TY - JOUR T1 - Patterns of individual variation in visual pathway structure and function in the sighted and blind JF - bioRxiv DO - 10.1101/065441 SP - 065441 AU - Geoffrey K. Aguirre AU - Ritobrato Datta AU - Noah C. Benson AU - Sashank Prasad AU - Samuel G. Jacobson AU - Artur V. Cideciyan AU - Holly Bridge AU - Kate E. Watkins AU - Omar H. Butt AU - Alexsandra S. Dain AU - Lauren Brandes AU - Efstathios D. Gennatas Y1 - 2016/01/01 UR - http://biorxiv.org/content/early/2016/07/23/065441.abstract N2 - Many structural and functional brain alterations accompany blindness. In normally sighted people, there is correlated individual variation in some visual pathway structures. Here we examined if the changes in brain anatomy produced by blindness alter this pattern of variation. We derived eight measures of central visual pathway anatomy from an MPRAGE image of the brain from 59 sighted and 53 blind people. These measures showed highly significant differences in mean size between the sighted and blind cohorts. When we examined the measurements across individuals within each group, we found three clusters of correlated variation, with V1 surface area and pericalcarine volume linked, and independent of the thickness of V1 cortex. These two clusters were in turn relatively independent of the volumes of the optic chiasm and lateral geniculate nucleus. This same pattern of variation in visual pathway anatomy was found in the sighted and the blind. Anatomical changes within these clusters were graded by the duration of blindness, with those subjects with a post-natal onset of blindness having alterations in brain anatomy that were intermediate to those seen in the sighted and congenitally blind. Many of the blind and sighted subjects also contributed BOLD fMRI measures of cross-modal responses within visual cortex, and a diffusion tensor imaging measure of fractional anisotropy within the optic radiations and the splenium of the corpus callosum. We again found group differences between the blind and sighted in these measures. The previously identified clusters of anatomical variation were also found to be differentially related to these additional measures: across subjects, V1 cortical thickness was related to cross-modal activation, and the volume of the optic chiasm and lateral geniculate was related to fractional anisotropy in the visual pathway. Our findings show that several of the structural and functional effects of blindness may be reduced to a smaller set of dimensions. It also seems that the changes in the brain that accompany blindness are on a continuum with normal variation found in the sighted. ER -