Skip to main content
Top
Published in: Clinical Neuroradiology 1/2018

01-03-2018 | Original Article

T2* Relaxometry in Patients with Parkinson’s Disease

Use of an Automated Atlas-based Approach

Authors: Karl Egger, Florian Amtage, Shan Yang, Markus Obmann, Ralf Schwarzwald, Lena Köstering, Irina Mader, Julia Koenigsdorf, Cornelius Weiller, Christoph P. Kaller, Horst Urbach

Published in: Clinical Neuroradiology | Issue 1/2018

Login to get access

Abstract

Background

Magnetic resonance (MR) relaxometry is of increasing scientific relevance in neurodegenerative disorders but is still not established in clinical routine. Several studies have investigated relaxation time alterations in disease-specific areas in Parkinson’s disease (PD), all using manually drawn regions of interest (ROI). Implementing MR relaxometry into the clinical setting involves the reduction of time needed for postprocessing using an investigator-independent and reliable approach. The aim of this study was to evaluate an automated, atlas-based ROI method for evaluating T2* relaxation times in patients with PD.

Method

Automated atlas-based ROI analysis of quantitative T2* maps were generated from 20 PD patients and 20 controls. To test for the accuracy of the atlas-based ROI segmentation, we evaluated the spatial overlap in comparison with manually segmented ROIs using the Dice similarity coefficient (DSC). Additionally, we tested for group differences using our automated atlas-based ROIs of the putamen, globus pallidus, and substantia nigra.

Results

A good spatial overlap accuracy was shown for the automated segmented putamen (mean DSC, 0.64 ± 0.04) and was inferior but still acceptable for the substantia nigra (mean DSC, 0.50 ± 0.17). Based on our automated defined ROI selection, a significant decrease of T2* relaxation time was found in the putamen as well as in the internal and external globus pallidus in PD patients compared with healthy controls.

Conclusion

Automated digital brain atlas-based approaches are reliable, more objective and time-efficient, and therefore have the potential to replace the time-consuming manual drawing of ROIs.
Literature
2.
go back to reference Halliday G, Lees A, Stern M. Milestones in Parkinson’s disease – clinical and pathologic features. Mov Disord. 2011;26:1015–21.CrossRefPubMed Halliday G, Lees A, Stern M. Milestones in Parkinson’s disease – clinical and pathologic features. Mov Disord. 2011;26:1015–21.CrossRefPubMed
3.
go back to reference Shtilbans A, Henchcliffe C. Biomarkers in Parkinson’s disease: an update. Curr Opin Neurol. 2012;25:460–5.CrossRefPubMed Shtilbans A, Henchcliffe C. Biomarkers in Parkinson’s disease: an update. Curr Opin Neurol. 2012;25:460–5.CrossRefPubMed
4.
go back to reference Dexter DT, Carayon A, Javoy-Agid F, Agid Y, Wells FR, Daniel SE, Lees AJ, Jenner P, Marsden CD. Alterations in the levels of iron, ferritin and other trace metals in Parkinson’s disease and other neurodegenerative diseases affecting the basal ganglia. Brain. 1991;114(4):1953–75.CrossRefPubMed Dexter DT, Carayon A, Javoy-Agid F, Agid Y, Wells FR, Daniel SE, Lees AJ, Jenner P, Marsden CD. Alterations in the levels of iron, ferritin and other trace metals in Parkinson’s disease and other neurodegenerative diseases affecting the basal ganglia. Brain. 1991;114(4):1953–75.CrossRefPubMed
5.
go back to reference Ulla M, Bonny JM, Ouchchane L, Rieu I, Claise B, Durif F. Is R2* a new MRI biomarker for the progression of Parkinson’s disease? A longitudinal follow-up. PLoS ONE. 2013;8:e57904.CrossRefPubMedPubMedCentral Ulla M, Bonny JM, Ouchchane L, Rieu I, Claise B, Durif F. Is R2* a new MRI biomarker for the progression of Parkinson’s disease? A longitudinal follow-up. PLoS ONE. 2013;8:e57904.CrossRefPubMedPubMedCentral
6.
go back to reference Baudrexel S, Nürnberger L, Rüb U, Seifried C, Klein JC, Deller T, Steinmetz H, Deichmann R, Hilker R. Quantitative mapping of T1 and T2* discloses nigral and brainstem pathology in early Parkinson’s disease. Neuroimage. 2010;51:512–20.CrossRefPubMed Baudrexel S, Nürnberger L, Rüb U, Seifried C, Klein JC, Deller T, Steinmetz H, Deichmann R, Hilker R. Quantitative mapping of T1 and T2* discloses nigral and brainstem pathology in early Parkinson’s disease. Neuroimage. 2010;51:512–20.CrossRefPubMed
7.
go back to reference Ordidge RJ, Gorell JM, Deniau JC, Knight RA, Helpern JA. Assessment of relative brain iron concentrations using T2-weighted and T2*-weighted MRI at 3 Tesla. Magn Reson Med. 1994;32:335–41.CrossRefPubMed Ordidge RJ, Gorell JM, Deniau JC, Knight RA, Helpern JA. Assessment of relative brain iron concentrations using T2-weighted and T2*-weighted MRI at 3 Tesla. Magn Reson Med. 1994;32:335–41.CrossRefPubMed
8.
go back to reference Du G, Lewis MM, Sen S, Wang J, Shaffer ML, Styner M, Yang QX, Huang X. Imaging nigral pathology and clinical progression in Parkinson’s disease. Mov Disord. 2012;27:1636–43.CrossRefPubMedPubMedCentral Du G, Lewis MM, Sen S, Wang J, Shaffer ML, Styner M, Yang QX, Huang X. Imaging nigral pathology and clinical progression in Parkinson’s disease. Mov Disord. 2012;27:1636–43.CrossRefPubMedPubMedCentral
9.
go back to reference Rossi M, Ruottinen H, Soimakallio S, Elovaara I, Dastidar P. Clinical MRI for iron detection in Parkinson’s disease. Clin Imaging. 2013;37:631–6.CrossRefPubMed Rossi M, Ruottinen H, Soimakallio S, Elovaara I, Dastidar P. Clinical MRI for iron detection in Parkinson’s disease. Clin Imaging. 2013;37:631–6.CrossRefPubMed
10.
go back to reference Martin, Wayne WR, Wieler M, Gee M. Midbrain iron content in early Parkinson disease: a potential biomarker of disease status. Neurology. 2008;70:1411–7.CrossRefPubMed Martin, Wayne WR, Wieler M, Gee M. Midbrain iron content in early Parkinson disease: a potential biomarker of disease status. Neurology. 2008;70:1411–7.CrossRefPubMed
11.
go back to reference Kaller CP, Reisert M, Katzev M, Umarova R, Mader I, Hennig J, Weiller C, Köstering L. Predicting planning performance from structural connectivity between left and right mid-dorsolateral prefrontal cortex: moderating effects of age during postadolescence and midadulthood. Cereb Cortex. 2015;25:869–83.CrossRefPubMed Kaller CP, Reisert M, Katzev M, Umarova R, Mader I, Hennig J, Weiller C, Köstering L. Predicting planning performance from structural connectivity between left and right mid-dorsolateral prefrontal cortex: moderating effects of age during postadolescence and midadulthood. Cereb Cortex. 2015;25:869–83.CrossRefPubMed
12.
go back to reference Thobois S. Proposed dose equivalence for rapid switch between dopamine receptor agonists in Parkinson’s disease: a review of the literature. Clin Ther. 2006;28:1–12.CrossRefPubMed Thobois S. Proposed dose equivalence for rapid switch between dopamine receptor agonists in Parkinson’s disease: a review of the literature. Clin Ther. 2006;28:1–12.CrossRefPubMed
13.
14.
15.
16.
go back to reference Dice LR. Measures of the amount of ecologic association between species. Ecology. 1945;26:297.CrossRef Dice LR. Measures of the amount of ecologic association between species. Ecology. 1945;26:297.CrossRef
17.
go back to reference Stroman PW, Figley CR, Cahill CM. Spatial normalization, bulk motion correction and coregistration for functional magnetic resonance imaging of the human cervical spinal cord and brainstem. Magn Reson Imaging. 2008;26:809–14.CrossRefPubMed Stroman PW, Figley CR, Cahill CM. Spatial normalization, bulk motion correction and coregistration for functional magnetic resonance imaging of the human cervical spinal cord and brainstem. Magn Reson Imaging. 2008;26:809–14.CrossRefPubMed
18.
go back to reference Baudrexel S, Volz S, Preibisch C, Klein JC, Steinmetz H, Hilker R, Deichmann R. Rapid single-scan T2*-mapping using exponential excitation pulses and image-based correction for linear background gradients. Magn Reson Med. 2009;62:263–8.CrossRefPubMed Baudrexel S, Volz S, Preibisch C, Klein JC, Steinmetz H, Hilker R, Deichmann R. Rapid single-scan T2*-mapping using exponential excitation pulses and image-based correction for linear background gradients. Magn Reson Med. 2009;62:263–8.CrossRefPubMed
19.
go back to reference Preibisch C, Volz S, Anti S, Deichmann R. Exponential excitation pulses for improved water content mapping in the presence of background gradients. Magn Reson Med. 2008;60:908–16.CrossRefPubMed Preibisch C, Volz S, Anti S, Deichmann R. Exponential excitation pulses for improved water content mapping in the presence of background gradients. Magn Reson Med. 2008;60:908–16.CrossRefPubMed
20.
go back to reference Zheng W, Nichol H, Liu S, Cheng YN, Haacke EM. Measuring iron in the brain using quantitative susceptibility mapping and X‑ray fluorescence imaging. Neuroimage. 2013;78:68–74.CrossRefPubMedPubMedCentral Zheng W, Nichol H, Liu S, Cheng YN, Haacke EM. Measuring iron in the brain using quantitative susceptibility mapping and X‑ray fluorescence imaging. Neuroimage. 2013;78:68–74.CrossRefPubMedPubMedCentral
21.
go back to reference Acosta-Cabronero J, Williams GB, Cardenas-Blanco A, Arnold RJ, Lupson V, Nestor PJ. In vivo quantitative susceptibility mapping (QSM) in Alzheimer’s disease. PLoS ONE. 2013;8:e81093.CrossRefPubMedPubMedCentral Acosta-Cabronero J, Williams GB, Cardenas-Blanco A, Arnold RJ, Lupson V, Nestor PJ. In vivo quantitative susceptibility mapping (QSM) in Alzheimer’s disease. PLoS ONE. 2013;8:e81093.CrossRefPubMedPubMedCentral
Metadata
Title
T2* Relaxometry in Patients with Parkinson’s Disease
Use of an Automated Atlas-based Approach
Authors
Karl Egger
Florian Amtage
Shan Yang
Markus Obmann
Ralf Schwarzwald
Lena Köstering
Irina Mader
Julia Koenigsdorf
Cornelius Weiller
Christoph P. Kaller
Horst Urbach
Publication date
01-03-2018
Publisher
Springer Berlin Heidelberg
Published in
Clinical Neuroradiology / Issue 1/2018
Print ISSN: 1869-1439
Electronic ISSN: 1869-1447
DOI
https://doi.org/10.1007/s00062-016-0523-2

Other articles of this Issue 1/2018

Clinical Neuroradiology 1/2018 Go to the issue