Dergiler / The Anatolian Journal of Cardiology / 2018 / Cilt: 19 - Sayı: 6

Study of the association of 17 lipid-related gene polymorphisms with coronary heart disease

Sayfa
360–367
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Conclusion: Our study revealed significant associations of APOE, PPAP2B, CETP, MLXIPL, PON2, and LEPR gene polymorphisms with CHD among the Han Chinese.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:Objective: Blood lipids are well-known risk factors for coronary heart disease (CHD).
📊
Temel Bulgular & Veri:The aim of this study was to explore the association between 17 lipid-related gene polymorphisms and CHD.
💡
Sonuç & Katkı:Conclusion: Our study revealed significant associations of APOE, PPAP2B, CETP, MLXIPL, PON2, and LEPR gene polymorphisms with CHD among the Han Chinese.
🔬Tür:Modelleme & Sayısal Simülasyon
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Özet

Objective: Blood lipids are well-known risk factors for coronary heart disease (CHD). The aim of this study was to explore the association between 17 lipid-related gene polymorphisms and CHD. Methods: The current study examined with 784 CHD cases and 739 non-CHD controls. Genotyping was performed on the MassARRAY iPLEX® assay platform. Results: Our analyses revealed a significant association of APOE rs7259620 with CHD (genotype: χ2 =6.353, df=2, p=0.042; allele: χ2 =5.05, df=1, p=0.025; recessive model: χ2 =5.57, df=1, p=0.018). A further gender-based subgroup analysis revealed significant associations of APOE rs7259620 and PPAP2B rs72664392 with CHD in males (genotype: χ2 =8.379, df=2, p=0.015; allele: χ2 =5.190, df=1, p=0.023; recessive model: χ2 =19.3, df=1, p<0.0001) and females (genotype: χ2 =9.878, df=2, p=0.007), respectively. Subsequent breakdown analysis by age showed that CETP rs4783961, MLXIPL rs35493868, and PON2 rs12704796 were significantly associated with CHD among individuals younger than 55 years of age (CETP rs4783961: χ2 =8.966, df=1, p=0.011 by genotype; MLXIPL rs35493868: χ2 =4.87, df=1, p=0.027 by allele; χ2 =4.88, df=1, p=0.027 by dominant model; PON2 rs12704796: χ2 =6.511, df=2, p=0.039 by genotype; χ2 =6.210, df=1, p=0.013 by allele; χ2 =5.03, df=1, p=0.025 by dominant model). Significant allelic association was observed between LEPR rs656451 and CHD among individuals older than 65 years of age (χ2 =4.410, df=1, p=0.036). Conclusion: Our study revealed significant associations of APOE, PPAP2B, CETP, MLXIPL, PON2, and LEPR gene polymorphisms with CHD among the Han Chinese.

🔖

Bu Makaleye Atıf Yap

WU, N., LİU, G., HUANG, Y., LİAO, Q., HAN, L., YE, H., DUAN, S., CHEN, X. (2018). Study of the association of 17 lipid-related gene polymorphisms with coronary heart disease. The Anatolian Journal of Cardiology, Cilt: 19 - Sayı: 6, 360–367. https://ajindex.com/articles/365328

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (2)

  1. Zhang H, Mo X, Hao Y, Huang J, Lu X, Cao J, et al. Adiponectin levels and risk of coronary heart disease: a meta-analysis of prospective studies. Am J Med Sci 2013; 345: 455-61. [CrossRef] Yan YL, Qiu B, Hu LJ, Jing XD, Liu YJ, Deng SB, et al. Efficacy and safety evaluation of intensive statin therapy in older patients with coronary heart disease: a systematic review and meta-analysis. Eur J Clin Pharmacol 2013; 69: 2001-9. [CrossRef] Petoumenos K, Worm SW. HIV infection, aging and cardiovascular disease: epidemiology and prevention. Sex Health 2011; 8: 465-73.
  2. Rai M, Baker WL, Parker MW, Heller GV. Meta-analysis of optimal risk stratification in patients >65 years of age. Am J Cardiol 2012; 110: 1092-9. [CrossRef] Ren H, Panchatcharam M, Mueller P, Escalante-Alcalde D, Morris AJ, Smyth SS. Lipid phosphate phosphatase (LPP3) and vascular development. Biochim Biophys Acta 2013; 1831: 126-32. [CrossRef] Schunkert H, König IR, Kathiresan S, Reilly MP, Assimes TL, Holm H, et al. Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nat Genet 2011; 43: 333-8. [CrossRef] Sun YX, Gao CY, Lu Y, Fu X, Jia JG, Zhao YJ, et al. Association between PPAP2B gene polymorphisms and coronary heart disease susceptibility in Chinese Han males and females. Oncotarget 2017; 8: 13166-73. [CrossRef] Wu C, Huang RT, Kuo CH, Kumar S, Kim CW, Lin YC, et al. Mechanosensitive PPAP2B Regulates Endothelial Responses to Atherorelevant Hemodynamic Forces. Circ Res 2015; 117: e41-e53. [CrossRef] Panchatcharam M, Miriyala S, Salous A, Wheeler J, Dong A, Mueller P, et al. Lipid phosphate phosphatase 3 negatively regulates smooth muscle cell phenotypic modulation to limit intimal hyperplasia. Arterioscler Thromb Vasc Biol 2013; 33: 52-9. [CrossRef] Touat-Hamici Z, Weidmann H, Blum Y, Proust C, Durand H, Iannacci F, et al. Role of lipid phosphate phosphatase 3 in human aortic endothelial cell function. Cardiovasc Res 2016; 112: 702-13. [CrossRef] Chouinard-Watkins R, Plourde M. Fatty acid metabolism in carriers of apolipoprotein E epsilon 4 allele: is it contributing to higher risk of cognitive decline and coronary heart disease? Nutrients 2014; 6: 4452-71. [CrossRef] Lim SS, Vos T, Flaxman AD, Danaei G, Shibuya K, Adair-Rohani H, et al. A comparative risk assessment of burden of disease and injury attributable to 67 risk factors and risk factor clusters in 21 regions, 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010. La