4.5 Article

Heritability of left ventricular dimensions and mass in American indians: The Strong Heart Study

Journal

JOURNAL OF HYPERTENSION
Volume 22, Issue 2, Pages 281-286

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/00004872-200402000-00011

Keywords

genetics; epidemiology; echocardiography; left ventricular mass; hypertension; diabetes mellitus

Funding

  1. NCRR NIH HHS [M10RR0047-34] Funding Source: Medline
  2. NHLBI NIH HHS [U01-HL41652, U01-HL41642, U01-HL41654] Funding Source: Medline

Ask authors/readers for more resources

Objective We sought to determine the heritability of left ventricular dimensions and mass in adult American Indians. Methods Echocardiograms were analysed in 1373 American Indian participants, from 445 families, in the Strong Heart Study (SHS) to determine the heritability of left ventricular dimensions and mass. Heritability calculations were performed using variance component analysis in SOLAR, a computer analysis program. Results The SHS participants analysed in this study included 1305 relative pairs, predominantly (n = 1077) sib-pairs. After simultaneously adjusting for sex, age and centre, the proportion of the residual phenotypic variance due to additive genetic effects or heritability (h(2)) of left ventricular mass was 0.27 (SE = 0.08, P < 0.001). Addition of body weight height, systolic blood pressure, heart rate, medications and diabetes into the polygenic model attenuated the residual h(2) of left ventricular mass to 0.17 (SE = 0.09, P < 0.05). The residual h(2) for left ventricular end-diastolic chamber diameter (LVID), after simultaneously adjusting for sex, age and centre was 0.36 (SE = 0.08, P < 0.001) for the analysed families. The residual h(2) for interventricular septal wall thickness was 0.26 (SE = 0.07), while that of left ventricular posterior wall thickness was 0.19 (SE = 0.08, both P < 0.001). While adjustment for body weight, height, systolic blood pressure, heart rate, medications and diabetes reduced the h(2) of LVID to 0.33 (SE = 0.09, P < 0.001), the h(2) of septal (0.12, SE = 0.10) and posterior wall thickness (0.09, SE = 0.09) were no longer significant after similar adjustment. The residual h(2) for relative wall thickness, a measure of left ventricular geometry, was 0.22 (SE = 0.07, P < 0.001) after adjusting for sex, age and centre, and 0.17 (SE = 0.08, P < 0.05) after additional adjustment for body weight, height, systolic blood pressure, heart rate, medications and diabetes. Conclusions A substantial proportion of the variance of left ventricular dimensions and mass can be explained by heredity, independent of the effects of sex, age, body size, blood pressure, heart rate, medications and diabetes. Identification of genes influencing left ventricular size and geometry may provide mechanistic and therapeutic targets to prevent left ventricular hypertrophy. (C) 2004 Lippincott Williams Wilkins.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available