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. 2019 May 16;8(5):692. doi: 10.3390/jcm8050692

Table 1.

Study characteristics of the rs700651 variant in multi-ethnic populations.

Study First Author (Year) Population Case/Control Female Age a N/R b RAF b OR (95% CI) c p Adjusted Covariates
Bilguvar (2008) [20] FIN 874/944 NA NA A/G 0.390/0.440 1.210 (1.057–1.386) 0.0058 NA
DUT 706/5332 NA NA A/G 0.350/0.400 1.230 (1.093–1.384) 5.8 × 10−4 NA
JPT 495/676 NA NA A/G 0.540/0.460 1.300 (1.107–1.526) 0.0011 NA
Deka (2010) [21] CEU 406/392 53.3 (45.7%) 50.5/63.4 A/G 0.340/0.339 1.000 (0.808–1.237) 0.973 age
Hashikata (2010) [22] JPT 419/408 66.1 (52.0%) 60.5/60.0 A/G 0.484/0.463 1.140 (0.940–1.390) 0.19 sex, age, smoking, HTN
Low (2012) [5] JPT 1359/5464 64.7 (42.7%) 60.1/56.9 A/G 0.490/0.488 1.001 (0.919–1.091) 0.975 sex, age, PCs
Hong (2019) [11] KOR 254/290 58.4 (52.0%) 59.3/52.1 A/G 0.476/0.449 1.415 (1.095–1.829) 0.0079 sex, age, smoking, HTN

CEU: Caucasian; DUT: Dutch; FIN: Finnish; GWAS: genome-wide association study; HLP: hyperlipidemia; HTN: hypertension; JPT: Japanese in Tokyo; KOR: Korean; NA: not available; PC: principal component; a Mean age of the case (left) and control (right) groups; b N/R: non-risk/risk allele type; RAF: risk allele frequency in the case (left) and control (right) groups; c odds ratio (OR), 95% confidence interval (CI), and p-values were estimated by multivariate logistic regression after adjustment for study-specific covariates under an additive effect model.