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. 2020 Feb 18;6(1):2055217320906844. doi: 10.1177/2055217320906844

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© The Author(s) 2020

Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).

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Figure 2. — Association between lesions at baseline in each region and the different disability scores. The estimates, odds ratios and the CIs plotted here were derived from the model defined as (2) using the whole dataset. The color associated with each estimate and CI derived from the bootstrap analysis indicates the percentage of times in which the association between lesions in specific locations and disability is stronger than the one between ‘average whole brain lesions’ and disability: values are 0–100%, higher values indicate better reproducibility. For the bootstrap analysis results, see Supplementary Table e-3. BR: supratentorial brain; BS: brainstem; CI: confidence interval; CR: cerebellum; EDSS: Expanded Disability Status Scale; EDSS-BB: EDSS bowel and bladder; EDSS-BS: EDSS brainstem; EDSS-CB: EDSS cerebellar; EDSS-CE: EDSS cerebral; EDSS-PY: EDSS pyramidal; EDSS-SE: EDSS sensory; EDSS-VI: EDSS visual; NHPT: 9-Hole Peg Test; PASAT: Paced Auditory Serial Addition Test; T25FWT: Timed 25-Foot Walk Test.