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Article type: Research Article
Authors: Kim, Hyeong Juna; 1 | Park, Kyung Wonb; 1 | Kim, Tae Euna | Im, Ji Younga | Shin, Ho Sika | Kim, Saeromia | Lee, Dong Hyuna | Ye, Byoung Seokc | Kim, Jong Hund | Kim, Eun-Jooe | Park, Kee Hyungf | Han, Hyun Jeongg | Jeong, Jee Hyangh | Choi, Seong Hyei | Park, Sun Aha; *
Affiliations: [a] Department of Neurology, Soonchunhyang University Bucheon Hospital, Bucheon, Korea | [b] Department of Neurology, Dong-A University College of Medicine, Dong-A University Hospital, Busan, Korea | [c] Department of Neurology, Yonsei University College of Medicine, Seoul, Korea | [d] Department of Neurology, Ilsan Hospital, National Health Insurance Corporation, Goyang, Korea | [e] Department of Neurology, Pusan National University Hospital, Busan, Korea | [f] Department of Neurology, Gachon University, College of Medicine, Incheon, Korea | [g] Department of Neurology, Myongii Hospital, Seonam University College of Medicine, Goyang, Korea | [h] Department of Neurology, Ewha Womans University Mokdong Hospital, Seoul, Korea | [i] Department of Neurology, Inha University School of Medicine, Incheon, Korea
Correspondence: [*] Correspondence to: Sun Ah Park, MD, PhD, Departments of Neurology, Soonchunhyang University Bucheon Hospital, 170 Jomaru-ro, Wonmi-gu, Bucheon, Republic of Korea, 420-767. Tel.: +82 32 621 5221; Fax: +82 32 621 5014; E-mail: sapark@schmc.ac.kr
Note: [] These two authors contributed equally to this work.
Abstract: Background: Although plasma amyloid-β (Aβ) levels have been evaluated as a possible diagnostic marker of Alzheimer’s disease (AD), the findings are inconsistent. Objective: The present study aimed to validate plasma levels of Aβ40, Aβ42, and the Aβ40/Aβ42 ratio as biomarkers of AD in subjects with early-onset AD (EOAD) without familial AD genetic mutations. Methods: Patients with sporadic EOAD (sEOAD) were prospectively recruited by nine neurology clinics. Plasma levels of Aβ40 and Aβ42 were measured using a sandwich enzyme-linked immunosorbent assay (ELISA) in 100 sEOAD (50–69 year-old) and 46 age-matched normal control subjects (50–72 year-old). Cerebrospinal fluid (CSF) was obtained from 32 sEOAD subjects and 25 controls. The integrity of the blood-brain barrier was assessed using the CSF/plasma albumin ratio. Results: The plasma levels of Aβ42 were significantly lower, while the Aβ40/Aβ42 ratio was significantly higher in sEOAD patients than in controls. The levels of Aβ40, Aβ42, and the Aβ40/Aβ42 ratio did not differ in relation to the APOE ɛ4 allele. The CSF/plasma albumin ratio was comparable between the two groups, and the plasma parameters of Aβ proteins were not significantly associated. A multivariate analysis revealed that an increased Aβ40/Aβ42 ratio is valuable for the discrimination of sEOAD from controls (β= 0.344, p = 0.000). The area under the ROC curve for the Aβ40/Aβ42 ratio was 0.76, and a cut-off ratio of 5.87 was suggested to have 70% sensitivity and 68% specificity. Conclusion: The plasma Aβ40/Aβ42 ratio had moderate validity for the discrimination of sEOAD patients from age-matched controls.
Keywords: Alzheimer’s disease, amyloid-β protein, biomarker, blood-brain barrier, plasma
DOI: 10.3233/JAD-143018
Journal: Journal of Alzheimer's Disease, vol. 48, no. 4, pp. 1043-1050, 2015
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