A comparison of the genetic and clinical risk factors for arterial hypertension between indigenous and non-indigenous people of the Shoria Mountain Region

References

• Bertuccio P, Levi F, Lucchini F, Chatenoud L, Bosetti C, Negri E, La Vecchia C. Coronary heart disease and cerebrovascular disease mortality in young adults: recent trends in Europe. Eur J Cardiovasc Prev Rehabil. 2011;18(4):627–34.
   PubMedGoogle Scholar
• Guoheng X. Role of perilipin phosphorylation on the control of lipolysis in adipocytes. Chin J Pathophysiology. 2006;22(13):69.
   Google Scholar
• Rubies-Prat J, Ordóñez-Llanos J, Martin S, Blanco-Vaca F, Molina L, Goday A, Pedro-Botet J. Low-density lipoprotein particle size, triglyceride-rich lipoproteins, and glucose tolerance in non-diabetic men with essential hypertension. Clin Exp Hypertens. 2001;23(6):489–500.
   PubMed Web of Science ®Google Scholar
• Kameda W, Daimon M, Oizumi T, Jimbu Y, Kimura M, Hirata A, Yamaguchi H, Ohnuma H, Igarashi M, Tominaga M, et al. Association of decrease in serum dehydroepiandrosterone sulfate levels with the progression to type 2 diabetes in men of a Japanese population: the Funagata Study. Metabolism. 2005;54(5):669–76.
   PubMed Web of Science ®Google Scholar
• Singh M, Singh AK, Pandey P, Chandra S, Singh KA, Gambhir IS. Molecular genetics of essential hypertension. Clin Exp Hypertens. 2016;38(3):268–77.
   PubMed Web of Science ®Google Scholar
• Yamada Y, Matsui K, Takeuchi I, Oguri M, Fujimaki T. Association of genetic variants with hypertension in a longitudinal population-based genetic epidemiological study. Int J Mol Med. 2015;35(5):1189–98.
   PubMed Web of Science ®Google Scholar
• Singh M, Singh AK, Singh S, Pandey P, Chandra S, Gambhir IS. Angiotensin-converting enzyme gene I/D polymorphism increases the susceptibility to hypertension and additive diseases: A study on North Indian patients. Clin Exp Hypertens. 2016;38(3):305–11.
   PubMed Web of Science ®Google Scholar
• Gao Y, Lin Y, Sun K, Wang Y, Chen J, Wang H, Zhou X, Fan X, Hui R. Orthostatic blood pressure dysregulation and polymorphisms of β-adrenergic receptor genes in hypertensive patients. J Clin Hypertens. 2014;16(3):207–13.
   Web of Science ®Google Scholar
• Yun L, Xu R, Li G, Yao Y, Li J, Cong D, Xu X, Zhang L. Homocysteine and the C677T gene polymorphism of its key metabolic enzyme MTHFR are risk factors of early renal damage in hypertension in a Chinese han population. Medicine. 2015;94(52):e2389.
   PubMed Web of Science ®Google Scholar
• Seidlerovа J, Filipovsky J, Mayer O, Kuсerovа A, Pesta M. Association between endothelial NO synthase polymorphisms and arterial properties in the general population. Nitric Oxide. 2015;44:47–51.
   PubMed Web of Science ®Google Scholar
• Cоwlеy АW. Thе gеnеtic dissеctiоn оf еssеntiаl hyреrtеnsiоn. Nаturе Rеv Gеnеtics. 2006;7(11):829–40.
   Google Scholar
• Еichlеr ЕЕ. Missing hеritаbility аnd strаtеgiеs fоr finding thе undеrlying cаusеs оf cоmрlех disеаsе. Nаt Rеv Gеnеt. 2010;11(6):446–50.
   Google Scholar
• Shakhtshneider EV, Yudin NS, Damba LD, Gubina MA, Maksimov VN, Barbarash OL, Ogarkov MY, Polikutina OM, Kazachek YV, Kulikov IV, et al. On the question of the ethnic characteristics of nuclear and mitochondrial gene pools Shor. The gene pool of the population of Siberia. Collection of scientific articles. Novosibirsk; 2003. С.174-176. (In Russ).
   Google Scholar
• Fox CS, Heard-Costa NL, Vasan RS, Murabito JM, D’Agostino RB, Atwood LD. Genome wide linkage analysis of weight change in the Framingham heart study. J Clin Endocrinol Metab. 2005;5:3197–201.
   Google Scholar
• Snapir A, Scheinin M, Groop LC, Orho-Melander M. The insertion/deletion variation in the α2B-adrenoceptor does not seem to modify the risk for acute myocardial infarction, but may modify the risk for hypertension in sib-pairs from families with type 2 diabetes. Cardiovasc Diabetol. 2003;2:15.
   PubMed Web of Science ®Google Scholar
• Lima JJ, Feng H, Duckworth L, Wang J, Sylvester JE, Kissoon N, Garg H. Association analyses of adrenergic receptor polymorphisms with obesity and metabolic alterations. Metabolism. 2007;56(6):757–65.
   PubMed Web of Science ®Google Scholar
• Salimi S, Firoozrai M, Nourmohammadi I, Shabani M, Mohebbi A. Endothelial nitric oxide synthase gene intron4 VNTR polymorphism in patients with coronary artery disease in Iran. Indian J Med Res. 2006;124(6):683–88.
   PubMed Web of Science ®Google Scholar
• Joffres M, Falaschetti E. Hypertension prevalence, awareness, treatment and control in national surveys from England, the USA and Canada, and correlation with stroke and ischemic heart disease mortality: a cross sectional study. BMJ Open. 2013;3:657–68.
   Web of Science ®Google Scholar
• Wolf-Maier K, Cooper RS, Kramer H, Banegas JR, Giampaoli S, Joffres MR, Poulter N, Primatesta P, Stegmayr B, Thamm M. Hypertension treatment and control in five European countries, Canada, and the United States. Hypertension. 2004;43:10–17.
   PubMed Web of Science ®Google Scholar
• Lim SS, Vos T, Flaxman AD, Danaei G, Shibuya K, 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. Lancet. 2012;38:2224–60.
   Google Scholar
• Chazova IE, Zhernakova I, Oshchepkova EV, Shalnova SA, Jarovaya EB, Konradi AO, Boitsov SA. Prevalence of risk factors for cardiovascular disease in the Russian population of patients with hypertension. Cardiology. 2014;10:4–12. (In Russ.).
   Google Scholar
• Muromtseva GA, Koncevaya AV, Konstantinov VV, Artamonova GV, Gatagonova TM, Duplyakov DV, Efanov A, Zhernakova Y, Ilyin VA, Conradi AO, et al. Prevalence of risk factors for noncommunicable diseases in the Russian population in 2012-2013. Results of the study ESSAY-RF. Cardiovascu Therapy Prev. 2014;13(6):4–11. (In Russ.).
   Google Scholar
• Redon J, Olsen MN, Cooper RS, Zurriaga O, Martinez-Beneito MA, Laurent S, Cifkova R, Coca A, Mancia G. Stroke mortality trends from 1990 to 2006 in 39 countries from Europe and Central Asia: implications for control of high blood pressure. Eur Heart J. 2011;32:1424–31.
   PubMed Web of Science ®Google Scholar
• Hubert HB, Fienleib M, McNamara PT, Castelli WP. Obesity as an independent risk factor for cardiovascular disease: a 26 year follow up of participants of the framingham heart study. Circulation. 1983;67:968–77.
   PubMed Web of Science ®Google Scholar
• Penesova A, Cizmarova E, Kvetnansky R, Koska J, Sedlakova B, Krizanova O. Insertion/deletion polymorphism on ACE gene is associated with endothelial dysfunction in young patients with hypertension. Horm Metab Res. 2006;8(9):592–97.
   Google Scholar
• O’Donnel CJ, Lindpainter K, Larson MG, Rao VS, Ordovas JM, Schaefer EJ, Myers RH, Levy D. Evidence for association and genetic linkage of the angiotensin-converting enzyme locus with hypertension and blood pressure in men but not women in the Framyngham Heart Study. Circulation. 1998;97(18):1766–72.
   PubMed Web of Science ®Google Scholar
• Glavnik N, Petrovic D. M235T polymorphism of the angiotensinogen gene and insertion/deletion polymorphism of the angiotensin-1 converting enzyme gene in essential arterial hypertension in Caucasians. Folia Biol (Praha). 2007;53(2):69–70.
   PubMed Web of Science ®Google Scholar
• Fatini C, Guazelli R, Manetti P, et al. RAS genes influence exercise-induced left ventricular hypertrophy: an elite athletes study. Med Sci Sports Exerc. 2000;32(11):1868–72.
   PubMed Web of Science ®Google Scholar
• Zee RY, Bennett CL, Schrader AP, Morris BJ. Frequenci.es of variants of candidate genes in different age groups of hypertensives. Clin Exp Pharmacol Physiol. 1994;21(11):925–30.
   PubMed Web of Science ®Google Scholar
• Vasudevan R. Association of insertion/deletion polymorphism of alpha-adrenoceptor gene in essential hypertension with or without type 2 diabetes mellitus in malaysian subjects. Int J Biol Sci. 2008;4(6):362–67.
   PubMed Web of Science ®Google Scholar
• Heinonen P, Koulu M, Pesonen U, Karvonen MK, Rissanen A, Laakso M, Valve R, Uusitupa M, Scheinin M. Identification of a three-amino acid deletion in the alpha2B-adrenergic receptor that is associated with reduced basal metabolic rate in obese subjects. J Clin Endocrinol Metab. 1999;84 (7):2429–33.
   PubMed Web of Science ®Google Scholar
• Baldwin CT, Schwartz F, Baima J. Identification of a polymorphic glutamic acid stretch in the alpha2B-adrenergic receptor and lack of linkage with essential hypertension. Am J Hypertens. 1999;12(9):853–57.
   PubMed Web of Science ®Google Scholar
• Etzel JP, Rana BK, Wen G, Parmer RJ, Schork NJ, O’Connor DT, Insel PA. Genetic variation at the human alpha2B-adrenergic receptor locus: role in blood pressure variation and yohimbine response. Hypertension. 2005;45(6):1207–13.
   PubMed Web of Science ®Google Scholar
• Nieminen T, Lehtimki T, Laiho J. Effects of polymorphisms in beta1-adrenoceptor and alpha-subunit of Gprotein on heart rate and blood pressure during exercise test. Finnish Cardiovasc Study J Appl Physiol. 2006;100(2):507–11.
   PubMed Web of Science ®Google Scholar
• Borodulin VB, Shevchenko OV, Bychkov EN. The value of genetic mutations in the development of metabolic disorders in hypertensive patients. Saratov J Med Scientific Res. 2012;3(8):751–56. (In Russ.).
   Google Scholar
• Bairova TA, Dolgich VV. Relationship polymorphism of endothelial nitric oxide synthase and hypertension in populations of Eastern Siberia. Bull East-Siberian Sci Center SB RAMS. 2007;3:64–65. (In Russ.).
   Google Scholar
• De Miranda JA, Lacchini R, Belo VA, Lanna CM, Sertorio JT, Luizon MR, Tanus-Santos JE. The effects of endothelial nitric oxide synthase tagSNPs on nitrite levels and risk of hypertension and obesity in children and adolescents. J Hum Hypertens. 2015;29(2):109–14.
   PubMed Web of Science ®Google Scholar
• Soudani NY, Fakhoury RM, Kaissi SS, Zgheib NK. The role of genetic polymorphisms in endothelial nitric oxide synthase and beta2-adrenergic receptors with risk of hypertension in a sample of Lebanese people. Saudi Med J. 2014;35 (3):255–60.
   PubMed Web of Science ®Google Scholar