AJDRAJNR - American Journal of Neuroradiology

This Article
Right arrow Abstract Freely available
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
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 CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ishii, K.
Right arrow Articles by Mori, E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ishii, K.
Right arrow Articles by Mori, E.

Voxel-Based Morphometric Comparison Between Early- and Late-Onset Mild Alzheimer’s Disease and Assessment of Diagnostic Performance of Z Score Images

Kazunari Ishiia, Takashi Kawachia,c, Hiroki Sasakia, Atsushi K Konoa, Tetsuya Fukudaa, Yoshio Kojimaa and Etsuro Morib

a Department of Radiology, Hyogo Brain and Heart Center, Himeji, Hyogo, Japan
b Institute for Aging Brain and Cognitive Disorders, Hyogo Brain and Heart Center, Himeji, Hyogo, Japan
c Department of Psychiatry, Kobe University, Kobe, Hyogo, Japan



View larger version (63K):

[in a new window]
 
FIG 1. Statistical parametric maps show specific pixels that indicate a negative correlation between aging and gray matter loss in healthy subjects. The gray matter loss in the hypothalamic region, perisylvian cortices, parahippocampal gyri, and pre- and postcentral gyri are significantly and negatively correlated with age (P < .05, corrected). L indicates left; R, right.



View larger version (35K):

[in a new window]
 
FIG 2. A, Statistical parametric maps show comparison of patients with early-onset AD with age-matched healthy volunteers (the younger control subjects). Highlighted areas are regions of significant gray matter loss in the patients with early-onset AD compared with age-matched control subjects at a threshold of P < .001, uncorrected. Bilateral medial temporal lobes, inferior parietal lobules, precuneus, and perisylvian cortices and the right inferior frontal gyrus and bilateral cingulate cortex are highlighted. L indicates left; R, right.

B, Statistical parametric maps show comparison of patients with late-onset AD and age-matched healthy volunteers (the older control subjects). Highlighted areas are regions of significant gray matter loss in patients with late-onset AD compared with age-matched control subjects at a threshold of P < .001, uncorrected. Bilateral medial temporal cortices are highlighted. L indicates left; R, right.



View larger version (53K):

[in a new window]
 
FIG 3. Statistical parametric maps show comparison of patients with early-onset AD and those with late-onset AD. Highlighted areas are regions of significant decreased density in patients with early-onset AD compared with those with late-onset AD at a threshold of P < .001, uncorrected. The gray matter densities in the bilateral precuneus, left parietal cortex, right middle temporal gyrus, and left fusiform gyrus were lower in the early-onset group than in the late-onset group. L indicates left; R, right.



View larger version (20K):

[in a new window]
 
FIG 4. ROC curves for patients with AD versus healthy subjects in the younger and older groups. Note the great differences in diagnostic performance between the younger and older groups. The Az value (0.94359) for early-onset AD was larger than that for late-onset AD (Az = 0.9018). True-positive fraction indicates sensitivity; false-positive fraction, 1 – specificity.



View larger version (72K):

[in a new window]
 
FIG 5. A and B, Conventional MR images (A) and Z score images (B) obtained in a 54-year-old patient with early-onset AD (MMSE score = 23). Mild right parietal lobular atrophy can be detected by visual inspection of the conventional T1-weighted images; however, the degree of atrophy was not estimated. By using the Z score map, the region and degree of atrophy can be detected easily, enabling this case to be diagnosed as AD. Areas with Z scores greater than 2 (indicated by rainbow color scale) in this subject were overlaid on the prototypic early-onset AD template map (overlaid on normal MR images with red area). L indicates left; R, right.



View larger version (71K):

[in a new window]
 
FIG 6. A and B, Conventional MR images (A) and Z score images (B) obtained in a 57-year-old healthy subject (MMSE score = 30). No atrophy is apparent on the MR images, and there are no areas with Z score greater than 2 overlaid on the prototypic early-onset AD template map. L indicates left; R, right.



View larger version (70K):

[in a new window]
 
FIG 7. A and B, Conventional MR images (A) and Z score images (B) obtained in a 73-year-old patient with late-onset AD (MMSE score = 23). Medial temporal atrophy can be detected by visual inspection of the conventional T1-weighted images. By using the Z score map, the region and degree of atrophy can be detected easily; note that the left hippocampal atrophy is stronger than the right. L indicates left; R, right.



View larger version (72K):

[in a new window]
 
FIG 8. A and B, Conventional MR images (A) and Z score images (B) in a 73-year-old healthy control subject (MMSE score = 30). The left parietal lobe seems to be atrophied on the conventional T1-weighted images, although the Z score map demonstrates that there is no significantly atrophied area