Neurology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


Published online before print January 2, 2008, doi:10.1212/01.wnl.0000286384.31050.b5)
This Article
Right arrow Full Text (Rapid PDF)
Right arrow All Versions of this Article:
01.wnl.0000286384.31050.b5v1
70/16_Part_2/1411    most recent
Right arrow Correspondence:
Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when Correspondence are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Martin, W. R. W.
Right arrow Articles by Gee, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Martin, W. R. W.
Right arrow Articles by Gee, M.
Received April 14, 2007
Accepted August 8, 2007

Midbrain iron content in early Parkinson disease. A potential biomarker of disease status

W. R. Wayne Martin MD*, Marguerite Wieler MSc, and Myrlene Gee PhD

From the Division of Neurology (W.R.W.M., M.W.), and Department of Biomedical Engineering (M.G.), University of Alberta, Edmonton, Canada.


* To whom correspondence should be addressed. E-mail: wayne.martin{at}ualberta.ca.

ABSTRACT

Background: Parkinson disease (PD) is a progressive neurodegenerative disorder in which the major pathologic substrate is a loss of dopaminergic neurons from the lateral substantia nigra pars compacta (SNc). Our objective was to determine whether, in patients with early PD, SNc changes evident on MRI sequences sensitive to iron content corresponded anatomically to the pathologic changes reported previously, and to correlate these changes to the duration and severity of clinical manifestations of PD.

Methods: Twenty-six untreated patients with early PD and 13 age- and gender-matched control subjects had MRI with a 3 tesla magnet using a multiple gradient echo sequence designed for rapid single-scan mapping of the proton transverse relaxation rate (R2*). R2* was calculated for midbrain and forebrain basal ganglia regions. Clinical features were rated with the Unified PD Rating Scale.

Results: A difference in measured R2* values between patients and controls was observed in the lateral SNc (p ≤ 0.005). Linear regression indicated a correlation between the lateralized motor score from the clinically most affected side and R2* values from the opposite lateral SNc (p = 0.01).

Conclusions: High field strength MRI demonstrates lateral substantia nigra pars compacta abnormalities in early Parkinson disease (PD) consistent with increased iron content and corresponding to the known distribution of neuronal loss occurring in this disorder. This may ultimately provide an imaging marker for disease progression in PD, although longitudinal studies are required.




This article has been cited by other articles:


Home page
J. Biol. Chem.Home page
D. W. Lee, S. Rajagopalan, A. Siddiq, R. Gwiazda, L. Yang, M. F. Beal, R. R. Ratan, and J. K. Andersen
Inhibition of Prolyl Hydroxylase Protects against 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced Neurotoxicity: MODEL FOR THE POTENTIAL INVOLVEMENT OF THE HYPOXIA-INDUCIBLE FACTOR PATHWAY IN PARKINSON DISEASE
J. Biol. Chem., October 16, 2009; 284(42): 29065 - 29076.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
A. E. Lang and D. Mikulis
A new sensitive imaging biomarker for Parkinson disease?
Neurology, April 21, 2009; 72(16): 1374 - 1375.
[Full Text] [PDF]


Home page
NeurologyHome page
D. E. Vaillancourt, M. B. Spraker, J. Prodoehl, I. Abraham, D. M. Corcos, X. J. Zhou, C. L. Comella, and D. M. Little
High-resolution diffusion tensor imaging in the substantia nigra of de novo Parkinson disease
Neurology, April 21, 2009; 72(16): 1378 - 1384.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Neuroradiol.Home page
S. Mittal, Z. Wu, J. Neelavalli, and E.M. Haacke
Susceptibility-Weighted Imaging: Technical Aspects and Clinical Applications, Part 2
AJNR Am. J. Neuroradiol., February 1, 2009; 30(2): 232 - 252.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Copyright © 2008 by AAN Enterprises, Inc.