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Original

The Univariation and Multiple Linear Regression Analyses for Seventeen SNPs in Thirteen Cardiovascular Disease-Predisposing Genes and Blood Pressure in Chinese Han Males

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Pages 648-661 | Received 08 Oct 2007, Accepted 08 Apr 2008, Published online: 03 Jul 2009

References

  • Luft FC. Geneticism of essential hypertension. Hypertension. 2004; 43: 1155–1159
  • Shimo NY, Urabe T, Hattori N, Hattori N, Watanabe Y, Nagao T, Yokochi M, Hamamoto M, Mizuno Y. Polymorphism of the lipoprotein lipase gene and risk of atherothrombotic cerebral infarction in the Japanese. Stroke. 2001; 32: 1481–1486
  • Klannemark M, Suurinkeroinen L, Orho MM, Groop L, Taskinen MR. Interaction between the Asn291Ser variant of the LPL gene and insulin resistance on dyslipidaemia in high risk individuals for Type 2 diabetes mellitus. Diabetes Med. 2000; 17: 599–605
  • Chu S, Zhu D, Xiong M. Linkage analysis of candidate genes for glucose and lipid metabolism with essential hypertension. Zhonghua Yi Xue Za Zhi. 2001; 81: 20–22
  • Lifton RP, Gharavi AG, Geller DS. Molecular mechanisms of human hypertension. Cell. 2001; 104: 545–556
  • Kato N. Genetic analysis in human hypertension. Hypertens Res. 2002; 25: 319–327
  • Wu KD, Hsiao CF, Ho LT, Sheu WH, Pei D, Chuang LM, Curb D, Chen YD, Tsai HJ, Dzau VJ, Cox D, Tai TY. Clustering and heritability of insulin resistance in Chinese and Japanese hypertensive families: A Stanford-Asian Pacific Program in hypertension and insulin resistance sibling study. Hypertens Res. 2002; 25: 529–536
  • Doris PA. Hypertension genetics, single nucleotide polymorphisms, and the common disease: Common variant hypothesis. Hypertension. 2002; 39: 323–331
  • Mingrone G, Henriksen FL, Greco AV, Krogh LN, Capristo E, Gastaldelli A, Castagneto M, Ferrannini E, Gasbarrini G, Beck-Nielsen H. Triglyceride-induced diabetes associated with familial lipoprotein lipase deficiency. Diabetes. 1999; 48: 1258–1263
  • Mondry A, Loh M, Liu P, Zhu AL, Nagel M. Polymorphisms of the insertion/deletion ACE and M235T AGT genes and hypertension: Surprising new findings and meta-analysis of data. BMC Nephrol. 2005; 6: 1–11
  • Say YH, Ling KH, Duraisamy G, Isaac S, Rosli R. Angiotensinogen M235T gene variants and its association with essential hypertension and plasma renin activity in Malaysian subjects: A case control study. BMC Cardiovasc Disord. 2005; 5: 7–17
  • Chen P, Jiang YF, Cheng K. Meta-analysis on the association of AGT M235T polymorphism and essential hypertension in Chinese population. Zhonghua Liu Xing Bing Xue Za Zhi. 2003; 24: 711–714
  • Wolff B, Grabe HJ, Schlüter C, Popowski K, Völzke H, Lüdemann J, John U, Felix SB, Cascorbi I. Endothelial nitric oxide synthase Glu298Asp gene polymorphism, blood pressure and hypertension in a general population sample. J Hypertens. 2005; 23: 1361–1366
  • Sharma P, Hingorani A, Jia H, Hopper R, Brown MJ. Quantitative association between a newly identified molecular variant in the endothelin-2 gene and human essential hypertension. J Hypertens. 1999; 17: 1281–1287
  • Kokubo Y, Tomoike H, Tanaka C, Banno M, Okuda T, Inamoto N, Kamide K, Kawano Y, Miyata T. Association of sixty-one non-synonymous polymorphisms in forty-one hypertension candidate genes with blood pressure variation and hypertension. Hypertens Res. 2006; 29: 611–619
  • Sass C, Cheng S, Siest G, Visvikis S. Genetic influences on blood pressure within the Stanislas cohort. J Hypertens. 2004; 22: 297–304

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