CSF and blood Kallikrein-8: a promising early biomarker for Alzheimer's disease.


Journal

Journal of neurology, neurosurgery, and psychiatry
ISSN: 1468-330X
Titre abrégé: J Neurol Neurosurg Psychiatry
Pays: England
ID NLM: 2985191R

Informations de publication

Date de publication:
01 2020
Historique:
received: 24 04 2019
revised: 15 07 2019
accepted: 23 07 2019
pubmed: 3 8 2019
medline: 7 7 2020
entrez: 3 8 2019
Statut: ppublish

Résumé

There is still an urgent need for supportive minimally invasive and cost-effective biomarkers for early diagnosis of Alzheimer's disease (AD). Previous work in our lab has identified Kallikrein-8 (KLK8) as a potential candidate since it shows an excessive increase in human brain in preclinical disease stages. The aim of this study was to evaluate the diagnostic performance of cerebrospinal fluid (CSF) and blood KLK8 for AD and mild cognitive impairment (MCI) due to AD. In this multi-centre trans-sectional study, clinical and laboratory data as well as CSF and/or blood serum samples of 237 participants, including 98 patients with mild AD, 21 with MCI due to AD and 118 controls were collected. CSF and/or serum KLK8 levels were analysed by ELISA. The diagnostic accuracy of KLK8 in CSF and blood was determined using receiver operating characteristic (ROC) analyses and compared with that of CSF core biomarkers Aβ42, P-tau and T-tau. The diagnostic accuracy of CSF KLK8 was as good as that of core CSF biomarkers for AD (area under the curve (AUC)=0.89) and in case of MCI (AUC=0.97) even superior to CSF Aβ42. Blood KLK8 was a similarly strong discriminator for MCI (AUC=0.94) but slightly weaker for AD (AUC=0.83). This is the first study to demonstrate the potential clinical utility of blood and CSF KLK8 as a biomarker for incipient AD. Future prospective validation studies are warranted.

Identifiants

pubmed: 31371645
pii: jnnp-2019-321073
doi: 10.1136/jnnp-2019-321073
pmc: PMC6952834
doi:

Substances chimiques

Amyloid beta-Peptides 0
Biomarkers 0
MAPT protein, human 0
tau Proteins 0
KLK8 protein, human EC 3.4.21.-
Kallikreins EC 3.4.21.-

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

40-48

Informations de copyright

© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: AH and KK are inventors on the pending patent ‘Agents inhibiting Kallikrein-8 for use in the prevention or treatment of Alzheimer's disease’, which is registered at the European Patent Agency since 09/2015 (EP 15003657/15003657.2) and at the US Patent and Trademark Office since 03/2018 (15/761,725).

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Auteurs

Sarah Teuber-Hanselmann (S)

Institute of Neuropathology, Faculty of Medicine, University of Duisburg-Essen, Essen, Germany.

Jan Rekowski (J)

Institute of Medical Informatics, Biometry and Epidemiology, Faculty of Medicine, University of Duisburg-Essen, Essen, Germany.

Jonathan Vogelgsang (J)

Department of Psychiatry and Psychotherapy, University Medical Center, Gottingen, Germany.

Christine von Arnim (C)

Department of Neurology, University of Ulm, Ulm, Germany.
Clinic for Neurogeriatrics and Neurological Rehabilitation, RKU-University and Rehabilitation Hospital Ulm, Ulm, Germany.

Kathrin Reetz (K)

Department of Neurology, RWTH Aachen University, Aachen, Germany.

Andreas Stang (A)

Center of Clinical Epidemiology, c/o Institute of Medical Informatics, Biometry and Epidemiology, Faculty of Medicine, University of Duisburg-Essen, Essen, Germany.

Karl-Heinz Jöckel (KH)

Institute of Medical Informatics, Biometry and Epidemiology, Faculty of Medicine, University of Duisburg-Essen, Essen, Germany.

Jens Wiltfang (J)

Department of Psychiatry and Psychotherapy, University Medical Center, Gottingen, Germany.
iBiMED, Medical Sciences Department, University of Aveiro, Aveiro, Portugal.

Herrmann Esselmann (H)

Department of Psychiatry and Psychotherapy, University Medical Center, Gottingen, Germany.

Markus Otto (M)

Department of Neurology, University of Ulm, Ulm, Germany.

Hayrettin Tumani (H)

Department of Neurology, University of Ulm, Ulm, Germany.

Arne Herring (A)

Institute of Neuropathology, Faculty of Medicine, University of Duisburg-Essen, Essen, Germany.

Kathy Keyvani (K)

Institute of Neuropathology, Faculty of Medicine, University of Duisburg-Essen, Essen, Germany kathy.keyvani@uk-essen.de.

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Classifications MeSH