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. 2017 Feb 16;7:42796. doi: 10.1038/srep42796

Table 4. Clinical characteristics in BM patients and genotypes and allele frequencies of TLR9 rs352139.

Characteristics Patients with symptoms or parameters defined (%)& OR (95%CI) P value#
Seizures Yes (n = 95) No (n = 122)    
GG 22 (23.2) 13 (10.7) 1 Ref.
GA 49 (51.6) 60 (49.2) 2.072 (0.947–4.532) 0.065
AA 24 (25.3) 49 (40.2) 0.289 (0.125–0.672) 0.003
G 93 (48.9) 86 (35.2) 1 Ref.
A 97 (51.1) 158 (64.8) 0.568 (0.386–0.836) 0.004
Bacteremia Yes (n = 65) No (n = 152)    
GG 5 (7.7) 30 (19.7) 1 Ref.
GA 33 (50.8) 76 (50.0) 2.604 (0.929–7.299) 0.062
AA 27 (41.5) 46 (30.3) 3.522 (1.221–10.158) 0.016
G 43 (33.1) 136 (44.7) 1 Ref.
A 87 (66.9) 168 (55.3) 1.637 (1.066–2.519) 0.024
Glucose in CSF (mmol/L)*  ≤ 1.5 (n = 61) >1.5 (n = 151)    
GG 8 (13.1) 26 (17.2) 1 Ref.
GA 32 (52.5) 75 (49.7) 1.387 (0.567–3.390) 0.472
AA 21 (34.4) 50 (33.1) 1.365 (0.532–3.502) 0.517
G 48 (39.3) 127 (42.1) 1 Ref.
A 74 (60.7) 175 (57.9) 0.894 (0.582–1.373) 0.608

There were no statistically significant differences between SNPs of TLR9 rs352139 in other clinical characteristics including consciousness, subdural effusion, hearing loss, CSF white cell numbers, CSF proteins and long-term prognosis (all p > 0.05).

*Information was only available in 212 subjects.

Abbreviations: CSF, cerebrospinal fluid; OR, odds ratio; CI, confidence interval.