Traducción y validación del «Cuestionario para investigación de resultados en queratocono» (KORQ) en población colombiana / Translation and validation of the "Questionnaire for research on keratoconus results" (KORQ) in the Colombian population

OBJETIVO: Se plantea realizar un proceso de traducción y adaptación del Cuestionario KORQ al castellano y su validación en una población hispanoparlante como es la colombiana. Con ello se pretende brindar una herramienta para la medición y control del compromiso en la calidad de vida de los pacientes con esta ectasia corneal. MATERIAL Y MÉTODOS: Estudio prospectivo, analítico, en el cual 200 sujetos con diagnóstico de queratocono completaron una versión traducida del cuestionario KORQ. La validez interna del cuestionario se evaluó por medio del Alfa de Cronbach, mientras que su construcción fue evaluada por un análisis exploratorio de factores, incluyendo un análisis paralelo de Horn para la selección del número de factores subyacentes. Posteriormente, 50 pacientes fueron seleccionados nuevamente para volver a completar el cuestionario una semana después. La repetibilidad del cuestionario fue medida por la prueba de Spearman. RESULTADOS: El cuestionario KORQ en su versión en castellano mostró cierta validez interna en ambas secciones. Tanto la sección de «habilidad visual» como la de «síntomas» mostraban un comportamiento esencialmente unidimensional. La repetibilidad test-retest de la prueba fue excelente (Spearman rho > 0,95). CONCLUSIONES: El cuestionario KORQ en su versión traducida es válido en población colombiana hispanoparlante

OBJECTIVE: It is proposed to carry out a process of translation and adaptation of the "Questionnaire for Research on Keratoconus Results" (KORQ) into Spanish and its validation in a Spanish-speaking population, such as Colombia. This is intended to provide a tool for measuring and monitoring the commitment to quality of life of patients with this corneal ectasia. MATERIAL AND METHODS: A prospective analytical study was carried out, in which 200 subjects diagnosed with keratoconus completed a translated version of the KORQ questionnaire. The internal validity of the questionnaire was evaluated using Cronbach's Alpha, while its construction was evaluated by an Exploratory Factor Analysis, including a Parallel Horn Analysis for the selection of the number of underlying factors. Subsequently, 50 patients were re-selected to complete the questionnaire one week later. The repeatability of the questionnaire was measured by the Spearman test. RESULTS: The KORQ questionnaire in its Spanish version showed some internal validity in both sections. Both sections of the questionnaire showed an essentially unidimensional behaviour. The test-retest repeatability of the test was excellent (Spearman rho > 0.95). CONCLUSIONS: The translated version of the KORQ is valid in Colombian population

Translation and validation of the "Questionnaire for research on keratoconus results" (KORQ) in the Colombian population. / Traducción y validación del «Cuestionario para investigación de resultados en queratocono¼ (KORQ) en población colombiana.

OBJECTIVE: It is proposed to carry out a process of translation and adaptation of the "Questionnaire for Research on Keratoconus Results" (KORQ) into Spanish and its validation in a Spanish-speaking population, such as Colombia. This is intended to provide a tool for measuring and monitoring the commitment to quality of life of patients with this corneal ectasia. MATERIAL AND METHODS: A prospective analytical study was carried out, in which 200 subjects diagnosed with keratoconus completed a translated version of the KORQ questionnaire. The internal validity of the questionnaire was evaluated using Cronbach's Alpha, while its construction was evaluated by an Exploratory Factor Analysis, including a Parallel Horn Analysis for the selection of the number of underlying factors. Subsequently, 50 patients were re-selected to complete the questionnaire one week later. The repeatability of the questionnaire was measured by the Spearman test. RESULTS: The KORQ questionnaire in its Spanish version showed some internal validity in both sections. Both sections of the questionnaire showed an essentially unidimensional behaviour. The test-retest repeatability of the test was excellent (Spearman rho> 0.95). CONCLUSIONS: The translated version of the KORQ is valid in Colombian population.

Identificación de nuevos genes candidatos para la retinopatía en diabéticos tipo 2. Estudio Valencia sobre Retinopatía Diabética (EVRD). Informe n.° 3 / Identification of new candidate genes for retinopathy in type 2 diabetics. Valencia Study on Diabetic Retinopathy (VSDR). Report number 3

OBJETIVO: Identificar genes implicados en los mecanismos patogénicos de la retinopatía diabética no proliferante, como estrés oxidativo, alteración de la matriz extracelular y/o apoptosis, para valorar el riesgo de desarrollo de la misma en una población de diabéticos tipo2 (DM2). MATERIAL Y MÉTODOS: Estudio de casos y controles en 81 participantes del Estudio Valencia sobre Retinopatía Diabética (EVRD), de ambos sexos y con edades comprendidas entre los 25 y 85 años, clasificados en: 1) grupo DM2 (n = 49), con RD (+RD; n = 14) y sin RD (−RD; n = 35), y 2)grupo control (GC; n=32). Se realizó entrevista personal, examen oftalmológico estandarizado y extracción de sangre que se procesó para analizar el ADN y determinar la expresión de: TP53, MMP9 y SLC23A2 en todos los participantes. El programa estadístico utilizado fue el SPSS v22.0. RESULTADOS: Los genes TP53 y MMP9 aumentaron su expresión en el grupo DM2 respecto al GC, aunque solo de manera significativa el gen MMP9 (TP53: 10,40 ± 1,20 vs. 8,23 ± 1,36, p = 0,084; MMP9: 1,45 ± 0,16 vs. 0,95 ± 0,16, p = 0,036) y el gen SLC23A2 disminuyó significativamente sus niveles en DM2 vs. GC (5,58 ± 0,64 vs. 11,66 ± 1,90, p = 0,026). Al subdividir el grupo DM2 según presencia de retinopatía, la expresión de los genes TP53, MMP9 y SLC23A2 mostró diferencias significativas entre los grupos DM2−RD, DM2+RD y GC (TP53: 9,95 ± 1,47 vs. 11,52 ± 2,05 vs. 8,23 ± 1,36, p = 0,038; MMP9: 1,47 ± 0,20 vs. 1,41 ± 0,27 vs. 0,95 ± 0,16, p = 0,021; SLC23A2: 5,61 ± 0,77 vs. 5,51 ± 1,21 vs. 11,66 ± 1,90, p = 0,018). CONCLUSIONES: Los genes reguladores de apoptosis (TP53) e integridad de la matriz extracelular (MMP9) podrían estar implicados en la susceptibilidad para el desarrollo/progresión de la RD, así como el gen SLC232A2 (transportador del ácido ascórbico) puede comportarse como protector del riesgo de padecer/progresar en la retinopatía

OBJECTIVE: To identify genes involved in the pathogenic mechanisms of non-proliferative diabetic retinopathy (NPDR), among which include oxidative stress, extracellular matrix changes, and/or apoptosis, in order to evaluate the risk of developing this retinal disease in a type2 diabetic (DM2) population. MATERIAL AND METHODS: A case-control study was carried out on 81 participants from the Valencia Study on Diabetic Retinopathy (VSDR) of both genders, with ages 25-85 years. They were classified into: (I) DM2 group (n = 49), with DR (+DR; n = 14) and without DR (-DR; n = 35), and (II) control group (GC; n = 32). The protocols included a personal interview, standardised ophthalmological examination, and blood collection (to analyse the DNA for determining the gene expression (TP53, MMP9, and SLC23A2) in the study groups. Statistical analyses were performed using the SPSS v22.0 program. RESULTS: The TP53 and MMP9 genes showed a higher expression in the DM2 group compared to the GC, although the difference was only significant for the MMP9 gene (TP53: 10.40 ± 1.20 V. 8.23 ± 1.36, P = .084; MMP9: 1.45 ± 0.16 vs. 0.95 ± 0.16, P = .036), and the SLC23A2 gene showed a significant lower expression in the DM2 vs CG (5.58 ± 0.64 vs. 11.66±1.90, P=.026). When sub-dividing the DM2 group according to the presence of retinopathy, the expression of the TP53, MMP9 and SLC23A2 genes showed significant differences between the DM2−RD, DM2+RD and GC groups (TP53: 9.95 ± 1.47 vs. 11.52 ± 2.05 vs. 8.23 ± 1.36, P = .038; MMP9: 1.47 ± 0.20 vs. 1.41 ± 0.27 vs. 0.95 ± 0.16, P = .021; SLC23A2: 5.61 ± 0.77 vs. 5.51 ± 1.21 vs. 11.66 ± 1.90, P = .018). CONCLUSIONS: Genes involved in extracellular matrix integrity (MMP9) and/or apoptosis (TP53), could be considered potential markers of susceptibility to the development/progression of NPDR. Interestingly, the SLC232A2 gene (ascorbic acid transporter) can be considered a protector of the risk of the development/progression of the retinopathy

Identification of new candidate genes for retinopathy in type 2 diabetics. Valencia Study on Diabetic Retinopathy (VSDR). Report number 3. / Identificación de nuevos genes candidatos para la retinopatía en diabéticos tipo 2. Estudio Valencia sobre Retinopatía Diabética (EVRD). Informe n.° 3.

OBJECTIVE: To identify genes involved in the pathogenic mechanisms of non-proliferative diabetic retinopathy (NPDR), among which include oxidative stress, extracellular matrix changes, and/or apoptosis, in order to evaluate the risk of developing this retinal disease in a type2 diabetic (DM2) population. MATERIAL AND METHODS: A case-control study was carried out on 81 participants from the Valencia Study on Diabetic Retinopathy (VSDR) of both genders, with ages 25-85years. They were classified into: (i)DM2 group (n=49), with DR (+DR; n=14) and without DR (-DR; n=35), and (ii)control group (GC; n=32). The protocols included a personal interview, standardised ophthalmological examination, and blood collection (to analyse the DNA for determining the gene expression (TP53, MMP9, and SLC23A2) in the study groups. Statistical analyses were performed using the SPSS v22.0 program. RESULTS: The TP53 and MMP9 genes showed a higher expression in the DM2 group compared to the GC, although the difference was only significant for the MMP9 gene (TP53: 10.40±1.20 vs. 8.23±1.36, P=.084; MMP9: 1.45±0.16 vs. 0.95±0.16, P=.036), and the SLC23A2 gene showed a significant lower expression in the DM2 vs CG (5.58±0.64 vs. 11.66±1.90, P=.026). When sub-dividing the DM2 group according to the presence of retinopathy, the expression of the TP53, MMP9 and SLC23A2 genes showed significant differences between the DM2-RD, DM2+RD and GC groups (TP53: 9.95±1.47 vs. 11.52±2.05 vs. 8.23±1.36, P=.038; MMP9: 1.47±0.20 vs. 1.41±0.27 vs. 0.95±0.16, P=.021; SLC23A2: 5.61±0.77 vs. 5.51±1.21 vs. 11.66±1.90, P=.018). CONCLUSIONS: Genes involved in extracellular matrix integrity (MMP9) and/or apoptosis (TP53), could be considered potential markers of susceptibility to the development/progression of NPDR. Interestingly, the SLC232A2 gene (ascorbic acid transporter) can be considered a protector of the risk of the development/progression of the retinopathy.

[Refractive surprise after LASIK]. / Sorpresa refractiva tras LASIK.

CASE REPORT: A female patient underwent laser in situ keratomileusis (LASIK) in both eyes. The final degree of astigmatism in her left eye was double the preoperative value due to an error in data management. Complex surgery to both eyes was necessary to resolve the mistake. DISCUSSION: Complications in refractive surgery can occur, however errors in data management must be minimized by double-checking. Solutions to resolve the errors made can be difficult and the entire staff must share responsibility to avoid these undesirable outcomes.

Sorpresa refractiva tras LASIK / Refractive surpris after LASIK

Caso clínico: Paciente intervenida de láser in situ keratomileusis (LASIK) en ambos ojos (AO). Debido a un error en el manejo de los datos, la refracción cilíndrica postoperatoria en el ojo izquierdo (OI) duplicó a la preoperatoria. La reparación del error exigió un planteamiento quirúrgico-refractivo que afectó a AO.Discusión: La cirugía refractiva no esta exenta de complicaciones. Los errores en el manejo de los datos deben de ser reducidos al máximo mediante la comprobación de los datos por personas distintas. Las soluciones refractivas pueden ser muy complejas y todo el personal debe compartir la responsabilidad de evitar estos errores (AU)

Case report: A female patient underwent laser in situ keratomileusis (LASIK) in both eyes. The final degree of astigmatism in her left eye was double the preoperative value due to an error in data management. Complex surgery to both eyes was necessary to resolve the mistake. Discussion: Complications in refractive surgery can occur, however errors in data management must be minimized by double-checking. Solutions to resolve the errors made can be difficult and the entire staff must share responsibility to avoid these undesirable outcomes (AU)