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

被引:64
作者
Bella, JN
MacCluer, JW
Roman, MJ
Almasy, L
North, KE
Best, LG
Lee, ET
Fabsitz, RR
Howard, BV
Devereux, RB
机构
[1] Cornell Univ, Weill Med Coll, New York, NY 10021 USA
[2] Medstar Res Inst, Washington, DC USA
[3] NHLBI, Bethesda, MD 20892 USA
[4] Univ Oklahoma, Sch Publ Hlth Serv, Oklahoma City, OK USA
[5] Missouri Breaks Ind Res Inc, Timber Lake, SD USA
[6] SW Fdn Biomed Res, San Antonio, TX 78284 USA
[7] Bronx Lebanon Hosp Ctr, Bronx, NY 10456 USA
关键词
genetics; epidemiology; echocardiography; left ventricular mass; hypertension; diabetes mellitus;
D O I
10.1097/00004872-200402000-00011
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
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.
引用
收藏
页码:281 / 286
页数:6
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