The relationship between genetic risk variants with brain structure and function in bipolar disorder: A systematic review of genetic-neuroimaging studies

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt


  • Licia P Pereira
  • Cristiano A Köhler
  • Rafael T de Sousa
  • Marco Solmi
  • Bárbara P de Freitas
  • Michele Fornaro
  • Rodrigo Machado-Vieira
  • Miskowiak, Kamilla
  • Eduard Vieta
  • Nicola Veronese
  • Brendon Stubbs
  • André F Carvalho

Genetic-neuroimaging paradigms could provide insights regarding the pathophysiology of bipolar disorder (BD). Nevertheless, findings have been inconsistent across studies. A systematic review of gene-imaging studies involving individuals with BD was conducted across electronic major databases from inception until January 9th, 2017. Forty-four studies met eligibility criteria (N=2122 BD participants). Twenty-six gene variants were investigated across candidate gene studies and 4 studies used a genome-wide association approach. Replicated evidence (i.e. in >2 studies) suggests that individuals with BD carrying the BDNF Val66Met risk allele could have reduced hippocampal volumes compared to non-carriers. This review underscores the potential of gene-neuroimaging paradigms to provide mechanistic insights for BD. However, this systematic review found a single replicated finding. Suggestions to improve the reproducibility of this emerging field are provided, including the adoption of a trans-diagnostic approach.

TidsskriftNeuroscience & Biobehavioral Reviews
Sider (fra-til)87-109
StatusUdgivet - aug. 2017

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