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Plasma levels of soluble tumor necrosis factor receptors are associated with cognitive performance in Parkinson's disease.

Authors :
Rocha NP
Teixeira AL
Scalzo PL
Barbosa IG
de Sousa MS
Morato IB
Vieira EL
Christo PP
Palotás A
Reis HJ
Source :
Movement disorders : official journal of the Movement Disorder Society [Mov Disord] 2014 Apr; Vol. 29 (4), pp. 527-31. Date of Electronic Publication: 2013 Dec 03.
Publication Year :
2014

Abstract

Inflammatory mechanisms have been implicated in a series of neuropsychiatric conditions, including behavioral disturbances, cognitive dysfunction, and affective disorders. Accumulating evidence also strongly suggests their involvement in the pathophysiology of Parkinson's disease (PD). This study aimed to evaluate plasma levels of inflammatory biomarkers, and their association with cognitive performance and other non-motor symptoms of PD. PD patients and control individuals were subjected to various psychometric tests, including the Mini-Mental State Examination (MMSE), Frontal Assessment Battery (FAB), and Beck's Depression Inventory (BDI). Biomarker plasma levels were measured by enzyme-linked immunosorbent assay (ELISA). PD patients exhibited worse performance on MMSE and the programming task of FAB, and presented higher soluble tumor necrosis factor receptor (sTNFR) plasma levels than control individuals. Among PD patients, increased sTNFR1 and sTNFR2 concentrations were associated with poorer cognitive test scores. After multiple linear regression, sTNFR1 and education remained a significant predictor for FAB scores. Our data suggest that PD is associated with a proinflammatory profile, and sTNFRs are putative biomarkers of cognitive performance, with elevated sTNFR1 levels predicting poorer executive functioning in PD patients.<br /> (© 2013 International Parkinson and Movement Disorder Society.)

Details

Language :
English
ISSN :
1531-8257
Volume :
29
Issue :
4
Database :
MEDLINE
Journal :
Movement disorders : official journal of the Movement Disorder Society
Publication Type :
Academic Journal
Accession number :
24301904
Full Text :
https://doi.org/10.1002/mds.25752