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2003 | 50 | 2 | 527-534
Article title

Carrier-state of D allele in ACE gene insertion/deletion polymorphism is associated with coronary artery disease, in contrast to the C677→T transition in the MTHFR gene.

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EN
Abstracts
EN
Angiotensin I-converting enzyme (ACE), which plays an important role in blood pressure regulation, and methylenetetrahydrofolate reductase (MTHFR) involved in homocysteine metabolism belong to a large group of polypeptides which may be potential risk factors for atherosclerosis and coronary artery disease (CAD). To assess whether polymorphisms of the genes encoding these peptides are associated with CAD in Silesian we conducted a study among 68 individuals suffering from CAD (including 52 cases after myocardial infarction), 51 subjects with positive family history of CAD and 111 controls. We analysed the distribution of genotypes and allele frequencies of the insertion/deletion (I/D) polymorphism in the ACE gene using PCR amplification, and the C677→T polymorphism in the MTHFR gene using PCR-RFLP analysis. We found that D allele frequency was significantly higher in CAD patients (61%) than in controls (43%) (P = 0.001, OR = 2.06). The D allele carriers (DD + ID genotypes) were more frequent in the CAD patients (85%) compared to control group (65%) (P = 0.003, OR = 3.14), whereas the familial CAD risk group shows the highest frequency of the ID genotype (57% vs 43% in controls). In contrast, the MTHFR polymorphism does not seem to be associated with the disease. Our data indicate that in Silesian CAD patients the disease is strongly associated with carrier-state of the ACE D allele, but not with the C677→T transition in the MTHFR gene.
Publisher

Year
Volume
50
Issue
2
Pages
527-534
Physical description
Dates
published
2003
received
2002-12-18
revised
2003-05-12
accepted
2003-05-21
Contributors
author
  • Department of Biochemistry and Medical Genetics, Medical University of Silesia, Katowice, Poland
  • Department of Biochemistry and Medical Genetics, Medical University of Silesia, Katowice, Poland
author
  • Department of Biochemistry and Medical Genetics, Medical University of Silesia, Katowice, Poland
  • Department of Biochemistry and Medical Genetics, Medical University of Silesia, Katowice, Poland
  • The First Department and Clinic of Cardiology, Medical University of Silesia, Katowice, Poland
author
  • Regional Blood Centre, Katowice, Poland
  • Regional Blood Centre, Katowice, Poland
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Document Type
Publication order reference
Identifiers
YADDA identifier
bwmeta1.element.bwnjournal-article-abpv50i2p527kz
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