: Methodology Validation
title_sort Tear Film Mediators After Corneal Cross-Linking: Methodology Validation
author Costa, Celso
author_facet Costa, Celso
Araújo, Mariana
Rosa, Andreia
Gil, João
Quadrado, Maria João
Tavares, Cristina
Costa, Esmeralda
Fernandes, Rosa
Costa, Lígia
Melo, Pedro
Murta, Joaquim
author_role author
author2 Araújo, Mariana
Rosa, Andreia
Gil, João
Quadrado, Maria João
Tavares, Cristina
Costa, Esmeralda
Fernandes, Rosa
Costa, Lígia
Melo, Pedro
Murta, Joaquim
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Costa, Celso
Araújo, Mariana
Rosa, Andreia
Gil, João
Quadrado, Maria João
Tavares, Cristina
Costa, Esmeralda
Fernandes, Rosa
Costa, Lígia
Melo, Pedro
Murta, Joaquim
dc.subject.por.fl_str_mv Artigos Originais
topic Artigos Originais
description Introduction: Currently, the gold-standard treatment of progressive keratoconus (KC) is corneal collagen cross-linking (CXL), in which riboflavin and ultraviolet-A radiation increase the corneal biomechanical rigidity, arresting progression. However, post-operatory results vary significantly among patients. Although it has been suggested that corneal thickness, cone location and patient’s age are important factors, their contribution is controversial. The reason for this variability remains obscure. This project aims to find biomarkers that could explain the variability within surgical results after corneal CXL by investigating the correlation between the local corneal inflammatory environment and these results. We hypothesize that better post-operatory results are related to a reduction in the inflammatory cytokine levels in the patients’ tear film. Ultimately, we aim to optimize the patients’ surgical outcomes according to their corneal inflammatory environment. Methodology: The research protocol was established after testing different sample collection methods. Patients are interviewed to assess their medical history and relevant habits. Their corneal tomographic and best corrected visual acuity data are registered before and 6 months after surgery. The patient´s tear film is sampled twice 6 months apart using Schirmer strips, as the volume yield is larger compared to direct methods (microcapillary tubes or micropipettes), which are more difficult to perform and require stimulation or the instillation of saline into the cul-de-sac, originating reflex tearing. The samples are analyzed for their total protein content (BCA Protein Assay Kit) and cytokine concentration using Multiplex technology (Th1/Th2/Th9/Th17 Cytokine 18-Plex Human Procarta-Plex™ Panel) and not ELISA, as we tried before. Statistical analysis to assess sample differences and the correlation between cytokine concentration and tomographic indexes and visual acuity values for each group and subgroup is performed at 6 months. Results: Twenty patients and eight control subjects have been enrolled in the study and the first collection of tears has been carried out. CXL surgeries for the twenty patients were per-formed from October 2020 to September 2021. Two samples were lost due to excessively length of dry Schirmer strip, which we improved by cutting the dry portion. Additionally, the tear fluid from the first eight samples from patients and from control participants was successfully processed for their total protein content. Conclusion: Tear film analysis poses several challenges concerning the small amount of material available without reflex production. This fact precludes the use of conventional ELISA, requiring multiplex modified technology. When dealing with tears it is also important to avoid contamination by using sterilized material, to avoid dilution and to establish an efficient flow of samples from the clinic to the laboratory. This pilot study enabled to identify several methodological frailties and to establish a solid research protocol that can be replicated by other researchers. Understanding the correlation between inflammatory cytokines and surgical outcomes of CXL may allow for the optimization and personalization of CXL. In addition, the results of this research protocol are expected to establish prognostic factors for CXL-related surgical outcomes, ultimately improving the quality of life of KC patients.
publishDate 2023
dc.date.none.fl_str_mv 2023-03-28
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