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1.
Am J Alzheimers Dis Other Demen ; 28(8): 769-75, 2013 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-24085246

RESUMO

In view of the paucity of data on cerebrospinal fluid (CSF) biomarkers in Chinese patients, we evaluated the validity of tau, phosphorylated tau 181 (p-tau-181), amyloid ß 42 (Aß42), and Aß40 proteins in Chinese patients with Alzheimer's disease (AD). We recruited 24 patients with AD, 12 nondemented controls, and 12 patients with non-AD dementia. We found the CSF levels of Aß42, tau, p-tau, Aß42-tau, and Aß42-p-tau ratios, except the Aß40 protein level, were significantly different among the 3 groups of patients. Patients with AD had higher levels of CSF tau and p-tau but lower levels of Aß42 proteins, Aß42-tau, and Aß42-p-tau ratios than the nondemented controls. In the diagnosis of AD versus nondementia, the sensitivity and specificity of the ratios of Aß42-tau and Aß42-p-tau were 96% and 83% versus 92% and 83%, respectively. Only the Aß42-p-tau ratio showed satisfactory sensitivity and specificity in the diagnosis of AD versus other dementia.


Assuntos
Doença de Alzheimer/líquido cefalorraquidiano , Peptídeos beta-Amiloides/líquido cefalorraquidiano , Fragmentos de Peptídeos/líquido cefalorraquidiano , Proteínas tau/líquido cefalorraquidiano , Idoso , Idoso de 80 Anos ou mais , Doença de Alzheimer/diagnóstico , Povo Asiático , Biomarcadores/líquido cefalorraquidiano , Estudos de Casos e Controles , Estudos Transversais , Demência/líquido cefalorraquidiano , Demência/diagnóstico , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Fosforilação , Projetos Piloto , Sensibilidade e Especificidade , Proteínas tau/metabolismo
2.
Geriatr Gerontol Int ; 12(4): 714-21, 2012 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-22469232

RESUMO

AIM: Rehabilitation using interactive virtual reality Wii (Wii-IVR) was shown to be feasible in patients with different medical problems, but there was no study examining its use in a geriatric day hospital (GDH). The aim of the present study was to test the feasibility, acceptability and efficacy of Wii-IVR in GDH. METHODS: It was a clinical trial with matched historic controls. Patients of a GDH were recruited to participate in Wii-IVR by playing "Wii Fit". Participants used a Wii controller to carry out movements involved in an arm ergometer. Each participant received eight sessions of Wii-IVR in addition to conventional GDH rehabilitation. Feasibility was assessed by the total time receiving Wii-IVR, the percentage of maximal heart rate reserve (%MHR) and Borg perceived exertion scale (BS) after participating in Wii-IVR. %MHR and BS were compared with those after carrying out an arm ergometer for the same duration. Acceptability was assessed by an interviewer-administered questionnaire. Efficacy was assessed by comparing improvements in Functional Independence Measure (FIM) between participants and matched historic controls, who received conventional GDH rehabilitations only. RESULTS: A total of 30 patients completed the study. Participants completed a total of 1941 min of event-free Wii-IVR. The mean %MHR was 15.9% ± 9.9% and the mean BS was 7.9 ± 2.3. There was no significant difference in %MHR and BS between participating in Wii-IVR and arm ergometer. Most participants found Wii-IVR similar to the arm ergometer, and would like to continue Wii-IVR if they had Wii at home. Improvements in FIM of participants were significantly more than that of historic controls. CONCLUSIONS: Wii-IVR in GDH was feasible and most participants accepted it. Participants had more improvements in FIM.


Assuntos
Modalidades de Fisioterapia , Extremidade Superior/fisiologia , Jogos de Vídeo , Atividades Cotidianas , Idoso , Idoso de 80 Anos ou mais , Assistência Ambulatorial , Estudos de Casos e Controles , Comorbidade , Estudos de Viabilidade , Feminino , Humanos , Masculino , Inquéritos e Questionários
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