Multiple genes for essential-hypertension susceptibility on chromosome 1q

Yen Pei Christy Chang, Xin Liu, James Dae Ok Kim, Morna A. Ikeda, Mamie R. Layton, Alan B. Weder, Richard S. Cooper, Sharon L.R. Kardia, D. C. Rao, Steve C. Hunt, Amy Luke, Eric Boerwinkle, Aravinda Chakravarti

Research output: Contribution to journalArticlepeer-review

96 Scopus citations


Essential hypertension, defined as elevated levels of blood pressure (BP) without any obvious cause, is a major risk factor for coronary heart disease, stroke, and renal disease. BP levels and susceptibility to development of essential hypertension are partially determined by genetic factors that are poorly understood. Similar to other efforts to understand complex, non-Mendelian phenotypes, genetic dissection of hypertension-related traits employs genomewide linkage analyses of families and association studies of patient cohorts, to uncover rare and common disease alleles, respectively. Family-based mapping studies of elevated BP cover the large intermediate ground for identification of genes with common variants of significant effect. Our genomewide linkage and candidate-gene-based association studies demonstrate that a replicated linkage peak for BP regulation on human chromosome 1q, homologous to mouse and rat quantitative trait loci for BP, contains at least three genes associated with BP levels in multiple samples: ATP1B1, RGS5, and SELE. Individual variants in these three genes account for 2-5-mm Hg differences in mean systolic BP levels, and the cumulative effect reaches 8-10 mm Hg. Because the associated alleles in these genes are relatively common (frequency >5%), these three genes are important contributors to elevated BP in the population at large.

Original languageEnglish
Pages (from-to)253-264
Number of pages12
JournalAmerican journal of human genetics
Issue number2
StatePublished - Feb 2007


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