The Metabolic Syndrome in Men study: a resource for studies of metabolic and cardiovascular diseases

被引:133
|
作者
Laakso, Markku [1 ,2 ]
Kuusisto, Johanna [1 ,2 ]
Stancakova, Alena [1 ]
Kuulasmaa, Teemu [1 ]
Pajukanta, Paivi [5 ]
Lusis, Aldons J. [3 ,4 ]
Collins, Francis S. [6 ]
Mohlke, Karen L. [7 ]
Boehnke, Michael [8 ,9 ]
机构
[1] Univ Eastern Finland, Inst Clin Med, Internal Med, Kuopio, Finland
[2] Kuopio Univ Hosp, Dept Med, Kuopio, Finland
[3] Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, Inst Mol Biol, Los Angeles, CA 90024 USA
[6] NHGRI, NIH, Bethesda, MD 20892 USA
[7] Univ N Carolina, Dept Genet, Chapel Hill, NC USA
[8] Univ Michigan, Dept Biostat, Ann Arbor, MI 48109 USA
[9] Univ Michigan, Ctr Stat Genet, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院; 芬兰科学院;
关键词
type; 2; diabetes; cardiovascular risk factors; metabolic disease; coronary artery disease; METSIM; GENOME-WIDE ASSOCIATION; BODY-MASS INDEX; INSULIN SENSITIVITY; FASTING GLUCOSE; GENETIC ARCHITECTURE; SUSCEPTIBILITY LOCI; COMMON VARIANTS; LOW-FREQUENCY; BLOOD-PRESSURE; FATTY-ACIDS;
D O I
10.1194/jlr.O072629
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Metabolic Syndrome in Men (METSIM) study is a population-based study including 10,197 Finnish men examined in 2005-2010. The aim of the study is to investigate nongenetic and genetic factors associated with the risk of T2D and CVD, and with cardiovascular risk factors. The protocol includes a detailed phenotyping of the participants, an oral glucose tolerance test, fasting laboratory measurements including proton NMR measurements, mass spectometry metabolomics, adipose tissue biopsies from 1,400 participants, and a stool sample. In our ongoing follow-up study, we have, to date, reexamined 6,496 participants. Extensive genotyping and exome sequencing have been performed for essentially all METSIM participants, and > 2,000 METSIM participants have been whole-genome sequenced. We have identified several nongenetic markers associated with the development of diabetes and cardiovascular events, and participated in several genetic association studies to identify gene variants associated with diabetes, hyperglycemia, and cardiovascular risk factors.jlr The generation of a phenotype and genotype resource in the METSIM study allows us to proceed toward a "systems genetics" approach, which includes statistical methods to quantitate and integrate intermediate phenotypes, such as transcript, protein, or metabolite levels, to provide a global view of the molecular architecture of complex traits.
引用
收藏
页码:481 / 493
页数:13
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