Association of increased genotypes risk for bipolar disorder with brain white matter integrity investigated with tract-based spatial statistics

被引:9
作者
Squarcina, L. [1 ]
Houenou, J. [2 ,3 ]
Altamura, A. C. [4 ]
Soares, J. [1 ,5 ]
Brambilla, P. [1 ,4 ,6 ]
机构
[1] IRCCS Medea Sci Inst, Bosisio Parini, Italy
[2] Univ Paris Est, Hop Univ Mondor, Fac Med, APHP, Creteil, France
[3] UNIACT, Psychiat Team, Neurospin Neuroimaging Platform, CEA Saclay, Gif Sur Yvette, France
[4] Univ Milan, Dept Neurosci & Mental Hlth, Fdn IRCCS Ca Granda Osped Maggiore Policli, Milan, Italy
[5] Univ Texas Hlth Sci Ctr, Dept Psychiat & Behav Sci, Houston, TX USA
[6] Univ Texas Houston, Dept Psychiat & Behav Neurosci, Houston, TX USA
关键词
Bipolar disorder; Polymorphisms; Diffusion tensor imaging; Tract-based spatial statistics; SEROTONIN TRANSPORTER GENE; POLYMORPHISM; MICROSTRUCTURE; SCHIZOPHRENIA; PSYCHOSIS; PROMOTER; ZNF804A; DEPRESSION; VARIANTS; EFFICACY;
D O I
10.1016/j.jad.2017.06.031
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Diffusion tensor imaging (DTI) studies, which allow the in-vivo investigation of brain tissue integrity, have shown that bipolar disorder (BD) patients present signs of white matter dysconnectivity. In parallel, genome-wide association studies (GWAS) identified several risk genetic variants for BD. I Methods: In this mini-review, we summarized DTI studies coupling tract-based spatial statistics (TBSS), a reliable technique exploring white matter axon bundles, and genetics in BD. We performed a bibliographic search on PUBMED, using the search terms "TBSS", "genetics", "genome", "genes", "polymorphism", "bipolar disorder". Results: Ten studies met these inclusion criteria. ANK3 and ZNF804A polymorphisms have shown the most consistent results, with the risk alleles showing abnormal white matter integrity in patients with BD. Limitations: Current studies are limited by the investigation of single SNPs in small and chronically treated samples. Conclusions: Most considered TBSS-DTI studies found associations between decreased white matter integrity and genetic risk variants. These results suggest an involvement of dysmyelination in the pathogenesis of BD. The combination of TBSS with genotyping can be powerful to unveil the role of white matter in BD, in conjunction with risk genes. Future DTI studies should combine TBSS and GWAS in large populations of drug-free or minimally treated patients with BD at the onset of the disease.
引用
收藏
页码:312 / 317
页数:6
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