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Brain-derived Neurotrophic Factor (BDNF) and gray matter volume in bipolar disorder
被引:22
|作者:
Poletti, S.
[1
,2
]
Aggio, V.
[1
]
Hoogenboezem, T. A.
[2
]
Ambree, O.
[3
]
de Wit, H.
[2
]
Wijkhuijs, A. J. M.
[2
]
Locatelli, C.
[1
]
Colombo, C.
[1
]
Arolt, V.
[3
]
Drexhage, H. A.
[2
]
Benedetti, F.
[1
,2
]
机构:
[1] Univ Vita Salute San Raffaele, Inst Sci, CERMAC, Dept Clin Neurosci, Milan, Italy
[2] Erasmus Univ, Med Ctr, Dept Immunol, Rotterdam, Netherlands
[3] Univ Munster, Dept Psychiat, Munster, Germany
基金:
欧盟第七框架计划;
关键词:
BDNF;
Gray matter;
Neuroinflammation;
Bipolar disorder;
VAL66MET POLYMORPHISM;
OXIDATIVE STRESS;
EXPRESSION;
DEPRESSION;
NEUROPROGRESSION;
SCHIZOPHRENIA;
REGISTRATION;
INFLAMMATION;
HIPPOCAMPUS;
PLATELETS;
D O I:
10.1016/j.eurpsy.2016.06.008
中图分类号:
R749 [精神病学];
学科分类号:
100205 ;
摘要:
Introduction: Bipolar Disorder (BD) is a severe psychiatric condition characterized by grey matter (GM) volumes reduction. Neurotrophic factors have been suggested to play a role in the neuroprogressive changes during the illness course. In particular peripheral brain-derived neurotrophic factor (BDNF) has been proposed as a potential biomarker related to disease activity and neuroprogression in BD. The aim of our study was to investigate if serum levels of BDNF are associated with GM volumes in BD patients and healthy controls (HC). Methods: We studied 36 inpatients affected by a major depressive episode in course of BD type I and 17 HC. Analysis of variance was performed to investigate the effect of diagnosis on GM volumes in the whole brain. Threshold for significance was P < 0.05, Family Wise Error (FWE) corrected for multiple comparisons. All the analyses were controlled for the effect of nuisance covariates known to influence GM volumes, such as age, gender and lithium treatment. Results: BD patients showed significantly higher serum BDNF levels compared with HC. Reduced GM volumes in BD patients compared to HC were observed in several brain areas, encompassing the caudate head, superior temporal gyrus, insula, fusiform gyrus, parahippocampal gyrus, and anterior cingulate cortex. The interaction analysis between BDNF levels and diagnosis showed a significant effect in the middle frontal gyrus. HC reported higher BDNF levels associated with higher GM volumes, whereas no association between BDNF and GM volumes was observed in BD. Discussion: Our study seems to suggest that although the production of BDNF is increased in BD possibly to prevent and repair neural damage, its effects could be hampered by underlying neuroinfiammatory processes interfering with the neurodevelopmental role of BDNF. (C) 2016 Elsevier Masson SAS. All rights reserved.
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页码:33 / 37
页数:5
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