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Endoplasmic Reticulum Stress-Regulated Chaperones as a Serum Biomarker Panel for Parkinson’s Disease

Examination of post-mortem brain tissues has previously revealed a strong association between Parkinson’s disease (PD) pathophysiology and endoplasmic reticulum (ER) stress. Evidence in the literature regarding the circulation of ER stress-regulated factors released from neurons provides a rationale...

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Autores principales: Mnich, Katarzyna, Moghaddam, Shirin, Browne, Patrick, Counihan, Timothy, Fitzgerald, Stephen P., Martin, Kenneth, Richardson, Ciaran, Samali, Afshin, Gorman, Adrienne M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9899193/
https://www.ncbi.nlm.nih.gov/pubmed/36478320
http://dx.doi.org/10.1007/s12035-022-03139-0
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author Mnich, Katarzyna
Moghaddam, Shirin
Browne, Patrick
Counihan, Timothy
Fitzgerald, Stephen P.
Martin, Kenneth
Richardson, Ciaran
Samali, Afshin
Gorman, Adrienne M.
author_facet Mnich, Katarzyna
Moghaddam, Shirin
Browne, Patrick
Counihan, Timothy
Fitzgerald, Stephen P.
Martin, Kenneth
Richardson, Ciaran
Samali, Afshin
Gorman, Adrienne M.
author_sort Mnich, Katarzyna
collection PubMed
description Examination of post-mortem brain tissues has previously revealed a strong association between Parkinson’s disease (PD) pathophysiology and endoplasmic reticulum (ER) stress. Evidence in the literature regarding the circulation of ER stress-regulated factors released from neurons provides a rationale for investigating ER stress biomarkers in the blood to aid diagnosis of PD. The levels of ER stress-regulated proteins in serum collected from 29 PD patients and 24 non-PD controls were measured using enzyme-linked immunosorbent assays. A panel of four biomarkers, protein disulfide-isomerase A1, protein disulfide-isomerase A3, mesencephalic astrocyte-derived neurotrophic factor, and clusterin, together with age and gender had higher ability (area under the curve 0.64, sensitivity 66%, specificity 57%) and net benefit to discriminate PD patients from the non-PD group compared with other analyzed models. Addition of oligomeric and total α-synuclein to the model did not improve the diagnostic power of the biomarker panel. We provide evidence that ER stress-regulated proteins merit further investigation for their potential as diagnostic biomarkers of PD. GRAPHICAL ABSTRACT: [Image: see text]
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spelling pubmed-98991932023-02-06 Endoplasmic Reticulum Stress-Regulated Chaperones as a Serum Biomarker Panel for Parkinson’s Disease Mnich, Katarzyna Moghaddam, Shirin Browne, Patrick Counihan, Timothy Fitzgerald, Stephen P. Martin, Kenneth Richardson, Ciaran Samali, Afshin Gorman, Adrienne M. Mol Neurobiol Article Examination of post-mortem brain tissues has previously revealed a strong association between Parkinson’s disease (PD) pathophysiology and endoplasmic reticulum (ER) stress. Evidence in the literature regarding the circulation of ER stress-regulated factors released from neurons provides a rationale for investigating ER stress biomarkers in the blood to aid diagnosis of PD. The levels of ER stress-regulated proteins in serum collected from 29 PD patients and 24 non-PD controls were measured using enzyme-linked immunosorbent assays. A panel of four biomarkers, protein disulfide-isomerase A1, protein disulfide-isomerase A3, mesencephalic astrocyte-derived neurotrophic factor, and clusterin, together with age and gender had higher ability (area under the curve 0.64, sensitivity 66%, specificity 57%) and net benefit to discriminate PD patients from the non-PD group compared with other analyzed models. Addition of oligomeric and total α-synuclein to the model did not improve the diagnostic power of the biomarker panel. We provide evidence that ER stress-regulated proteins merit further investigation for their potential as diagnostic biomarkers of PD. GRAPHICAL ABSTRACT: [Image: see text] Springer US 2022-12-07 2023 /pmc/articles/PMC9899193/ /pubmed/36478320 http://dx.doi.org/10.1007/s12035-022-03139-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Mnich, Katarzyna
Moghaddam, Shirin
Browne, Patrick
Counihan, Timothy
Fitzgerald, Stephen P.
Martin, Kenneth
Richardson, Ciaran
Samali, Afshin
Gorman, Adrienne M.
Endoplasmic Reticulum Stress-Regulated Chaperones as a Serum Biomarker Panel for Parkinson’s Disease
title Endoplasmic Reticulum Stress-Regulated Chaperones as a Serum Biomarker Panel for Parkinson’s Disease
title_full Endoplasmic Reticulum Stress-Regulated Chaperones as a Serum Biomarker Panel for Parkinson’s Disease
title_fullStr Endoplasmic Reticulum Stress-Regulated Chaperones as a Serum Biomarker Panel for Parkinson’s Disease
title_full_unstemmed Endoplasmic Reticulum Stress-Regulated Chaperones as a Serum Biomarker Panel for Parkinson’s Disease
title_short Endoplasmic Reticulum Stress-Regulated Chaperones as a Serum Biomarker Panel for Parkinson’s Disease
title_sort endoplasmic reticulum stress-regulated chaperones as a serum biomarker panel for parkinson’s disease
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9899193/
https://www.ncbi.nlm.nih.gov/pubmed/36478320
http://dx.doi.org/10.1007/s12035-022-03139-0
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