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Structural neuroimaging correlates of allelic variation of the BDNF val66met polymorphism.

  • Natalie J. Forde
  • , Lisa Ronan
  • , John Suckling
  • , Cathy Scanlon
  • , Simon Neary
  • , Laurena Holleran
  • , Alexander Leemans
  • , Roger Tait
  • , Catarina Rua
  • , Paul C. Fletcher
  • , Ben Jeurissen
  • , Chris M. Dodds
  • , Sam R. Miller
  • , Edward T. Bullmore
  • , Colm Mcdonald
  • , Pradeep J. Nathan
  • , Dara Cannon
  • University of Galway
  • University of Cambridge
  • Behavioural and Clinical Neuroscience Institute
  • Cambridge and Peterborough NHS Foundation Trust
  • University Medical Centre Utrecht
  • University of Antwerp
  • GlaxoSmithKline plc.
  • Monash University

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

37 Citations (Scopus)

Abstract

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. 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. 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. 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 Alzheimers disease and depression.
Original languageEnglish (Ireland)
Pages (from-to)280-289
Number of pages10
JournalNeuroimage
Volume90
DOIs
Publication statusPublished - 1 Apr 2014

Keywords

  • BDNF
  • Diffusion
  • Intrinsic curvature
  • MRI
  • Structural
  • Val66met

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