Executive dysfunction in euthymic bipolar disorder patients and its association with plasma biomarkers

被引:89
作者
Barbosa, Izabela Guimaraes [1 ,2 ,3 ,4 ]
Rocha, Natalia Pessoa [2 ,3 ]
Huguet, Rodrigo Barreto [3 ]
Ferreira, Rodrigo A. [2 ,3 ]
Salgado, Joao Vinicius [2 ]
Carvalho, Livia A. [4 ]
Pariante, Carmine M. [1 ]
Teixeira, Antonio Lucio [2 ,3 ]
机构
[1] Kings Coll London, Sect & Lab Stress Psychiat & Immunol SPI Lab, Div Psychol Med, Inst Psychiat, London SE5 9NU, England
[2] Univ Fed Minas Gerais, Programa Posgrad Neurociencias, Belo Horizonte, MG, Brazil
[3] Univ Fed Minas Gerais, Inst Ciencias Biol, Lab Imunofarmacol, Belo Horizonte, MG, Brazil
[4] Roehampton Univ, Psychoneuroimmunol Translat Lab, London, England
关键词
Bipolar disorder; Executive function; Frontal assessment battery; BDNF; Inflammatory parameters; NEUROTROPHIC FACTOR; VAL66MET POLYMORPHISM; COGNITION; BDNF;
D O I
10.1016/j.jad.2011.12.034
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Despite the old Kraepelinean concept that bipolar disorder (BD) does not evolve with cognitive decline, the presence of cognitive impairment, especially executive dysfunction has been recognized in BD patients. Brain-derived neurotrophic factor (BDNF) and pro-inflammatory molecules are important contributors to the pathophysiology of BD, and imbalance in peripheral levels of these molecules may be implicated in the cognitive decline observed in BD patients. We aimed to investigate the executive performance of BD type I euthymic patients and its relation with the plasma levels of BDNF. TNF-alpha and its related soluble receptors (sTNFR1 and sTNFR2). Methods: We evaluated executive functioning through the Frontal Assessment Battery (FAB). Plasma levels of BDNF, TNF-alpha, sTNFR1 and sTNFR2 were measured using enzyme-linked immunosorbent assay (ELISA) in 25 euthymic type I BD patients and 25 age and gender matched healthy controls. Results: BD patients had an impairment in executive functioning (p < 0.006), particularly sensitivity of interference (p = 0.02), inhibitory control (p = 0.02), and increased BDNF plasma levels (p = 0.001) in comparison with controls. Plasma levels of TNF-alpha were correlated with inhibitory control in BD patients (p = 0.50, p = 0.02) while motor programming was negatively correlated with sTNFR2 plasma levels (p = -0.47, p = 0.02) in controls. Executive function correlated with age and MMSE, but not with BDNF, neither was influenced by psychiatric and clinical comorbidities nor medications in use. Conclusion: BDNF is altered in BD but do not correlate with executive functioning. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:151 / 155
页数:5
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