Source:http://linkedlifedata.com/resource/pubmed/id/12189485
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
2
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| pubmed:dateCreated |
2002-8-21
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| pubmed:abstractText |
Elevated levels of homocysteine is a risk factor for coronary artery disease. Polymorphic alleles in the MTHFR genes that cause recessively inherited increased homocysteine level can explain only a small proportion of the observed variation in homocysteine level. To investigate additional genetic influences, we examined environmental, familial, and genetic influences on serum homocysteine levels in 661 family members of 112 probands who underwent elective coronary arteriography. Maximum likelihood methods were used to fit several genetic and non-genetic models of inheritance to these data to determine if an unobserved Mendelian major gene could explain the familial homocysteine distribution. Adjustments for age, lifestyle (smoking and alcohol consumption), serum folate and vitamin B12, and the measured genotype effect of the MTHFR C677T mutation was carried out separately for males and females using multiple regression models for homocysteine, before and after log-transformation prior to this segregation analysis. After excluding the effects of mutations in the MTHFR genes, we found evidence of a major gene acting in a co-dominant manner. Estimated mean homocysteine levels for the three putative genotypes (LL, LH, and HH) were 8.0, 10.1, and 15.9 micro mol/l, respectively, with relative frequencies of 56.8%, 37.2%, and 6%, respectively. Our analysis suggested the presence of a co-dominantly expressed major gene, in addition to the effects of the MTHFR C677T mutation. The results of this study also indicated that multifactorial inheritance was supported more strongly than Mendelian inheritance alone. Our findings may have implications for attempts to identify new homocysteine susceptible genes.
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| pubmed:grant | |
| pubmed:language |
eng
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| pubmed:journal | |
| pubmed:citationSubset |
IM
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| pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Folic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Homocysteine,
http://linkedlifedata.com/resource/pubmed/chemical/Methylenetetrahydrofolate...,
http://linkedlifedata.com/resource/pubmed/chemical/Oxidoreductases Acting on CH-NH...,
http://linkedlifedata.com/resource/pubmed/chemical/Vitamin B 12
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| pubmed:status |
MEDLINE
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| pubmed:month |
Aug
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| pubmed:issn |
0340-6717
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| pubmed:author | |
| pubmed:issnType |
Print
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| pubmed:volume |
111
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| pubmed:owner |
NLM
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| pubmed:authorsComplete |
Y
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| pubmed:pagination |
128-35
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| pubmed:dateRevised |
2007-11-15
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| pubmed:meshHeading |
pubmed-meshheading:12189485-Adolescent,
pubmed-meshheading:12189485-Adult,
pubmed-meshheading:12189485-Aged,
pubmed-meshheading:12189485-Aged, 80 and over,
pubmed-meshheading:12189485-Child,
pubmed-meshheading:12189485-Chromosome Segregation,
pubmed-meshheading:12189485-Coronary Angiography,
pubmed-meshheading:12189485-Coronary Artery Disease,
pubmed-meshheading:12189485-Family,
pubmed-meshheading:12189485-Female,
pubmed-meshheading:12189485-Folic Acid,
pubmed-meshheading:12189485-Genotype,
pubmed-meshheading:12189485-Homocysteine,
pubmed-meshheading:12189485-Humans,
pubmed-meshheading:12189485-Male,
pubmed-meshheading:12189485-Methylenetetrahydrofolate Reductase (NADPH2),
pubmed-meshheading:12189485-Middle Aged,
pubmed-meshheading:12189485-Mutation,
pubmed-meshheading:12189485-Oxidoreductases Acting on CH-NH Group Donors,
pubmed-meshheading:12189485-Pedigree,
pubmed-meshheading:12189485-Vitamin B 12
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| pubmed:year |
2002
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| pubmed:articleTitle |
Major gene evidence after MTHFR-segregation analysis of serum homocysteine in families of patients undergoing coronary arteriography.
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| pubmed:affiliation |
Department of Epidemiology and Health Promotion, Graduate School of Health Science and Management, Yonsei University, Seoul 120-752, South Korea. jsunha@yumc.yonsei.ac.kr
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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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