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Plasma Aß42/Aß40 and p-tau181 Predict Long-Term Clinical Progression in a Cohort with Amnestic Mild Cognitive Impairment.
Xiao, Zhenxu; Wu, Wanqing; Ma, Xiaoxi; Liang, Xiaoniu; Lu, Jiaying; Zheng, Li; Ding, Saineng; Lei, Qiqi; Luo, Jianfeng; Chen, Keliang; Ding, Ding; Zhao, Qianhua.
Afiliação
  • Xiao Z; Institute of Neurology, Huashan Hospital, Fudan University, Shanghai, China.
  • Wu W; National Clinical Research Center for Aging and Medicine, Huashan Hospital, Fudan University, Shanghai, China.
  • Ma X; National Center for Neurological Disorders, Huashan Hospital, Fudan University, Shanghai, China.
  • Liang X; Institute of Neurology, Huashan Hospital, Fudan University, Shanghai, China.
  • Lu J; National Clinical Research Center for Aging and Medicine, Huashan Hospital, Fudan University, Shanghai, China.
  • Zheng L; National Center for Neurological Disorders, Huashan Hospital, Fudan University, Shanghai, China.
  • Ding S; Institute of Neurology, Huashan Hospital, Fudan University, Shanghai, China.
  • Lei Q; National Clinical Research Center for Aging and Medicine, Huashan Hospital, Fudan University, Shanghai, China.
  • Luo J; National Center for Neurological Disorders, Huashan Hospital, Fudan University, Shanghai, China.
  • Chen K; Institute of Neurology, Huashan Hospital, Fudan University, Shanghai, China.
  • Ding D; National Clinical Research Center for Aging and Medicine, Huashan Hospital, Fudan University, Shanghai, China.
  • Zhao Q; National Center for Neurological Disorders, Huashan Hospital, Fudan University, Shanghai, China.
Clin Chem ; 68(12): 1552-1563, 2022 12 06.
Article em En | MEDLINE | ID: mdl-36208187
ABSTRACT

BACKGROUND:

Previous studies reported the value of blood-based biomarkers in predicting Alzheimer disease (AD) progression among individuals with different disease stages. However, evidence regarding the value of these markers in those with amnestic mild cognitive impairment (aMCI) is insufficient.

METHODS:

A cohort with 251 aMCI individuals were followed for up to 8 years. Baseline blood biomarkers were measured on a single-molecule array platform. Multipoint clinical diagnosis and domain-specific cognitive functions were assessed to investigate the longitudinal relationship between blood biomarkers and clinical AD progression.

RESULTS:

Individuals with low Aß42/Aß40 and high p-tau181 at baseline demonstrated the highest AD risk (hazard ratio = 4.83, 95% CI 2.37-9.86), and the most dramatic decline across cognitive domains. Aß42/Aß40 and p-tau181, combined with basic characteristics performed the best in predicting AD conversion (AUC = 0.825, 95% CI 0.771-0.878).

CONCLUSIONS:

Combining Aß42/Aß40 and p-tau181 may be a feasible indicator for AD progression in clinical practice, and a potential composite marker in clinical trials.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Alzheimer / Disfunção Cognitiva Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Doença de Alzheimer / Disfunção Cognitiva Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article