Pregled bibliografske jedinice broj: 383499
C-reactive protein gene polymorphisms affect plasma CRP and homocysteine concentrations in subjects with and without angiographically confirmed coronary artery disease
C-reactive protein gene polymorphisms affect plasma CRP and homocysteine concentrations in subjects with and without angiographically confirmed coronary artery disease // Molecular Biology Reports, 36 (2009), 4; 775-780 doi:10.1007/s11033-008-9244-1 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 383499 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
C-reactive protein gene polymorphisms affect plasma CRP and homocysteine concentrations in subjects with and without angiographically confirmed coronary artery disease
Autori
Pašalić, Daria ; Marinković, Natalija ; Gršković, Branka, Ferenčak, Goran ; Bernat, Robert ; Stavljenić Rukavina, Ana
Izvornik
Molecular Biology Reports (0301-4851) 36
(2009), 4;
775-780
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
Coronary artery disease ; CRP ; genetic polymorphism ; homocysteine
Sažetak
Abstract Human C-reactive protein (CRP) is a reactant involved in the acute phase response and one of the many molecular factors involved in pathogenesis of coronary artery disease (CAD). CRP gene variants potentially mediate CRP plasma concentrations and the development of CAD. 220 Croatian subjects with angiographically confirmed CAD and 132 control subjects were included in the study. CRP gene polymorphisms 1059G/C and -717G/ A were determined by RFLPs, using MaeIII and KspI endonuclease, respectively. Plasma concentrations of CRP and homocysteine were determined by immunoturbidimetry and FPIA, respectively. CRP 1059G/C gene variants were significantly associated with CAD (OR = 0.50 ; 95% CI = 0.27, 0.94 ; P = 0.032). Wild GG genotype and rare allele C carrier genotypes were 184 and 22 in CAD(+) group, and 101 and 24 in CAD(-) group, respectively. Multivariate analysis with age, gender, BMI, smoking status, hypertension and diabetes as covariates showed that 1059C carriers had lower CRP concentrations in CAD(-) (P = 0.010) and CAD(+) subjects (P = 0.028). This allele was also significantly associated with lower plasma homocysteine concentrations in both groups (P = 0.018) for CAD(-) and 0.002 for CAD(+). There was no significant difference between CAD(+) and CAD(-) subjects in absolute frequencies for CRP -717A/G gene variant, but multivariate analysis showed that carriers of the rarer G allele had significantly higher CRP plasma concentrations in CAD(-) subjects (P = 0.031) and higher omocysteine concentrations in CAD(+) group (P<0.001). Atherosclerosis is an inflammatory disease resulting from different genetic and environmental factors. Results presented here support the contribution of CRP genetic variations in the development of CAD.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti, Kliničke medicinske znanosti, Javno zdravstvo i zdravstvena zaštita
POVEZANOST RADA
Projekti:
108-1080316-0298 - Molekularna osnova aterogeneze
Ustanove:
Medicinski fakultet, Zagreb,
Sveučilište Libertas
Profili:
Branka Gršković
(autor)
Robert Bernat
(autor)
Daria Pašalić
(autor)
Ana Stavljenić
(autor)
Natalija Marinković
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE
Uključenost u ostale bibliografske baze podataka::
- EMBASE (Excerpta Medica)
- Genetics Abstracts
- Nucleic Acids Abstracts