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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1997-10-23
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pubmed:abstractText |
Two hundred and thirty-five survivors of myocardial infarction (MI) were compared to 384 controls with respect to distribution of genotypes and gene frequencies in the A1166C polymorphism at the angiotensin II type 1 receptor (AT1R) locus. No differences in allele frequencies or genotype distribution were observed when all patients were compared with all controls. When comparing CC homozygotes with the combined group of CA heterozygotes and AA homozygotes (CA/AA), a difference in borderline significance between the MI group and controls was observed (p=0.05). In males alone, this difference was much more pronounced because of the larger proportion of males with the CC genotype in MI cases than in male controls (p=0.01). No significant differences were observed between female cases and controls. No interaction between the insertion/deletion (I/D) polymorphism at the angiotensin I-converting enzyme (ACE) locus and the polymorphism at the AT1R locus was detected. When subdividing the subjects into a "low-risk" and a "high-risk" group, based on levels of apolipoprotein B (apoB) and body mass index (BMI), and whether or not the person used lipid-lowering drugs, the frequency of CC homozygotes in male cases of the "low-risk" group differed significantly compared to the frequency in male controls of the "low-risk" group (p<0.001). No differences were observed in females, but the number of "low-risk" group female cases was low (n=3). Thus, CC homozygosity appears to be associated with MI in Norwegian males, especially among those with a "low-risk" phenotype.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Apolipoproteins B,
http://linkedlifedata.com/resource/pubmed/chemical/Peptidyl-Dipeptidase A,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Angiotensin, Type 1,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Angiotensin, Type 2,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Angiotensin
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0009-9163
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
52
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
71-6
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:9298740-Apolipoproteins B,
pubmed-meshheading:9298740-Body Mass Index,
pubmed-meshheading:9298740-Case-Control Studies,
pubmed-meshheading:9298740-Female,
pubmed-meshheading:9298740-Gene Frequency,
pubmed-meshheading:9298740-Genotype,
pubmed-meshheading:9298740-Humans,
pubmed-meshheading:9298740-Male,
pubmed-meshheading:9298740-Middle Aged,
pubmed-meshheading:9298740-Myocardial Infarction,
pubmed-meshheading:9298740-Norway,
pubmed-meshheading:9298740-Peptidyl-Dipeptidase A,
pubmed-meshheading:9298740-Polymorphism, Genetic,
pubmed-meshheading:9298740-Receptor, Angiotensin, Type 1,
pubmed-meshheading:9298740-Receptor, Angiotensin, Type 2,
pubmed-meshheading:9298740-Receptors, Angiotensin,
pubmed-meshheading:9298740-Risk Factors
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pubmed:year |
1997
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pubmed:articleTitle |
A DNA polymorphism at the angiotensin II type 1 receptor (AT1R) locus and myocardial infarction.
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pubmed:affiliation |
Institute of Medical Genetics, University of Oslo, Norway.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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