dc.contributor.author | Ghaffari, MA | |
dc.contributor.author | Sede, SA | |
dc.contributor.author | Rashtchizadeh, N | |
dc.contributor.author | Mohammadzadeh, G | |
dc.contributor.author | Majidi, S | |
dc.date.accessioned | 2018-08-26T08:36:19Z | |
dc.date.available | 2018-08-26T08:36:19Z | |
dc.date.issued | 2014 | |
dc.identifier | 10.15171/bi.2014.006 | |
dc.identifier.uri | http://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/52731 | |
dc.description.abstract | Introduction: We evaluated the association between four polymorphisms in the CRP gene with serum C-reactive protein (CRP) levels, prevalence and severity of coronary artery disease (CAD) in type 2 diabetes mellitus (T2DM) patients. Methods: We performed coronary angiography for 308 T2DM patients and classified them into two groups: T2DM with CAD and T2DM without CAD. All patients were from Ahvaz, Iran. serum levels of CRP, glucose and lipid profile were measured. Genotyping was performed by PCR/RFLP, and the severity of coronary artery disease was determined by Gensini score. Results: The GG genotype of SNP rs279421 was associated with the increased risk of CAD (OR= 2.38; 95% CI: 1.12- 5.8; p= 0.02) and CA, TT, TA genotypes and A allele of SNP rs3091244 and GA genotypes and A allele of SNP rs3093062 were significantly associated with increased CRP levels. None of genotypes or alleles was associated with Gensini score. We found that the haplotype 7 (AGCG) was associated with decreased risk of CAD (OR= 0.11; 95% CI: 0.02, 0.66; p= 0.017) and the Gensini score was correlated with increased levels of CRP, only in CAD group. Conclusion: Although genetic polymorphisms were influenced on serum RP levels, none of the alleles and genotypes raising or falling C-reactive protein levels was consistently associated with an increased prevalence of CAD or protected from that. é 2014 The Author(s). | |
dc.language.iso | English | |
dc.relation.ispartof | BioImpacts | |
dc.subject | C reactive protein | |
dc.subject | glucose | |
dc.subject | lipid | |
dc.subject | adult | |
dc.subject | angiocardiography | |
dc.subject | Article | |
dc.subject | clinical evaluation | |
dc.subject | coronary artery disease | |
dc.subject | CRP gene | |
dc.subject | disease severity | |
dc.subject | female | |
dc.subject | gene frequency | |
dc.subject | gene location | |
dc.subject | genetic association | |
dc.subject | genetic risk | |
dc.subject | genetic variability | |
dc.subject | genotype | |
dc.subject | glucose blood level | |
dc.subject | haplotype | |
dc.subject | human | |
dc.subject | Iran | |
dc.subject | lipid blood level | |
dc.subject | major clinical study | |
dc.subject | male | |
dc.subject | marker gene | |
dc.subject | non insulin dependent diabetes mellitus | |
dc.subject | polymerase chain reaction | |
dc.subject | protein blood level | |
dc.subject | restriction fragment length polymorphism | |
dc.subject | single nucleotide polymorphism | |
dc.title | Association of CRP gene polymorphism with CRP levels and coronary artery disease in type 2 diabetes in Ahvaz, southwest of Iran | |
dc.type | Article | |
dc.citation.volume | 4 | |
dc.citation.issue | 3 | |
dc.citation.spage | 133 | |
dc.citation.epage | 139 | |
dc.citation.index | Scopus | |
dc.identifier.DOI | 10.15171/bi.2014.006 | |