• Sinead Kelly, Derek W Morris, Omar Mothersill, Emma Jane Rose, Ciara Fahey, Carol O'Brien, Erik O'Hanlon, Michael Gill, Aiden P Corvin, and Gary Donohoe.
• Neuropsychiatric Genetics Group, Department of Psychiatry, Trinity Centre for health Sciences, St. James's Hospital, Dublin 8, Ireland; Trinity College Institute for Neuroscience, Trinity College Dublin, Ireland.
• Neurosci. Lett. 2014 Jun 27; 574: 6-10.

AbstractA single nucleotide polymorphism (SNP rs1625579) within the micro-RNA 137 (MIR137) gene recently achieved strong genome-wide association with schizophrenia (SZ). However, the mechanisms by which SZ risk may be mediated by this variant are unknown. As miRNAs have the potential to influence oligodendrocyte development, we investigated whether this SNP was associated with variability in white matter (WM) microstructure. Diffusion tensor imaging (DTI) was conducted on 123 healthy participants genotyped for rs1625579. The analysis consisted of whole-brain tract-based spatial statistics and atlas-based tractography analysis of six major WM tracts known to be affected in SZ - the inferior longitudinal fasciculus, the uncinate fasciculus, the inferior fronto-occipital fasciculus, the anterior thalamic radiation, the cingulum bundle and the corpus callosum. No significant differences in either whole-brain fractional anisotropy or mean diffusivity between MIR137 genotype groups were observed (p>0.05). Similarly, atlas-based tractography of particular tracts implicated in SZ failed to reveal any significant differences between MIR137 genotype groups on measures of WM connectivity (p>0.05). In the absence of WM effects comparable to those reported for other SZ associated genes, these data suggest that MIR137 alone may not confer variability in these WM measures and therefore may not act in isolation for any effects that the variant may have on WM microstructure in SZ samples. Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.

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