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Quantitative Appraisal of Ventricular Cerebrospinal Fluid Biomarkers in Neuropathologically Diagnosed Parkinson’s Disease Cases Lacking Alzheimer’s Disease Pathology

Identifying biomarkers that distinguish Parkinson’s disease (PD) from normal control (NC) individuals has the potential to increase diagnostic sensitivity for the detection of early-stage PD. A previous proteomic study identified potential biomarkers in postmortem ventricular cerebrospinal fluid (V-...

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Autores principales: Maarouf, Chera L., Beach, Thomas G., Adler, Charles H., Malek-Ahmadi, Michael, Kokjohn, Tyler A., Dugger, Brittany N., Walker, Douglas G., Shill, Holly A., Jacobson, Sandra A., Sabbagh, Marwan N., Roher, Alex E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Libertas Academica 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3603385/
https://www.ncbi.nlm.nih.gov/pubmed/23533154
http://dx.doi.org/10.4137/BMI.S11422
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author Maarouf, Chera L.
Beach, Thomas G.
Adler, Charles H.
Malek-Ahmadi, Michael
Kokjohn, Tyler A.
Dugger, Brittany N.
Walker, Douglas G.
Shill, Holly A.
Jacobson, Sandra A.
Sabbagh, Marwan N.
Roher, Alex E.
author_facet Maarouf, Chera L.
Beach, Thomas G.
Adler, Charles H.
Malek-Ahmadi, Michael
Kokjohn, Tyler A.
Dugger, Brittany N.
Walker, Douglas G.
Shill, Holly A.
Jacobson, Sandra A.
Sabbagh, Marwan N.
Roher, Alex E.
author_sort Maarouf, Chera L.
collection PubMed
description Identifying biomarkers that distinguish Parkinson’s disease (PD) from normal control (NC) individuals has the potential to increase diagnostic sensitivity for the detection of early-stage PD. A previous proteomic study identified potential biomarkers in postmortem ventricular cerebrospinal fluid (V-CSF) from neuropathologically diagnosed PD subjects lacking Alzheimer’s disease (AD) neuropathology. In the present study, we assessed these biomarkers as well as p-tau(181), Aβ42, and S100B by ELISA in PD (n = 43) and NC (n = 49) cases. The p-tau(181)/Aβ42 ratio and ApoA-1 showed statistically significant differences between groups. Multiple regression analysis demonstrated that p-tau(181)/Aβ42 had a significant odds ratio: OR = 1.42 (95% confidence interval [CI], 1.12–1.84), P = 0.006. Among the molecules investigated, intriguing correlations were observed that require further investigation. Our results suggest coexistent AD CSF biomarkers within the PD group notwithstanding that it was selected to minimize AD neuropathological lesions.
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spelling pubmed-36033852013-03-25 Quantitative Appraisal of Ventricular Cerebrospinal Fluid Biomarkers in Neuropathologically Diagnosed Parkinson’s Disease Cases Lacking Alzheimer’s Disease Pathology Maarouf, Chera L. Beach, Thomas G. Adler, Charles H. Malek-Ahmadi, Michael Kokjohn, Tyler A. Dugger, Brittany N. Walker, Douglas G. Shill, Holly A. Jacobson, Sandra A. Sabbagh, Marwan N. Roher, Alex E. Biomark Insights Original Research Identifying biomarkers that distinguish Parkinson’s disease (PD) from normal control (NC) individuals has the potential to increase diagnostic sensitivity for the detection of early-stage PD. A previous proteomic study identified potential biomarkers in postmortem ventricular cerebrospinal fluid (V-CSF) from neuropathologically diagnosed PD subjects lacking Alzheimer’s disease (AD) neuropathology. In the present study, we assessed these biomarkers as well as p-tau(181), Aβ42, and S100B by ELISA in PD (n = 43) and NC (n = 49) cases. The p-tau(181)/Aβ42 ratio and ApoA-1 showed statistically significant differences between groups. Multiple regression analysis demonstrated that p-tau(181)/Aβ42 had a significant odds ratio: OR = 1.42 (95% confidence interval [CI], 1.12–1.84), P = 0.006. Among the molecules investigated, intriguing correlations were observed that require further investigation. Our results suggest coexistent AD CSF biomarkers within the PD group notwithstanding that it was selected to minimize AD neuropathological lesions. Libertas Academica 2013-03-12 /pmc/articles/PMC3603385/ /pubmed/23533154 http://dx.doi.org/10.4137/BMI.S11422 Text en © 2013 the author(s), publisher and licensee Libertas Academica Ltd. This is an open access article. Unrestricted non-commercial use is permitted provided the original work is properly cited.
spellingShingle Original Research
Maarouf, Chera L.
Beach, Thomas G.
Adler, Charles H.
Malek-Ahmadi, Michael
Kokjohn, Tyler A.
Dugger, Brittany N.
Walker, Douglas G.
Shill, Holly A.
Jacobson, Sandra A.
Sabbagh, Marwan N.
Roher, Alex E.
Quantitative Appraisal of Ventricular Cerebrospinal Fluid Biomarkers in Neuropathologically Diagnosed Parkinson’s Disease Cases Lacking Alzheimer’s Disease Pathology
title Quantitative Appraisal of Ventricular Cerebrospinal Fluid Biomarkers in Neuropathologically Diagnosed Parkinson’s Disease Cases Lacking Alzheimer’s Disease Pathology
title_full Quantitative Appraisal of Ventricular Cerebrospinal Fluid Biomarkers in Neuropathologically Diagnosed Parkinson’s Disease Cases Lacking Alzheimer’s Disease Pathology
title_fullStr Quantitative Appraisal of Ventricular Cerebrospinal Fluid Biomarkers in Neuropathologically Diagnosed Parkinson’s Disease Cases Lacking Alzheimer’s Disease Pathology
title_full_unstemmed Quantitative Appraisal of Ventricular Cerebrospinal Fluid Biomarkers in Neuropathologically Diagnosed Parkinson’s Disease Cases Lacking Alzheimer’s Disease Pathology
title_short Quantitative Appraisal of Ventricular Cerebrospinal Fluid Biomarkers in Neuropathologically Diagnosed Parkinson’s Disease Cases Lacking Alzheimer’s Disease Pathology
title_sort quantitative appraisal of ventricular cerebrospinal fluid biomarkers in neuropathologically diagnosed parkinson’s disease cases lacking alzheimer’s disease pathology
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3603385/
https://www.ncbi.nlm.nih.gov/pubmed/23533154
http://dx.doi.org/10.4137/BMI.S11422
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