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Diffusion tensor analysis of corpus callosum in progressive supranuclear palsy

  • Functional Neuroradiology
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Abstract

Introduction

Progressive supranuclear palsy (PSP) is a neurodegenerative disease featuring parkinsonism, supranuclear ophthalmoplegia, dysphagia, and frontal lobe dysfunction. The corpus callosum which consists of many commissure fibers probably reflects cerebral cortical function. Several previous reports showed atrophy or diffusion abnormalities of anterior corpus callosum in PSP patients, but partitioning method used in these studies was based on data obtained in nonhuman primates. In this study, we performed a diffusion tensor analysis using a new partitioning method for the human corpus callosum.

Methods

Seven consecutive patients with PSP were compared with 29 age-matched patients with Parkinson’s Disease (PD) and 19 age-matched healthy control subjects. All subjects underwent diffusion tensor magnetic resonance imaging, and the corpus callosum was partitioned into five areas on the mid-sagittal plane according to a recently established topography of human corpus callosum (CC1—prefrontal area, CC2—premotor and supplementary motor area, CC3—motor area, CC4—sensory area, CC5—parietal, temporal, and occipital area). Fractional anisotropy (FA) and apparent diffusion coefficient (ADC) were measured in each area and differences between groups were analyzed.

Results

In the PSP group, FA values were significantly decreased in CC1 and CC2, and ADC values were significantly increased in CC1 and CC2. Receiver operating characteristic analysis showed excellent reliability of FA and ADC analyses of CC1 for differentiating PSP from PD.

Conclusion

The anterior corpus callosum corresponding to the prefrontal, premotor, and supplementary motor cortices is affected in PSP patients. This analysis can be an additional test for further confirmation of the diagnosis of PSP.

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References

  1. Gröschel K, Hauser TK, Luft A, Patronas N, Dichgans J, Litvan I et al (2004) Magnetic resonance imaging-based volumetry differentiates progressive supranuclear palsy from corticobasal degeneration. Neuroimage 21:714–724 doi:10.1016/j.neuroimage.2003.09.070

    Article  PubMed  Google Scholar 

  2. Boxer AL, Geschwind MD, Belfor N, Gorno-Tempini ML, Schauer GF, Miller BL et al (2006) Patterns of brain atrophy that differentiate corticobasal degeneration syndrome from progressive supranuclear palsy. Arch Neurol 63:81–86 doi:10.1001/archneur.63.1.81

    Article  PubMed  Google Scholar 

  3. Brenneis C, Seppi K, Schocke M, Benke T, Wenning GK, Poewe W (2004) Voxel based morphometry reveals a distinct pattern of frontal atrophy in progressive supranuclear palsy. J Neurol Neurosurg Psychiatry 75:246–249

    PubMed  CAS  Google Scholar 

  4. Padovani A, Borroni B, Brambati SM, Agosti C, Broli M, Alonso R et al (2006) Diffusion tensor imaging and voxel based morphometry study in early progressive supranuclear palsy. J Neurol Neurosurg Psychiatry 77:457–463 doi:10.1136/jnnp.2005.075713

    Article  PubMed  CAS  Google Scholar 

  5. Yamauchi H, Fukuyama H, Nagahama Y, Katsumi Y, Dong Y, Konishi J et al (1997) Atrophy of corpus callosum, cognitive impairment, and cortical hypometabolism in progressive supranuclear palsy. Ann Neurol 41:606–614 doi:10.1002/ana.410410509

    Article  PubMed  CAS  Google Scholar 

  6. Yamauchi H, Fukuyama H, Nagahama Y, Katsumi Y, Hayashi T, Oyanagi C et al (2000) Comparison of the pattern of atrophy of the corpus callosum in frontotemporal dementia, progressive supranuclear palsy, and Alzheimer’s disease. J Neurol Neurosurg Psychiatry 69:623–629 doi:10.1136/jnnp.69.5.623

    Article  PubMed  CAS  Google Scholar 

  7. Arai K (2006) MRI of progressive supranuclear palsy, corticobasal degeneration and multiple system atrophy. J Neurol 253(Suppl 3):III25–III29 doi:10.1007/s00415-006-3005-7

    Article  Google Scholar 

  8. Paviour DC, Thornton JS, Lees AJ, Jäger HR (2007) Diffusion-weighted magnetic resonance imaging differentiates parkinsonian variant of multiple system atrophy from progressive supranuclear palsy. Mov Disord 22:68–74 doi:10.1002/mds.21204

    Article  PubMed  Google Scholar 

  9. Witelson SF (1989) Hand and sex differences in the isthmus and genu of the human corpus callosum. A postmortem morphological study. Brain 112:799–835 doi:10.1093/brain/112.3.799

    Article  PubMed  Google Scholar 

  10. Hofer S, Frahma J (2006) Topography of the human corpus callosum revisited: comprehensive fiber tractography using diffusion tensor magnetic resonance imaging. Neuroimage 32:989–994 doi:10.1016/j.neuroimage.2006.05.044

    Article  PubMed  Google Scholar 

  11. Litvan I, Agid Y, Calne D, Campbell G, Dubois B, Duvoisin RC et al (1996) Clinical research criteria for the diagnosis of progressive supranuclear palsy (Steele–Richardson–Olszewski syndrome): report of the NINDS-SPSP international workshop. Neurology 47:1–9 doi:10.1159/000113224

    Article  PubMed  CAS  Google Scholar 

  12. Litvan I, Bhatia KP, Burn DJ, Goetz CG, Lang AE, McKeith I et al (2003) SIC task force appraisal of clinical diagnostic criteria for Parkinsonian disorders. Mov Disord 18:467–486 doi:10.1002/mds.10459

    Article  PubMed  Google Scholar 

  13. Aoki S, Iwata NK, Masutani Y, Yoshida M, Abe O, Ugawa Y et al (2005) Quantitative evaluation of the pyramidal tract segmented by diffusion tensor tractography: feasibility study in patients with amyotrophic lateral sclerosis. Radiat Med 23:195–199

    PubMed  Google Scholar 

  14. Ohshita T, Oka M, Imon Y, Yamaguchi S, Mimori Y, Nakamura S (2000) Apparent diffusion coefficient measurements in progressive supranuclear palsy. Neuroradiology 42:643–647 doi:10.1007/s002340000372

    Article  PubMed  CAS  Google Scholar 

  15. Dubois B, Slachevsky A, Litvan I, Pillon B (2000) The FAB: a Frontal Assessment Battery at bedside. Neurology 55:1621–1626

    PubMed  CAS  Google Scholar 

  16. Martinez-Martin P, Gil-Nagel A, Gracia LM, Gomez JB, Martinez-Sarries J, Bermejo F (1994) Unified Parkinson’s Disease Rating Scale characteristics and structure. The Cooperative Multicentric Group. Mov Disord 9:76–83 doi:10.1002/mds.870090112

    Article  PubMed  CAS  Google Scholar 

  17. Abe O, Aoki S, Hayashi N, Yamada H, Kunimatsu A, Mori H et al (2002) Normal aging in the central nervous system: quantitative MR diffusion-tensor analysis. Neurobiol Aging 23:433–441 doi:10.1016/S0197-4580(01)00318-9

    Article  PubMed  Google Scholar 

  18. Pfefferbaum A, Adalsteinsson E, Sullivan EV (2005) Frontal circuitry degradation marks healthy adult aging: evidence from diffusion tensor imaging. Neuroimage 26:891–899 doi:10.1016/j.neuroimage.2005.02.034

    Article  PubMed  Google Scholar 

  19. Salat DH, Tuch DS, Greve DN, van der Kouwe AJW, Hevelone ND, Zaleta AK et al (2005) Age-related alterations in white matter microstructure measured by diffusion tensor imaging. Neurobiol Aging 26:1215–1227 doi:10.1016/j.neurobiolaging.2004.09.017

    Article  PubMed  CAS  Google Scholar 

  20. Sullivan EV, Adalsteinsson E, Pfefferbaum A (2006) Selective age-related degradation of anterior callosal fiber bundles quantified in vivo with fiber tracking. Cereb Cortex 16:1030–1039 doi:10.1093/cercor/bhj045

    Article  PubMed  Google Scholar 

  21. Càmara E, Bodammer N, Rodríguez-Fornells A, Tempelmann C (2007) Age-related diffusion changes in human brain: a voxel-based approach. Neuroimage 34:1588–1599 doi:10.1016/j.neuroimage.2006.09.045

    Article  PubMed  Google Scholar 

  22. Wiltshire K, Foster S, Kaye JA, Small BJ, Camicioli R (2005) Corpus callosum in neurodegenerative diseases: findings in Parkinson’s disease. Dement Geriatr Cogn Disord 20:345–351 doi:10.1159/000088526

    Article  PubMed  Google Scholar 

  23. Ni H, Kavcic V, Zhu T, Ekholm S, Zhong J (2006) Effects of number of diffusion gradient directions on derived diffusion tensor imaging indices in human brain. AJNR Am J Neuroradiol 27:1776–1781

    PubMed  CAS  Google Scholar 

  24. Oouchi H, Yamada K, Sakai K, Kizu O, Kubota T, Ito H et al (2007) Diffusion anisotropy measurement of brain white matter is affected by voxel size: underestimation occurs in areas crossing fibers. AJNR Am J Neuroradiol 28:1102–1106 doi:10.3174/ajnr.A0488

    Article  PubMed  CAS  Google Scholar 

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We declare that we have no conflict of interest.

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Correspondence to Shoichi Ito.

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Ito, S., Makino, T., Shirai, W. et al. Diffusion tensor analysis of corpus callosum in progressive supranuclear palsy. Neuroradiology 50, 981–985 (2008). https://doi.org/10.1007/s00234-008-0447-x

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  • DOI: https://doi.org/10.1007/s00234-008-0447-x

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