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Plasma contact factors as novel biomarkers for diagnosing Alzheimer’s disease

BACKGROUND: Alzheimer’s disease (AD) is the most common cause of dementia and most of AD patients suffer from vascular abnormalities and neuroinflammation. There is an urgent need to develop novel blood biomarkers capable of diagnosing Alzheimer’s disease (AD) at very early stage. This study was per...

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Autores principales: Park, Jung Eun, Lim, Do Sung, Cho, Yeong Hee, Choi, Kyu Yeong, Lee, Jang Jae, Kim, Byeong C., Lee, Kun Ho, Lee, Jung Sup
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7796542/
https://www.ncbi.nlm.nih.gov/pubmed/33422144
http://dx.doi.org/10.1186/s40364-020-00258-5
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author Park, Jung Eun
Lim, Do Sung
Cho, Yeong Hee
Choi, Kyu Yeong
Lee, Jang Jae
Kim, Byeong C.
Lee, Kun Ho
Lee, Jung Sup
author_facet Park, Jung Eun
Lim, Do Sung
Cho, Yeong Hee
Choi, Kyu Yeong
Lee, Jang Jae
Kim, Byeong C.
Lee, Kun Ho
Lee, Jung Sup
author_sort Park, Jung Eun
collection PubMed
description BACKGROUND: Alzheimer’s disease (AD) is the most common cause of dementia and most of AD patients suffer from vascular abnormalities and neuroinflammation. There is an urgent need to develop novel blood biomarkers capable of diagnosing Alzheimer’s disease (AD) at very early stage. This study was performed to find out new accurate plasma diagnostic biomarkers for AD by investigating a direct relationship between plasma contact system and AD. METHODS: A total 101 of human CSF and plasma samples from normal and AD patients were analyzed. The contact factor activities in plasma were measured with the corresponding specific peptide substrates. RESULTS: The activities of contact factors (FXIIa, FXIa, plasma kallikrein) and FXa clearly increased and statistically correlated as AD progresses. We present here, for the first time, the FXIIa cut-off scores to as: > 26.3 U/ml for prodromal AD [area under the curve (AUC) = 0.783, p < 0.001] and > 27.2 U/ml for AD dementia (AUC = 0.906, p < 0.001). We also describe the cut-off scores from the ratios of CSF Aβ(1–42) versus the contact factors. Of these, the representative ratio cut-off scores of Aβ(1–42)/FXIIa were to be: < 33.8 for prodromal AD (AUC = 0.965, p < 0.001) and < 27.44 for AD dementia (AUC = 1.0, p < 0.001). CONCLUSION: The activation of plasma contact system is closely associated with clinical stage of AD, and FXIIa activity as well as the cut-off scores of CSF Aβ(1–42)/FXIIa can be used as novel accurate diagnostic AD biomarkers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40364-020-00258-5.
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spelling pubmed-77965422021-01-11 Plasma contact factors as novel biomarkers for diagnosing Alzheimer’s disease Park, Jung Eun Lim, Do Sung Cho, Yeong Hee Choi, Kyu Yeong Lee, Jang Jae Kim, Byeong C. Lee, Kun Ho Lee, Jung Sup Biomark Res Research BACKGROUND: Alzheimer’s disease (AD) is the most common cause of dementia and most of AD patients suffer from vascular abnormalities and neuroinflammation. There is an urgent need to develop novel blood biomarkers capable of diagnosing Alzheimer’s disease (AD) at very early stage. This study was performed to find out new accurate plasma diagnostic biomarkers for AD by investigating a direct relationship between plasma contact system and AD. METHODS: A total 101 of human CSF and plasma samples from normal and AD patients were analyzed. The contact factor activities in plasma were measured with the corresponding specific peptide substrates. RESULTS: The activities of contact factors (FXIIa, FXIa, plasma kallikrein) and FXa clearly increased and statistically correlated as AD progresses. We present here, for the first time, the FXIIa cut-off scores to as: > 26.3 U/ml for prodromal AD [area under the curve (AUC) = 0.783, p < 0.001] and > 27.2 U/ml for AD dementia (AUC = 0.906, p < 0.001). We also describe the cut-off scores from the ratios of CSF Aβ(1–42) versus the contact factors. Of these, the representative ratio cut-off scores of Aβ(1–42)/FXIIa were to be: < 33.8 for prodromal AD (AUC = 0.965, p < 0.001) and < 27.44 for AD dementia (AUC = 1.0, p < 0.001). CONCLUSION: The activation of plasma contact system is closely associated with clinical stage of AD, and FXIIa activity as well as the cut-off scores of CSF Aβ(1–42)/FXIIa can be used as novel accurate diagnostic AD biomarkers. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40364-020-00258-5. BioMed Central 2021-01-09 /pmc/articles/PMC7796542/ /pubmed/33422144 http://dx.doi.org/10.1186/s40364-020-00258-5 Text en © The Author(s) 2021 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/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Park, Jung Eun
Lim, Do Sung
Cho, Yeong Hee
Choi, Kyu Yeong
Lee, Jang Jae
Kim, Byeong C.
Lee, Kun Ho
Lee, Jung Sup
Plasma contact factors as novel biomarkers for diagnosing Alzheimer’s disease
title Plasma contact factors as novel biomarkers for diagnosing Alzheimer’s disease
title_full Plasma contact factors as novel biomarkers for diagnosing Alzheimer’s disease
title_fullStr Plasma contact factors as novel biomarkers for diagnosing Alzheimer’s disease
title_full_unstemmed Plasma contact factors as novel biomarkers for diagnosing Alzheimer’s disease
title_short Plasma contact factors as novel biomarkers for diagnosing Alzheimer’s disease
title_sort plasma contact factors as novel biomarkers for diagnosing alzheimer’s disease
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7796542/
https://www.ncbi.nlm.nih.gov/pubmed/33422144
http://dx.doi.org/10.1186/s40364-020-00258-5
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