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Effects of ankyrin 3 gene risk variants on brain structures in patients with bipolar disorder and healthy subjects
Author(s) -
Ota Miho,
Hori Hiroaki,
Sato Noriko,
Yoshida Fuyuko,
Hattori Kotaro,
Teraishi Toshiya,
Kunugi Hiroshi
Publication year - 2016
Publication title -
psychiatry and clinical neurosciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.609
H-Index - 74
eISSN - 1440-1819
pISSN - 1323-1316
DOI - 10.1111/pcn.12431
Subject(s) - bipolar disorder , ankyrin repeat , ankyrin , neuroscience , psychology , medicine , psychiatry , gene , genetics , biology , cognition
Aim The intronic single‐nucleotide polymorphism rs10994336 of the ankyrin 3 gene ( ANK3 ) is one of the genome‐wide supported risk variants for bipolar disorder ( BD ), and the T ‐allele of rs10761482 is also reported to have relevance to BD . We investigated the effect of ANK3 rs10761482 genetic variation on brain structure. Methods Subjects were 43 BD patients and 229 healthy volunteers. We evaluated the effects of ANK3 rs10761482 genetic variation on diagnosis, and of the genotype‐by‐diagnosis interaction on the brain structure and the degree of age‐related brain atrophy on magnetic resonance imaging data evaluated by voxel‐based morphometry. Results BD patients showed significantly lower fractional anisotropy value in the bilateral parietal regions, left fronto‐occipital fasciculus, and corpus callosum, compared to healthy subjects. Further, we found considerable decreases of fractional anisotropy in the forceps minor in non‐ T ‐allele BD patients compared with the T ‐carrier patient group. We also found significant lessening of age‐related brain atrophy in the T ‐allele carrier groups compared with the non‐ T ‐allele carrier groups in the area around the cerebrospinal space, cingulate cortices, and cerebellum. Conclusion Our results suggest the influence of the ANK3 on age‐related brain atrophy. The ankyrin 3 genotype may be associated with pathogenesis of age‐related neurodegeneration, and, in part, of BD .