Serum BDNF levels in unaffected first-degree relatives of patients with bipolar disorder

被引:6
作者
Nery, Fabiano G. [1 ,2 ]
Gigante, Alexandre D. [1 ]
Amaral, Jose A. [1 ]
Fernandes, Francy B. [1 ]
Berutti, Mariangeles [1 ]
Almeida, Karla M. [1 ]
Stertz, Laura [3 ]
Bristot, Giovana [3 ,4 ]
Kapczinski, Flavio [3 ,5 ]
Lafer, Beny [1 ]
机构
[1] Univ Sao Paulo, Fac Med, Dept Psiquiatria, Programa Transtorno Bipolar, Sao Paulo, SP, Brazil
[2] Univ Cincinnati, Coll Med, Dept Psychiat & Behav Neurosci, Cincinnati, OH USA
[3] HCPA, INCT TM, Ctr Pesquisas Expt, Lab Psiquiatria Mol, Porto Alegre, RS, Brazil
[4] Univ Fed Rio Grande do Sul, Programa Posgrad Ciencias Biol Bioquim, Porto Alegre, RS, Brazil
[5] Univ Fed Rio Grande do Sul, Programa Posgrad Med, Psiquiatria, Porto Alegre, RS, Brazil
基金
巴西圣保罗研究基金会;
关键词
Bipolar disorder; endophenotypes; cerebral cortex; hippocampus; brain-derived neurotrophic factor; NEUROTROPHIC FACTOR LEVELS; UNIPOLAR DEPRESSION; INFLAMMATORY MARKERS; BRAIN; PLATELETS; EPISODES; PLASMA; TWINS;
D O I
10.1590/1516-4446-2015-1801
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: Unaffected relatives of bipolar disorder (BD) patients have been investigated for the identification of endophenotypes in an attempt to further elucidate the pathophysiology of the disease. Brain-derived neurotrophic factor (BDNF) is considered to be implicated in the pathophysiology of BD, but its role as an endophenotype has been poorly studied. We investigated abnormal serum BDNF levels in BD patients, in their unaffected relatives, and in healthy controls. Methods: BDNF levels were obtained from 25 DSM-IV bipolar I disorder patients, 23 unaffected relatives, and 27 healthy controls. All BD patients were in remission. The unaffected subjects were first-degree relatives of the proband who had no lifetime DSM-IV diagnosis of axis I disorder. BDNF serum levels were determined by sandwich ELISA using monoclonal BDNF-specific antibodies. Results: There were no statistical differences in BDNF levels among BD patients, relatives, and healthy controls. Conclusion: Serum BDNF levels may not indicate high genetic risk for BD, possibly acting as state markers rather than trait markers of the disease.
引用
收藏
页码:197 / 200
页数:4
相关论文
共 32 条
[1]   THE GENETICS OF BIPOLAR DISORDER [J].
Barnett, J. H. ;
Smoller, J. W. .
NEUROSCIENCE, 2009, 164 (01) :331-343
[2]   Serum brain-derived neurotrophic factor is decreased in bipolar disorder during depressive and manic episodes [J].
Cunha, Angelo B. M. ;
Frey, Benicio N. ;
Andreazza, Ana C. ;
Goi, Julia D. ;
Rosa, Adriane R. ;
Goncalves, Carlos A. ;
Santin, Aida ;
Kapczinski, Flavio .
NEUROSCIENCE LETTERS, 2006, 398 (03) :215-219
[3]   A neurotrophic model for stress-related mood disorders [J].
Duman, Ronald S. ;
Monteggia, Lisa M. .
BIOLOGICAL PSYCHIATRY, 2006, 59 (12) :1116-1127
[4]   Brain-derived neurotrophic factor as a state-marker of mood episodes in bipolar disorders: A systematic review and meta-regression analysis [J].
Fernandes, Brisa Simoes ;
Gama, Clarissa Severino ;
Cereser, Keila Maria ;
Yatham, Lakshmi N. ;
Fries, Gabriel Rodrigo ;
Colpo, Gabriela ;
de Lucena, David ;
Kunz, Mauricio ;
Gomes, Fabiano Alves ;
Kapczinski, Flavio .
JOURNAL OF PSYCHIATRIC RESEARCH, 2011, 45 (08) :995-1004
[5]  
First M, 2002, STRUCTURED CLIN INTE
[6]   Toward Clinically Applicable Biomarkers in Bipolar Disorder: Focus on BDNF, Inflammatory Markers, and Endothelial Function [J].
Goldstein, Benjamin I. ;
Young, L. Trevor .
CURRENT PSYCHIATRY REPORTS, 2013, 15 (12)
[7]   The endophenotype concept in psychiatry: Etymology and strategic intentions [J].
Gottesman, II ;
Gould, TD .
AMERICAN JOURNAL OF PSYCHIATRY, 2003, 160 (04) :636-645
[8]  
Hamilton M., 1976, ECDEU Assessment manual for psychopharmacology, P179
[9]   Toward constructing an endophenotype strategy for bipolar disorders [J].
Hasler, Gregor ;
Drevets, Wayne C. ;
Gould, Todd D. ;
Gottesman, Irving I. ;
Manji, Husseini K. .
BIOLOGICAL PSYCHIATRY, 2006, 60 (02) :93-105
[10]   Neurotrophins: Roles in neuronal development and function [J].
Huang, EJ ;
Reichardt, LF .
ANNUAL REVIEW OF NEUROSCIENCE, 2001, 24 :677-736