Abstract
Abstract
Stroke is the leading cause of adult disability worldwide, with up to two-thirds of individuals experiencing long-term disabilities. Large-scale neuroimaging studies have shown promise in identifying robust biomarkers (e.g., measures of brain structure) of long-term stroke recovery following rehabilitation. However, analyzing large rehabilitation-related datasets is problematic due to barriers in accurate stroke lesion segmentation. Manually-traced lesions are currently the gold standard for lesion segmentation on T1-weighted MRIs, but are labor intensive and require anatomical expertise. While algorithms have been developed to automate this process, the results often lack accuracy. Newer algorithms that employ machine-learning techniques are promising, yet these require large training datasets to optimize performance. Here we present ATLAS (Anatomical Tracings of Lesions After Stroke), an open-source dataset of 304 T1-weighted MRIs with manually segmented lesions and metadata. This large, diverse dataset can be used to train and test lesion segmentation algorithms and provides a standardized dataset for comparing the performance of different segmentation methods. We hope ATLAS release 1.1 will be a useful resource to assess and improve the accuracy of current lesion segmentation methods.
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References
32
[1]
Heart Disease and Stroke Statistics—2017 Update: A Report From the American Heart Association

Emelia J. Benjamin, Michael J. Blaha, Stephanie E. Chiuve et al.

Circulation 2017 10.1161/cir.0000000000000485
[2]
Global and regional burden of stroke during 1990–2010: findings from the Global Burden of Disease Study 2010

Valery L Feigin, Mohammad H Forouzanfar, Rita Krishnamurthi et al.

The Lancet 2014 10.1016/s0140-6736(13)61953-4
[3]
Kwakkel, G., Kollen, B. J., Van der Grond, J. V. & Prevo, A. J. H. Probability of regaining dexterity in the flaccid upper limb: Impact of severity of paresis and time since onset in acute stroke. Stroke 34, 2181–2186 (2003). 10.1161/01.str.0000087172.16305.cd
[4]
Ren, J., Kaplan, P. L., Charette, M. F., Speller, H. & Finklestein, S. P. Time window of intracisternal osteogenic protein-1 in enhancing functional recovery after stroke. Neuropharmacology 39, 860–865 (2000). 10.1016/s0028-3908(99)00261-0
[6]
Burke Quinlan, E. et al. Neural function, injury, and stroke subtype predict treatment gains after stroke. Ann Neurol 77, 132–145 (2015). 10.1002/ana.24309
[7]
Marie-Héléne, M. & Cramer, S. C. Biomarkers of recovery after stroke. Current opinion in neurology 21, 654–659 (2008). 10.1097/wco.0b013e3283186f96
[8]
Nijland, R. H. M., van Wegen, E. E. H., Harmeling-van der Wel, B. C. & Kwakkel, G. Presence of finger extension and shoulder abduction within 72 Hours after stroke predicts functional recovery. Stroke 41, 745–750 (2010). 10.1161/strokeaha.109.572065
[9]
Riley, J. D. et al. Anatomy of stroke injury predicts gains from therapy. Stroke 42, 421–426 (2011). 10.1161/strokeaha.110.599340
[10]
Cramer, S. C. et al. Predicting functional gains in a stroke trial. Stroke 38, 2108–2114 (2007). 10.1161/strokeaha.107.485631
[11]
Jongbloed, L. Y. N. Prediction of function after stroke: a critical review. Stroke 17, 765–776 (1986). 10.1161/01.str.17.4.765
[12]
Nouri, S. & Cramer, S. C. Anatomy and physiology predict response to motor cortex stimulation after stroke. Neurology 77, 1076–1083 (2011). 10.1212/wnl.0b013e31822e1482
[13]
Inter-individual Variability in the Capacity for Motor Recovery After Ischemic Stroke

Shyam Prabhakaran, Eric Zarahn, Claire Riley et al.

Neurorehabilitation and Neural Repair 2007 10.1177/1545968307305302
[14]
Stinear, C. Prediction of recovery of motor function after stroke. The Lancet Neurology 9, 1228–1232 (2010). 10.1016/s1474-4422(10)70247-7
[15]
Lesion Load of the Corticospinal Tract Predicts Motor Impairment in Chronic Stroke

Lin L. Zhu, Robert Lindenberg, Michael P. Alexander et al.

Stroke 2010 10.1161/strokeaha.109.577023
[16]
Fiez, J. A., Damasio, H. & Grabowski, T. J. Lesion segmentation and manual warping to a reference brain: Intra- and interobserver reliability. Human Brain Mapping 9, 192–211 (2000). 10.1002/(sici)1097-0193(200004)9:4<192::aid-hbm2>3.0.co;2-y
[17]
Montaner, J. et al. Plasmatic level of neuroinflammatory markers predict the extent of diffusion-weighted image lesions in hyperacute stroke. Journal of Cerebral Blood Flow & Metabolism 23, 1403–1407 (2003). 10.1097/01.wcb.0000100044.07481.97
[18]
Sakamoto, Y. et al. Early ischaemic diffusion lesion reduction in patients treated with intravenous tissue plasminogen activator: infrequent, but significantly associated with recanalization. International Journal of Stroke 8, 321–326 (2013). 10.1111/j.1747-4949.2012.00902.x
[19]
Thomas, R. G. R. et al. Apparent diffusion coefficient thresholds and diffusion lesion volume in acute stroke. Journal of Stroke and Cerebrovascular Diseases 22, 906–909 (2013). 10.1016/j.jstrokecerebrovasdis.2012.09.018
[20]
Wittsack, H.-J. et al. MR Imaging in Acute Stroke: Diffusion-weighted and Perfusion Imaging Parameters for Predicting Infarct Size. Radiology 222, 397–403 (2002). 10.1148/radiol.2222001731
[21]
Pustina, D. et al. Automated segmentation of chronic stroke lesions using LINDA: Lesion identification with neighborhood data analysis. Human Brain Mapping 37, 1405–1421 (2016). 10.1002/hbm.23110
[22]
de Haan, B., Clas, P., Juenger, H., Wilke, M. & Karnath, H.-O. Fast semi-automated lesion demarcation in stroke. NeuroImage. Clinical 9, 69–74 (2015). 10.1016/j.nicl.2015.06.013
[23]
Maier, O. et al. ISLES 2015—A public evaluation benchmark for ischemic stroke lesion segmentation from multispectral MRI. Medical Image Analysis 35, 250–269 (2017). 10.1016/j.media.2016.07.009
[24]
Rorden, C. & Brett, M. Stereotaxic display of brain lesions. Behav Neurol 12, 191–200 (2000). 10.1155/2000/421719
[25]
Fazekas, F., Chawluk, J., Alavi, A., Hurtig, H. & Zimmerman, R. MR signal abnormalities at 1.5 T in Alzheimer's dementia and normal aging. American Journal of Roentgenology 149, 351–356 (1987). 10.2214/ajr.149.2.351
[26]
Sled, J. G., Zijdenbos, A. P. & Evans, A. C. A nonparametric method for automatic correction of intensity nonuniformity in MRI data. IEEE Transactions on Medical Imaging 17, 87–97 (1998). 10.1109/42.668698
[27]
Automatic 3D Intersubject Registration of MR Volumetric Data in Standardized Talairach Space

D. Louis Collins, Peter Neelin, Terrence M. Peters et al.

Journal of Computer Assisted Tomography 1994 10.1097/00004728-199403000-00005
[28]
Cox, R. W. et al. A (sort of) new image data format standard: Nifti-1. Neuroimage 22, e1440 (2004).
[29]
Heuer, K., Ghosh, S., Robinson Sterling, A. & Toro, R. Open Neuroimaging Laboratory. Research Ideas and Outcomes 2, e9113 (2016). 10.3897/rio.2.e9113
[30]
Ito, K., Anglin, J. & Liew, S.-L. Semi-automated Robust Quantification of Lesions (SRQL) Toolbox. Research Ideas and Outcomes 3, e12259 (2017). 10.3897/rio.3.e12259
[31]
Liew, S.-L. ICPSR—Interuniversity Consortium for Political and Social Research https://doi.org/10.3886/ICPSR36684.v1 (2017) 10.3886/icpsr36684.v1
[32]
Liew, S.-L. Child Mind Institute https://doi.org/10.15387/fcp_indi.atlas (2017) 10.15387/fcp_indi.atlas
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Published
Feb 20, 2018
Vol/Issue
5(1)
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Cite This Article
Sook-Lei Liew, Julia M. Anglin, Nick W. Banks, et al. (2018). A large, open source dataset of stroke anatomical brain images and manual lesion segmentations. Scientific Data, 5(1). https://doi.org/10.1038/sdata.2018.11
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