Peripheral brain-derived neurotrophic factor in schizophrenia and the role of antipsychotics: meta-analysis and implications

被引:203
作者
Fernandes, B. S. [1 ,2 ]
Steiner, J. [3 ]
Berk, M. [4 ,5 ,6 ]
Molendijk, M. L. [7 ,8 ]
Gonzalez-Pinto, A. [9 ]
Turck, C. W. [10 ]
Nardin, P. [1 ,2 ]
Goncalves, C-A [1 ,2 ]
机构
[1] Univ Fed Rio Grande do Sul, Dept Biochem, Lab Calcium Binding Prot Cent Nervous Syst, Ramiro Barcelos St, BR-2600 Porto Alegre, RS, Brazil
[2] Univ Fed Rio Grande do Sul, Postgrad Program Biol Sci Biochem, BR-2600 Porto Alegre, RS, Brazil
[3] Univ Magdeburg, Dept Psychiat, D-39106 Magdeburg, Germany
[4] Deakin Univ, Sch Med, Barwon Hlth, IMPACT Strateg Res Ctr, Geelong, Vic 3217, Australia
[5] Univ Melbourne, Florey Inst Neurosci & Mental Hlth, Dept Psychiat, Parkville, Vic 3052, Australia
[6] Univ Melbourne, Orygen Res Ctr, Parkville, Vic 3052, Australia
[7] Leiden Univ, Inst Psychol, Dept Clin Psychol, Leiden, Netherlands
[8] Leiden Univ, Med Ctr, Leiden Inst Brain & Cognit, Leiden, Netherlands
[9] Univ Basque Country, Dept Neurosci, Biomed Res Ctr Mental HealthNet CIBERSAM, Vitoria, Spain
[10] Max Planck Inst Psychiat, D-80804 Munich, Germany
基金
澳大利亚国家健康与医学研究理事会;
关键词
FACTOR SERUM CONCENTRATIONS; FACTOR BDNF LEVELS; BIPOLAR DISORDER; PLASMA-LEVELS; CATECHOLAMINE METABOLITES; PUBLICATION BIAS; HUMAN PLATELETS; DECREASED BDNF; 1ST-EPISODE SCHIZOPHRENIA; ELECTROCONVULSIVE-THERAPY;
D O I
10.1038/mp.2014.117
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
It has been postulated that schizophrenia (SZ) is related to a lower expression of brain-derived neurotrophic factor (BDNF). In the past few years, an increasing number of divergent clinical studies assessing BDNF in serum and plasma have been published. It is now possible to verify the relationship between BDNF levels and severity of symptoms in SZ as well as the effects of antipsychotic drugs on BDNF using meta-analysis. The aims of this study were to verify if peripheral BDNF is decreased in SZ, whether its levels are correlated with positive and negative symptomatology and if BDNF levels change after antipsychotic treatment. This report consists of two distinct meta-analyses of peripheral BDNF in SZ including a total of 41 studies and more than 7000 participants: (1) peripheral BDNF levels in serum and plasma were moderately reduced in SZ compared with controls. Notably, this decrease was accentuated with the disease duration. However, the extent of peripheral BDNF level decrease did not correlate with the severity of positive and negative symptoms. (2) In plasma, but not serum, peripheral BDNF levels are consistently increased after antipsychotic treatment irrespective of the patient's response to medication. In conclusion, there is compelling evidence that there are decreased levels of peripheral BDNF in SZ, in parallel to previously described reduced cerebral BDNF expression. It remains unclear whether these systemic changes are causally related to the development of SZ or if they are merely a pathologic epiphenomenon.
引用
收藏
页码:1108 / 1119
页数:12
相关论文
共 101 条
[1]   Changes in Serum Levels of Brain Derived Neurotrophic Factor and Nerve Growth Factor-Beta in Schizophrenic Patients Before and After Treatment [J].
Ajami, A. ;
Hosseini, S. H. ;
Taghipour, M. ;
Khalilian, A. .
SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 2014, 80 (01) :36-42
[2]   CORRELATIONAL STUDIES OF THE SCALE FOR THE ASSESSMENT OF NEGATIVE SYMPTOMS AND THE SCALE FOR THE ASSESSMENT OF POSITIVE SYMPTOMS - AN OVERVIEW AND UPDATE [J].
ANDREASEN, NC ;
ARNDT, S ;
MILLER, D ;
FLAUM, M ;
NOPOULOS, P .
PSYCHOPATHOLOGY, 1995, 28 (01) :7-17
[3]   Neurotrophic factors and CNS disorders:: findings in rodent models of depression and schizophrenia [J].
Angelucci, F ;
Mathé, AA ;
Aloe, L .
NGF AND RELATED MOLECULES IN HEALTH AND DISEASE, 2004, 146 :151-165
[4]  
[Anonymous], 2019, DIAGN STAT MAN MENT
[5]  
[Anonymous], NEWCASTLE OTTAWA SCA
[6]   Neuroplasticity signaling pathways linked to the pathophysiology of schizophrenia [J].
Balu, Darrick T. ;
Coyle, Joseph T. .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2011, 35 (03) :848-870
[7]   Pathways underlying neuroprogression in bipolar disorder: Focus on inflammation, oxidative stress and neurotrophic factors [J].
Berk, M. ;
Kapczinski, F. ;
Andreazza, A. C. ;
Dean, O. M. ;
Giorlando, F. ;
Maes, M. ;
Yuecel, M. ;
Gama, C. S. ;
Dodd, S. ;
Dean, B. ;
Magalhaes, P. V. S. ;
Amminger, P. ;
McGorry, P. ;
Malhi, G. S. .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 2011, 35 (03) :804-817
[8]   Quantifying, displaying and accounting for heterogeneity in the meta-analysis of RCTs using standard and generalised Q statistics [J].
Bowden, Jack ;
Tierney, Jayne F. ;
Copas, Andrew J. ;
Burdett, Sarah .
BMC MEDICAL RESEARCH METHODOLOGY, 2011, 11
[9]   Brain derived neurotropic factor in first-episode psychosis [J].
Buckley, Peter F. ;
Pillai, Anilkumar ;
Evans, Denise ;
Stirewalt, Edna ;
Mahadik, Sahebarao .
SCHIZOPHRENIA RESEARCH, 2007, 91 (1-3) :1-5
[10]   Low serum truncated-BDNF isoform correlates with higher cognitive impairment in schizophrenia [J].
Carlino, Davide ;
Leone, Emiliano ;
Di Cola, Francesco ;
Baj, Gabriele ;
Marin, Raffaella ;
Dinelli, Giacomo ;
Tongiorgi, Enrico ;
De Vanna, Maurizio .
JOURNAL OF PSYCHIATRIC RESEARCH, 2011, 45 (02) :273-279