Brain iron is a major contributor to magnetic resonance imaging (MRI)
contrast in normal gray matter, and its role in the pathogenesis of di
fferent neurological disorders has also become apparent. Non-heme brai
n iron is present in the brain mainly in the form of ferritin, The uni
que magnetic properties of ferritin determine different signal changes
on both T1- and T2 weighted images, and the T2 relaxation rates have
a linear dependence on applied field strength, This finding is typical
for ferric oxyhydroxide cores. The resulting T2-shortening also depen
ds on echo-spacing used in the imaging sequence as well as on the wate
r diffusion coefficient and the size of the ferritin cluster, Quantita
tion of non-heme brain iron by MRI aids in the diagnosis and monitorin
g of different neurological diseases.