TY - JOUR
T1 - Genetic influences on brain asymmetry
T2 - A DTI study of 374 twins and siblings
AU - Jahanshad, Neda
AU - Lee, Agatha D.
AU - Barysheva, Marina
AU - McMahon, Katie L.
AU - de Zubicaray, Greig I.
AU - Martin, Nicholas G.
AU - Wright, Margaret J.
AU - Toga, Arthur W.
AU - Thompson, Paul M.
N1 - Funding Information:
This study was supported by grant number RO1 HD050735 from the National Institute of Child Health and Human Development, USA , T15 LM07356 from the NIH/National Library of Medicine , and Project Grant 496682 from the National Health and Medical Research Council, Australia . Additional support for algorithm development was provided by the NIA , NIBIB , and the National Center for Research Resources ( EB008432 , EB008281 , EB007813 , AG016570 , and RR013642 to PT). Zygosity typing was supported by the Australian Research Council ( A7960034 , A79906588 , A79801419 , and DP0212016 ). We are extremely grateful to the twins for their participation, to the radiographer, Matt Meredith, Centre for Magnetic Resonance, University of Queensland, for image acquisition, and research nurses, Marlene Grace and Ann Eldridge, Queensland Institute of Medical Research, for twin recruitment.
PY - 2010/8
Y1 - 2010/8
N2 - Brain asymmetry, or the structural and functional specialization of each brain hemisphere, has fascinated neuroscientists for over a century. Even so, genetic and environmental factors that influence brain asymmetry are largely unknown. Diffusion tensor imaging (DTI) now allows asymmetry to be studied at a microscopic scale by examining differences in fiber characteristics across hemispheres rather than differences in structure shapes and volumes. Here we analyzed 4. Tesla DTI scans from 374 healthy adults, including 60 monozygotic twin pairs, 45 same-sex dizygotic pairs, and 164 mixed-sex DZ twins and their siblings; mean age: 24.4 years ± 1.9 SD). All DTI scans were nonlinearly aligned to a geometrically-symmetric, population-based image template. We computed voxel-wise maps of significant asymmetries (left/right differences) for common diffusion measures that reflect fiber integrity (fractional and geodesic anisotropy; FA, GA and mean diffusivity, MD). In quantitative genetic models computed from all same-sex twin pairs (N=210 subjects), genetic factors accounted for 33% of the variance in asymmetry for the inferior fronto-occipital fasciculus, 37% for the anterior thalamic radiation, and 20% for the forceps major and uncinate fasciculus (all L > R). Shared environmental factors accounted for around 15% of the variance in asymmetry for the cortico-spinal tract (R > L) and about 10% for the forceps minor (L > R). Sex differences in asymmetry (men > women) were significant, and were greatest in regions with prominent FA asymmetries. These maps identify heritable DTI-derived features, and may empower genome-wide searches for genetic polymorphisms that influence brain asymmetry.
AB - Brain asymmetry, or the structural and functional specialization of each brain hemisphere, has fascinated neuroscientists for over a century. Even so, genetic and environmental factors that influence brain asymmetry are largely unknown. Diffusion tensor imaging (DTI) now allows asymmetry to be studied at a microscopic scale by examining differences in fiber characteristics across hemispheres rather than differences in structure shapes and volumes. Here we analyzed 4. Tesla DTI scans from 374 healthy adults, including 60 monozygotic twin pairs, 45 same-sex dizygotic pairs, and 164 mixed-sex DZ twins and their siblings; mean age: 24.4 years ± 1.9 SD). All DTI scans were nonlinearly aligned to a geometrically-symmetric, population-based image template. We computed voxel-wise maps of significant asymmetries (left/right differences) for common diffusion measures that reflect fiber integrity (fractional and geodesic anisotropy; FA, GA and mean diffusivity, MD). In quantitative genetic models computed from all same-sex twin pairs (N=210 subjects), genetic factors accounted for 33% of the variance in asymmetry for the inferior fronto-occipital fasciculus, 37% for the anterior thalamic radiation, and 20% for the forceps major and uncinate fasciculus (all L > R). Shared environmental factors accounted for around 15% of the variance in asymmetry for the cortico-spinal tract (R > L) and about 10% for the forceps minor (L > R). Sex differences in asymmetry (men > women) were significant, and were greatest in regions with prominent FA asymmetries. These maps identify heritable DTI-derived features, and may empower genome-wide searches for genetic polymorphisms that influence brain asymmetry.
KW - Brain asymmetry
KW - DTI
KW - Fractional anisotropy
KW - Geodesic anisotropy
KW - Path analysis
KW - Quantitative genetics
KW - Structural equation model
KW - Twins
UR - http://www.scopus.com/inward/record.url?scp=77953715731&partnerID=8YFLogxK
U2 - 10.1016/j.neuroimage.2010.04.236
DO - 10.1016/j.neuroimage.2010.04.236
M3 - Article
C2 - 20430102
AN - SCOPUS:77953715731
SN - 1053-8119
VL - 52
SP - 455
EP - 469
JO - NeuroImage
JF - NeuroImage
IS - 2
ER -