Myelination shapes functional activity in the developing brain

NeuroImage

Volumn 38, Issue 3, 2007, Pages 511-518

  Fornari, Eleonora ^a   Knyazeva, Maria G ^a   Meuli, Reto ^a   Maeder, Philippe ^a  

^a LAUSANNE UNIVERSITY HOSPITAL   (Switzerland)

Author keywords

Children; fMRI BOLD; MTI; Myelination; Spatial integration; Splenium

Indexed keywords

ADOLESCENT; ARTICLE; BRAIN CORTEX; BRAIN FUNCTION; BRAIN REGION; BRAIN SCINTISCANNING; CHILD; CINGULATE GYRUS; CORPUS STRIATUM; CORRELATION FUNCTION; FEMALE; FIBER; FUNCTIONAL MAGNETIC RESONANCE IMAGING; GESTALT THERAPY; GRATING; HEMISPHERE; HUMAN; HUMAN TISSUE; MALE; MATURATION; MORPHOLOGY; MYELINATION; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; SPATIAL ORIENTATION; STIMULUS;

BRAIN; BRAIN MAPPING; CHILD; GYRUS CINGULI; HUMANS; MAGNETIC RESONANCE IMAGING; MAGNETICS; MYELIN SHEATH; REFERENCE VALUES;

EID: 35148853153     PISSN: 10538119     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuroimage.2007.07.010     Document Type: Article

References (48)

1. Aboitiz F., Lopez J., Montiel J., Aboitiz F., Scheibel A.B., Fisher R.S., and Zaidel E. Individual differences in brain asymmetries and fiber composition in the human corpus callosum. Biol. Res. 598 (1992) 154-161
2. Ashburner J., and Friston K.J. Voxel-based morphometry-The methods. NeuroImage 11 (2000) 805-821
3. Atkinson J. The Developing Visual Brain (2000), Oxford Univ. Press, USA
4. Bengtsson S.L., Nagy Z., Skare S., Forsman L., Forssberg H., and Ullén F. Extensive piano practicing has regionally specific effects on white matter development. Nat. Neurosci. 8 (2005) 1148-1150
5. Casey B.J., Giedd J.N., and Thomas K.M. Structural and functional brain development and its relation to cognitive development. Biol. Psychol. 54 (2000) 241-257
6. Cissé Y., Crochet S., Timofeev I., and Steriade M. Synaptic enhancement induced through callosal pathways in cat association cortex. J. Neurophysiol. 92 (2004) 3221-3232
7. Conner I.P., Sharma S., Lemieux S.K., and Mendola J.D. Retinotopic organization in children measured with fMRI. J. Vis. 4 (2004) 509-523
8. Dougherty R.F., Ben-Shachar M., Bammer R., Brewer A.A., and Wandell B.A. Functional organization of human occipital-callosal fiber tracts. Proc. Natl. Acad. Sci. U. S. A. 102 (2005) 7350-7355
9. Eng J., Ceckler T.L., and Balaban R.S. Quantitative 1H magnetization transfer imaging in vivo. Magn. Reson. Med. 17 (1991) 304-314
10. Farber D., and Knyazeva M. Electrophysiological. correlates of interhemispheric interaction in ontogenesis. In: Ramaekers G., and Njiokiktjien C. (Eds). Pediatric Behavioural Neurology, Developing Brain and Cognition (1993), Suyi Publ. 86-99
11. Fields R.D. Myelination: an overlooked mechanism of synaptic plasticity?. Neuroscientist 11 (2005) 528-531
12. Filippi M., Campi A., Dousset V., Baratti C., Martinelli V., Canal N., Scotti G., and Comi G. A magnetization transfer imaging study of normal-appearing white matter in multiple sclerosis. Neurology 45 (1995) 478-482
13. Friede R.L., and Hu K.H. Proximo-distal differences in myelin development in human optic fibers. Z. Zellforsch. Mikrosk. Anat. 79 (1967) 259-264
14. Giedd J.N., Blumenthal J., Jeffries N.O., Castellanos F.X., Liu H., Zijdenbos A., Paus T., Evans A.C., and Rapoport J.L. Brain development during childhood and adolescence: a longitudinal MRI study. Nat. Neurosci. 2 (1999) 861-863
15. Gilbert C.D., Das A., Ito M., Kapadia M., and Westheimer G. Spatial integration and cortical dynamics. Proc. Natl. Acad. Sci. U. S. A. 93 (1996) 615-622
16. Henkelman R.M., Stanisz G.J., and Graham S.J. Magnetization transfer in MRI: a review. NMR Biomed. 14 (2001) 57-64
17. Huttenlocher P.R. Synaptic density in human frontal cortex-Developmental changes and effects of aging. Brain Res. 163 (1979) 195-205
18. Kabani N.J., Sled J.G., and Chertkow H. Magnetization transfer ratio in mild cognitive impairment and dementia of Alzheimer's type. NeuroImage 15 (2002) 604-610
19. Knyazeva M.G., Fornari E., Meuli R., Innocenti G., and Maeder P. Imaging of a synchronous neuronal assembly in the human visual brain. NeuroImage 29 (2006) 593-604
20. Knyazeva M.G., Fornari E., Meuli R., and Maeder P. Interhemispheric integration at different spatial scales: the evidence from EEG coherence and fMRI. J. Neurophysiol. 96 (2006) 259-275
21. Kourtzi Z., Augath M., Logothetis N.K., Movshon J.A., and Kiorpes L. Development of visually evoked cortical activity in infant macaque monkeys studied longitudinally with fMRI. Magn. Reson. Imaging 24 (2006) 359-366
22. Kovács I., Kozma P., Fehér A., and Benedek G. Late maturation of visual spatial integration in humans. Proc. Natl. Acad. Sci. U. S. A. 96 (1999) 12204-12209
23. Logothetis N.K., Pauls J., Augath M., Trinath T., and Oeltermann A. Neurophysiological investigation of the basis of the fMRI signal. Nature 412 (2001) 150-157
24. McGowan J.C. The physical basis of magnetization transfer imaging. Neurology 53 (1999) S3-S7
25. Mizuhara H., Wang L., Kobayashi K., and Yamaguchi Y. Long-range EEG phase synchronization during an arithmetic task indexes a coherent cortical network simultaneously measured by fMRI. NeuroImage 27 (2005) 553-563
26. Nagy Z., Westerberg H., and Klingberg T. Maturation of white matter is associated with the development of cognitive functions during childhood. J. Cogn. Neurosci. 16 (2004) 1227-1233
27. Norcia A. Development of spatial selectivity and response timing in humans. In: Chalupa L.M., and Werner J.S. (Eds). The Visual Neurosciences (2003), MIT Press, Cambridge, USA 1603-1615
28. Olesen P.J., Nagy Z., Westerberg H., and Klingberg T. Combined analysis of DTI and fMRI data reveals a joint maturation of white and grey matter in a fronto-parietal network. Brain Res. Cogn. Brain Res. 18 (2003) 48-57
29. Paus T. Mapping brain maturation and cognitive development during adolescence. Trends Cogn. Sci. 9 (2005) 60-68
30. Rademacher J., Engelbrecht V., Bürgel U., Freund H., and Zilles K. Measuring in vivo myelination of human white matter fiber tracts with magnetization transfer MR. NeuroImage 9 (1999) 393-406
31. Rauch R.A., and Jinkins J.R. Analysis of cross-sectional area measurements of the corpus callosum adjusted for brain size in male and female subjects from childhood to adulthood. Behav. Brain Res. 64 (1994) 65-78
32. Rovaris M., Horsfield M.A., and Filippi M. Correlations between magnetization transfer metrics and other magnetic resonance abnormalities in multiple sclerosis. Neurology 53 (1999) S40-S45
33. Schmidt K.E., Goebel R., Löwel S., and Singer W. The perceptual grouping criterion of colinearity is reflected by anisotropies of connections in the primary visual cortex. Eur. J. Neurosci. 9 (1997) 1083-1089
34. Schmithorst V.J., Wilke M., Dardzinski B.J., and Holland S.K. Cognitive functions correlate with white matter architecture in a normal pediatric population: a diffusion tensor MRI study. Hum. Brain Mapp. 26 (2005) 139-147
35. Sireteanu R., and Rieth C. Texture segregation in infants and children. Behav. Brain Res. 49 (1992) 133-139
36. Stanisz G.J., Kecojevic A., Bronskill M.J., and Henkelman R.M. Characterizing white matter with magnetization transfer and T(2). Magn. Reson. Med. 42 (1999) 1128-1136
37. Stiles J., Moses P., Passarotti A., Dick F.K., and Buxton R. Exploring developmental change in the neural bases of higher cognitive functions: the promise of functional magnetic resonance imaging. Dev. Neuropsychol. 24 (2003) 641-668
38. Thompson P.M., Giedd J.N., Woods R.P., MacDonald D., Evans A.C., and Toga A.W. Growth patterns in the developing brain detected by using continuum mechanical tensor maps. Nature 404 (2000) 190-193
39. van Buchem M.A., Steens S.C., Vrooman H.A., Zwinderman A.H., McGowan J.C., Rassek M., and Engelbrecht V. Global estimation of myelination in the developing brain on the basis of magnetization transfer imaging: a preliminary study. AJNR Am. J. Neuroradiol. 22 (2001) 762-766
40. van der Flier W.M., van den Heuvel D.M.J., Weverling-Rijnsburger A.W.E., Bollen E.L.E.M., Westendorp R.G.J., van Buchem M.A., and Middelkoop H.A.M. Magnetization transfer imaging in normal aging, mild cognitive impairment, and Alzheimer's disease. Ann. Neurol. 52 (2002) 62-67
41. Winterer G., Carver F.W., Musso F., Mattay V., Weinberger D.R., and Coppola R. Complex relationship between BOLD signal and synchronization/desynchronization of human brain MEG oscillations. Hum. Brain Mapp. 28 (2007) 805-816
42. Witelson S.F. Hand and sex differences in the isthmus and genu of the human corpus callosum. A postmortem morphological study. Brain 112 Pt 3 (1989) 799-835
43. Wolff S.D., and Balaban R.S. Magnetization transfer contrast (MTC) and tissue water proton relaxation in vivo. Magn. Reson. Med. 10 (1989) 135-144
44. Wozniak J.R., and Lim K.O. Advances in white matter imaging: a review of in vivo magnetic resonance methodologies and their applicability to the study of development and aging. Neurosci. Biobehav. Rev. 30 (2006) 762-774
45. Xydis V., Astrakas L., Zikou A., Pantou K., Andronikou S., and Argyropoulou M.I. Magnetization transfer ratio in the brain of preterm subjects: age-related changes during the first 2 years of life. Eur. Radiol. 16 (2006) 215-220
46. Yakovlev P., and Lecours A. The myelogenetic cycles of regional maturation of the brain. In: Minkrowski A. (Ed). Regional Development of the Brain in Early Life (1967), Blackwell, Oxford 3-70
47. Yurgelun-Todd D.A., Killgore W.D.S., and Young A.D. Sex differences in cerebral tissue volume and cognitive performance during adolescence. Psychol. Rep. 91 (2002) 743-757
48. Zaidel E., Iacoboni M., and Pacual-Leone A.P. The Role of the Human Corpus Callosum in Sensory Motor Integration: Anatomy, Physiology, and Behavior; Individual Differences and Clinical Applications (1998), Plenum Press, New York