CSF and blood Kallikrein-8: a promising early biomarker for Alzheimer's disease.
Aged
Alzheimer Disease
/ blood
Amyloid beta-Peptides
/ cerebrospinal fluid
Biomarkers
/ blood
Cognitive Dysfunction
/ blood
Cross-Sectional Studies
Disease Progression
Female
Humans
Kallikreins
/ blood
Male
Middle Aged
Neuropsychological Tests
Prognosis
Reproducibility of Results
tau Proteins
/ blood
Alzheimer’s disease
KLK8
Kallikrein-8
Parkinson’s disease
affective disorders
biomarker
blood
cerebrospinal fluid
mild cognitive impairment
neuropsin
psychiatric 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
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
40-48Informations 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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