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Kallikrein-related peptidases 6 and 10 are elevated in cerebrospinal fluid of patients with Alzheimer’s disease and associated with CSF-TAU and FDG-PET

BACKGROUND: Alterations in the expression of human kallikrein-related peptidases (KLKs) have been described in patients with Alzheimer’s disease (AD). We elucidated the suitability of KLK6, KLK8 and KLK10 to distinguish AD from NC and explored associations with established AD biomarkers. METHODS: KL...

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Autores principales: Goldhardt, Oliver, Warnhoff, Inanna, Yakushev, Igor, Begcevic, Ilijana, Förstl, Hans, Magdolen, Viktor, Soosaipillai, Antoninus, Diamandis, Eleftherios, Alexopoulos, Panagiotis, Grimmer, Timo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6712703/
https://www.ncbi.nlm.nih.gov/pubmed/31467673
http://dx.doi.org/10.1186/s40035-019-0168-6
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author Goldhardt, Oliver
Warnhoff, Inanna
Yakushev, Igor
Begcevic, Ilijana
Förstl, Hans
Magdolen, Viktor
Soosaipillai, Antoninus
Diamandis, Eleftherios
Alexopoulos, Panagiotis
Grimmer, Timo
author_facet Goldhardt, Oliver
Warnhoff, Inanna
Yakushev, Igor
Begcevic, Ilijana
Förstl, Hans
Magdolen, Viktor
Soosaipillai, Antoninus
Diamandis, Eleftherios
Alexopoulos, Panagiotis
Grimmer, Timo
author_sort Goldhardt, Oliver
collection PubMed
description BACKGROUND: Alterations in the expression of human kallikrein-related peptidases (KLKs) have been described in patients with Alzheimer’s disease (AD). We elucidated the suitability of KLK6, KLK8 and KLK10 to distinguish AD from NC and explored associations with established AD biomarkers. METHODS: KLK levels in cerebrospinal fluid (CSF), as determined by ELISA, were compared between 32 AD patients stratified to A/T/(N) system with evidence for amyloid pathology and of 23 normal controls with normal AD biomarkers. Associations between KLK levels and clinical severity, CSF and positron emission tomography (PET) based AD biomarkers were tested for. RESULTS: Levels of KLK6 and KLK10 were significantly increased in AD. KLK6 differed significantly between AD A+/T+/N+ and AD A+/T−/N+ or NC with an AUC of 0.922. CSF pTau and tTau levels were significantly associated with KLK6 in AD. CONCLUSIONS: KLK6 deserves further investigations as a potential biomarker of Tau pathology in AD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40035-019-0168-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-67127032019-08-29 Kallikrein-related peptidases 6 and 10 are elevated in cerebrospinal fluid of patients with Alzheimer’s disease and associated with CSF-TAU and FDG-PET Goldhardt, Oliver Warnhoff, Inanna Yakushev, Igor Begcevic, Ilijana Förstl, Hans Magdolen, Viktor Soosaipillai, Antoninus Diamandis, Eleftherios Alexopoulos, Panagiotis Grimmer, Timo Transl Neurodegener Research BACKGROUND: Alterations in the expression of human kallikrein-related peptidases (KLKs) have been described in patients with Alzheimer’s disease (AD). We elucidated the suitability of KLK6, KLK8 and KLK10 to distinguish AD from NC and explored associations with established AD biomarkers. METHODS: KLK levels in cerebrospinal fluid (CSF), as determined by ELISA, were compared between 32 AD patients stratified to A/T/(N) system with evidence for amyloid pathology and of 23 normal controls with normal AD biomarkers. Associations between KLK levels and clinical severity, CSF and positron emission tomography (PET) based AD biomarkers were tested for. RESULTS: Levels of KLK6 and KLK10 were significantly increased in AD. KLK6 differed significantly between AD A+/T+/N+ and AD A+/T−/N+ or NC with an AUC of 0.922. CSF pTau and tTau levels were significantly associated with KLK6 in AD. CONCLUSIONS: KLK6 deserves further investigations as a potential biomarker of Tau pathology in AD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40035-019-0168-6) contains supplementary material, which is available to authorized users. BioMed Central 2019-08-27 /pmc/articles/PMC6712703/ /pubmed/31467673 http://dx.doi.org/10.1186/s40035-019-0168-6 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Research
Goldhardt, Oliver
Warnhoff, Inanna
Yakushev, Igor
Begcevic, Ilijana
Förstl, Hans
Magdolen, Viktor
Soosaipillai, Antoninus
Diamandis, Eleftherios
Alexopoulos, Panagiotis
Grimmer, Timo
Kallikrein-related peptidases 6 and 10 are elevated in cerebrospinal fluid of patients with Alzheimer’s disease and associated with CSF-TAU and FDG-PET
title Kallikrein-related peptidases 6 and 10 are elevated in cerebrospinal fluid of patients with Alzheimer’s disease and associated with CSF-TAU and FDG-PET
title_full Kallikrein-related peptidases 6 and 10 are elevated in cerebrospinal fluid of patients with Alzheimer’s disease and associated with CSF-TAU and FDG-PET
title_fullStr Kallikrein-related peptidases 6 and 10 are elevated in cerebrospinal fluid of patients with Alzheimer’s disease and associated with CSF-TAU and FDG-PET
title_full_unstemmed Kallikrein-related peptidases 6 and 10 are elevated in cerebrospinal fluid of patients with Alzheimer’s disease and associated with CSF-TAU and FDG-PET
title_short Kallikrein-related peptidases 6 and 10 are elevated in cerebrospinal fluid of patients with Alzheimer’s disease and associated with CSF-TAU and FDG-PET
title_sort kallikrein-related peptidases 6 and 10 are elevated in cerebrospinal fluid of patients with alzheimer’s disease and associated with csf-tau and fdg-pet
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6712703/
https://www.ncbi.nlm.nih.gov/pubmed/31467673
http://dx.doi.org/10.1186/s40035-019-0168-6
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