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APOE: a potential marker of disease progression in ALS.
Lacomblez, L; Doppler, V; Beucler, I; Costes, G; Salachas, F; Raisonnier, A; Le Forestier, N; Pradat, P-F; Bruckert, E; Meininger, V.
Afiliação
  • Lacomblez L; Fédération de Neurologie Mazarin, Service de Pharmacologie, AP-HP, Hôpital de la Salpêtrière, Paris, France.
Neurology ; 58(7): 1112-4, 2002 Apr 09.
Article em En | MEDLINE | ID: mdl-11940705
ABSTRACT
Although documented in AD, the role of APOE remains unclear in ALS. APOE phenotype and plasma levels were measured in 403 patients with ALS and were correlated with clinical parameters and survival time. No correlations were observed between the APOE phenotype and these variables. In contrast, APOE plasma levels were correlated with both rate of deterioration and survival time and appeared to be an important risk factor for decreased survival time with a relative risk of 0.647 (95% CI 0.465 to 0.901; p = 0.01).
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Apolipoproteínas E / Esclerose Lateral Amiotrófica Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Neurology Ano de publicação: 2002 Tipo de documento: Article País de afiliação: França
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Apolipoproteínas E / Esclerose Lateral Amiotrófica Tipo de estudo: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Neurology Ano de publicação: 2002 Tipo de documento: Article País de afiliação: França