- Author:
Sun Ah PARK
1
;
Jung Hun KIM
;
Hyeong Jun KIM
;
Tae Eun KIM
;
Yoon Jeong KIM
;
Dong Hyun LEE
;
Jeong Ho PARK
;
Won Seok CHAE
;
Soo Jae YIM
;
Sang Won SEO
;
Duk L NA
;
Seong Hye CHOI
Author Information
- Publication Type:Multicenter Study ; Original Article
- Keywords: Alzheimer's disease; Amyloid beta protein; Biomarker; Enzyme-linked immunosorbent assay; Cerebrospinal fluid; Tau
- MeSH: Academies and Institutes; Adoption; Alzheimer Disease; Amyloid beta-Peptides; Biomarkers; Dementia; Enzyme-Linked Immunosorbent Assay; Logistic Models; Pyridines; ROC Curve; Sensitivity and Specificity; Thiazoles
- From:Dementia and Neurocognitive Disorders 2013;12(1):1-8
- CountryRepublic of Korea
- Language:Korean
- Abstract: BACKGROUND: The usefulness of cerebrospinal fluid (CSF) concentrations of amyloid beta protein 1-42 (Abeta42), phosphorylated tau (pTau) and total tau (tTau) have been increasing in Alzheimer's disease (AD). However, the direct adoption of previously reported standard values is not appropriate due to interlaboratory variability. We started this study to set up an accessible system to measure CSF biomarkers in our country with high reproducibility and validity. METHODS: Including CSFs from four different institutes the levels of Abeta42, pTau181 and tTau were measured in one lab. The intertest variability and difference in the levels of biomarkers depending on diseases were assessed. Through analysis of receiver operating characteristic cut points and binary logistic regression the cut-off values of Abeta42, pTau and tTau level were obtained, and their validity was evaluated. RESULTS: The intertest consistency was high in measuring CSF biomarkers. The value of Abeta42 was markedly decreased in AD (n= 17) and other dementia (n= 9) compared to normal control (n= 12). The levels of pTau181 and tTau were high in AD, but not in other dementia and normal control. The threshold values of Abeta42, pTau181 and tTau were 290.3 pg/mL, 54.3 pg/mL, and 320.7 pg/mL in differentiating AD from normal control showing high sensitivity and specificity. Especially, the ratios of pTau181/Abeta42 (> 0.16) and tTau/Abeta42 (> 0.76) showed the prime validity. CONCLUSIONS: Our data of CSF Abeta42, pTau181, and tTau levels were highly reproducible. PTau181/Abeta42 and tTau/Abeta42 ratios were the greatly helpful in differentiating AD from normal control.