Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 3 de 3
Filtrar
Más filtros











Base de datos
Intervalo de año de publicación
1.
Eur Arch Psychiatry Clin Neurosci ; 270(7): 911-919, 2020 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-31760473

RESUMEN

For patients with depression treated with electroconvulsive therapy (ECT), the novel seizure quality index (SQI) can predict the risk of non-response (and non-remission)-as early as after the second ECT session-based the extent of several ictal parameters of the seizure. We aim to test several CSF markers on their ability to predict the degree of seizure quality, measured by the SQI to identify possible factors, that could explain some variability of the seizure quality. Baseline CSF levels of metabolites from the kynurenine pathway, markers of neurodegeneration (tau proteins, ß-amyloids and neurogranin), elements of the innate immune system, endocannabinoids, sphingolipids, neurotrophic factors (VEGF) and Klotho were measured before ECT in patients with depression (n = 12) to identify possible correlations with the SQI by Pearson's partial correlation. Negative, linear relationships with the SQI for response were observed for CSF levels of T-tau (rpartial = - 0.69, p = 0.019), phosphatidylcholines (rpartial = - 0.52, p = 0.038) and IL-8 (rpartial = - 0.67, p = 0.047). Regarding the SQI for remission, a negative, linear relationship was noted with CSF levels of the endocannabinoid AEA (rpartial = - 0.70, p = 0.024) and CD163 (rpartial = - 0.68, p = 0.029). In sum, CSF Markers for the innate immune system, for neurodegeneration and from lipids were found to be associated with the SQI for response and remission after adjusting for age. Consistently, higher CSF levels of the markers were always associated with lower seizure quality. Based on these results, further research regarding the mechanism of seizure quality in ECT is suggested.


Asunto(s)
Trastorno Bipolar/líquido cefalorraquídeo , Trastorno Bipolar/terapia , Trastorno Depresivo Mayor/líquido cefalorraquídeo , Trastorno Depresivo Mayor/terapia , Trastorno Depresivo Resistente al Tratamiento/líquido cefalorraquídeo , Trastorno Depresivo Resistente al Tratamiento/terapia , Terapia Electroconvulsiva , Evaluación de Resultado en la Atención de Salud , Adulto , Anciano , Biomarcadores/líquido cefalorraquídeo , Electromiografía , Femenino , Humanos , Masculino , Persona de Mediana Edad , Inducción de Remisión
2.
J Affect Disord ; 253: 449-453, 2019 06 15.
Artículo en Inglés | MEDLINE | ID: mdl-31103810

RESUMEN

BACKGROUND: Several lines of evidence are pointing towards an involvement of the vascular endothelial growth factor (VEGF) in the pathophysiology of depression. There are studies analyzing blood levels of VEGF in patients with depression compared to controls, but a data on cerebrospinal fluid (CSF) levels of VEGF in patients with depression are lacking. METHOD: CSF VEGF levels were measured in patients (n = 12) with a severe, treatment-resistant depressive episode before and after the antidepressant treatment by a course of electroconvulsive therapy (ECT) and compared to age- and sex-matched controls (n = 20). RESULTS: The patients with depression showed lower mean VEGF levels in the CSF prior to ECT than the controls (p = 0.041). Regarding the patients, CSF VEGF concentration at baseline and after the complete ECT treatment did not differ from each other (p = 0.78). LIMITATIONS: Major limitations of this study are the small sample size and that data from corresponding serum levels cannot be provided. Another limitation is that the controls were not completely healthy, as they were recruited from a memory clinic with subjective complaints. The timing of the second sample might have been suboptimal, when taking into account that there might be an on-going phase of re-equilibrating after ECT. CONCLUSIONS: CSF VEGF concentrations were lower in a clinical sample of patients with treatment-resistant depression compared with matched controls. Additionally, no change in CSF VEGF levels during a course of ECT could be detected.


Asunto(s)
Trastorno Depresivo Mayor/líquido cefalorraquídeo , Trastorno Depresivo Mayor/terapia , Trastorno Depresivo Resistente al Tratamiento/líquido cefalorraquídeo , Trastorno Depresivo Resistente al Tratamiento/terapia , Terapia Electroconvulsiva , Factor A de Crecimiento Endotelial Vascular/líquido cefalorraquídeo , Adulto , Antidepresivos , Depresión , Femenino , Humanos , Masculino , Persona de Mediana Edad , Proyectos Piloto
3.
World J Biol Psychiatry ; 19(5): 379-389, 2018 08.
Artículo en Inglés | MEDLINE | ID: mdl-28714751

RESUMEN

OBJECTIVES: A bidirectional link between the antidepressant effects of electroconvulsive therapy (ECT) and the modulation of the immune system has been proposed. To elucidate the interplay between antidepressant treatment and macrophage/microglia activation in humans, we performed a study on the effects of the antidepressant treatment by ECT on markers of macrophage/microglia activation in patients with depression. METHODS: We measured six different markers (IL-6, neopterin, sCD14, sCD163 MIF and MCP1) of macrophage/microglia activation in the cerebrospinal fluid (CSF) and blood of 12 patients with a severe, treatment-resistant depressive episode before and after a course of ECT. RESULTS: Some markers in the CSF of remitters were reduced after the ECT course and differed from non-remitters, but no differences were found before and after ECT independently from the antidepressant efficacy. CSF baseline levels of some markers could predict the reduction of depressive psychopathology during ECT. Higher CSF levels indicating increased macrophage/microglia activation at baseline predicted a better treatment response to ECT. CONCLUSIONS: Although the sample size was small, our data suggest that macrophages/microglia are involved in the pathophysiology of major depression and that antidepressant efficacy by ECT might be partly explained by the modulation of the innate immune system within the brain.


Asunto(s)
Antígenos CD/líquido cefalorraquídeo , Antígenos de Diferenciación Mielomonocítica/líquido cefalorraquídeo , Quimiocina CCL2/líquido cefalorraquídeo , Trastorno Depresivo Mayor/terapia , Trastorno Depresivo Resistente al Tratamiento/terapia , Terapia Electroconvulsiva/métodos , Interleucina-6/líquido cefalorraquídeo , Receptores de Lipopolisacáridos/metabolismo , Macrófagos/inmunología , Microglía/inmunología , Neopterin/líquido cefalorraquídeo , Adulto , Anciano , Anciano de 80 o más Años , Antígenos CD/sangre , Antígenos de Diferenciación Mielomonocítica/sangre , Quimiocina CCL2/sangre , Trastorno Depresivo Mayor/líquido cefalorraquídeo , Trastorno Depresivo Mayor/inmunología , Trastorno Depresivo Resistente al Tratamiento/líquido cefalorraquídeo , Trastorno Depresivo Resistente al Tratamiento/inmunología , Femenino , Humanos , Inmunidad Innata/inmunología , Interleucina-6/sangre , Receptores de Lipopolisacáridos/sangre , Masculino , Persona de Mediana Edad , Neopterin/sangre , Evaluación de Resultado en la Atención de Salud , Receptores de Superficie Celular/sangre , Adulto Joven
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA