A Quantitative Trait Locus for SBP Maps Near KCNB1 and PTGIS in a Population Isolate

作者:Barbalic Maja*; Narancic Nina Smolej; Skaric Juric Tatjana; Salihovic Marijana Pericic; Klaric Irena Martinovic; Lauc Lovorka Barac; Janicijevic Branka; Farrall Martin; Rudan Igor; Campbell Harry; Wright Alan F; Hastie Nicholas D; Rudan Pavao
来源:American Journal of Hypertension, 2009, 22(6): 663-668.
DOI:10.1038/ajh.2009.46

摘要

BACKGROUND Population isolates are characterized by simplified genetic background and as such present promising opportunities for studying complex diseases. We performed a genome-wide linkage analysis for systolic (SBP) and diastolic blood pressure (DBP) followed up by the association analysis in the Croatian isolated island of Vis, where a very high prevalence of hypertension was reported (75%). METHODS Variance-components linkage analysis was used to map quantitative trait loci (QTL) for SBP and DBP in 125 families with 1,389 members. Follow-up association analysis was performed in a sample of 421 subjects from the island of Vis. The 15 top-ranking single nucleotide polymorphisms (SNPs) were selected and tested for the association by in silico replication in the British 1958 Birth Cohort DNA Collection. RESULTS Linkage results showed evidence for a QTL influencing DBP (Iod = 1.89) on chromosome 7p14.2 and two QTL influencing SBP (Iod = 2.03 on chromosome 1p36 and Iod = 1.75 on chromosome 20q13). For the association results, the replication was observed for the rs237484 polymorphism on chromosome 20 that was associated with SBP with the effect size beta = -5.2 (P = 0.001; per A allele) in Vis population and beta = -1.1 (P = 0.04) in the British 1958 Birth Cohort. rs237484 is in proximity to the potassium voltage gate channel gene (KCNB1) and close to the prostaglandin 12 (prostacyclin) synthase gene (PTGIS). CONCLUSIONS These results provide evidence of a QTL influencing blood pressure (BP) variability in this region and support the notion that the isolated population of the island of Vis is a suitable population for conducting linkage and association analyses of cardiovascular-related phenotypes.

  • 出版日期2009-6