Structural neuroimaging correlates of allelic variation of the BDNF val66met polymorphism

被引:34
作者
Forde, Natalie J. [1 ]
Ronan, Lisa [2 ]
Suckling, John [2 ,4 ,7 ]
Scanlon, Cathy [1 ]
Neary, Simon [1 ]
Holleran, Laurena [1 ]
Leemans, Alexander [3 ]
Tait, Roger [4 ]
Rua, Catarina [2 ]
Fletcher, Paul C. [2 ,4 ,7 ]
Jeurissen, Ben [5 ]
Dodds, Chris M.
Miller, Sam R.
Bullmore, Edward T. [2 ,4 ,7 ]
McDonald, Colm [1 ]
Nathan, Pradeep J. [2 ,6 ]
Cannon, Dara M. [1 ]
机构
[1] Natl Univ Ireland Galway, Coll Med Nursing & Hlth Sci, Sch Med, Clin Neuroimaging Lab, Galway, Ireland
[2] Univ Cambridge, Dept Psychiat, Brain Mapping Unit, Cambridge, England
[3] Univ Med Ctr Utrecht, Image Sci Inst, Utrecht, Netherlands
[4] Univ Cambridge, Dept Expt Psychol, Behav & Clin Neurosci Inst, Cambridge CB2 3EB, England
[5] Univ Antwerp, iMinds Vis Lab, Antwerp, Belgium
[6] Monash Univ, Sch Psychol & Psychiat, Clayton, Vic 3800, Australia
[7] Cambridge & Peterborough NHS Fdn Trust, Cambridge, England
关键词
BDNF; Structural; Diffusion; MRI; Val66met; Intrinsic curvature; ACTIVITY-DEPENDENT SECRETION; SURFACE-BASED ANALYSIS; NEUROTROPHIC FACTOR; WHITE-MATTER; HIPPOCAMPAL VOLUME; CORTICAL SURFACE; VAL(66)MET POLYMORPHISM; SPATIAL STATISTICS; ALZHEIMERS-DISEASE; COORDINATE SYSTEM;
D O I
10.1016/j.neuroimage.2013.12.050
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Background: The brain-derived neurotrophic factor (BDNF) val66met polymorphism is associated with altered activity dependent secretion of BDNF and a variable influence on brain morphology and cognition. Although a met-dose effect is generally assumed, to date the paucity of met-homozygotes have limited our understanding of the role of the met-allele on brain structure. Methods: To investigate this phenomenon, we recruited sixty normal healthy subjects, twenty in each genotypic group (val/val, val/met and met/met). Global and local morphology were assessed using voxel based morphometry and surface reconstruction methods. White matter organisation was also investigated using tract-based spatial statistics and constrained spherical deconvolution tractography. Results: Morphological analysis revealed an "inverted-U" shaped profile of cortical changes, with val/met heterozygotes most different relative to the two homozygous groups. These results were evident at a global and local level as well as in tractography analysis of white matter fibre bundles. Conclusion: In contrast to our expectations, we found no evidence of a linear met-dose effect on brain structure, rather our results support the view that the heterozygotic BDNF val66met genotype is associated with cortical morphology that is more distinct from the BDNF val66met homozygotes. These results may prove significant in furthering our understanding of the role of the BDNF met-allele in disorders such as Alzheimer's disease and depression. (C) 2014 The Authors. Published by Elsevier Inc All rights reserved.
引用
收藏
页码:280 / 289
页数:10
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