One major hallmark of the Alzheimer's disease (AD) is the loss of neurons in the brain. In many cases, medical experts
use magnetic resonance imaging (MRI) to qualitatively measure the neuronal loss by the shrinkage or enlargement of the
structures-of-interest. Brain ventricle is one of the popular choices. It is easily detectable in clinical MR images due to the
high contrast of the cerebro-spinal fluid (CSF) with the rest of the parenchyma. Moreover, atrophy in any periventricular
structure will directly lead to ventricle enlargement. For quantitative analysis, volume is the common choice. However,
volume is a gross measure and it cannot capture the entire complexity of the anatomical shape. Since most existing shape
descriptors are complex and difficult-to-reproduce, more straightforward and robust ways to extract ventricle shape features
are preferred in the diagnosis. In this paper, a novel ventricle shape based classification method for Alzheimer's disease has
been proposed. Training process is carried out to generate two probability maps for two training classes: healthy controls
(HC) and AD patients. By subtracting the HC probability map from the AD probability map, we get a 3D ventricle
discriminant map. Then a matching coefficient has been calculated between each training subject and the discriminant
map. An adjustable cut-off point of the matching coefficients has been drawn for the two classes. Generally, the higher
the cut-off point that has been drawn, the higher specificity can be achieved. However, it will result in relatively lower
sensitivity and vice versa. The benchmarked results against volume based classification show that the area under the ROC
curves for our proposed method is as high as 0.86 compared with only 0.71 for volume based classification method.
Access to the requested content is limited to institutions that have purchased or subscribe to SPIE eBooks.
You are receiving this notice because your organization may not have SPIE eBooks access.*
*Shibboleth/Open Athens users─please
sign in
to access your institution's subscriptions.
To obtain this item, you may purchase the complete book in print or electronic format on
SPIE.org.
INSTITUTIONAL Select your institution to access the SPIE Digital Library.
PERSONAL Sign in with your SPIE account to access your personal subscriptions or to use specific features such as save to my library, sign up for alerts, save searches, etc.