Skip to main content
Top
Published in: Annals of Nuclear Medicine 2/2012

01-02-2012 | Original article

Correlated regions of cerebral blood flow with clinical parameters in Parkinson’s disease; comparison using ‘Anatomy’ and ‘Talairach Daemon’ software

Authors: Hyun Jin Yoon, Sang Myung Cheon, Young Jin Jeong, Do-Young Kang

Published in: Annals of Nuclear Medicine | Issue 2/2012

Login to get access

Abstract

Objectives

We assign the anatomical names of functional activation regions in the brain, based on the probabilistic cyto-architectonic atlas by Anatomy 1.7 from an analysis of correlations between regional cerebral blood flow (rCBF) and clinical parameters of the non-demented Parkinson’s disease (PD) patients by SPM8. We evaluated Anatomy 1.7 of SPM toolbox compared to ‘Talairach Daemon’ (TD) Client 2.4.2 software.

Methods

One hundred and thirty-six patients (mean age 60.0 ± 9.09 years; 73 women and 63 men) with non-demented PD were selected. Tc-99m-HMPAO brain single-photon emission computed tomography (SPECT) scans were performed on the patients using a two-head gamma-camera. We analyzed the brain image of PD patients by SPM8 and found the anatomical names of correlated regions of rCBF perfusion with the clinical parameters using TD Client 2.4.2 and Anatomy 1.7. The SPM8 provided a correlation coefficient between clinical parameters and cerebral hypoperfusion by a simple regression method. To the clinical parameters were added age, duration of disease, education period, Hoehn and Yahr (H&Y) stage and Korean mini-mental state examination (K-MMSE) score.

Results

Age was correlated with cerebral perfusion in the Brodmann area (BA) 6 and BA 3b assigned by Anatomy 1.7 and BA 6 and pyramis in gray matter by TD Client 2.4.2 with p < 0.001 uncorrected. Also, assigned significant correlated regions were found in the left and right lobules VI (Hem) with duration of disease, in left and right lobules VIIa crus I (Hem) with education, in left insula (Ig2), left and right lobules VI (Hem) with H&Y, and in BA 4a and 6 with K-MMSE score with p < 0.05 uncorrected by Anatomy 1.7, respectively. Most areas of correlation were overlapped by two different anatomical labeling methods, but some correlation areas were found with different names.

Conclusion

Age was the most significantly correlated clinical parameter with rCBF. TD Client found the exact anatomical name by the peak intensity position of the cluster while Anatomy 1.7 of SPM8 toolbox, using the cyto-architectonic probability maps, assigned the anatomical name by percentage value of the probability.
Literature
1.
go back to reference Tolosa E, Wenning G, Poewe W. The diagnosis of Parkinson’s disease. Lancet Neurol. 2006;5(1):75–86.PubMedCrossRef Tolosa E, Wenning G, Poewe W. The diagnosis of Parkinson’s disease. Lancet Neurol. 2006;5(1):75–86.PubMedCrossRef
2.
go back to reference Van Laere K, Santens P, Bosman T, De Reuck J, Mortelmans L, Dierckx R. Statistical parametric mapping of 99mTc-ECD SPECT in idiopathic Parkinson’s disease and multiple system atrophy with predominant parkinsonian features: correlation with clinical parameters. J Nucl Med. 2004;45(6):933–42.PubMed Van Laere K, Santens P, Bosman T, De Reuck J, Mortelmans L, Dierckx R. Statistical parametric mapping of 99mTc-ECD SPECT in idiopathic Parkinson’s disease and multiple system atrophy with predominant parkinsonian features: correlation with clinical parameters. J Nucl Med. 2004;45(6):933–42.PubMed
3.
go back to reference Imon Y, Matsuda H, Ogawa M, Kogure D, Sunohara N. SPECT image analysis using statistical parametric mapping in patients with Parkinson’s disease. J Nucl Med. 1999;40(10):1583–9.PubMed Imon Y, Matsuda H, Ogawa M, Kogure D, Sunohara N. SPECT image analysis using statistical parametric mapping in patients with Parkinson’s disease. J Nucl Med. 1999;40(10):1583–9.PubMed
4.
go back to reference Janvin CC, Larsen JP, Aarsland D, Hugdahl K. Subtypes of mild cognitive impairment in Parkinson’s disease: progression to dementia. Mov Disord. 2006;21(9):1343–9.PubMedCrossRef Janvin CC, Larsen JP, Aarsland D, Hugdahl K. Subtypes of mild cognitive impairment in Parkinson’s disease: progression to dementia. Mov Disord. 2006;21(9):1343–9.PubMedCrossRef
5.
go back to reference Kim JW, Jo HY, Park MJ, Cheon SM. Mild cognitive impairment in Parkinson’s disease. J Mov Disord. 2008;1(1):19–25. Kim JW, Jo HY, Park MJ, Cheon SM. Mild cognitive impairment in Parkinson’s disease. J Mov Disord. 2008;1(1):19–25.
6.
go back to reference Kim JW, Cheon SM, Park MJ, Kim SY, Jo HY. Cognitive impairment in Parkinson’s disease without dementia: subtypes and influences of age. J Clin Neurol. 2009;5:133–138. Kim JW, Cheon SM, Park MJ, Kim SY, Jo HY. Cognitive impairment in Parkinson’s disease without dementia: subtypes and influences of age. J Clin Neurol. 2009;5:133–138.
7.
go back to reference Pillon B, Dubois B, Agid Y. Testing cognition may contribute to the diagnosis of movement disorders. Neurology. 1996;46(2):329–34.PubMed Pillon B, Dubois B, Agid Y. Testing cognition may contribute to the diagnosis of movement disorders. Neurology. 1996;46(2):329–34.PubMed
8.
go back to reference Antonini A, De Notaris R, Benti R, De Gaspari D, Pezzoli G. Perfusion ECD/SPECT in the characterization of cognitive deficits in Parkinson’s disease. Neurol Sci. 2001;22(1):45–6.PubMedCrossRef Antonini A, De Notaris R, Benti R, De Gaspari D, Pezzoli G. Perfusion ECD/SPECT in the characterization of cognitive deficits in Parkinson’s disease. Neurol Sci. 2001;22(1):45–6.PubMedCrossRef
9.
go back to reference Eickhoff SB, Stephan KE, Mohlberg H, Grefkes C, Fink GR, Amunts K, et al. A new SPM toolbox for combining probabilistic cytoarchitectonic maps and functional imaging data. Neuroimage. 2005;25(4):1325–35.PubMedCrossRef Eickhoff SB, Stephan KE, Mohlberg H, Grefkes C, Fink GR, Amunts K, et al. A new SPM toolbox for combining probabilistic cytoarchitectonic maps and functional imaging data. Neuroimage. 2005;25(4):1325–35.PubMedCrossRef
10.
go back to reference Eickhoff SB, Heim S, Zilles K, Amunts K. Testing anatomically specified hypotheses in functional imaging using cytoarchitectonic maps. Neuroimage. 2006;32(2):570–82.PubMedCrossRef Eickhoff SB, Heim S, Zilles K, Amunts K. Testing anatomically specified hypotheses in functional imaging using cytoarchitectonic maps. Neuroimage. 2006;32(2):570–82.PubMedCrossRef
11.
go back to reference Eickhoff SB, Paus T, Caspers S, Grosbras MH, Evans AC, Zilles K, et al. Assignment of functional activations to probabilistic cytoarchitectonic areas revisited. Neuroimage. 2007;36(3):511–21.PubMedCrossRef Eickhoff SB, Paus T, Caspers S, Grosbras MH, Evans AC, Zilles K, et al. Assignment of functional activations to probabilistic cytoarchitectonic areas revisited. Neuroimage. 2007;36(3):511–21.PubMedCrossRef
12.
go back to reference Benoit M, Clairet S, Koulibaly P, Darcourt J, Robert P. Brain perfusion correlates of the apathy inventory dimensions of Alzheimer’s disease. Int J Geriatr Psychiatry. 2004;19(9):864–9.PubMedCrossRef Benoit M, Clairet S, Koulibaly P, Darcourt J, Robert P. Brain perfusion correlates of the apathy inventory dimensions of Alzheimer’s disease. Int J Geriatr Psychiatry. 2004;19(9):864–9.PubMedCrossRef
14.
go back to reference Chang L. A method for attenuation correction in radionuclide computed tomography. IEEE Trans Nucl Sci. 1978;25(1):638–43.CrossRef Chang L. A method for attenuation correction in radionuclide computed tomography. IEEE Trans Nucl Sci. 1978;25(1):638–43.CrossRef
15.
go back to reference Friston KJ, Holmes AP, Worsley KJ, Poline JP, Frith CD, Frackowiak RSJ. Statistical parametric maps in functional imaging: a general linear approach. Hum Brain Mapp. 1994;2(4):189–210.CrossRef Friston KJ, Holmes AP, Worsley KJ, Poline JP, Frith CD, Frackowiak RSJ. Statistical parametric maps in functional imaging: a general linear approach. Hum Brain Mapp. 1994;2(4):189–210.CrossRef
16.
go back to reference Friston KJ, Ashburner J, Frith CD, Poline JB, Heather JD, Frackowiak RSJ. Spatial registration and normalization of images. Hum Brain Mapp. 1995;3(3):165–89.CrossRef Friston KJ, Ashburner J, Frith CD, Poline JB, Heather JD, Frackowiak RSJ. Spatial registration and normalization of images. Hum Brain Mapp. 1995;3(3):165–89.CrossRef
17.
go back to reference Friston K, Holmes A, Poline J, Price C, Frith C. Detecting activations in PET and fMRI: levels of inference and power. Neuroimage. 1996;4(3):223–35.PubMedCrossRef Friston K, Holmes A, Poline J, Price C, Frith C. Detecting activations in PET and fMRI: levels of inference and power. Neuroimage. 1996;4(3):223–35.PubMedCrossRef
18.
go back to reference Talairach J, Tournoux P. Co-planar stereotaxic atlas of the human brain. New York: Thieme; 1988. Talairach J, Tournoux P. Co-planar stereotaxic atlas of the human brain. New York: Thieme; 1988.
20.
go back to reference Lancaster JL, Woldorff MG, Parsons LM, Liotti M, Freitas CS, Rainey L, et al. Automated Talairach atlas labels for functional brain mapping. Hum Brain Mapp. 2000;10(3):120–31.PubMedCrossRef Lancaster JL, Woldorff MG, Parsons LM, Liotti M, Freitas CS, Rainey L, et al. Automated Talairach atlas labels for functional brain mapping. Hum Brain Mapp. 2000;10(3):120–31.PubMedCrossRef
21.
go back to reference Morbelli S, Rodriguez G, Mignone A, Altrinetti V, Brugnolo A, Piccardo A, et al. The need of appropriate brain SPECT templates for SPM comparisons. Q J Nucl Med Mol Imaging. 2008;52(1):89–98.PubMed Morbelli S, Rodriguez G, Mignone A, Altrinetti V, Brugnolo A, Piccardo A, et al. The need of appropriate brain SPECT templates for SPM comparisons. Q J Nucl Med Mol Imaging. 2008;52(1):89–98.PubMed
22.
go back to reference Lee JS, Lee DS, Oh SH, Kim CS, Kim JW, Hwang CH, et al. PET evidence of neuroplasticity in adult auditory cortex of postlingual deafness. J Nucl Med. 2003;44(9):1435–9.PubMed Lee JS, Lee DS, Oh SH, Kim CS, Kim JW, Hwang CH, et al. PET evidence of neuroplasticity in adult auditory cortex of postlingual deafness. J Nucl Med. 2003;44(9):1435–9.PubMed
24.
go back to reference Schleicher A, Palomero-Gallagher N, Morosan P, Eickhoff S, Kowalski T, Vos K, et al. Quantitative architectural analysis: a new approach to cortical mapping. Anat Embryol. 2005;210(5):373–86.PubMedCrossRef Schleicher A, Palomero-Gallagher N, Morosan P, Eickhoff S, Kowalski T, Vos K, et al. Quantitative architectural analysis: a new approach to cortical mapping. Anat Embryol. 2005;210(5):373–86.PubMedCrossRef
25.
go back to reference Schleicher A, Morosan P, Amunts K, Zilles K. Quantitative architectural analysis: a new approach to cortical mapping. J Autism Dev Disord. 2009;39(11):1568–81.PubMedCrossRef Schleicher A, Morosan P, Amunts K, Zilles K. Quantitative architectural analysis: a new approach to cortical mapping. J Autism Dev Disord. 2009;39(11):1568–81.PubMedCrossRef
26.
go back to reference Osaki Y, Morita Y, Fukumoto M, Akagi N, Yoshida S, Doi Y. Three-dimensional stereotactic surface projection SPECT analysis in Parkinson’s disease with and without dementia. Mov Disord. 2005;20(8):999–1005.PubMedCrossRef Osaki Y, Morita Y, Fukumoto M, Akagi N, Yoshida S, Doi Y. Three-dimensional stereotactic surface projection SPECT analysis in Parkinson’s disease with and without dementia. Mov Disord. 2005;20(8):999–1005.PubMedCrossRef
27.
go back to reference Hu M, Taylor-Robinson S, Chaudhuri K, Bell J, Labbe C, Cunningham V, et al. Cortical dysfunction in non-demented Parkinson’s disease patients: a combined 31P-MRS and 18FDG-PET study. Brain. 2000;123(2):340–52.PubMedCrossRef Hu M, Taylor-Robinson S, Chaudhuri K, Bell J, Labbe C, Cunningham V, et al. Cortical dysfunction in non-demented Parkinson’s disease patients: a combined 31P-MRS and 18FDG-PET study. Brain. 2000;123(2):340–52.PubMedCrossRef
28.
go back to reference Oishi N, Udaka F, Kameyama M, Sawamoto N, Hashikawa K, Fukuyama H. Regional cerebral blood flow in Parkinson disease with nonpsychotic visual hallucinations. Neurology. 2005;65(11):1708–15.PubMedCrossRef Oishi N, Udaka F, Kameyama M, Sawamoto N, Hashikawa K, Fukuyama H. Regional cerebral blood flow in Parkinson disease with nonpsychotic visual hallucinations. Neurology. 2005;65(11):1708–15.PubMedCrossRef
29.
go back to reference Mito Y, Yoshida K, Yabe I, Makino K, Hirotani M, Tashiro K, et al. Brain 3D-SSP SPECT analysis in dementia with Lewy bodies, Parkinson’s disease with and without dementia, and Alzheimer’s disease. Clin Neurol Neurosurg. 2005;107(5):396–403.PubMedCrossRef Mito Y, Yoshida K, Yabe I, Makino K, Hirotani M, Tashiro K, et al. Brain 3D-SSP SPECT analysis in dementia with Lewy bodies, Parkinson’s disease with and without dementia, and Alzheimer’s disease. Clin Neurol Neurosurg. 2005;107(5):396–403.PubMedCrossRef
30.
go back to reference Lee MC, Bae SK, Lee MH, Chung JK, Koh CS, Roh JK, et al. Quantitative analysis of regional cerebral blood flow using 99mTc-HMPAO SPECT in Parkinson’s disease. Korean J Nucl Med. 1992;26:251–6. Lee MC, Bae SK, Lee MH, Chung JK, Koh CS, Roh JK, et al. Quantitative analysis of regional cerebral blood flow using 99mTc-HMPAO SPECT in Parkinson’s disease. Korean J Nucl Med. 1992;26:251–6.
31.
go back to reference Wolf U, Rapoport MJ, Schweizer TA. Evaluating the affective component of the cerebellar cognitive affective syndrome. J Neuropsychiatry Clin Neurosci. 2009;21(3):245–53.PubMedCrossRef Wolf U, Rapoport MJ, Schweizer TA. Evaluating the affective component of the cerebellar cognitive affective syndrome. J Neuropsychiatry Clin Neurosci. 2009;21(3):245–53.PubMedCrossRef
Metadata
Title
Correlated regions of cerebral blood flow with clinical parameters in Parkinson’s disease; comparison using ‘Anatomy’ and ‘Talairach Daemon’ software
Authors
Hyun Jin Yoon
Sang Myung Cheon
Young Jin Jeong
Do-Young Kang
Publication date
01-02-2012
Publisher
Springer Japan
Published in
Annals of Nuclear Medicine / Issue 2/2012
Print ISSN: 0914-7187
Electronic ISSN: 1864-6433
DOI
https://doi.org/10.1007/s12149-011-0547-2

Other articles of this Issue 2/2012

Annals of Nuclear Medicine 2/2012 Go to the issue