Analysis of metabolic syndrome phenotypes in Framingham Heart Study families from Genetic Analysis Workshop 13

被引:11
作者
Goldin, LR
Camp, NJ
Keen, KJ
Martin, LJ
Moslehi, R
Ghosh, S
North, KE
Wyszynski, DF
Blacker, D
机构
[1] NCI, DCEG, Genet Epidemiol Branch, Bethesda, MD 20892 USA
[2] Univ Utah, Sch Med, Dept Med Informat, Div Genet Epidemiol, Salt Lake City, UT USA
[3] Case Western Reserve Univ, Dept Epidemiol, Cleveland, OH 44106 USA
[4] Cincinnati Childrens Hosp Med Ctr, Ctr Biostat & Epidemiol, Cincinnati, OH USA
[5] NCI, Genet Epidemiol Branch, Div Canc Epidemiol & Genet, DHHS,NIH, Bethesda, MD 20892 USA
[6] Washington Univ, Sch Med, Dept Psychiat, St Louis, MO 63110 USA
[7] Indian Stat Inst, Appl Stat Unit, Kolkata 700035, W Bengal, India
[8] Univ N Carolina, Dept Epidemiol, Chapel Hill, NC 27599 USA
[9] Boston Univ, Sch Med, Dept Med, Genet Program, Boston, MA 02118 USA
[10] Massachusetts Gen Hosp, Dept Psychiat, Charlestown, MA USA
关键词
metabolic syndrome; longitudinal measures; linkage methods; susceptibility genes;
D O I
10.1002/gepi.10288
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Twelve teams of investigators constituted a group which analyzed phenotypes related to metabolic syndrome, making use of the available longitudinal measurements from the family component of the Framingham Heart Study or the simulated data, as distributed by Genetic Analysis Workshop 13 (GAW13). Body mass index, obesity, lipid abnormalities, glucose, or combinations of these traits were analyzed by this group. A wide variety of approaches were taken to construct phenotypes from the longitudinal measurements, including considering single or multiple cross-sectional time points, single ages, minimum values, maximum values, means, other lifetime values, ever/never dichotomy, or age at onset of some threshold value. Approaches also differed in the family structures utilized (sib pairs to full extended pedigrees), the genetic data considered (two-point or multipoint), and the statistics calculated (model-free and parametric), and led to a diverse set of analyses being performed. Inferences were made about heritability, and attempts were made to map underlying genes. Over 40 genome-wide linkage analyses were conducted. Despite the broad range of approaches, several regions of the genome were repeatedly identified across multiple analyses. Published 2003 Wiley-Liss, Inc dagger.
引用
收藏
页码:S78 / S89
页数:12
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