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The QPLEX™ Plus Assay Kit for the Early Clinical Diagnosis of Alzheimer's Disease.
Na, Hunjong; Shin, Ki Young; Lee, Dokyung; Yoon, Changsik; Han, Sun-Ho; Park, Jong-Chan; Mook-Jung, Inhee; Jang, Jisung; Kwon, Sunghoon.
Afiliação
  • Na H; Department of Electrical and Computer Engineering, Seoul National University, Seoul 08826, Republic of Korea.
  • Shin KY; QuantaMatrix Inc., Seoul 08506, Republic of Korea.
  • Lee D; Bio-MAX Institute, Seoul National University, Seoul 08826, Republic of Korea.
  • Yoon C; QuantaMatrix Inc., Seoul 08506, Republic of Korea.
  • Han SH; QuantaMatrix Inc., Seoul 08506, Republic of Korea.
  • Park JC; Department of Biochemistry and Biomedical Sciences, College of Medicine, Seoul National University, Seoul 03080, Republic of Korea.
  • Mook-Jung I; Neuroscience Research Institute, Medical Research Center, College of Medicine, Seoul National University, Seoul 03080, Republic of Korea.
  • Jang J; SNU Dementia Research Center, College of Medicine, Seoul National University, Seoul 03080, Republic of Korea.
  • Kwon S; Department of Biochemistry and Biomedical Sciences, College of Medicine, Seoul National University, Seoul 03080, Republic of Korea.
Int J Mol Sci ; 24(13)2023 Jul 05.
Article em En | MEDLINE | ID: mdl-37446296
ABSTRACT
We recently developed a multiplex diagnostic kit, QPLEX™ Alz plus assay kit, which captures amyloid-ß1-40, galectin-3 binding protein, angiotensin-converting enzyme, and periostin simultaneously using microliters of peripheral blood and utilizes an optimized algorithm for screening Alzheimer's disease (AD) by correlating with cerebral amyloid deposition. Owing to the demand for early AD detection, we investigate the potential of our kit for the early clinical diagnosis of AD. A total of 1395 participants were recruited, and their blood samples were analyzed with the QPLEX™ kit. The average of QPLEX™ algorithm values in each group increased gradually in the order of the clinical progression continuum of AD cognitively normal (0.382 ± 0.150), subjective cognitive decline (0.452 ± 0.130), mild cognitive impairment (0.484 ± 0.129), and AD (0.513 ± 0.136). The algorithm values between each group showed statistically significant differences among groups divided by Mini-Mental State Examination and Clinical Dementia Rating. The QPLEX™ algorithm values could be used to distinguish the clinical continuum of AD or cognitive function. Because blood-based diagnosis is more accessible, convenient, and cost- and time-effective than cerebral spinal fluid or positron emission tomography imaging-based diagnosis, the QPLEX™ kit can potentially be used for health checkups and the early clinical diagnosis of AD.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos Cognitivos / Doença de Alzheimer / Disfunção Cognitiva Tipo de estudo: Diagnostic_studies / Etiology_studies / Screening_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transtornos Cognitivos / Doença de Alzheimer / Disfunção Cognitiva Tipo de estudo: Diagnostic_studies / Etiology_studies / Screening_studies Limite: Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article