Abstract
Imparting functional meaning to neuroanatomical location has been among the greatest challenges to neuroscientists. The characterization of the brain architecture responsible in human cognition received a boost in momentum with the emergence of in vivo functional and structural neuroimaging technology over the past 30 years. Yet, individual variability in cortical gyrification as well as the patterns of blood flow-related activity measured using fMRI and positron emission tomography complicated direct comparisons across subjects without spatially accounting for overall brain size and shape. This realization resulted in considerable effort now involving the collective efforts of neuroscientists, computer scientists, and mathematicians to develop common brain atlas spaces against which the regions of activity may be accurately referenced. We examine recent developments in brain imaging and computational anatomy that have greatly expanded our ability to analyze brain structure and function. The enormous diversity of brain maps and imaging methods has spurred the development of population-based digital brain atlases. Atlases store information on how the brain varies across age and gender, across time, in health and disease, and in large human populations. We describe how brain atlases, and the computational tools that align new datasets with them, facilitate comparison of brain data across experiments, laboratories, and from different imaging devices. The major philosophies are presented that underlie the construction of probabilistic atlases, which store information on anatomic and functional variability in a population. Algorithms which create composite brain maps and atlases based on multiple subjects are examined. We show that group patterns of cortical organization, asymmetry, and disease-specific trends can be resolved that may not be apparent in individual brain maps. Finally, we describe the development of four-dimensional maps that store information on the dynamics of brain change in development and disease.
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References
Haas LF (2001) Phineas Gage and the science of brain localisation. J Neurol Neurosurg Psychiatry 71:761
Cowie SE (2000) A place in history: Paul Broca and cerebral localization. J Invest Surg 13:297–298
Goedert M, Ghetti B (2007) Alois Alzheimer: his life and times. Brain Pathol 17:57–62
Roland PE, Zilles K (1994) Brain atlases – a new research tool. Trends Neurosci 17:458–467
Toga AW, Thompson PM (2001) Maps of the brain. Anat Rec 265:37–53
Toga AW, Thompson PM (2002) New approaches in brain morphometry. Am J Geriatr Psychiatry 10:13–23
Thompson P, Cannon TD, Toga AW (2002) Mapping genetic influences on human brain structure. Ann Med 34:523–536
Narr KL, Thompson PM, Sharma T, Moussai J, Cannestra AF, Toga AW (2000) Mapping morphology of the corpus callosum in schizophrenia. Cereb Cortex 10:40–49
Davatzikos C (1996) Spatial normalization of 3D brain images using deformable models. J Comput Assist Tomogr 20:656–665
Davatzikos C (1997) Spatial transformation and registration of brain images using elastically deformable models. Comput Vis Image Underst 66:207–222
Thompson PM, Woods RP, Mega MS, Toga AW (2000) Mathematical/computational challenges in creating deformable and probabilistic atlases of the human brain. Hum Brain Mapp 9:81–92
Weaver JB, Healy DM Jr, Periaswamy S, Kostelec PJ (1998) Elastic image registration using correlations. J Digit Imaging 11:59–65
Barillot C, Lemoine D, Le Briquer L, Lachmann F, Gibaud B (1993) Data fusion in medical imaging: merging multimodal and multipatient images, identification of structures and 3D display aspects. Eur J Radiol 17:22–27
Woods RP, Grafton ST, Holmes CJ, Cherry SR, Mazziotta JC (1998) Automated image registration. I. General methods and intrasubject, intramodality validation. J Comput Assist Tomogr 22:139–152
Toga AW, Thompson PM, Mori S, Amunts K, Zilles K (2006) Towards multimodal atlases of the human brain. Nat Rev Neurosci 7:952–966
Woods RP (2003) Characterizing volume and surface deformations in an atlas framework: theory, applications, and implementation. Neuroimage 18:769–788
Avants B, Gee JC (2004) Geodesic estimation for large deformation anatomical shape averaging and interpolation. Neuroimage 23(Suppl 1):S139–S150
Avants BB, Schoenemann PT, Gee JC (2006) Lagrangian frame diffeomorphic image registration: morphometric comparison of human and chimpanzee cortex. Med Image Anal 10:397–412
Evans AC, Collins DL, Milner B (1992) An MRI-based stereotactic atlas from 250 young normal subjects. J Neurosci Abstr 18:408
Durrleman S, Pennec X, Trouve A, Ayache N (2007) Measuring brain variability via sulcal lines registration: a diffeomorphic approach. Med Image Comput Comput Assist Interv 10(Pt 1):675–682
Alayon S, Robertson R, Warfield SK, Ruiz-Alzola J (2007) A fuzzy system for helping medical diagnosis of malformations of cortical development. J Biomed Inform 40:221–235
Rohlfing T, Maurer CR Jr (2007) Shape-based averaging. IEEE Trans Image Process 16:153–161
Narr KL, Bilder RM, Luders E et al (2007) Asymmetries of cortical shape: effects of handedness, sex and schizophrenia. Neuroimage 34:939–948
Thompson PM, Giedd JN, Woods RP, MacDonald D, Evans AC, Toga AW (2000) Growth patterns in the developing brain detected by using continuum mechanical tensor maps. Nature 404:190–193
Corouge I, Dojat M, Barillot C (2004) Statistical shape modeling of low level visual area borders. Med Image Anal 8:353–360
Cardenas VA, Boxer AL, Chao LL et al (2007) Deformation-based morphometry reveals brain atrophy in frontotemporal dementia. Arch Neurol 64:873–877
Leow AD, Klunder AD, Jack CR Jr et al (2006) Longitudinal stability of MRI for mapping brain change using tensor-based morphometry. Neuroimage 31:627–640
Diedrichsen J (2006) A spatially unbiased atlas template of the human cerebellum. Neuroimage 33:127–138
Toga AW, Thompson PM (2005) Genetics of brain structure and intelligence. Annu Rev Neurosci 28:1–23
Toga AW, Thompson PM, Sowell ER (2006) Mapping brain maturation. Trends Neurosci 29:148–159
Apostolova LG, Thompson PM (2007) Brain mapping as a tool to study neurodegeneration. Neurotherapeutics 4(3):387–400
Apostolova LG, Akopyan GG, Partiali N et al (2007) Structural correlates of apathy in Alzheimer’s disease. Dement Geriatr Cogn Disord 24:91–97
Apostolova LG, Lu P, Rogers S et al (2008) 3D mapping of language networks in clinical and pre-clinical Alzheimer’s disease. Brain Lang 104:33–41
Scher AI, Xu Y, Korf ES et al (2007) Hippocampal shape analysis in Alzheimer’s disease: a population-based study. Neuroimage 36:8–18
Thompson PM, Hayashi KM, Dutton RA et al (2007) Tracking Alzheimer’s disease. Ann N Y Acad Sci 1097:183–214
Mazziotta JC, Toga AW, Evans AC, Fox PT, Lancaster JL (1995) Digital brain atlases. Trends Neurosci 18:210–211
Toga AW, Thompson PM, Mega MS, Narr KL, Blanton RE (2001) Probabilistic approaches for atlasing normal and disease-specific brain variability. Anat Embryol (Berl) 204:267–282
Wakana S, Jiang H, Nagae-Poetscher LM, van Zijl PC, Mori S (2004) Fiber tract-based atlas of human white matter anatomy. Radiology 230:77–87
Van Essen DC (2005) A Population-Average, Landmark- and Surface-based (PALS) atlas of human cerebral cortex. Neuroimage 15:635–662
Fox PT, Perlmutter JS, Raichle ME (1984) Stereotactic method for determining anatomical localization in physiological brain images. J Cereb Blood Flow Metab 4:634
Evans AC, Marrett S, Neelin P et al (1992) Anatomical mapping of functional activation in stereotactic coordinate space. Neuroimage 1:43–53
Nowinski WL, Thirunavuukarasuu A (2001) Atlas-assisted localization analysis of functional images. Med Image Anal 5:207–220
Crivello F, Schormann T, Tzourio-Mazoyer N, Roland PE, Zilles K, Mazoyer BM (2002) Comparison of spatial normalization procedures and their impact on functional maps. Hum Brain Mapp 16:228–250
Swallow KM, Braver TS, Snyder AZ, Speer NK, Zacks JM (2003) Reliability of functional localization using fMRI. Neuroimage 20:1561–1577
Tu Z, Zheng S, Yuille AL et al (2007) Automated extraction of the cortical sulci based on a supervised learning approach. IEEE Trans Med Imaging 26:541–552
Luders E, Thompson PM, Narr KL, Toga AW, Jancke L, Gaser C (2006) A curvature-based approach to estimate local gyrification on the cortical surface. Neuroimage 29:1224–1230
Ashburner J, Friston KJ (1999) Nonlinear spatial normalization using basis functions. Hum Brain Mapp 7:254–266
Friston KJ, Stephan KE, Lund TE, Morcom A, Kiebel S (2005) Mixed-effects and fMRI studies. Neuroimage 24:244–252
Miller MB, Van Horn JD, Wolford GL et al (2002) Extensive individual differences in brain activations associated with episodic retrieval are reliable over time. J Cogn Neurosci 14:1200–1214
Fox PT, Parsons LM, Lancaster JL (1998) Beyond the single study: function/location metanalysis in cognitive neuroimaging. Curr Opin Neurobiol 8:178–187
Nowinski WL (2005) The cerefy brain atlases: continuous enhancement of the electronic talairach-tournoux brain atlas. Neuroinformatics 3:293–300
Amunts K, Schleicher A, Zilles K (2007) Cytoarchitecture of the cerebral cortex – more than localization. Neuroimage 37:1061–1065, discussion 6–8
Mazziotta J, Toga AW, Evans A et al (2001) A probabilistic atlas and reference system for the human brain: International Consortium for Brain Mapping (ICBM). Philos Trans R Soc Lond B Biol Sci 356:1293–1322
Nowinski WL (2001) Modified Talairach landmarks. Acta Neurochir (Wien) 143:1045–1057
Bookstein FL (2001) Voxel-based morphometry” should not be used with imperfectly registered images. Neuroimage 14:1454–1462
Talairach J, Tournoux P (1988) Co-planar stereotactic atlas of the human brain. Tieme, New York
Maldjian JA, Laurienti PJ, Burdette JH (2004) Precentral gyrus discrepancy in electronic versions of the Talairach atlas. Neuroimage 21:450–455
Shattuck DW, Mirza M, Adisetiyo V et al (2008) Construction of a 3D probabilistic atlas of human cortical structures. Neuroimage 39:1064–1080
Woods RP, Grafton ST, Watson JD, Sicotte NL, Mazziotta JC (1998) Automated image registration. II. Intersubject validation of linear and nonlinear models. J Comput Assist Tomogr 22:153–165
Rex DE, Ma JQ, The TAW, LONI (2003) Pipeline processing environment. Neuroimage 19:1033–1048
Smith SM, Jenkinson M, Woolrich MW et al (2004) Advances in functional and structural MR image analysis and implementation as FSL. Neuroimage 23(Suppl 1):S208–S219
Ashburner J, Friston KJ (2005) Unified segmentation. Neuroimage 26:839–851
Van Essen DC (2002) Windows on the brain: the emerging role of atlases and databases in neuroscience. Curr Opin Neurobiol 12:574–579
Mazziotta J, Toga A, Evans A et al (2001) A four-dimensional probabilistic atlas of the human brain. J Am Med Inform Assoc 8:401–430
Mega MS, Dinov ID, Mazziotta JC et al (2005) Automated brain tissue assessment in the elderly and demented population: construction and validation of a sub-volume probabilistic brain atlas. Neuroimage 26:1009–1018
Yoon U, Lee JM, Koo BB et al (2005) Quantitative analysis of group-specific brain tissue probability map for schizophrenic patients. Neuroimage 26:502–512
Cannon TD, Thompson PM, van Erp TG et al (2006) Mapping heritability and molecular genetic associations with cortical features using probabilistic brain atlases: methods and applications to schizophrenia. Neuroinformatics 4:5–19
Wilke M, Schmithorst VJ, Holland SK (2002) Assessment of spatial normalization of whole-brain magnetic resonance images in children. Hum Brain Mapp 17:48–60
Jelacic S, de Regt D, Weinberger E (2006) Interactive digital MR atlas of the pediatric brain. Radiographics 26:497–501
Joshi S, Davis B, Jomier M, Gerig G (2004) Unbiased diffeomorphic atlas construction for computational anatomy. Neuroimage 23(Suppl 1):S151–S160
Mazziotta J, Toga A, Evans A et al (2001) A four-dimensional probabilistic atlas of the human brain. J Am Med Inform Assoc 8:401–430
Narr K, Thompson P, Sharma T et al (2001) Three-dimensional mapping of gyral shape and cortical surface asymmetries in schizophrenia: gender effects. Am J Psychiatry 158:244–255
Amunts K, Hawrylycz MJ, Van Essen DC et al (2014) Interoperable atlases of the human brain. Neuroimage 99:525–532
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Van Horn, J.D., Toga, A.W. (2016). Brain Atlases: Their Development and Role in Functional Inference. In: Filippi, M. (eds) fMRI Techniques and Protocols. Neuromethods, vol 119. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-5611-1_9
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DOI: https://doi.org/10.1007/978-1-4939-5611-1_9
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