Premium
Correlation of iron in the hippocampus with MMSE in patients with Alzheimer's disease
Author(s) -
Ding Bei,
Chen KeMin,
Ling HuaWei,
Sun Fei,
Li Xia,
Wan Tao,
Chai WeiMin,
Zhang Huan,
Zhan Ying,
Guan YongJing
Publication year - 2009
Publication title -
journal of magnetic resonance imaging
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.563
H-Index - 160
eISSN - 1522-2586
pISSN - 1053-1807
DOI - 10.1002/jmri.21730
Subject(s) - hippocampus , putamen , coronal plane , medicine , globus pallidus , correlation , fornix , cardiology , magnetic resonance imaging , pathology , gastroenterology , nuclear medicine , nuclear magnetic resonance , basal ganglia , radiology , physics , central nervous system , geometry , mathematics
Abstract Purpose To investigate the brain iron deposits in patients with Alzheimer's disease (AD) and healthy age‐matched controls using phase imaging. Materials and Methods Twenty‐six AD patients and 24 healthy controls were recruited. A three‐dimensional high‐resolution, gradient‐echo sequence was used to acquire phase data in the coronal plane. A high‐pass filter was used to remove the phase variation caused by field inhomogeneity. The regions evaluated included the bilateral putamen, globus pallidus, and the head and body of the hippocampus. Results Significantly lower phase values in both the basal ganglion and hippocampus were revealed in the AD group compared to the normal controls ( P < 0.05). The phase value in the right side of the head of the hippocampus had a moderate positive correlation with the MMSE score ( r = 0.603, P = 0.000) and a negative correlation with the duration of the disease ( r = −0.677, P = 0.013). Using −0.0972 radians as an optimal cutoff value, the sensitivity and specificity for differentiation between AD and normal controls reached 95.8 and 80.8%, respectively. Conclusion Phase imaging proved to be a useful method for the differentiation between normal controls and AD patients. An investigation of the excessive accumulation of iron in the hippocampus may help us better understand the pathologic process and neuropsychological dysfunction of AD disease. J. Magn. Reson. Imaging 2009;29:793–798. © 2009 Wiley‐Liss, Inc.