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1.
Acta Psychiatr Scand ; 138(6): 581-590, 2018 12.
Artículo en Inglés | MEDLINE | ID: mdl-30264457

RESUMEN

OBJECTIVE: Metabolic syndrome (MS) is highly prevalent in schizophrenia and often a consequence of unhealthy behaviour. Reward-related brain areas might be associated with MS, since they play a major role in regulating health behaviour. This study examined the relationship between MS and brain volumes related to the reward system in schizophrenia. METHOD: We included patients with schizophrenia, with MS (MS+; n = 23), patients with schizophrenia, without MS (MS-; n = 48), and healthy controls (n = 54). Global brain volumes and volumes of (sub)cortical areas, part of the reward circuit, were compared between patients and controls. In case of a significant brain volume difference between patients and controls, the impact of MS in schizophrenia was examined. RESULTS: Patients had smaller total brain (TB; P = 0.001), GM (P = 0.010), larger ventricles (P = 0.026), and smaller reward circuit volume (P < 0.001) than controls. MS+ had smaller TB (P = 0.017), GM (P = 0.008), larger ventricles (P = 0.015), and smaller reward circuit volume (P = 0.002) than MS-. MS+ had smaller orbitofrontal cortex (OFC; P = 0.002) and insula volumes (P = 0.005) and smaller OFC (P = 0.008) and insula cortical surface area (P = 0.025) compared to MS-. CONCLUSION: In schizophrenia, structural brain volume reductions in areas of the reward circuitry appear to be related to comorbid MS.


Asunto(s)
Encéfalo/patología , Síndrome Metabólico/patología , Red Nerviosa/patología , Recompensa , Esquizofrenia/patología , Adulto , Encéfalo/diagnóstico por imagen , Ventrículos Cerebrales/diagnóstico por imagen , Ventrículos Cerebrales/patología , Comorbilidad , Femenino , Sustancia Gris/diagnóstico por imagen , Sustancia Gris/patología , Humanos , Imagen por Resonancia Magnética , Masculino , Síndrome Metabólico/diagnóstico por imagen , Síndrome Metabólico/epidemiología , Red Nerviosa/diagnóstico por imagen , Esquizofrenia/diagnóstico por imagen , Esquizofrenia/epidemiología , Adulto Joven
2.
Acta Psychiatr Scand ; 133(4): 289-97, 2016 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-26558719

RESUMEN

OBJECTIVE: More than 40% of patients with schizophrenia have an additional diagnosis of the metabolic syndrome (MS), possibly related to poor cognition. This study investigated premorbid and current cognitive functioning in schizophrenia and co-occurrence of MS. METHOD: A total of 104 participants with schizophrenia with MS and 142 without MS were included. Neuropsychological assessment was carried out using the Wechsler Adult Intelligence Scale-III, Word Learning Task, and Continuous Performance Test-HQ. Premorbid functioning was assessed retrospectively with the Premorbid Adjustment Scale. anovas were used to examine differences between participants with and without MS. RESULTS: Subjects with and without MS did not differ concerning current, lifetime and amount substance use, duration/severity of illness, parental socioeconomic status (SES), and type/amount of antipsychotic medication. We found that poor school performance between the ages 12 and 16 is associated with MS in schizophrenia. Educational level and current cognitive functioning in participants with MS deviate as compared to those without MS. CONCLUSION: Subjects with MS had impaired premorbid cognition in adolescence and lower educational achievement, irrespective of parental SES. This suggests poor premorbid cognitive functioning is a risk factor for metabolic complications later in life. Future studies are needed to examine whether cognitive interventions have beneficial effects on general health in schizophrenia.


Asunto(s)
Trastornos del Conocimiento/diagnóstico , Síndrome Metabólico/psicología , Esquizofrenia/metabolismo , Adolescente , Adulto , Factores de Edad , Trastornos del Conocimiento/metabolismo , Trastornos del Conocimiento/psicología , Estudios Transversales , Humanos , Estudios Longitudinales , Persona de Mediana Edad , Pruebas Neuropsicológicas , Estudios Retrospectivos , Ajuste Social , Adulto Joven
3.
Schizophr Res ; 173(3): 166-173, 2016 06.
Artículo en Inglés | MEDLINE | ID: mdl-25843919

RESUMEN

Emerging evidence suggests schizophrenia to involve widespread alterations in the macroscale wiring architecture of the human connectome. Recent findings of attenuated connectome alterations in unaffected siblings of schizophrenia patients suggest that altered connectome organization may relate to the vulnerability to develop the disorder, but whether it relates to progression of illness after disease onset is currently unknown. Here, we examined the interaction between connectome structure and longitudinal changes in general functioning, clinical symptoms and IQ in the 3years following MRI assessment in a group of chronically ill schizophrenia patients. Effects in patients were compared to associations between connectome organization and changes in subclinical symptoms and IQ in healthy controls and unaffected siblings of schizophrenia patients. Analyzing the patient sample revealed a relationship between structural connectivity-particularly among central 'brain hubs'-and progressive changes in general functioning (p=0.007), suggesting that more prominent impairments of hub connectivity may herald future functional decline. Our findings further indicate that affected local connectome organization relates to longitudinal increases in overall PANSS symptoms (p=0.013) and decreases in total IQ (p=0.003), independent of baseline symptoms and IQ. No significant associations were observed in controls and siblings, suggesting that the findings in patients represent effects of ongoing illness, as opposed to normal time-related changes. In all, our findings suggest connectome structure to have predictive value for the course of illness in schizophrenia.


Asunto(s)
Encéfalo/diagnóstico por imagen , Encéfalo/fisiopatología , Conectoma , Esquizofrenia/diagnóstico por imagen , Esquizofrenia/fisiopatología , Psicología del Esquizofrénico , Adulto , Trastorno Bipolar/diagnóstico por imagen , Trastorno Bipolar/tratamiento farmacológico , Trastorno Bipolar/fisiopatología , Trastorno Bipolar/psicología , Enfermedad Crónica , Femenino , Estudios de Seguimiento , Humanos , Inteligencia , Pruebas de Inteligencia , Estudios Longitudinales , Imagen por Resonancia Magnética , Masculino , Persona de Mediana Edad , Vías Nerviosas/diagnóstico por imagen , Vías Nerviosas/fisiopatología , Escalas de Valoración Psiquiátrica , Trastornos Psicóticos/diagnóstico por imagen , Trastornos Psicóticos/tratamiento farmacológico , Trastornos Psicóticos/fisiopatología , Trastornos Psicóticos/psicología , Esquizofrenia/tratamiento farmacológico , Hermanos , Adulto Joven
4.
Acta Derm Venereol ; 63(6): 476-82, 1983.
Artículo en Inglés | MEDLINE | ID: mdl-6198835

RESUMEN

We report a patient who developed a vesiculobullous eruption which clinically and histologically showed features of pemphigoid and dermatitis herpetiformis, responded to prednisone but doubtfully to dapsone, and demonstrated 'classical' immunopathologic characteristics of phemphigoid and dermatitis herpetiformis. Peribullous and unaffected skin featured deposition of IgG and C3c in a homogeneous-linear pattern at the epidermal basement membrane, while the unaffected skin demonstrated concomitantly granular IgA deposits in the dermal papillae. Circulating IgG class anti-basement membrane antibody was found in a titre of 1:80 when using guinea-pig oesophagus, and of 1:320 when using human oral mucosa as antigenic substrate. Our findings add another piece to the puzzle that continues to stimulate discussion among dermatologists as how to classify patients with overlapping features of pemphigoid and dermatitis herpetiformis. (Received February 18, 1983.)


Asunto(s)
Dermatitis Herpetiforme/inmunología , Penfigoide Ampolloso/inmunología , Enfermedades Cutáneas Vesiculoampollosas/inmunología , Anciano , Autoanticuerpos/análisis , Biopsia , Dermatitis Herpetiforme/patología , Antígenos HLA/análisis , Histocitoquímica , Humanos , Inmunoquímica , Inmunoglobulinas/análisis , Yeyuno/patología , Masculino , Penfigoide Ampolloso/patología , Piel/patología
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