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Seed Amplification Assay as a Diagnostic Tool in Newly-Diagnosed Parkinson’s Disease

Seed amplification assays (SAA) are the first credible molecular assay for Parkinson’s disease (PD). However, the value of SAA to support the clinicians’ initial diagnosis of PD is not clear. In our study, we analyzed cerebrospinal fluid samples from 121 PD patients recruited through population scre...

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Autores principales: Oftedal, Linn, Maple-Grødem, Jodi, Tysnes, Ole-Bjørn, Alves, Guido, Lange, Johannes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473053/
https://www.ncbi.nlm.nih.gov/pubmed/37393438
http://dx.doi.org/10.3233/JPD-230065
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author Oftedal, Linn
Maple-Grødem, Jodi
Tysnes, Ole-Bjørn
Alves, Guido
Lange, Johannes
author_facet Oftedal, Linn
Maple-Grødem, Jodi
Tysnes, Ole-Bjørn
Alves, Guido
Lange, Johannes
author_sort Oftedal, Linn
collection PubMed
description Seed amplification assays (SAA) are the first credible molecular assay for Parkinson’s disease (PD). However, the value of SAA to support the clinicians’ initial diagnosis of PD is not clear. In our study, we analyzed cerebrospinal fluid samples from 121 PD patients recruited through population screening methods and taken within a median delay of 38 days from diagnosis and 51 normal controls without neurodegenerative disease. SAA yielded a sensitivity of 82.6% (95% CI, 74.7% – 88.9%) and specificity of 88.2% (95% CI, 76.1% – 95.6%). These results highlight the potential of SAA to support the initial diagnosis of PD in clinical practice and research.
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spelling pubmed-104730532023-09-02 Seed Amplification Assay as a Diagnostic Tool in Newly-Diagnosed Parkinson’s Disease Oftedal, Linn Maple-Grødem, Jodi Tysnes, Ole-Bjørn Alves, Guido Lange, Johannes J Parkinsons Dis Short Communication Seed amplification assays (SAA) are the first credible molecular assay for Parkinson’s disease (PD). However, the value of SAA to support the clinicians’ initial diagnosis of PD is not clear. In our study, we analyzed cerebrospinal fluid samples from 121 PD patients recruited through population screening methods and taken within a median delay of 38 days from diagnosis and 51 normal controls without neurodegenerative disease. SAA yielded a sensitivity of 82.6% (95% CI, 74.7% – 88.9%) and specificity of 88.2% (95% CI, 76.1% – 95.6%). These results highlight the potential of SAA to support the initial diagnosis of PD in clinical practice and research. IOS Press 2023-07-25 /pmc/articles/PMC10473053/ /pubmed/37393438 http://dx.doi.org/10.3233/JPD-230065 Text en © 2023 – The authors. Published by IOS Press https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC 4.0) License (https://creativecommons.org/licenses/by-nc/4.0/) , which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Oftedal, Linn
Maple-Grødem, Jodi
Tysnes, Ole-Bjørn
Alves, Guido
Lange, Johannes
Seed Amplification Assay as a Diagnostic Tool in Newly-Diagnosed Parkinson’s Disease
title Seed Amplification Assay as a Diagnostic Tool in Newly-Diagnosed Parkinson’s Disease
title_full Seed Amplification Assay as a Diagnostic Tool in Newly-Diagnosed Parkinson’s Disease
title_fullStr Seed Amplification Assay as a Diagnostic Tool in Newly-Diagnosed Parkinson’s Disease
title_full_unstemmed Seed Amplification Assay as a Diagnostic Tool in Newly-Diagnosed Parkinson’s Disease
title_short Seed Amplification Assay as a Diagnostic Tool in Newly-Diagnosed Parkinson’s Disease
title_sort seed amplification assay as a diagnostic tool in newly-diagnosed parkinson’s disease
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10473053/
https://www.ncbi.nlm.nih.gov/pubmed/37393438
http://dx.doi.org/10.3233/JPD-230065
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