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Hersberger, M.* ; Müller, M. ; Marti-Jaun, J. ; Heid, I.M.* ; Coassin, S.* ; Young, T.F.* ; Waechter, V.* ; Hengstenberg, C.* ; Meisinger, C. ; Peters, A. ; König, W.* ; Holmer, S.* ; Schunkert, H.* ; Klopp, N. ; Kronenberg, F.* ; Illig, T.

No association of two functional polymorphisms in human ALOX15 with myocardial infarction.

Atherosclerosis 205, 192-196 (2009)
DOI PMC
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
The 12/15-lipoxygenase plays a janus-role in inflammation with pro-inflammatory and anti-inflammatory effects in cell systems and even opposite effects on atherosclerosis in two different animal species. Screening of the human 15-lipoxygenase (ALOX15) gene detected a polymorphic C to T substitution at position c.-292, which led to three times higher ALOX15 activity in macrophages and showed a trend to be atheroprotective in a small case-control study for coronary artery disease (CAD). A second polymorphism at position c.1693C>T leading to an T560M exchange and an inactive enzyme was recently associated with increased CAD. We now investigated whether these polymorphisms or a certain haplotype of ALOX15 are associated with myocardial infarction (MI) in a case-control subset from the population-based MONIKA/KORA cohort S3. Six polymorphisms in ALOX15 were analyzed in 2629 participants to cover all major haplotypes with a frequency higher than 1% in the Caucasian population. None of the polymorphism was associated with MI but a rare ALOX15 haplotype showed a significant protective effect on the risk for MI (p=0.03). However, none of the polymorphisms or haplotypes was associated with CRP levels. These data suggest that ALOX15 may play a less prominent role during later stages of atherosclerosis involving atherothrombotic mechanisms than eventually during early plaque development.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter 15-Lipoxygenase; 12-Lipoxygenase; 15-LOX; 12-LOX; ALOX15; ALOX12; Inflammation; Atherosclerosis; Myocardial infarction; Genetics; Haplotype; Polymorphism; Acetylcholine-induced hypotension; Coronary-artery-disease; Low-density-lipoprotein; e-deficient mice; 15-lipoxygenase; Gene; Atherosclerosis; Macrophages; Involvement; Rabbits
Sprache
Veröffentlichungsjahr 2009
HGF-Berichtsjahr 2010
ISSN (print) / ISBN 0021-9150
e-ISSN 1879-1484
Zeitschrift Atherosclerosis
Quellenangaben Band: 205, Heft: 1, Seiten: 192-196 Artikelnummer: , Supplement: ,
Verlag Elsevier
Verlagsort Amsterdam
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Epidemiology (EPI)
POF Topic(s) 30503 - Chronic Diseases of the Lung and Allergies
30202 - Environmental Health
Forschungsfeld(er) Genetics and Epidemiology
PSP-Element(e) G-503900-003
G-504090-001
PubMed ID 19131063
DOI 10.1016/j.atherosclerosis.2008.11.017
Scopus ID 67349191171
Erfassungsdatum 2009-12-31
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