Association study of candidate genes in Croatian myocardial infarction patients (CROSBI ID 739447)
Prilog sa skupa u časopisu | izvorni znanstveni rad
Podaci o odgovornosti
Ferenčak, Goran ; Cheng, Suzanne ; Fijal, Bonnie ; Gršković, Branka ; Skodlar, Jasna ; Šesto, Mihajlo ; Stavljenić Rukavina, Ana
engleski
Association study of candidate genes in Croatian myocardial infarction patients
Association of 65 biallelic polymorphisms or mutations within 36 genes, selected from pathways of lipid and homocysteine metabolism, regulation of blood pressure and coagulation, inflammation, cellular adhesion, and matrix integrity, with myocardial infarction was investigated in a case-control study. Multiplex assay genotyping was done in 257 subjects with a history of myocardial infarction (MI+) and 490 control subjects (MI-). The analyzed genes were LPA, APOA4, APOB, APOC3, APOE, ADRB3, PPARG, LIPC, LPL, PON1, PON2, LDLR, CETP, CBS, MTHFR, NOS3, DCP1, AGTR1, AGT, NPPA, ADD1, SCNN1A, GNB3, ADRB2, MMP3, F2, F5, F7, PAI1, FGB, ITGA2, ITGB3, SELE, ICAM1, TNF, and LTA. After adjusting for age, sex, smoking, hypertension, plasma homocysteine, lipids and glucose, we found an association (P less than or equal to 0.05) of polymorphisms in ADRB3 (OR 1.649, 95% CI 1.063-2.558), PPARG (OR 0.530, 95% CI 0.371-0.756), AGTR1 (OR 1.824, 95% CI 1.306-2.547), NPPA (OR 2.344, 95% CI 1.108-4.961), and FGB genes (OR 2.167, 95% CI 1.044-4.499) with myocardial infarction. The results are strongly supporting the hypothesis of the polygenic inheritance of susceptibility to myocardial infarction as a result of an interaction between various metabolic pathways involved in the pathogenesis of atherosclerosis.
gene polymorphism; myocardial infarction
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Podaci o prilogu
A52-x.
2002.
nije evidentirano
objavljeno
Podaci o matičnoj publikaciji
Clinical chemistry and laboratory medicine
1434-6621
1437-4331
Podaci o skupu
Nepoznat skup
ostalo
29.02.1904-29.02.2096
Povezanost rada
Temeljne medicinske znanosti