Peripheral biomarkers and illness activity in bipolar disorder

被引:189
作者
Kapczinski, Flavio [1 ,2 ]
Dal-Pizzol, Felipe [3 ]
Teixeira, Antonio Lucio [4 ]
Magalhaes, Pedro V. S. [2 ]
Kauer-Sant'Anna, Marcia [2 ]
Klamt, Fabio [5 ]
Moreira, Jose Claudio F. [5 ]
de Bittencourt Pasquali, Mateus Augusto [5 ]
Fries, Gabriel Rodrigo [2 ]
Quevedo, Joao [6 ]
Gama, Clarissa Severino [2 ]
Post, Robert [7 ]
机构
[1] Univ Fed Rio Grande do Sul, Lab Psiquiatria Mol, HCPA, Bipolar Disorders Program, BR-90035003 Porto Alegre, RS, Brazil
[2] Univ Fed Rio Grande do Sul, INCT Translat Med, HCPA, BR-90035003 Porto Alegre, RS, Brazil
[3] Univ Extremo Catarinense, Unidade Acad Ciencias Saude, Lab Fisiopatol Expt, Criciuma, SC, Brazil
[4] Univ Fed Minas Gerais, Inst Biol Sci, Lab Immunopharmacol, Belo Horizonte, MG, Brazil
[5] Univ Fed Rio Grande do Sul, Dept Bioquim, Ctr Estudos Estresse Oxidat, BR-90035003 Porto Alegre, RS, Brazil
[6] Univ Extremo Catarinense, Lab Neurociencias, Programa Posgrad Ciencias Saude, Criciuma, Brazil
[7] Bipolar Collaborat Network, Bethesda, MD USA
关键词
Bipolar disorder; Biomarkers; Allostatic load; Oxidative stress; Inflammation; Neurotrophins; Sepsis; Illness activity; CORTICOTROPIN-RELEASING HORMONE; NEUROTROPHIC FACTOR; DEPRESSIVE EPISODES; OXIDATIVE STRESS; ALLOSTATIC LOAD; MOOD DISORDERS; MEDICAL BURDEN; SERUM-LEVELS; FOLLOW-UP; PATHOPHYSIOLOGY;
D O I
10.1016/j.jpsychires.2010.05.015
中图分类号
R749 [精神病学];
学科分类号
100204 [神经病学];
摘要
Recent evidence suggests that peripheral markers related to oxidative stress, inflammation and neurotrophins may be altered during mood episodes in bipolar disorder. These can be seen as proxies of peripheral toxicity or markers of illness activity. Here we report an en bloc assessment of a set of previously described biomarkers in different mood states (n = 60) as well as in healthy subjects (n = 80). To make the point that these are ominous changes, we obtained the same measures from a group of septic patients (n = 15) as a "positive" control group. In this sample, we measured serum levels of brain derived neurotrophic factor, neurotrophin 3, tumor necrosis factor a., interleukin 6, interleukin 10, total reactive antioxidant potential, thiobarbituric acid reactive substances and protein carbonyl content. Several of the markers discriminated between the bipolar and control groups, especially when patients were in acute episodes. In some cases, toxicity was as high in bipolar disorder as that seen in patients with sepsis. We believe these findings highlight the potential of using biomarkers to assess illness activity in bipolar disorder. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:156 / 161
页数:6
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