Table 2.
Factor | Genotype | CDMS | p | Relapse | p | ||
---|---|---|---|---|---|---|---|
N | HR (95% CI) | N | HR (95% CI) | ||||
Baseline HHV6 | CC | 23 | 0.63 (0.14, 2.77) | .54 | 27 | 0.58 (0.20, 1.64) | .30 |
CT + TT | 16 | 6.95 (1.11, 43.31) | .04 | 23 | 3.00 (1.19, 7.53) | .02 | |
p interaction | .05 | p interaction | .02 | ||||
Baseline EBNA1 | CC | 23 | 1.30 (0.57, 2.99) | .54 | 27 | 1.10 (0.57, 2.12) | .77 |
CT + TT | 16 | 3.01 (1.15, 7.87) | .02 | 23 | 1.28 (0.88, 1.87) | .19 | |
p interaction | .28 | p interaction | .66 | ||||
Baseline EBNA2 | CC | 23 | 1.12 (0.59, 2.14) | .73 | 27 | 1.13 (0.74, 1.73) | .57 |
CT + TT | 16 | 4.14 (1.62, 10.56) | .003 | 23 | 1.52 (0.90, 2.56) | .12 | |
p interaction | .19 | p interaction | .68 |
HR, hazard ratio; CI, confidence interval; FDE, first demyelinating event.
Due to the smaller number people carrying TT genotype converted to CDMS (N = 2), we recoded the genotype as CT + TT. Results were adjusted for age, sex and study site, and presented as HR (95% CI) for CDMS and relapse. N refers to the number of events for each related clinical course. p value <0.05 bolded.