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1.
J Nerv Ment Dis ; 207(4): 232-238, 2019 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-30865075

RESUMEN

The aim of this study was to investigate the effectiveness of cognitive behavioral therapy (CBT) on improving the cognitive function in minor depression (MiD) and major depression (MaD). The study will constitute a placebo-controlled single-blind parallel-group randomized controlled trial. The selected participants will be randomly allocated into one of two parallel groups with a 1:1 ratio: the CBT-based group and the general health education group. CBT significantly alleviated depressive symptoms of MiD and MaD at 12 weeks (p < 0.001), and the treatment effect was maintained for at least 12 months (p < 0.001). Interestingly, CBT significantly promotes more cognitive function of MiD and partial cognitive function of MaD at 12 weeks in the intervention group than in the control group (p < 0.01). CBT can alleviate depressive symptoms of both minor and MaDs. The effectiveness of CBT is different on improving the cognitive function in MiD and MaD.


Asunto(s)
Terapia Cognitivo-Conductual , Disfunción Cognitiva/terapia , Depresión/terapia , Trastorno Depresivo Mayor/terapia , Adulto , Disfunción Cognitiva/etiología , Depresión/complicaciones , Trastorno Depresivo Mayor/complicaciones , Femenino , Estudios de Seguimiento , Humanos , Masculino , Método Simple Ciego , Adulto Joven
2.
Compr Psychiatry ; 68: 24-33, 2016 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-27234179

RESUMEN

BACKGROUND: Neurocognitive impairment is a contributor to major depressive disorder (MDD). However, MDD patients show great variability in the level and course of deficits. The present longitudinal study was to identify predictors of neurocognitive impairment in first-episode MDD patients. METHODS: Neurocognitive performance was analyzed in a cohort of 100 patients at 2years after a first-episode MDD. Subgroups, deficit type vs. non-deficit type, were compared on baseline clinical, neuropsychological, premorbid and sociodemographic characteristics. The analysis was performed using the multivariate logistic regression to obtain a model for neurocognitive impairment determination. The predicted probabilities of multivariate logistic regression were analyzed using receiver operating characteristic (ROC) curve. RESULTS: Fifty-two percent of MDD participants presented general neurocognitive impairment. The regression analyses demonstrated that clinical and sociodemographic characteristics were not predictive variables. A model composed of processing speed, executive function, and attention, dexterity correctly classified 85.8% of the MDD patients with deficit type. ROC curve indicated that the changes of these three cognitions could identify MDD with deficit type from MDD with non-deficit type. In addition, ROC curve also indicated that processing speed and executive function could identify MDD from CN subjects. Finally, processing speed performance was negatively correlated with Hamilton Depression Scale scores in both MDD with deficit and non-deficit type. CONCLUSION: The present study provides novel insights on frequency and neurocognitive profile of subtypes of patients showing impairment. Our results suggest that processing speed impairment is a trait dimension of the disorder related to specific cognitive dysfunctions and the severity of depression.


Asunto(s)
Trastornos del Conocimiento/etiología , Trastornos del Conocimiento/psicología , Trastorno Depresivo Mayor/complicaciones , Trastorno Depresivo Mayor/psicología , Adulto , Atención , Cognición , Función Ejecutiva , Femenino , Humanos , Modelos Logísticos , Estudios Longitudinales , Masculino , Persona de Mediana Edad , Pruebas Neuropsicológicas , Valor Predictivo de las Pruebas , Escalas de Valoración Psiquiátrica , Curva ROC , Análisis de Regresión , Factores Socioeconómicos
3.
Bioorg Med Chem Lett ; 21(20): 6203-5, 2011 Oct 15.
Artículo en Inglés | MEDLINE | ID: mdl-21889341

RESUMEN

A series of novel N-glycoside analogues with 4-azasteroid moiety bearing sugar-like D ring were conveniently synthesized by constructing the core dihydropyran ring embedded in 4-azasteroidal skeleton which was prepared from 4-aza-5α-androst-3,17-dione 1 in four steps. The structure of 6b were unambiguously proved by the appropriate X-ray structural analysis. Anticancer activity was found for all of the analogues with purinyl moiety against breast cancer (MCF-7), human neuroblastoma (SK-N-SH), cervical cancer cell (HeLa) and prostatic cancer (PC-3), while the analogue 7 containing 1,2,4-triazole heterocycle as the nucleobase was inactive against all of the tested cancer cell lines. The biology results showed the purinyl moiety attached to the pyran ring of 6a-d, substituent at 6'-position of purine base and introduction of a halogen atom at 2'-position of 6'-chloropurine had obviously effect on the evaluated anticancer activity.


Asunto(s)
Antineoplásicos/química , Antineoplásicos/farmacología , Azaesteroides/química , Azaesteroides/farmacología , Glicósidos/química , Glicósidos/farmacología , Antineoplásicos/síntesis química , Azaesteroides/síntesis química , Línea Celular Tumoral , Supervivencia Celular/efectos de los fármacos , Femenino , Glicósidos/síntesis química , Humanos , Masculino , Neoplasias/tratamiento farmacológico
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