Source:http://linkedlifedata.com/resource/pubmed/id/15336915
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions |
umls-concept:C0001792,
umls-concept:C0002085,
umls-concept:C0003595,
umls-concept:C0021753,
umls-concept:C0021760,
umls-concept:C0025266,
umls-concept:C0027051,
umls-concept:C0031928,
umls-concept:C0035647,
umls-concept:C0150312,
umls-concept:C0205217,
umls-concept:C0332281,
umls-concept:C0521115,
umls-concept:C1274040,
umls-concept:C1882417
|
pubmed:issue |
8
|
pubmed:dateCreated |
2004-8-31
|
pubmed:abstractText |
Genetic background of inflammatory or anti-inflammatory molecules may be helpful in identifying subjects with increased or decrease risk of developing cardiovascular disease. Bi-allele polymorphism (C > T) in the promoter region (-511) of the interleukin-1beta (IL-1beta) gene and the bi-allele polymorphism (G > C) in the promoter region (-174) of interleukin-6 (IL-6) gene were determined in elderly men patients with myocardial infarction (MI) and healthy controls. Each subject was also genotyped for the triallelic polymorphism of the apolipoprotein E epsilon gene. The IL-6C and APOE epsilon4 alleles were independently associated with a mild or moderate increased risk of MI, whilst the allele C of the IL-1beta was not independently linked to MI risk. However, the simultaneous presence of the allele C of IL-1beta, the allele C of IL-6 and epsilon4 allele of APOE was strongly associated with the disease. Data from this cross-sectional study suggest that the functional interaction of these three genes affects pathogenetic mechanisms of MI and an impaired regulation of immune responses plays a pivotal role in the disease. Furthermore, genetic background of inflammatory genes may influence longevity of human species by affecting inflammatory responses associated to cardiovascular diseases. The administration of anti-inflammatory compounds to middle age healthy subjects with increased genetic susceptibility of developing MI might decrease the incidence and prevalence of cardiovascular events in aging.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
0047-6374
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
125
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
575-9
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:15336915-Aged,
pubmed-meshheading:15336915-Alleles,
pubmed-meshheading:15336915-Apolipoproteins E,
pubmed-meshheading:15336915-Humans,
pubmed-meshheading:15336915-Inflammation,
pubmed-meshheading:15336915-Interleukin-1,
pubmed-meshheading:15336915-Interleukin-6,
pubmed-meshheading:15336915-Male,
pubmed-meshheading:15336915-Middle Aged,
pubmed-meshheading:15336915-Myocardial Infarction,
pubmed-meshheading:15336915-Pilot Projects,
pubmed-meshheading:15336915-Polymorphism, Genetic,
pubmed-meshheading:15336915-Risk
|
pubmed:year |
2004
|
pubmed:articleTitle |
The concomitant presence of polymorphic alleles of interleukin-1beta, interleukin-6 and apolipoprotein E is associated with an increased risk of myocardial infarction in elderly men. Results from a pilot study.
|
pubmed:affiliation |
Department of Experimental Pathology, Via S. Giacomo 14, 40126 Bologna, Italy. licastro@alma.unibo.it
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|