Disease progression and oxidative stress are associated with higher serum ferritin levels in patients with multiple sclerosis

被引:26
作者
Zanin Ferreira, Katerine Panichi [1 ]
Oliveira, Sayonara R. [2 ]
Kallaur, Ana Paula [1 ]
Kaimen-Maciel, Damacio R. [3 ]
Lozovoy, Marcell Alysson B. [2 ]
Delicato de Almeida, Elaine Regina [2 ]
Morimoto, Helena Kaminami [2 ]
Mezzaroba, Leda [2 ]
Dichi, Isaias [3 ]
Vissoci Reiche, Edna Maria [2 ]
Colado Simao, Andrea Name [2 ]
机构
[1] Univ Londrina, Ctr Biol Sci, Postgrad Program, Londrina, Parana, Brazil
[2] Univ Londrina, Hlth Sci Ctr, Dept Pathol Clin Anal & Toxicol, Londrina, Parana, Brazil
[3] Univ Londrina, Dept Internal Med, Londrina, Parana, Brazil
关键词
Ferritin; Multiple sclerosis; Oxidative stress; Disease progression; Hyperferritinemia; DISABILITY STATUS SCALE; IRON; PLASMA; INFLAMMATION; TRANSFERRIN; ACTIVATION; DAMAGE; BRAIN;
D O I
10.1016/j.jns.2016.12.039
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Hyperferritinemia and oxidative stress have been implicated in the pathogenesis of multiple sclerosis (MS). The aim of the present study was to evaluate the serum levels of ferritin and to verify their association with oxidative stress markers and MS progression. This study included 164 MS patients, which were divided in two groups according to their levels of ferritin (cut off 125.6 mu g/L). Oxidative stress was evaluated by tert-butyl hydroperoxideinitiated chemiluminescence (CL-LOOH), advanced oxidation protein products (AOPP), carbonyl protein, nitric oxide metabolites (NOx), sulfhydryl groups of protein and total radical-trapping antioxidant parameter (TRAP). MS patients with elevated levels of ferritin showed higher disease progression (p = 0.030), AOPP (p = 0.001), and lower plasma NOx levels (p = 0.031) and TRAP (p = 0.006) than MS patients with lower ferritin levels. The multivariate binary logistic regression analysis showed that increased AOPP and progression of disease were significantly and positively associated with increase of ferritin. The combination of serum ferritin levels and oxidative stress markers were responsible for 13,9% in the disease progression. In conclusion, our results suggest that ferritin could aggravate oxidative stress in patients with MS and contribute to progression of disease. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:236 / 241
页数:6
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