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Chapter 41 - Iron imaging in neurodegenerative disorders

from Section 6 - Psychiatric and neurodegenerative diseases

Published online by Cambridge University Press:  05 March 2013

By
Prashanthi Vemuri  and
Clifford R. Jack Jr.
Edited by
Jonathan H. Gillard ,
Adam D. Waldman  and
Peter B. Barker
Jonathan H. Gillard
Affiliation:
University of Cambridge
Adam D. Waldman
Affiliation:
Imperial College London
Peter B. Barker
Affiliation:
The Johns Hopkins University School of Medicine
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Summary

Introduction

Iron plays an important role in normal neuronal metabolism. Excessive iron is, however, considered to be harmful because of its role in causing oxidative stress. It is well established in the literature that abnormal non-heme iron deposits (in different forms) occur in neurodegenerative disorders, including Alzheimer’s disease (AD), Huntington’s disease (HD), Parkinson’s disease (PD), multiple sclerosis, and neurodegenerative brain iron accumulation (NBIA). This suggests that oxidative stress resulting from imbalance in iron regulation may contribute to the pathological cascade in these diseases. The metabolism of brain iron and its potential role in causing various neurodegenerative disorders has been discussed in detail in Moos and Morgan [1] and Berg and Youdim.[2] Iron imaging will play an important role in understanding the mechanisms and may be useful for early diagnosis of neurodegenerative disorders. This chapter has two objectives: to present the basics of iron signal detection using magnetic resonance imaging (MRI) and to examine the potential of MRI techniques for imaging abnormal iron deposits in various neurodegenerative disorders.

Iron signal in MRI

The MRI approach utilizes the nuclear magnetic resonance of atomic nuclei and, because of the abundance of protons in the human body (primarily in tissue water), MRI machines use signal from protons for imaging. The signal contrast in MR images mainly originates from differences in the proton density, longitudinal relaxation (T1) and transverse relaxation (T2) of protons in different tissues. Additionally in sequences such as gradient echo sequences where there is no 180° radiofrequency pulse to refocus the dephasing resulting from magnetic field inhomogeneity, the amplitude of the gradient echo carries a 1/T2* weighting where 1/T2* = 1/T2 + 1/T2′ where T2′ is the reversible contribution resulting from local magnetic field inhomogeneity. Since MRI detects changes in electromagnetic signals, changes in local magnetic field inhomogeneities caused by the presence of iron alter the signal contrast in the images. The presence of iron is mainly associated with reduction of T1, T2, and T2* relaxation of protons. There has been some recent work on using additional MRI contrasts such as diffusion tensor imaging (DTI) metrics and rotating frame relaxation constants, longitudinal (T1ρ) and transverse (T2ρ), to measure local iron content.

Type
Chapter
Information
Clinical MR Neuroimaging
Physiological and Functional Techniques
 , pp. 642 - 652
Publisher: Cambridge University Press
Print publication year: 2009

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