Kynurenic Acid Levels are Increased in the CSF of Alzheimer's Disease Patients

被引:66
作者
Gonzalez-Sanchez, Marta [1 ,2 ]
Jimenez, Javier [3 ]
Narvaez, Arantzazu [3 ]
Antequera, Desiree [1 ,2 ]
Llamas-Velasco, Sara [1 ,2 ]
Herrero-San Martin, Alejandro [1 ,2 ]
Molina Arjona, Jose Antonio [1 ,2 ]
Lopez de Munain, Adolfo [2 ,4 ]
Lleo Bisa, Alberto [2 ,5 ]
Marco, M-Pilar [6 ,7 ]
Rodriguez-Nunez, Montserrat [6 ,7 ]
Andres Perez-Martinez, David [1 ,2 ]
Villarejo-Galende, Alberto [1 ,2 ]
Bartolome, Fernando [1 ,2 ]
Dominguez, Elena [3 ]
Carro, Eva [1 ,2 ]
机构
[1] Hosp 12 Octubre, Grp Neurodegenerat Dis, Res Inst Imas12, Madrid 28041, Spain
[2] Biomed Res Networking Ctr Neurodegenerat Dis CIBE, Madrid 28031, Spain
[3] Univ Alcala, Dept Analyt Chem Phys Chem & Chem Engn, Alcala De Henares 28871, Spain
[4] Biodonostia Hlth Res Inst, Neurosci Res Area, San Sebastian 20014, Spain
[5] Hosp Santa Creu & Sant Pau, Neurol Dept, Barcelona 08041, Spain
[6] CSIC, Inst Adv Chem Catalonia IQAC, Nanobiotechnol Diagnost Grp Nb4D, Barcelona 08034, Spain
[7] Ctr Invest Biomed Red CIBER Bioingn Biomat & Nano, Barcelona 08034, Spain
关键词
Alzheimer's disease; kynurenine pathway; cerebrospinal fluid; biomarkers; amyloid-beta; tau protein; QUINOLINIC ACID; CEREBROSPINAL-FLUID; PATHWAY METABOLISM; ASSOCIATION WORKGROUPS; DIAGNOSTIC GUIDELINES; NATIONAL INSTITUTE; HUMAN ASTROCYTES; BRAIN; TRYPTOPHAN; DEMENTIA;
D O I
10.3390/biom10040571
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
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收藏
页数:15
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