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. Author manuscript; available in PMC: 2011 May 23.
Published in final edited form as: Lancet Neurol. 2009 Oct 29;8(12):1111–1119. doi: 10.1016/S1474-4422(09)70275-3

Table 1a.

Clinical characteristics of the derivation samples

Analysis stratum US UK

Subject Source BWH WU ACP UCSF RUSH UC 1958 BC

Number of controls 4071 13 35 142 489 - 1030
Number of Cases 227 152 597 407 - 831 -
Female: Male ratio 2.8:1.0 3.1:1.0 3.1:1.0 5.6:1.0 - 2.28:1.0 -
Mean Disease Duration, years (range) 12 (<1–58) 13 (<1–39) 15 (1–56) 12(<1–47) - 14 (<1–54) -
Mean age at onset, years (range) 33 (8–59) 33 (13–71) 33 (1–70) 42 (3–60) - 32 (10–67) -

Disease course, n (%)
- -
“Bout onset” 178 (78%) 128 (84%) 463 (78%) 345 (85%) - 732 (88%) -
Relapse Remitting 136 (60%) 106 (70%) 358 (60%) 237 (58%) - NA2 -
Secondary Progressive 42 (19%) 22 (14%) 105 (18%) 111 (27%) - NA2 -
Primary Progressive 17 (8%) 17 (11%) 36 (6%) 23 (6%) - 84 (10%) -
Clinically Isolated Syndrome 25 (11%) 7 (4%) 75 (13%) 10 (2%) - 0 (0%) -
Unknown 7 (3%) 0 23 (4%) 26 (6%) - 15 (2%) -
1

BWH controls – these subjects of European ancestry recruited in the Boston area include (1) unaffected spouses from our MS Genetics collections (n=14), (2) The BWH PhenoGenetic Project subjects (n=292), and healthy subjects from the HPCGG collection (n=101) (see methods for details). These subjects do not overlap with BWH control subjects used in the meta-analysis.

2

NA – the breakdown of remitting relapsing and secondary progressive subjects is not available in this cohort.

Glossary: 1958 BC – 1958 birth cohort; ACP – Accelerated Cure Project; BWH – Brigham & Women’s Hospital; RUSH – RUSH University; UC – University of Cambridge, UK; UCSF – University California, San Francisco; UK – United Kingdom; US – United States; WU – Washington University, St. Louis