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1.
Acta Neurol Belg ; 112(3): 249-54, 2012 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-22527789

RESUMO

Although the disclosure of the diagnosis of Alzheimer's disease (AD) is recommended by several guidelines, many clinicians do not announce the diagnosis to their patient. One of the main arguments against disclosure is the fear of a depressive reaction. Our aim was to report the experience and agreement of patients and their caregivers regarding the disclosure of the diagnosis of AD. All the patients with a diagnosis of AD attending our memory clinic were screened during 1 year. The patients and their caregivers were interviewed with a structured questionnaire. We included 108 patients (mean age = 77; Mini-Mental State Examination = 21) and matched caregivers (mean age 65). Twenty-nine percent of patients said they had suffered when the diagnosis was disclosed and 5% wished they had not been informed. Four percent felt more sad or depressed and 14% more anxious since the disclosure. The caregivers reported that 32% of patients had suffered from the disclosure, but only 15% were still suffering. In 85% of cases, the caregivers thought that the disclosure was useful. If they could go back in time and decide whether to disclose or not the diagnosis, only 4% of caregivers would retrospectively disagree to disclose the diagnosis to the patient. The disclosure of AD can induce anxiety and sadness. However, these negative feelings seem to persist only in a minority of patients. The vast majority of patients and caregivers agrees with the disclosure.


Assuntos
Doença de Alzheimer/diagnóstico , Doença de Alzheimer/psicologia , Cuidadores/psicologia , Revelação , Idoso , Idoso de 80 Anos ou mais , Doença de Alzheimer/enfermagem , Bélgica , Estudos de Casos e Controles , Feminino , Humanos , Masculino , Entrevista Psiquiátrica Padronizada , Pessoa de Meia-Idade , Estudos Retrospectivos , Inquéritos e Questionários
2.
Insect Mol Biol ; 16(2): 155-66, 2007 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-17298559

RESUMO

The alternative pathway of complement is an important innate defence against pathogens including ticks. This component of the immune system has selected for pathogens that have evolved countermeasures. Recently, a salivary protein able to inhibit the alternative pathway was cloned from the American tick Ixodes scapularis (Valenzuela et al., 2000; J. Biol. Chem. 275, 18717-18723). Here, we isolated two different sequences, similar to Isac, from the transcriptome of I. ricinus salivary glands. Expression of these sequences revealed that they both encode secreted proteins able to inhibit the complement alternative pathway. These proteins, called I. ricinus anticomplement (IRAC) protein I and II, are coexpressed constitutively in I. ricinus salivary glands and are upregulated during blood feeding. Also, we demonstrated that they are the products of different genes and not of alleles of the same locus. Finally, phylogenetic analyses demonstrate that ticks belonging to the Ixodes ricinus complex encode a family of relatively small anticomplement molecules undergoing diversification by positive Darwinian selection.


Assuntos
Proteínas Inativadoras do Complemento/química , Ixodes/química , Proteínas e Peptídeos Salivares/química , Sequência de Aminoácidos , Animais , Evolução Biológica , Proteínas Inativadoras do Complemento/genética , Proteínas Inativadoras do Complemento/metabolismo , Feminino , Imuno-Histoquímica , Ixodes/genética , Ixodes/metabolismo , Dados de Sequência Molecular , Família Multigênica , Glândulas Salivares/metabolismo , Homologia de Sequência de Aminoácidos
3.
Protein Eng ; 12(3): 217-23, 1999 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-10235622

RESUMO

A methodology is proposed to solve a difficult modeling problem related to the recently sequenced P39 protein. This sequence shares no similarity with any known 3D structure, but a fold is proposed by several threading tools. The difficulty in aligning the target sequence on one of the proposed template structures is overcome by combining the results of several available prediction methods and by refining a rational consensus between them. In silico validation of the obtained model and a preliminary cross-check with experimental features allow us to state that this borderline prediction is at least reasonable. This model raises relevant hypotheses on the main structural features of the protein and allows the design of site-directed mutations. Knowing the genetic context of the P39 reading frame, we are now able to suggest a function for the P39 protein: it would act as a periplasmic substrate-binding protein.


Assuntos
Proteínas de Bactérias , Brucella abortus/metabolismo , Proteínas de Transporte/metabolismo , Proteínas de Membrana/metabolismo , Proteínas Periplásmicas de Ligação , Sequência de Aminoácidos , Proteínas de Transporte/química , Proteínas de Membrana/química , Modelos Moleculares , Dados de Sequência Molecular , Fases de Leitura Aberta , Estrutura Secundária de Proteína , Homologia de Sequência de Aminoácidos , Relação Estrutura-Atividade
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