Book of abstracts - British Neuroscience Association
Book of abstracts - British Neuroscience Association
Book of abstracts - British Neuroscience Association
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69.06<br />
Comparison <strong>of</strong> data analysis techniques for direct<br />
pharmacological challenge fMRI (phMRI)<br />
McKie S (1), Lees J (1), Richardson P(1), Elliott R(1), Anderson I (1),<br />
Deakin B (1), Williams S(2)<br />
(1) <strong>Neuroscience</strong> and Psychiatry Unit (2) Imaging Science and<br />
Biomedical Engineering, , University <strong>of</strong> Manchester<br />
Direct pharmacological challenge-fMRI (direct phMRI) is used to study<br />
the dynamic effects <strong>of</strong> drugs on brain haemodynamics. A common<br />
analysis approach is to use subjective-ratings (subjective effects<br />
scales, SES) to measure subject-specific changes while a drug is<br />
being infused. However, there are several problems with this method.<br />
Therefore, we have developed an alternative based on the<br />
conventional block analysis <strong>of</strong> fMRI data – the pseudo-block analysis<br />
method (p-block).<br />
The infused drugs were mCPP and ketamine. Each subject underwent<br />
a 9 minute fMRI scan during which they self-assessed their mental<br />
state using SES. After 1 minute the drug/saline was infused. Images<br />
were acquired on a 1.5T Philips scanner with a multi-slice, single shot<br />
EPI sequence to achieve whole brain coverage. Data were analysed<br />
using SPM5. The SES analysis involved creating a regressor based<br />
on significant ratings from the SES and a random effects two-sample<br />
t-test. The p-block analysis involved dividing the 9 minute fMRI scan<br />
into 9 one-minute time-bins (T0 to T8). The average signal for each<br />
time-bin (Tn) was compared to the pre-infusion average (T0) and a<br />
random effects ANOVA was used to investigate significant signal<br />
changes.<br />
Both analysis methods resulted in the detection <strong>of</strong> similar areas for<br />
each drug, however more areas were present in the p-block analysis.<br />
This is thought to be due to individual differences in drug-induced<br />
BOLD signal time courses as well as latency effects between different<br />
brain regions. The p-block method can also be applied when no<br />
regressor is available such as animal studies.<br />
69.07<br />
Structural correlates <strong>of</strong> autistic features in young people with special<br />
educational needs: a voxel-based morphometric analysis<br />
Spencer M D, Moorhead T W J, Hoare P, Muir W J, Owens D G C, Lawrie<br />
S M, Johnstone E C<br />
Division <strong>of</strong> Psychiatry, Royal Edinburgh Hospital, Morningside Park,<br />
Edinburgh, EH10 5HF, UK<br />
Background: A strong association exists between intellectual disability<br />
and autism spectrum disorders (ASD). Although previous studies have<br />
investigated the neural correlates <strong>of</strong> ASD in intellectually unimpaired<br />
subjects, the present study is the first to address these issues in<br />
intellectually impaired subjects.<br />
Methods: We used structural MRI and voxel-based morphometry to study<br />
63 intellectually disabled adolescents receiving additional learning support,<br />
recruited via their place <strong>of</strong> education. Participants comprised 34 males and<br />
29 females with mean age 16.0 years (SD: 1.8 years) and mean IQ 59.7<br />
(SD: 7.7). We used the Social Communication Questionnaire to classify<br />
participants according to their parentally reported degree <strong>of</strong> autistic<br />
features, as scoring 1) below the threshold for ASD (n=32); 2) within the<br />
pervasive developmental disorder (PDD) range (n=16); and 3) above the<br />
threshold for autism (n=15). Groups did not differ significantly in terms<br />
<strong>of</strong> gender, age or IQ. We report tissue density differences at cluster level<br />
with adjustment for underlying smoothness.<br />
Results: We detected a reduction in grey matter density in the thalamus <strong>of</strong><br />
subjects with autistic features scoring within the PDD range as compared to<br />
subjects below the threshold for ASD (p