[No authors listed]
We performed genome-wide analyses to identify genomic loci that interact with sodium to influence blood pressure (BP) using single-marker-based (1 and 2 df joint tests) and gene-based tests among 1876 Chinese participants of the Genetic Epidemiology Network of Salt-Sensitivity (GenSalt) study. Among GenSalt participants, the average of 3 urine samples was used to estimate sodium excretion. Nine BP measurements were taken using a random zero sphygmomanometer. A total of 2.05 million single-nucleotide polymorphisms were imputed using Affymetrix 6.0 genotype data and the Chinese Han of Beijing and Japanese of Tokyo HapMap reference panel. Promising findings (P<1.00Ã10(-4)) from GenSalt were evaluated for replication among 775 Chinese participants of the Multi-Ethnic Study of Atherosclerosis (MESA). Single-nucleotide polymorphism and gene-based results were meta-analyzed across the GenSalt and MESA studies to determine genome-wide significance. The 1 df tests identified interactions for UST rs13211840 on diastolic BP (P=3.13Ã10(-9)). The 2 df tests additionally identified associations for CLGN rs2567241 (P=3.90Ã10(-12)) and LOC105369882 rs11104632 (P=4.51Ã10(-8)) with systolic BP. The CLGN variant rs2567241 was also associated with diastolic BP (P=3.11Ã10(-22)) and mean arterial pressure (P=2.86Ã10(-15)). Genome-wide gene-based analysis identified MKNK1 (P=6.70Ã10(-7)), C2orf80 (P<1.00Ã10(-12)), EPHA6 (P=2.88Ã10(-7)), SCOC-AS1 (P=4.35Ã10(-14)), SCOC (P=6.46Ã10(-11)), CLGN (P=3.68Ã10(-13)), MGAT4D (P=4.73Ã10(-11)), ARHGAP42 (Pâ¤1.00Ã10(-12)), CASP4 (P=1.31Ã10(-8)), and LINC01478 (P=6.75Ã10(-10)) that were associated with at least 1 BP phenotype. In summary, we identified 8 novel and 1 previously reported BP loci through the examination of single-nucleotide polymorphism and gene-based interactions with sodium. © 2016 American Heart Association, Inc.
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