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J Am Heart Assoc ; 5(2)2016 Feb 12.
Artigo em Inglês | MEDLINE | ID: mdl-26873692

RESUMO

BACKGROUND: Animal and human studies indicate that ABCA1-mediated cholesterol transport is important in Alzheimer's disease (AD). We hypothesized that the efficiency of cerebrospinal fluid (CSF) to facilitate ABCA1-mediated cholesterol efflux would be reduced in participants with mild cognitive impairment (MCI) or AD compared with cognitively healthy participants. METHODS AND RESULTS: CSF was collected from a cross-sectional study of cognitively healthy participants (n=47) and participants with MCI (n=35) or probable AD (n=26).The capacity of CSF to mediate cholesterol transport was assessed using a BHK cell line that can be induced to express the ABCA1 transporter. ABCA1-mediated cholesterol efflux capacity was 30% less in participants with MCI or AD compared with cognitively healthy participants (P<0.001 for both). Cholesterol efflux capacity correlated with CSF cholesterol content (r=0.37, P<0.001). CSF phosphatidylcholine decreased in participants with MCI and AD compared with cognitively healthy participants (9% less in MCI and 27% less in AD compared with cognitively healthy participants, P=0.01) and correlated with CSF efflux capacity (r=0.3, P=0.001). CSF sphingomyelin also correlated with the efflux capacity (r=0.24, P=0.02). Concentrations of CSF apoA-I and apoE did not significantly correlate with measures of efflux capacity. CONCLUSIONS: In people with MCI and AD, the capacity of CSF to facilitate ABCA1-mediated cholesterol efflux is impaired. This lesser cholesterol efflux in MCI supports a pathophysiological role for ABCA1-mediated cholesterol transport in early neurodegeneration.


Assuntos
Transportador 1 de Cassete de Ligação de ATP/líquido cefalorraquidiano , Doença de Alzheimer/líquido cefalorraquidiano , Colesterol/líquido cefalorraquidiano , Disfunção Cognitiva/líquido cefalorraquidiano , Transportador 1 de Cassete de Ligação de ATP/genética , Idoso , Idoso de 80 Anos ou mais , Doença de Alzheimer/diagnóstico , Animais , Transporte Biológico , Biomarcadores/líquido cefalorraquidiano , Estudos de Casos e Controles , Linhagem Celular , Disfunção Cognitiva/diagnóstico , Cricetinae , Estudos Transversais , Regulação para Baixo , Feminino , Humanos , Masculino , Fosfatidilcolinas/líquido cefalorraquidiano , Transfecção
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