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1.
Neurol Sci ; 45(2): 693-698, 2024 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-37698786

RESUMEN

BACKGROUND: Neuromyelitis optica spectrum disorders (NMOSD) are autoantibody-mediated inflammatory diseases of the central nervous system predominantly targeting optic nerves and the spinal cord. Two distinct phenotypes are recognized based on the presence of serum aquaporin-4 (AQP4-IgG) antibodies. However, contrasting clinical course patterns have been identified between AQP4-IgG-positive and AQP4-IgG-negative patients. AIMS: This study aimed to present demographic and clinical characteristics of patients with NMOSD in Slovakia and to evaluate the significance of differences between AQP4-IgG-seropositive and AQP4-IgG-seronegative patients. METHODS: We performed a longitudinal multi-centric retrospective study and analysed the clinical and demographic characteristics of a cohort of 63 Slovak NMOSD patients. RESULTS: Eighty-six percent of patients were women, and ninety-four patients were Caucasian. The median age at diagnosis was 37 years. The most frequent initial manifestations were optic neuritis (47.6% of patients) and transverse myelitis (39.7% of patients). The median EDSS score deteriorated from the initial 3.0 to 4.0 at the last follow-up. Sixty-eight percent of patients were AQP4-IgG positive; 10% of patients were MOG-IgG positive; 27% of patients had no NMOSD-specific antibodies detected. There was a higher prevalence of autoimmune thyroiditis among AQP4-IgG-positive patients (25.6%) compared to AQP4-IgG-negative patients (0%) (p = 0.01). CONCLUSION: This study provides a detailed overview of the clinical and demographic characteristics of NMOSD based on a retrospective analysis of a Slovak cohort of 63 NMOSD patients and extends information provided by similar recently published studies. The most important finding is that there is a high prevalence of autoimmune thyroiditis among AQP4-IgG-negative patients (25%).


Asunto(s)
Enfermedad de Hashimoto , Neuromielitis Óptica , Humanos , Femenino , Adulto , Masculino , Estudios Retrospectivos , Eslovaquia/epidemiología , Glicoproteína Mielina-Oligodendrócito , Acuaporina 4 , Autoanticuerpos , Inmunoglobulina G , Demografía
2.
Neurol Res ; 44(1): 38-46, 2022 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-34261427

RESUMEN

OBJECTIVE: : Neuromyelitis optica spectrum disorders (NMOSDs) are a group of rare, inflammatory, demyelinating diseases that affect the central nervous system. Neither the incidence nor the prevalence of NMOSD has been determined in Slovakia thus far. The aim of this study was to determine both the incidence and the prevalence of NMOSD in Slovakia using the 2015 International Panel of NMOSD diagnosis (IPND) criteria. METHODS: : We performed a population-based study in Slovakia to estimate both the incidence and the prevalence of NMOSD during the period from 1 January 2006 through 31 December 2019. NMOSD cases were reported from multiple sources and the diagnosis was subsequently verified using the IPND criteria by a joint commitee of three neurologists. The prevalence is reported as number of cases per 100,000 inhabitans and the incidence as number of new cases per 1,000,000 person-years. Age-adjusted rates to the WHO standard population 2005-2025 were also calculated. RESULTS: : We identified 63 NMOSD cases. The crude point-prevalence rate was 1.37 (95% CI 1.03-1.71) per 100,000 inhabitants. The crude indidence rate was 0.88 (95% CI 0.65-1.12) per 1,000,000 person-years. The age-adjusted point-prevalence rate was 1.42 (95% CI 1.07-1.84) per 100,000 persons and the age-adjusted incidence rate was 0.96 (95% CI 0.72-1.25) per 1,000,000 person-years. CONCLUSION: : The NMOSD epidemiological situation in Slovakia is comparable to those reported from other Caucasian populations.


Asunto(s)
Neuromielitis Óptica , Acuaporina 4 , Autoanticuerpos , Humanos , Incidencia , Neuromielitis Óptica/diagnóstico , Neuromielitis Óptica/epidemiología , Prevalencia , Eslovaquia/epidemiología , Población Blanca
4.
Clin Biochem ; 48(1-2): 24-8, 2015 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-25304914

RESUMEN

BACKROUND: Oxidative stress plays a role in multiple sclerosis. Saliva can be potentially used to study the disease progression or treatment, because of its non-invasiveness and easy collection. But studies on saliva and multiple sclerosis are missing. The aim of this study was to compare the concentrations of salivary oxidative stress markers in patients and healthy controls. OBJECTIVE: Whole saliva and blood samples were collected from 29 patients and 29 healthy controls. Samples were collected during relapse, after corticosteroid therapy, and after three months. Markers of oxidative, carbonyl stress and antioxidant status were measured. RESULTS: In plasma, thiobarbituric acid reacting substances, advanced oxidation protein products and fructosamine were significantly higher in patients compared to controls (by 271%, 46% and 24%, respectively; p<0.01). Total antioxidant capacity in plasma was lower by 20% (p<0.01) in patients versus controls. In saliva, higher levels of thiobarbituric acid reacting substances and advanced glycation end-products were observed in patients when compared to controls (by 51% and 49% respectively; p<0.01). Ferric reducing ability was reduced by 38% (p<0.05) in patients with multiple sclerosis. CONCLUSION: According to our knowledge, this is the first report showing higher markers of oxidative stress and lower antioxidant status in patients with multiple sclerosis in saliva.


Asunto(s)
Biomarcadores/análisis , Esclerosis Múltiple/sangre , Estrés Oxidativo , Saliva/metabolismo , Adulto , Anciano , Antioxidantes/metabolismo , Biomarcadores/sangre , Estudios de Casos y Controles , Femenino , Humanos , Masculino , Persona de Mediana Edad , Carbonilación Proteica , Adulto Joven
5.
Acta Neurochir (Wien) ; 154(7): 1255-62, 2012 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-22555551

RESUMEN

We report a case of awake resection of temporal low-grade glioma infiltrating the optic radiation (OR). The OR was localized by direct electrical stimulation (DES) and the tumor was delineated by navigated intraoperative 3D ultrasound. Ultrasound artifacts were eliminated by 3D-ultrasound data acquisition with a miniature probe inserted into the resection cavity. A total of 97 % resection was achieved, and small tumor portion involving OR was intentionally left in place. Functional result was partial quadrantanopia instead of more profound visual deficit, which would follow gross-total resection. To our knowledge, DES of OR was reported once; the aforementioned method of ultrasound artifact elimination has not been reported before.


Asunto(s)
Neoplasias Encefálicas/cirugía , Imagen de Difusión Tensora/métodos , Interpretación de Imagen Asistida por Computador/métodos , Imagenología Tridimensional/métodos , Microcirugia/métodos , Monitoreo Intraoperatorio/métodos , Neuronavegación/métodos , Oligodendroglioma/patología , Oligodendroglioma/cirugía , Nervio Óptico/patología , Nervio Óptico/cirugía , Reconocimiento Visual de Modelos/fisiología , Lóbulo Temporal/cirugía , Ultrasonografía Intervencional/métodos , Campos Visuales/fisiología , Adulto , Neoplasias Encefálicas/diagnóstico , Neoplasias Encefálicas/patología , Craneotomía/métodos , Imagen de Difusión por Resonancia Magnética , Estimulación Eléctrica , Humanos , Aumento de la Imagen , Masculino , Clasificación del Tumor , Invasividad Neoplásica/patología , Neoplasia Residual/diagnóstico , Oligodendroglioma/diagnóstico , Complicaciones Posoperatorias/diagnóstico , Lóbulo Temporal/patología
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