BioFINDER-1
The Swedish BioFINDER Study (Biomarkers For Identifying Neurodegenerative Disorders Early and Reliably), BioFINDER-1
Brain MRI, amyloid and tau PET with CSF, blood and cognitive tests from older adults who are cognitively healthy or have memory complaints, dementia or parkinsonism, followed for up to 10 years to find early markers of Alzheimer's and Parkinson's disease. Data on request.
Overview
BioFINDER-1 is the first Swedish BioFINDER cohort, run by Lund University and Skåne University Hospital to find early and reliable markers of Alzheimer's disease, Parkinson's disease and related disorders. Participants were examined repeatedly with clinical and cognitive testing, CSF and blood sampling, MRI and, in subsets, amyloid and tau PET. The study has stopped enrolling and following participants. A second, independent cohort (BioFINDER-2) started in 2017 and is not covered by this entry.
Composition
The study website gives more than 1,600 participants in four cohorts. Cognitively healthy adults aged 60 or older were sampled at random from the Malmö Diet and Cancer Study (2010 to 2016). People referred to the memory clinics of Skåne University Hospital and Ängelholm Hospital with subjective cognitive decline or mild cognitive impairment (MCI) were enrolled consecutively (2010 to 2015). A dementia cohort of 300 patients covers Alzheimer's disease, vascular dementia, dementia with Lewy bodies, Parkinson's disease dementia and frontotemporal dementia, with 50 more patients with familial Alzheimer's disease. A parkinsonian cohort from the neurology clinic in Lund, recruited from 2008, covers Parkinson's disease, progressive supranuclear palsy and multiple system atrophy. The ClinicalTrials.gov record of the healthy and SCD/MCI arms lists an actual enrollment of 1,150. Vogel et al. (2019) analysed 123 participants with MRI and [18F]flortaucipir PET: 55 controls, 21 amyloid-positive MCI and 47 amyloid-positive Alzheimer's dementia patients.
Acquisition
All cohorts except the parkinsonian one were scanned on one 3 T Siemens Trio: T1-weighted spin echo and MPRAGE, FLAIR, T2*-weighted gradient echo, diffusion tensor and kurtosis imaging, resting-state fMRI, arterial spin labelling and single-voxel MR spectroscopy. The parkinsonian cohort used a 3 T Siemens Skyra with T2-weighted spin echo, FLAIR, SWI, MPRAGE, multi-shell diffusion, resting-state fMRI and ASL. Amyloid PET with [18F]flutemetamol and tau PET with [18F]flortaucipir, repeated every two years, ran on a Philips Gemini TF 16. The methods page also lists F-DOPA PET without any details, so it is not counted here. MRI was repeated every 24 months.
Known limitations
- Images are not publicly released; data are shared only on request for replicating a published article.
- Per-cohort counts on the website read as cohort sizes, and the number of participants with each scan type is not published.
- PET was done only in subsets, and tau PET was added after the study had started.
Cohort
Aggregate numbers from the sources below. Bars are relative to the largest value.
PET tracer
- [18F]flortaucipir 123
Condition by pet tracer
Reported cross table. A dot marks a cell the source does not give.
| [18F]flortaucipir | |
|---|---|
| Healthy control | 55 |
| Alzheimer's disease | 47 |
| Mild cognitive impairment | 21 |
Condition
Groups can overlap
- Dementia 300
Dementia cohort in BioFINDER website, BioFINDER One population and study design
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
Ask the authors or the data holder. No published process or terms, and access is at their discretion
No data access page is published. Papers from the study state that anonymized data are shared on request with qualified academic investigators to replicate the published results, under a material transfer agreement.
Swedish BioFINDER data availability statement (sharing on request under a material transfer agreement)
BioFINDER publishes no license or data use agreement. Its papers state that anonymized data are shared on request with qualified academic investigators, only to replicate the procedures and results of the article, when the transfer complies with the GDPR and Swedish ethics and Region Skåne decisions, under a material transfer agreement whose terms are not published.
What you can do
- No
- Not stated
- Conditional
- Not stated
- Publish results Not stated
What you can share
- Not stated
- Share derived data Not stated
- Share trained models Not stated
What you must do
- No
- Share alike No
- Yes
- Conditional
- Manuscript review No
- Release code No
- Return results No
- Delete after use No
Limits
- No
- Conditional
Citation
No dataset citation is requested. Cite the BioFINDER papers whose results you use, e.g. Vogel JW, et al. Data-driven approaches for tau-PET imaging biomarkers in Alzheimer's disease. Human Brain Mapping 40, 638-651 (2019). doi:10.1002/hbm.24401
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.
- BioFINDER website, BioFINDER One overview website
- BioFINDER website, BioFINDER One population and study design website
- BioFINDER website, BioFINDER One methods website
- ClinicalTrials.gov record NCT01208675, The Swedish BioFINDER Study website
- Vogel JW et al. 2019, Data-driven approaches for tau-PET imaging biomarkers in Alzheimer's disease, Human Brain Mapping paper
- Smith R et al. 2020, The accumulation rate of tau aggregates is higher in females and younger amyloid-positive subjects, Brain paper