TY - JOUR
T1 - Kynurenic acid levels are increased in the CSF of Alzheimer's disease patients
AU - Lleó, Alberto
AU - González-Sánchez, M.
AU - Jiménez, J.
AU - Narváez, A.
AU - Antequera, D.
AU - Llamas-Velasco, S.
AU - Martín, A.H.S.
AU - Arjona, J.A.M.
AU - Munain, A.L.d.
AU - Marco, M.P.
AU - Rodríguez-Núñez, M.
AU - Pérez-Martínez, D.A.
AU - Villarejo-Galende, A.
AU - Bartolome, F.
AU - Domínguez, E.
AU - Carro, E.
PY - 2020
Y1 - 2020
N2 - Kynurenic acid (KYNA) is a product of the tryptophan (TRP) metabolism via the kynurenine pathway (KP). This pathway is activated in neurodegenerative disorders, such as Alzheimer's disease (AD). KYNA is primarily produced by astrocytes and is considered neuroprotective. Thus, altered KYNA levels may suggest an inflammatory response. Very recently, significant increases in KYNA levels were reported in cerebrospinal fluid (CSF) from AD patients compared with normal controls. In this study, we assessed the accuracy of KYNA in CSF for the classification of patients with AD, cognitively healthy controls, and patients with a variety of other neurodegenerative diseases, including frontotemporal dementia (FTD), amyotrophic lateral sclerosis (ALS), and progressive supranuclear palsy (PSP). Averaged KYNA concentration in CSF was higher in patients with AD when compared with healthy subjects and with all the other differentially diagnosed groups. There were no significant differences in KYNA levels in CSF between any other neurodegenerative groups and controls. These results suggest a specific increase in KYNA concentration in CSF from AD patients not seen in other neurodegenerative diseases.
AB - Kynurenic acid (KYNA) is a product of the tryptophan (TRP) metabolism via the kynurenine pathway (KP). This pathway is activated in neurodegenerative disorders, such as Alzheimer's disease (AD). KYNA is primarily produced by astrocytes and is considered neuroprotective. Thus, altered KYNA levels may suggest an inflammatory response. Very recently, significant increases in KYNA levels were reported in cerebrospinal fluid (CSF) from AD patients compared with normal controls. In this study, we assessed the accuracy of KYNA in CSF for the classification of patients with AD, cognitively healthy controls, and patients with a variety of other neurodegenerative diseases, including frontotemporal dementia (FTD), amyotrophic lateral sclerosis (ALS), and progressive supranuclear palsy (PSP). Averaged KYNA concentration in CSF was higher in patients with AD when compared with healthy subjects and with all the other differentially diagnosed groups. There were no significant differences in KYNA levels in CSF between any other neurodegenerative groups and controls. These results suggest a specific increase in KYNA concentration in CSF from AD patients not seen in other neurodegenerative diseases.
KW - Alzheimer's disease
KW - Amyloid-β
KW - Biomarkers
KW - Cerebrospinal fluid
KW - Kynurenine pathway
KW - Tau protein
UR - https://www.scopus.com/pages/publications/85083215100
U2 - 10.3390/biom10040571
DO - 10.3390/biom10040571
M3 - Article
C2 - 32276479
SN - 2218-273X
VL - 10
JO - Biomolecules
JF - Biomolecules
IS - 4
ER -