Scottish Bipolar Family Study fMRI (Whalley 2013)
Scottish Bipolar Family Study, baseline task fMRI of young relatives at high familial risk of bipolar disorder and controls (Whalley et al. 2013, PLOS ONE)
Task fMRI and structural brain MRI of young unaffected relatives of people with bipolar disorder and matched controls, followed for about two years to test whether baseline brain activation predicts later major depression.
Overview
This entry covers the baseline functional MRI sample of the Scottish Bipolar Family Study, run by the Division of Psychiatry at the University of Edinburgh. Psychiatrists across Scotland identified patients with bipolar I disorder, who named relatives aged 16 to 25. Relatives with no mood or psychotic illness themselves were scanned once and reassessed about two years later. Whalley and colleagues (PLOS ONE, 2013) used the sample to ask whether brain activation at baseline separates the relatives who went on to develop major depression from those who stayed well. They reported higher insula activation with rising task difficulty in those who later became ill.
Composition
Baseline scans exist for 110 high-risk relatives (at least one first-degree or two second-degree relatives with bipolar I disorder) and 70 unrelated controls drawn from the relatives' social networks and matched for age, sex and premorbid IQ. Follow-up status could not be established for 10 relatives and 8 controls, and 4 controls who developed depression were dropped. The analysed sample is 156: 58 controls, 78 relatives who stayed well and 20 who developed major depression. Two further relatives developed bipolar disorder. Mean age per group is about 21 years. Clinical measures include the Hamilton depression and Young mania scales, TEMPS-A temperament and the NEO five-factor inventory.
Acquisition
All scans were acquired on a GE 1.5 T Signa scanner at the Scottish Brain Imaging Research Centre in Edinburgh. The functional run was gradient-echo EPI (TR 2 s, TE 40 ms, 27 axial 5 mm slices, 404 volumes) during a block-design Hayling sentence completion task with four difficulty levels. A T1-weighted volume with 180 coronal 1.2 mm slices served for registration. Processing used SPM5.
Annotations
No image annotations. Labels are group membership, follow-up diagnosis from structured interview or health records, and the clinical and personality scores.
Known limitations
- The scans have no public release and the paper gives no data access route or terms.
- The figshare record holds supplementary documents only, not imaging data.
- Sex counts cover the 156 analysed subjects, not all 180 scanned.
- Follow-up for 33 subjects came from written contact with the health service rather than an interview.
Cohort
Aggregate numbers from the sources below. Bars are relative to the 180 subjects.
Contrast / sequence
Groups can overlap
- BOLD fMRI 180 100%
- T1-weighted 156 87%
Methods: Main analysis in Whalley et al. 2013, PLOS ONE; Scanning procedure; Image processing and analysis in Whalley et al. 2013, PLOS ONE, Supplementary Text S1 (methods)
Scanner vendor
- GE HealthCare 180 100%
Scanning procedure in Whalley et al. 2013, PLOS ONE, Supplementary Text S1 (methods)
Condition
Groups can overlap
- Healthy control 70 39%
- Major depressive disorder 20 11%
- Bipolar disorder 2 1%
Methods: Main analysis, Results in Whalley et al. 2013, PLOS ONE
Field strength
- 1.5 T 180 100%
Scanning procedure in Whalley et al. 2013, PLOS ONE, Supplementary Text S1 (methods)
License and access
Our reading of the license, not legal advice. Before you use the data, read the original license and confirm that your use is allowed. We take no responsibility for how you use a dataset. Full disclaimer
The data are not available outside the institution or study that holds them
The paper has no data availability statement and names no repository for the scans. The PLOS figshare record (https://plos.figshare.com/articles/dataset/645725) holds only the supplementary methods text, one table and two figure documents, not imaging data.
No published license or data use terms
The data holder has published no license and no data use terms. Any use, sharing or commercial right has to be agreed with the data holder, and nothing can be assumed to be allowed. Default copyright and data protection law still apply.
Neither the paper nor its figshare supplement states terms for the imaging data. The CC BY license on the article covers the publication, not the scans.
What you can do
- Commercial use Not stated
- Not stated
- Train ML models Not stated
- Create derived data Not stated
- Publish results Not stated
What you can share
- Share the data Not stated
- Share derived data Not stated
- Share trained models Not stated
What you must do
- Cite or credit Not stated
- Share alike Not stated
- Sign an agreement Not stated
- Ethics approval Not stated
- Manuscript review Not stated
- Release code Not stated
- Return results Not stated
- Delete after use Not stated
Limits
- No re-identification Not stated
- Location limits Not stated
Citation
Whalley HC, Sussmann JE, Romaniuk L, Stewart T, Papmeyer M, Sprooten E, Hackett S, Hall J, Lawrie SM, McIntosh AM. Prediction of Depression in Individuals at High Familial Risk of Mood Disorders Using Functional Magnetic Resonance Imaging. PLoS ONE 8(3): e57357 (2013). doi:10.1371/journal.pone.0057357
Sources
Every number on this page comes from one of these documents. Each chart names the table or page it is taken from. The raw numbers are in stats.csv.