Autoantibodies against myelin sheath and S100β are associated with cognitive dysfunction in patients with rheumatoid arthritis

被引:34
|
作者
Almeida Baptista, Talita Siara [1 ]
Petersen, Laura Esteves [1 ]
Molina, Julia K. [2 ]
de Nardi, Tatiana [2 ]
Wieck, Andrea [1 ]
do Prado, Aline [3 ]
Piovesan, Deise Marcela [3 ]
Keisermann, Mauro [3 ]
Grassi-Oliveira, Rodrigo [2 ]
Bauer, Moises Evandro [1 ,4 ]
机构
[1] Pontifical Catholic Univ Rio Grande do Sul PUCRS, Inst Biomed Res, Lab Immunosenescence, Porto Alegre, RS, Brazil
[2] Pontificia Univ Catolica Rio Grande do Sul, Postgrad Program Psychol, Ctr Studies & Res Traumat Stress NEPTE, Cognit Neurosci Res Grp GNCD, Porto Alegre, RS, Brazil
[3] Pontificia Univ Catolica Rio Grande do Sul, Hosp Sao Lucas, Rheumatol Unit, Porto Alegre, RS, Brazil
[4] Pontificia Univ Catolica Rio Grande do Sul, Fac Biosci, Inst Pesquisas Biomed, Ave Ipiranga 6690,2 Andar,POB 1429, BR-90610000 Porto Alegre, RS, Brazil
关键词
Autoantibodies; Cognitive dysfunction; Myelin sheath; Rheumatoid arthritis; S100; beta; SYSTEMIC-LUPUS-ERYTHEMATOSUS; GLIAL-DERIVED ANTIGENS; ALZHEIMERS-DISEASE; EXTRAARTICULAR MANIFESTATIONS; CEREBROSPINAL-FLUID; MULTIPLE-SCLEROSIS; PATHOGENIC ROLE; BASIC-PROTEIN; ANTIBODIES; SERUM;
D O I
10.1007/s10067-017-3724-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rheumatoid arthritis (RA) has been associated with cognitive impairment and peripheral production of autoantibodies. Autoantibodies against central nervous system (CNS) proteins and S100 calcium-binding beta (S100 beta) were found increased in diseases characterized by cognitive impairment like Alzheimer disease and Neuropsychiatric Systemic Lupus Erythematosus (NPSLE). The aim of this study was to investigate the plasma levels of autoantibodies against myelin basic protein (anti-MBP), myelin oligodendrocyte glycoprotein (anti-MOG) and S100 beta, and their relationships with cognitive performance in RA patients. Twenty patients with active rheumatoid arthritis and 19 age-, sex-, and schooling-matched healthy controls were recruited. Multiple dimensions of cognitive function were evaluated by structured clinical questionnaires. Autoantibodies and S100 beta levels were assessed by ELISAs. Patients had significantly higher levels of anti-MBP IgG (17.51 +/- 1.36 vs. 5.24 +/- 0.53 ng/mL), anti-MOG IgG (5.68 +/- 1.34 vs. 0.51 +/- 0.49 ng/mL), and S100 beta protein (2.24 +/- 0.50 vs. 0.47 +/- 0.06) than controls (all p < 0.0001). After adjusting for potential confounders, RA group presented worse cognitive performance involving the working memory and executive functions such as inhibition, flexibility, and mental control in parallel to higher autoantibodies and S100 beta levels than healthy controls (all p < 0.001). Levels of anti-MBP were negatively associated with delayed verbal recall (DVR; r = -0.42, p = 0.005), Stroop Color-Word (r = -0.48, p = 0.004), and N-Back Total scores (r = -0.59, p < 0.0001) and positively with Trail Making Test B (TMB, r = 0.53, p = 0.001). Negative correlation was found between levels of anti-MOG and DVR (r = -0.64, p < 0.0001), N-Back Total scores (r = -0.35, p = 0.03), Stroop Color-Word (r = -0.51, p = 0.001), and positively with TMB (r = 0.50, p = 0.003). S100 beta levels were associated with DVR (r = -0.51, p = 0.002), TMB (r = 0.46, p = 0.008), Stroop Color-Word (r = -0.67, p < 0.0001), and N-Back Total (r = -0.52, p = 0.003). RA is associated with impaired cognitive performance associated with higher levels of CNS-related autoantibodies and S100 beta levels. Given the importance of myelin integrity to cognition, our data indicate that these autoantibodies may be harmful to proper cognitive function.
引用
收藏
页码:1959 / 1968
页数:10
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