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. Author manuscript; available in PMC: 2017 Jul 26.
Published in final edited form as: Nature. 2017 Jan 18;541(7638):481–487. doi: 10.1038/nature21029

Extended Data Table 3.

Clinical and pathological characteristics of human post mortem tissue samples from multiple sclerosis patients and age-matched controls.

Sex Age (years) PMD (hours) Disease duration (years) Disease course FDX
F 51 10 23 SP active
F 35 9 5 SP active
M 40 27 16 SP active
F 50 22 23 SP active, chronic inactive
F 42 11 6 PP chronic active
F 34 12 11 SP chronic active
F 59 21 39 SP chronic active
F 59 21 39 SP chronic active
F 53 17 28 SP chronic inactive
M 53 13 16 SP chronic inactive
F 57 12 19 SP chronic inactive
M 82 21 NA NA control, unknown
M 35 22 NA NA control, carcinoma of the tongue
M 84 5 NA NA control, carcinoma of the bladder
M 82 21 NA NA control, myelodysplastic syndrome

Inflammatory staging of subcortical MS lesions was carried out according to established histological criteria: active – presence of MOG+/LFB+ phagocytes and strong microglia activation; early inactive – presence of PAS+ phagocytes and strong microglia activation; late inactive – no macrophages and diffuse microglia activation79. Abbreviations: F, female; FDX, functional diagnosis; LFB, Luxol fast blue; M, male; MOG, myelin oligodendrocyte glycoprotein; MS, multiple sclerosis; NA, not applicable; PAS, periodic acid Schiff; PMD, postmortem delay; PP, primary progressive MS; SP, secondary progressive MS.