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Docteur de l'université Automatic Segmentation and Shape Analysis ...

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Chapter 5 Quantitative shape analysis of hippocampus in AD 127<br />

Sensitivity<br />

0.78 0.82 0.86<br />

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1e−04 1e−03 1e−02 1e−01 1e+00<br />

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1e−04 1e−03 1e−02 1e−01 1e+00<br />

(a) Testing set sensitivity, LR, MR (b) Testing set sensitivity, LR, MS<br />

Sensitivity<br />

0.55 0.65 0.75 0.85<br />

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Threshold α<br />

(c) Testing set sensitivity, LS, MR<br />

Sensitivity<br />

Sensitivity<br />

0.78 0.80 0.82 0.84 0.86<br />

0.60 0.70 0.80<br />

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(d) Testing set sensitivity, LS, MS<br />

Figure 5.8: The sensitivity of the disease classification using bagged support<br />

vector machines (SVMs) with varying thresholds in the l<strong>and</strong>mark selection on<br />

a separated testing set. Black circles: shape features from the Statistical <strong>Shape</strong><br />

Mo<strong>de</strong>l (SSM) only; red circles: shape features with additional volume features.<br />

of significant shape difference between the two groups revealed a different profile<br />

with more localized effects mainly located in the posterior hippocampus. Because<br />

global changes were mainly driven by the predominant effects in the CA1 <strong>and</strong><br />

subiculum subfields, it is not surprising that the changes in<strong>de</strong>pen<strong>de</strong>nt from these<br />

main effects reveals a different pattern.<br />

It should be pointed out that the hippocampal subregions affected by AD were<br />

i<strong>de</strong>ntified by comparing the AD subpopulation with NC, which did not take into<br />

account the association of AD <strong>and</strong> its cognitive outcome with other factors such<br />

as age <strong>and</strong> level of education. Hippocampal atrophy has been shown to <strong>de</strong>velop<br />

during the course of normal aging (Jack et al., 1998; Malykhin et al., 2008; Chételat<br />

et al., 2008; La Joie et al., 2010). The shape changes <strong>and</strong> variations reflect the<br />

combined effect of aging <strong>and</strong> AD, which may limit the discrimination ability of<br />

the shape analysis. In the future work it will be of interest to explicitly control<br />

the effects of normal aging on the hippocampus <strong>and</strong> other variables such as years<br />

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