Source:http://linkedlifedata.com/resource/pubmed/id/11884284
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2002-3-8
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pubmed:abstractText |
Coronary artery disease (CAD) is the leading cause of mortality in the developed world. Although several CAD risk factors, including measures of lipid metabolism, obesity, and blood pressure, have a genetic basis, many genes for CAD susceptibility have yet to be identified. Coronary atherosclerosis is the major cause of CAD, but many with coronary atherosclerosis lack symptoms. Thus, a major limitation of using symptomatic CAD endpoints (eg, sudden coronary death, myocardial infarction) as a study outcome is substantial disease misclassification. Coronary artery calcification (CAC) is part of the atherosclerotic process and is an independent predictor of CAD endpoints. In the present study, CAC was noninvasively quantified by electron beam computed tomography. We performed genome-wide multipoint mode-of-inheritance-free linkage analysis on affected sib pairs, defined as being > or = the 70th sex- and age-specific percentile for CAC quantity, in a sample of 29 families enriched for hypertension. Almost 95% of participants were asymptomatic for CAD. Our LOD score (log10 odds in favor of linkage) results provide evidence that chromosomal regions 6p21.3 (maximum LOD score=2.22, P=0.00070) and 10q21.3 (maximum LOD score=3.24, P=0.000057) may harbor genes associated with subclinical coronary atherosclerosis.
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pubmed:grant |
http://linkedlifedata.com/resource/pubmed/grant/M01 RR00585,
http://linkedlifedata.com/resource/pubmed/grant/R01 HL46292,
http://linkedlifedata.com/resource/pubmed/grant/U01 HL054457,
http://linkedlifedata.com/resource/pubmed/grant/U01 HL054464,
http://linkedlifedata.com/resource/pubmed/grant/U01 HL054481
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pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1524-4636
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pubmed:author |
pubmed-author:BielakLawrence FLF,
pubmed-author:BoerwinkleEricE,
pubmed-author:KardiaSharon LSL,
pubmed-author:LangeEthan MEM,
pubmed-author:LangeLeslie ALA,
pubmed-author:LangefeldCarl DCD,
pubmed-author:PeyserPatricia APA,
pubmed-author:RoystonPatrickP,
pubmed-author:SheedyPatrick FPF2nd,
pubmed-author:TurnerStephen TST
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pubmed:issnType |
Electronic
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pubmed:day |
1
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pubmed:volume |
22
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
418-23
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:11884284-Adult,
pubmed-meshheading:11884284-Aged,
pubmed-meshheading:11884284-Calcinosis,
pubmed-meshheading:11884284-Chromosome Mapping,
pubmed-meshheading:11884284-Coronary Artery Disease,
pubmed-meshheading:11884284-Family Health,
pubmed-meshheading:11884284-Female,
pubmed-meshheading:11884284-Genetic Linkage,
pubmed-meshheading:11884284-Genetic Predisposition to Disease,
pubmed-meshheading:11884284-Genome, Human,
pubmed-meshheading:11884284-Humans,
pubmed-meshheading:11884284-Hypertension,
pubmed-meshheading:11884284-Male,
pubmed-meshheading:11884284-Middle Aged,
pubmed-meshheading:11884284-Tomography, X-Ray Computed
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pubmed:year |
2002
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pubmed:articleTitle |
Autosomal genome-wide scan for coronary artery calcification loci in sibships at high risk for hypertension.
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pubmed:affiliation |
Sections on Epidemiology and Biostatistics, Department of Public Health Sciences, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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