Table 1.
Group | CCR5 Genotype Prevalence a | CCR5 Allele Prevalence | ||
---|---|---|---|---|
wt/wt | wt/ Δ32 | Δ32/ Δ32 | (wt/Δ32 Allele) | |
Healthy controls (n = 265) | 212 (82.5%) | 41 (16.0%) | 4 (1.6%) | 0.905/0.095 |
TBE (n = 205) | 166 (81.0%) | 36 (17.6%) | 3 (1.5%) | 0.898/0.102 |
Clinical presentation | ||||
meningitis (M) (n = 109) | 88 (80.7%) | 19 (17.4%) | 2 (1.8%) | 0.894/0.106 |
meningoencephalitis (ME) (n = 77) | 63 (81.8%) | 13 (16.9%) | 1 (1.3%) | 0.903/0.097 |
meningoencephalomyelitis (MEM) (n = 19) | 15 (78.9%) | 4 (21.1%) | 0 (0.0%) | 0.895/0.105 |
Severity of ME/MEM | ||||
mild (n = 43) | 36 (83.7%) | 6 (14.0%) | 1 (2.3%) | 0.907/0.093 |
moderate (n = 36) | 30 (83.3%) | 6 (16.7%) | 0 (0.0%) | 0.917/0.083 |
severe (n = 17) | 12 (70.6%) | 5 (29.4%) | 0 (0.0%) | 0.853/0.147 |
Consciousness abnormalities | ||||
absent (n = 155) | 128 (82.6%) | 24 (15.4%) | 3 (1.9%) | 0.903/0.097 |
present (n = 50): | 38 (76.0%) | 12 (24.0%) | 0 (0.0%) | 0.880/0.120 |
mild (n = 33) | 26 (78.8%) | 7 (21.2%) | 0 (0.0%) | 0.894/0.106 |
moderate (n = 9) | 6 (66.7%) | 3 (33.3%) | 0 (0.0%) | 0.833/0.167 |
severe (n = 8) | 6 (75.0%) | 2 (25.0%) | 0 (0.0%) | 0.875/0.125 |
Paresis | ||||
absent (n = 187) | 152 (81.3%) | 32 (17.1%) | 3 (1.6%) | 0.898/0.102 |
present (n = 18) | 14 (77.8%) | 4 (22.2%) | 0 (0.0%) | 0.889/0.111 |
Cerebellar syndrome | ||||
absent (n = 166) | 134 (80.7%) | 30 (18.1%) | 2 (1.2%) | 0.898/0.102 |
present (n = 39) | 32 (82.1%) | 6 (15.4%) | 1 (2.6%) | 0.897/0.103 |
Disease course | ||||
monophasic (n = 110) | 87 (79.1%) | 21 (19.1%) | 2 (1.8%) | 0.886/0.114 |
biphasic (n = 92) | 78 (84.8%) | 13 (14.1%) | 1 (1.1%) | 0.918/0.082 |
a number of cases (frequency of a genotype in %); wt—wild type.