Cargando…

Multiplex Analysis of Cytokines in the Serum and Cerebrospinal Fluid of Patients With Alzheimer's Disease by Color-Coded Bead Technology

BACKGROUND AND PURPOSE: The availability and promise of effective treatments for neurodegenerative disorders are increasing the importance of early diagnosis. Having molecular and biochemical markers of Alzheimer's disease (AD) would complement clinical approaches, and further the goals of earl...

Descripción completa

Detalles Bibliográficos
Autores principales: Choi, Chulhee, Jeong, Jee-Hyang, Jang, Joong Sik, Choi, Kyungsun, Lee, Jungsul, Kwon, Jongbum, Choi, Kyoung-Gyu, Lee, Jong-Seo, Kang, Sang Won
Formato: Texto
Lenguaje:English
Publicado: Korean Neurological Association 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2686871/
https://www.ncbi.nlm.nih.gov/pubmed/19513308
http://dx.doi.org/10.3988/jcn.2008.4.2.84
_version_ 1782167485727899648
author Choi, Chulhee
Jeong, Jee-Hyang
Jang, Joong Sik
Choi, Kyungsun
Lee, Jungsul
Kwon, Jongbum
Choi, Kyoung-Gyu
Lee, Jong-Seo
Kang, Sang Won
author_facet Choi, Chulhee
Jeong, Jee-Hyang
Jang, Joong Sik
Choi, Kyungsun
Lee, Jungsul
Kwon, Jongbum
Choi, Kyoung-Gyu
Lee, Jong-Seo
Kang, Sang Won
author_sort Choi, Chulhee
collection PubMed
description BACKGROUND AND PURPOSE: The availability and promise of effective treatments for neurodegenerative disorders are increasing the importance of early diagnosis. Having molecular and biochemical markers of Alzheimer's disease (AD) would complement clinical approaches, and further the goals of early and accurate diagnosis. Combining multiple biomarkers in evaluations significantly increases the sensitivity and specificity of the biochemical tests. METHODS: In this study, we used color-coded bead-based Luminex technology to test the potential of using chemokines and cytokines as biochemical markers of AD. We measured the levels of 22 chemokines and cytokines in the serum and cerebrospinal fluid (CSF) of 32 de novo patients (13 controls, 11 AD, and 8 Parkinson's disease [PD]). RESULTS: MCP-1 was the only cytokine detectable in CSF, and its levels did not differ between control and disease groups. However, the serum concentration of eotaxin was significantly higher in AD patients than in the control group. CONCLUSIONS: The analysis of multiple inflammatory mediators revealed marginal differences in their CSF and serum concentrations for the differential diagnosis of AD and PD. These results provide evidence that immunological responses are not major contributors to the pathogenesis of AD and PD.
format Text
id pubmed-2686871
institution National Center for Biotechnology Information
language English
publishDate 2008
publisher Korean Neurological Association
record_format MEDLINE/PubMed
spelling pubmed-26868712009-06-09 Multiplex Analysis of Cytokines in the Serum and Cerebrospinal Fluid of Patients With Alzheimer's Disease by Color-Coded Bead Technology Choi, Chulhee Jeong, Jee-Hyang Jang, Joong Sik Choi, Kyungsun Lee, Jungsul Kwon, Jongbum Choi, Kyoung-Gyu Lee, Jong-Seo Kang, Sang Won J Clin Neurol Original Article BACKGROUND AND PURPOSE: The availability and promise of effective treatments for neurodegenerative disorders are increasing the importance of early diagnosis. Having molecular and biochemical markers of Alzheimer's disease (AD) would complement clinical approaches, and further the goals of early and accurate diagnosis. Combining multiple biomarkers in evaluations significantly increases the sensitivity and specificity of the biochemical tests. METHODS: In this study, we used color-coded bead-based Luminex technology to test the potential of using chemokines and cytokines as biochemical markers of AD. We measured the levels of 22 chemokines and cytokines in the serum and cerebrospinal fluid (CSF) of 32 de novo patients (13 controls, 11 AD, and 8 Parkinson's disease [PD]). RESULTS: MCP-1 was the only cytokine detectable in CSF, and its levels did not differ between control and disease groups. However, the serum concentration of eotaxin was significantly higher in AD patients than in the control group. CONCLUSIONS: The analysis of multiple inflammatory mediators revealed marginal differences in their CSF and serum concentrations for the differential diagnosis of AD and PD. These results provide evidence that immunological responses are not major contributors to the pathogenesis of AD and PD. Korean Neurological Association 2008-06 2008-06-20 /pmc/articles/PMC2686871/ /pubmed/19513308 http://dx.doi.org/10.3988/jcn.2008.4.2.84 Text en Copyright © 2008 Korean Neurological Association
spellingShingle Original Article
Choi, Chulhee
Jeong, Jee-Hyang
Jang, Joong Sik
Choi, Kyungsun
Lee, Jungsul
Kwon, Jongbum
Choi, Kyoung-Gyu
Lee, Jong-Seo
Kang, Sang Won
Multiplex Analysis of Cytokines in the Serum and Cerebrospinal Fluid of Patients With Alzheimer's Disease by Color-Coded Bead Technology
title Multiplex Analysis of Cytokines in the Serum and Cerebrospinal Fluid of Patients With Alzheimer's Disease by Color-Coded Bead Technology
title_full Multiplex Analysis of Cytokines in the Serum and Cerebrospinal Fluid of Patients With Alzheimer's Disease by Color-Coded Bead Technology
title_fullStr Multiplex Analysis of Cytokines in the Serum and Cerebrospinal Fluid of Patients With Alzheimer's Disease by Color-Coded Bead Technology
title_full_unstemmed Multiplex Analysis of Cytokines in the Serum and Cerebrospinal Fluid of Patients With Alzheimer's Disease by Color-Coded Bead Technology
title_short Multiplex Analysis of Cytokines in the Serum and Cerebrospinal Fluid of Patients With Alzheimer's Disease by Color-Coded Bead Technology
title_sort multiplex analysis of cytokines in the serum and cerebrospinal fluid of patients with alzheimer's disease by color-coded bead technology
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2686871/
https://www.ncbi.nlm.nih.gov/pubmed/19513308
http://dx.doi.org/10.3988/jcn.2008.4.2.84
work_keys_str_mv AT choichulhee multiplexanalysisofcytokinesintheserumandcerebrospinalfluidofpatientswithalzheimersdiseasebycolorcodedbeadtechnology
AT jeongjeehyang multiplexanalysisofcytokinesintheserumandcerebrospinalfluidofpatientswithalzheimersdiseasebycolorcodedbeadtechnology
AT jangjoongsik multiplexanalysisofcytokinesintheserumandcerebrospinalfluidofpatientswithalzheimersdiseasebycolorcodedbeadtechnology
AT choikyungsun multiplexanalysisofcytokinesintheserumandcerebrospinalfluidofpatientswithalzheimersdiseasebycolorcodedbeadtechnology
AT leejungsul multiplexanalysisofcytokinesintheserumandcerebrospinalfluidofpatientswithalzheimersdiseasebycolorcodedbeadtechnology
AT kwonjongbum multiplexanalysisofcytokinesintheserumandcerebrospinalfluidofpatientswithalzheimersdiseasebycolorcodedbeadtechnology
AT choikyounggyu multiplexanalysisofcytokinesintheserumandcerebrospinalfluidofpatientswithalzheimersdiseasebycolorcodedbeadtechnology
AT leejongseo multiplexanalysisofcytokinesintheserumandcerebrospinalfluidofpatientswithalzheimersdiseasebycolorcodedbeadtechnology
AT kangsangwon multiplexanalysisofcytokinesintheserumandcerebrospinalfluidofpatientswithalzheimersdiseasebycolorcodedbeadtechnology