11 research outputs found
Improving the Quality of EEG Data in Patients With Alzheimers Disease Using ICA
Does Independent Component Analysis (ICA) denature EEG
signals? We applied ICA to two groups of subjects (mild Alzheimer
patients and control subjects). The aim of this study was to examine
whether or not the ICA method can reduce both group di®erences and
within-subject variability. We found that ICA diminished Leave-One-
Out root mean square error (RMSE) of validation (from 0.32 to 0.28),
indicative of the reduction of group di®erence. More interestingly, ICA
reduced the inter-subject variability within each group (¾ = 2:54 in the
± range before ICA, ¾ = 1:56 after, Bartlett p = 0.046 after Bonfer-
roni correction). Additionally, we present a method to limit the impact
of human error (' 13:8%, with 75.6% inter-cleaner agreement) during
ICA cleaning, and reduce human bias. These ¯ndings suggests the novel
usefulness of ICA in clinical EEG in Alzheimer's disease for reduction of
subject variability
Formal derivation to object-oriented implementation of financial policies
International Journal of Computer Applications in Technology105-6316-326IJCT
Corpus callosum morphology in first-episode and chronic schizophrenia: Combined magnetic resonance and diffusion tensor imaging study of Chinese Singaporean patients
10.1192/bjp.bp.113.127886British Journal of Psychiatry204155-60BJPY
Duration of illness, regional brain morphology and neurocognitive correlates in schizophrenia
Annals of the Academy of Medicine Singapore385388-395AAMS
Plasma fatty acids, oxylipins, and risk of myocardial infarction: the Singapore Chinese Health Study
We aimed to examine the prospective association between plasma FAs, oxylipins, and risk of acute myocardial infarction (AMI) in a Singapore Chinese population. A nested case-control study with 744 incident AMI cases and 744 matched controls aged 47–83 years was conducted within the Singapore Chinese Health Study. Nineteen plasma FAs and 12 oxylipins were quantified using MS. These were grouped into 12 FA clusters and 5 oxylipin clusters using hierarchical clustering, and their associations with AMI risk were assessed. Long-chain n-3 FAs [odds ratio (OR) = 0.67 per SD increase, 95% confidence interval (CI): 0.53–0.84, P < 0.001] and stearic acid (OR = 0.65, 95% CI: 0.44–0.97, P = 0.03) were inversely associated with AMI risk, whereas arachidonic acid (AA) was positively associated with AMI risk (OR = 1.25, 95% CI: 1.03–1.52, P = 0.02) in the multivariable model with adjustment for other FAs. Further adjustment for oxylipins did not substantially change these associations. An inverse association was observed between AA-derived oxylipin, thromboxane (TX)B(2), and AMI risk (OR = 0.81, 95% CI: 0.71–0.93, P = 0.003). Circulating long-chain n-3 FAs and stearic acid were associated with a lower and AA was associated with a higher AMI risk in this Chinese population. The association between the oxylipin TXB(2) and AMI requires further research