Journals / The Anatolian Journal of Cardiology / 2015 / Cilt: 15 - Sayı: 9

Association of the rs10757274 SNP with coronary artery disease in a small group of a Pakistani population

Pages
709–715
DOI
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⚡ TL;DR(Too Long; Didn't Read)

Results for the association between the genotype on the basis of rs10757274 showed a strong association between the GG genotype and the occurrence of CAD (OR: 9.603; 95% CI: 5.746-16.05).Conclusion: The present results suggest the importance of the 9p21 locus in modulating the chances of CAD

📌 3 Key Takeaways

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Objective & Hypothesis:Objective: The present study aimed to investigate the association between the rs10757274 SNP (present on locus 9p21 in the gene for CDKN2BAS1) and coronary artery disease (CAD) in a local population of Pakistan.Methods: It was a case-control study.
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Key Findings & Data:An allele-specific PCR-based strategy was used for the identification of genotypes.
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Conclusion & Impact:Results for the association between the genotype on the basis of rs10757274 showed a strong association between the GG genotype and the occurrence of CAD (OR: 9.603; 95% CI: 5.746-16.05).Conclusion: The present results suggest the importance of the 9p21 locus in modulating the chances of CAD
🔬Design:Research Article
📍Scope:350 samples
⚙️Variables:Domain Parameters

Abstract

Objective: The present study aimed to investigate the association between the rs10757274 SNP (present on locus 9p21 in the gene for CDKN2BAS1) and coronary artery disease (CAD) in a local population of Pakistan.Methods: It was a case-control study. An allele-specific PCR-based strategy was used for the identification of genotypes. A total of 350 samples were used for the investigation, out of which 220 samples were CAD patients and 130 samples were normal healthy individuals. Effects of parameters, like family history of CAD, smoking, presence of diabetes, and hypertension, in changing the chances of CAD were studied. Odds ratio was estimated with 95% confidence interval.Results: A strong association was observed between CAD and factors, like smoking (OR: 1.666; 95% CI: 1.042-2.664), presence of hypertension (OR: 26.55; 95% CI: 15.95-44.20), diabetes (OR: 3.009; 95% CI: 1.841-4.920), and family history of CAD (OR: 4.9; 95% CI: 2.965-8.099). Results for the association between the genotype on the basis of rs10757274 showed a strong association between the GG genotype and the occurrence of CAD (OR: 9.603; 95% CI: 5.746-16.05).Conclusion: The present results suggest the importance of the 9p21 locus in modulating the chances of CAD

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Cite This Article

NAWAZ, S. K., NOREEN, A., RANİ, A., ARSHAD, M. (2015). Association of the rs10757274 SNP with coronary artery disease in a small group of a Pakistani population. The Anatolian Journal of Cardiology, Cilt: 15 - Sayı: 9, 709–715. https://ajindex.com/articles/367261

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References (12)

  1. Slack J, Evans KA. The increased risk of death from ischaemic heart disease in first degree relatives of 121 men and 96 women with ischaemic heart disease. J Med Genet 1966
  2. [CrossRef] 2. Levy S, Sutton G, Ng PC, Feuk L, Halpern AL, Walenz BP, et al. The diploid genome sequence of an individual human. PLoS Biol 2007
  3. E254. [CrossRef] 3. Wheeler DA, Srinivasan M, Egholm M, Shen Y, Chen L, McGuire A, et al. The complete genome of an individual by massively parallel DNA sequencing. Nature 2008
  4. [CrossRef] 4. Peyser PA, Bielak LF, Chu JS, Turner ST, Ellsworth DL, Boerwinkle E, et al. Heritability of coronary artery calcium quantity measured by electron beam computed tomography in asymptomatic adults. Circulation 2002
  5. [CrossRef] 5. Goldstein JL, Brown MS. Familial hypercholesterolemia: identification of a defect in the regulation of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity associated with overproduction of cholesterol. Proc Natl Acad Sci USA 1973
  6. [CrossRef] 6. Ridker PM, Stampfer MJ, Rifai N. Novel risk factors for systemic atherosclerosis: a comparison of C-reactive protein, fibrinogen, homocysteine, lipoprotein(a), and standard cholesterol screening as predictors of peripheral arterial disease. JAMA 2001
  7. [CrossRef] 7. Samani NJ, Burton P, Mangino M, Ball SG, Balmforth AJ, Barrett J, et al. A genomewide linkage study of 1,933 families affected by premature coronary artery disease: The British Heart Foundation (BHF) Family Heart Study. Am J Hum Genet 2005
  8. [CrossRef] 8. Wellcome Trust Case Control Consortium. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 2007
  9. [CrossRef] 9. Singh NN, Ramji DP. The role of transforming growth factor-β in atherosclerosis. Cytokine Growth Factor Rev 2006
  10. [CrossRef] 10. Dorn GW, Sharon Cresci S. Genome-wide association studies of coronary artery disease and heart failure: where are we going? Pharmacogenomics 2009
  11. [CrossRef] 11. Broadbent HM, Peden JF, Lorkowski S, Goel A, Öngen H, Green F, et al. Susceptibility to coronary artery disease and diabetes is encoded by distinct, tightly linked SNPs in the ANRIL locus on chromosome 9p. Hum Mol Genet 2008
  12. [CrossRef] 12. Holdt LM, Sass K, Gäbel G, Bergert H, Thiery J, Teupser D. Expression of Chr9p21 genes CDKN2B (p15(INK4b)), CDKN2A (p16(INK4a), p14(ARF)) and MTAP in human atherosclerotic