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. 2016 Apr 1;44(3):444–452. doi: 10.1177/0300060516635385

Table 3.

Distribution of ECE1 gene polymorphism genotypes and their associations with risks of intracerebral haemorrhage (ICH) in patients with ICH and healthy control subjects.

Polymorphism Genotypes Patients with ICH n = 389 Control subjects n = 404 Statistical significancea Adjusted ORb (95% CI)
rs212528 AA 265 (68.1) 258 (63.9) 1.00 (reference)
AG 110 (28.3) 128 (31.7) NS 1.361 (0.374, 4.362)
GG 14 (3.6) 18 (4.5) NS 1.173 (0.301, 3.687)
A allele 640 (82.3) 644 (79.7) NS
G allele 138 (17.7) 164 (20.3)
rs213045 GG 118 (30.3) 145 (35.9) 1.00 (reference)
GT 200 (51.4) 184 (45.5) NS 0.915 (0.432, 1.746)
TT 71 (18.3) 75 (18.6) NS 1.259 (0.594, 2.361)
G allele 436 (56.0) 474 (58.7) NS
T allele 342 (44.0) 334 (41.3)

Data presented as n of patients (%) or n of alleles (%).

a

Two-sided χ2-test test for distribution between the patients and control subjects.

b

Adjusted for age, sex, ischaemic heart disease, hypertension, type 2 diabetes mellitus, smoking and alcohol drinking status, systolic blood pressure, diastolic blood pressure, and fasting blood glucose in the binary logistic regression analysis.

OR, odds ratio; CI, confidence interval; NS, no statistically significant difference (P ≥ 0.05).