Decline in corpus callosum volume among pediatric patients with medulloblastoma: longitudinal MR imaging study.

BACKGROUND AND PURPOSE A decline in intrahemispheric cerebral white matter volume in children treated for brain tumors with cranial irradiation has been well documented. It was hypothesized that the development of the corpus callosum, the largest white matter commissure of the brain, would also be adversely affected after treatment with cranial irradiation in pediatric patients treated for medulloblastoma. METHODS After diagnosis, 35 patients (22 male and 13 female patients) with histologically proved medulloblastoma were treated by maximal surgical resection, risk-adapted craniospinal irradiation, and chemotherapy. Using quantitative measurement techniques with MR imaging, corpus callosum volume was measured at multiple time points for each patient during a 4-year period. RESULTS Quantitative MR imaging analyses of 239 examinations in 35 patients showed, in contrast to normal development, that the total midsagittal corpus callosum area decreased with time from craniospinal irradiation (-18.0 mm(2)/y; P <.0001). After examination of seven corpus callosum subregions, significant declines were also observed: genu (-2.2 mm(2)/y; P =.03), rostral body (-2.0 mm(2)/y; P =.04), anterior midbody (-1.4 mm(2)/y; P =.005), posterior midbody (-1.2 mm(2)/y; P =.004), isthmus (-2.4 mm(2)/y; P =.001), and splenium (-5.0 mm(2)/y; P =.007). CONCLUSION The greatest deviation from normal development occurred in the most posterior subregions of the corpus callosum: the isthmus and the splenium. These corpus callosum subregions, associated with fibers traversing from the temporal, posterior parietal, and occipital lobes, are normally expected to have the highest rate of growth during childhood. However, these regions also received the highest total dose of irradiation, providing a possible explanation for atypical corpus callosum development observed in these 35 patients treated for medulloblastoma.

[1]  Ralph L. Rosnow,et al.  Essentials of Behavioral Research: Methods and Data Analysis , 1984 .

[2]  S Ekholm,et al.  Adverse effects of brain irradiation correlated with MR and CT imaging. , 1987, International journal of radiation oncology, biology, physics.

[3]  J. Juraska,et al.  Sex and environmental influences on the size and ultrastructure of the rat corpus callosum , 1988, Brain Research.

[4]  S. F. Witelson Hand and sex differences in the isthmus and genu of the human corpus callosum. A postmortem morphological study. , 1989, Brain : a journal of neurology.

[5]  Shayle R. Searle,et al.  Linear Models for Unbalanced Data. , 1990 .

[6]  Trevor Hastie,et al.  Statistical Models in S , 1991 .

[7]  Heikki Lyytinen,et al.  Corpus Callosum Morphology in Attention Deficit-Hyperactivity Disorder: Morphometric Analysis of MRI , 1991, Journal of learning disabilities.

[8]  Richard H. Jones,et al.  Longitudinal Data with Serial Correlation : A State-Space Approach , 1994 .

[9]  R M Elashoff,et al.  Analysis of longitudinal data: random coefficient regression modelling. , 1994, Statistics in medicine.

[10]  B. J. Casey,et al.  Quantitative morphology of the corpus callosum in attention deficit hyperactivity disorder. , 1994, The American journal of psychiatry.

[11]  T E Schultheiss,et al.  Radiation response of the central nervous system. , 1995, International journal of radiation oncology, biology, physics.

[12]  R. Littell SAS System for Mixed Models , 1996 .

[13]  A L Reiss,et al.  Corpus callosum morphology in children with Tourette syndrome and attention deficit hyperactivity disorder , 1996, Neurology.

[14]  J C Rajapakse,et al.  A quantitative MRI study of the corpus callosum in children and adolescents. , 1996, Brain research. Developmental brain research.

[15]  Edwin N. Cook,et al.  Automated segmentation and classification of multispectral magnetic resonance images of brain using artificial neural networks , 1997, IEEE Transactions on Medical Imaging.

[16]  W. Reddick,et al.  A hybrid neural network analysis of subtle brain volume differences in children surviving brain tumors. , 1998, Magnetic resonance imaging.

[17]  S. Schmidt,et al.  Effects of prenatal gamma irradiation on the development of the corpus callosum of Swiss mice , 1999, International Journal of Developmental Neuroscience.

[18]  Amar Gajjar,et al.  Neurocognitive deficits in medulloblastoma survivors and white matter loss , 1999, Annals of neurology.

[19]  Jagath C. Rajapakse,et al.  Development of the human corpus callosum during childhood and adolescence: A longitudinal MRI study , 1999, Progress in Neuro-Psychopharmacology and Biological Psychiatry.

[20]  W. Reddick,et al.  NEUROCOGNITIVE DEFICITS IN MEDULLOBLASTOMA SURVIVORS ASSOCIATED WITH WHITE MATTER LOSS , 1999 .

[21]  N. Minshew,et al.  Corpus callosum size in autism , 2000, Neurology.

[22]  N. J. Minshew,et al.  332. Corpus callosum size in autism , 2000, Biological Psychiatry.

[23]  W E Reddick,et al.  Subtle white matter volume differences in children treated for medulloblastoma with conventional or reduced dose craniospinal irradiation. , 2000, Magnetic resonance imaging.

[24]  S Eliez,et al.  MRI neuroimaging of childhood psychiatric disorders: a selective review. , 2000, Journal of child psychology and psychiatry, and allied disciplines.

[25]  I. Wilkinson,et al.  A Study of Three Cases of Familial Related Agenesis of the Corpus Callosum , 2000, Journal of clinical and experimental neuropsychology.

[26]  A. Barkovich Concepts of myelin and myelination in neuroradiology. , 2000, AJNR. American journal of neuroradiology.

[27]  Barkovich Aj Concepts of Myelin and Myelination in Neuroradiology , 2000 .

[28]  U Bellugi,et al.  Corpus callosum morphology of Williams syndrome: relation to genetics and behavior. , 2001, Developmental medicine and child neurology.

[29]  W E Reddick,et al.  Patterns of intellectual development among survivors of pediatric medulloblastoma: a longitudinal analysis. , 2001, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[30]  W E Reddick,et al.  Risks of young age for selected neurocognitive deficits in medulloblastoma are associated with white matter loss. , 2001, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[31]  R. Krance,et al.  Feasibility of four consecutive high-dose chemotherapy cycles with stem-cell rescue for patients with newly diagnosed medulloblastoma or supratentorial primitive neuroectodermal tumor after craniospinal radiotherapy: results of a collaborative study. , 2001, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[32]  H S Levin,et al.  Correlation of atrophy measures on MRI with neuropsychological sequelae in children and adolescents with traumatic brain injury. , 2001, Brain injury.

[33]  Stefan Pollmann,et al.  Dichotic listening in patients with splenial and nonsplenial callosal lesions. , 2002, Neuropsychology.