Exp Mol Med.  2009 Nov;41(11):841-848. 10.3858/emm.2009.41.11.090.

Analysis of genetic and non-genetic factors that affect the QTc interval in a Mongolian population: the GENDISCAN study

Affiliations
  • 1Department of Biochemistry and Molecular Biology, Seoul National University College of Medicine, Seoul 110-799, Korea.
  • 2Psoma Therapeutics, Inc, Seoul 153-023, Korea. jeongsun@snu.ac.kr, jongil@snu.ac.kr
  • 3Department of Epidemiology, Graduate School of Public Health and Institute of Health and Environment, Seoul National University College of Medicine, Seoul 110-799, Korea.
  • 4Department of Internal Medicine, Seoul National University College of Medicine, Seoul 110-799, Korea.
  • 5Department of Biochemistry, Ewha Womans University School of Medicine, Seoul 158-710, Korea.
  • 6ILCHUN Genomic Medicine Institute, Medical Research Center, Seoul National University, Seoul 110-799, Korea.

Abstract

The QTc interval is a complex quantitative trait and a strong prognostic indicator of cardiovascular mortality in general, healthy people. The aim of this study was to identify non-genetic factors and quantitative trait loci that govern the QTc interval in an isolated Mongolian population. We used multiple regression analysis to determine the relationship between the QTc interval and non-genetic factors including height, blood pressure, and the plasma lipid level. Whole genome linkage analyses were performed to reveal quantitative trait loci for the QTc interval with 349 microsatellite markers from 1,080 Mongolian subjects. Among many factors previously known for association with the QTc interval, age, sex, heart rate, QRS duration of electrocardiogram and systolic blood pressure were also found to have influence on the QTc interval. A genetic effect for the QTc interval was identified based on familial correlation with a heritability value of 0.31. In a whole genome linkage analysis, we identified the four potential linkage regions 7q31-34, 5q21, 4q28, and 2q36.

Keyword

electrocardiography; linkage (genetics); long QT syndrome; quantitative trait, heritable; quantitative trait loci; regression analysis

MeSH Terms

Adolescent
Adult
Age Factors
Aged
Aged, 80 and over
Blood Pressure/genetics
Body Height/genetics
Cardiovascular Diseases/*genetics/mortality/pathology/*physiopathology
Child
Child, Preschool
Chromosomes, Human/genetics
*Electrocardiography
Female
*Genome-Wide Association Study
Heart Rate/genetics
Humans
Male
Microsatellite Repeats/*genetics
Middle Aged
Mongolia/epidemiology
Quantitative Trait Loci/*genetics
Sex Factors
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