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Shadrina A.S.

Institute of Chemical Biology and Fundamental Medicine, Novosibirsk, Russia;
Novosibirsk State University, Novosibirsk, Russia

Smetanina M.A.

Institute of Chemical Biology and Fundamental Medicine, Novosibirsk, Russia

Sevost'ianova K.S.

Institut khimicheskoĭ biologii i fundamental'noĭ meditsiny SO RAN, Novosibirsk

Sokolova E.A.

Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia;
Novosibirsk State University, Novosibirsk, Russia

Shevela A.I.

The Center of New Medical Technologies Institute of Chemical Biology and Fundamental Medicine, The Russian Academy of Sciences, Siberian Branch Novosibirsk, Russia

Soldatsky E.Yu.

Department of Intermediate Level Surgery No1, Faculty of General Medicine, N.I. Pirogov Russian National Research Medical University, Moscow

Seliverstov E.I.

Russian National Research Medical University named after N.I. Pirogov, Moscow, Russia

Demekhova M.Yu.

Medalp Ltd, Sankt-Petersburg

Shonov O.A.

Medalp Ltd, Sankt-Petersburg

Iliukhin E.A.

Sankt-Peterburg

Voronina E.N.

Institut khimicheskoĭ biologii i fundamental'noĭ meditsiny SO RAN, Novosibirsk

Pikalov I.V.

Novosibirsk State Medical University, Novosibirsk, Russia

Zolotukhin I.A.

Pirogov Russian National Research Medical University, Moscow, Russia

Kirienko A.I.

Russian National Research Medical University nabbed after N.I. Pirogov, Moscow, Russia

Filipenko M.L.

Institute of Chemical Biology and Fundamental Medicine, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russia;
Novosibirsk State University, Novosibirsk, Russia

The Association of Single Nucleotide Polymorphisms with the Risk of Varicose Veins of the Lower Extremities: A Study of the Russian Population of the Russian Federation

Authors:

Shadrina A.S., Smetanina M.A., Sevost'ianova K.S., Sokolova E.A., Shevela A.I., Soldatsky E.Yu., Seliverstov E.I., Demekhova M.Yu., Shonov O.A., Iliukhin E.A., Voronina E.N., Pikalov I.V., Zolotukhin I.A., Kirienko A.I., Filipenko M.L.

More about the authors

Journal: Journal of Venous Disorders. 2016;10(2): 68‑76

Read: 2095 times


To cite this article:

Shadrina AS, Smetanina MA, Sevost'ianova KS, et al. . The Association of Single Nucleotide Polymorphisms with the Risk of Varicose Veins of the Lower Extremities: A Study of the Russian Population of the Russian Federation. Journal of Venous Disorders. 2016;10(2):68‑76. (In Russ.)
https://doi.org/10.17116/flebo201610268-74

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References:

  1. Beebe-Dimmer JL, Pfeifer JR, Engle JS, Schottenfeld D. The epidemiology of chronic venous insufficiency and varicose veins. Annals of Epidemiology. 2005;15(3):175-184.  doi: 10.1016/j.annepidem.2004.05.015.
  2. Lim CS, Davies AH. Pathogenesis of primary varicose veins. The British journal of surgery. 2009;96(11):1231-1242. doi: 10.1002/bjs.6798.
  3. Pfisterer L, König G, Hecker M, Korff T. Pathogenesis of varicose veins — lessons from biomechanics. VASA. Zeitschrift für Gefässkrankheiten. 2014;43(2):88-99.  doi: 10.1024/0301-1526/a000335.
  4. Raffetto JD, Khalil RA. Mechanisms of varicose vein formation: valve dysfunction and wall dilation. Phlebology. 2008;23(2):85-98.  doi: 10.1258/phleb.2007.007027
  5. Segiet OA, Brzozowa M, Piecuch A, Dudek D, Reichman-Warmusz E, Wojnicz R. Biomolecular mechanisms in varicose veins development. Annals of vascular surgery. 2015;29(2):377-384.  doi: 10.1016/j.avsg.2014.10.009.
  6. Krysa J, Jones GT, van Rij AM. Evidence for a genetic role in varicose veins and chronic venous insufficiency. Phlebology. 2012;27(7):329-335.  doi: 10.1258/phleb.2011.011030.
  7. Bharath V, Kahn SR, Lazo-Langner A. Genetic polymorphisms of vein wall remodeling in chronic venous disease: a narrative and systematic review. Blood. 2014;124(8):1242-1250. doi: 10.1182/blood-2014-03-558478.
  8. Fan C, Ouyang P, Timur AA, He P, You SA, Hu Y, Ke T, Driscoll D J, Chen Q, Wang QK. Novel roles of GATA1 in regulation of angiogenic factor AGGF1 and endothelial cell function. The Journal of biological chemistry. 2009;284(35):23331-23343. doi: 10.1074/jbc.M109.036079.
  9. Chen D, Li L, Tu X, Yin Z, Wang Q. Functional characterization of Klippel—Trenaunay syndrome gene AGGF1 identifies a novel angiogenic signaling pathway for specification of vein differentiation and angiogenesis during embryogenesis. Human Molecular Genetics. 2013;22(5):963-976.  doi: 10.1093/hmg/dds501.
  10. Hu Y, Li L, Seidelmann SB, Timur AA, Shen PH, Driscoll DJ, Wang QK. Identification of association of common AGGF1 variants with susceptibility for Klippel—Trenaunay syndrome using the structure association program. Annals of human genetics. 2008;72(Pt 5):636-643.  doi: 10.1111/j.1469-1809.2008.00458.x.
  11. Feder JN, Gnirke A, Thomas W, Tsuchihashi Z, Ruddy DA, Basava A, Dormishian F, Domingo R, Ellis MC, Fullan A, Hinton LM, Jones NL, Kimmel BE, Kronmal GS, Lauer P, Lee VK, Loeb DB, Mapa FA, McClelland E, Meyer NC, Mintier GA, Moeller N, Moore T, Morikang E, Prass CE, Quintana L, Starnes SM, Schatzman RC, Brunke KJ, Drayna DT, Risch NJ, Bacon BR, Wolff RK. A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis. Nature genetics. 1996;13(4):399-408.  doi: 10.1038/ng0896-399.
  12. Kartikasari AE, Georgiou NA, Visseren FL, van Kats-Renauld H, van Asbeck BS, Marx JJ. Endothelial activation and induction of monocyte adhesion by nontransferrin-bound iron present in human sera. FASEB journal. 2005;20(2):353-355.  doi: 10.1096/fj.05-4700fje.
  13. Fredriksen A, Meyer K, Ueland PM, Vollset SE, Grotmol T, Schneede J. Large-scale population-based metabolic phenotyping of thirteen genetic polymorphisms related to one-carbon metabolism. Human mutation. 2007;28(9):856-865.  doi: 10.1002/humu.20522.
  14. Austin RC, Lentz SR, Werstuck GH. Role of hyperhomocysteinemia in endothelial dysfunction and atherothrombotic disease. Cell death and differentiation. 2004;11(suppl1):S56-S64.  doi: 10.1038/sj.cdd.4401451.
  15. Wu S, Gao X, Yang S, Meng M, Yang X, Ge B. The role of endoplasmic reticulum stress in endothelial dysfunction induced by homocysteine thiolactone. Fundamental & clinical pharmacology. 2015;29(3):252-259.  doi: 10.1111/fcp.12101.
  16. Zhang D, Chen Y, Xie X, Liu J, Wang Q, Kong W, Zhu Y. Homocysteine activates vascular smooth muscle cells by DNA demethylation of platelet-derived growth factor in endothelial cells. Journal of molecular and cellular cardiology. 2012;53(4):487-496.  doi: 10.1016/j.yjmcc.2012.07.010.
  17. Brice G, Mansour S, Bell R, Collin JR, Child AH, Brady AF, Sarfarazi M, Burnand KG, Jeffery S, Mortimer P, Murday VA. Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24. Journal of medical genetics. 2002;39(7):478-483.  doi: 10.1136/jmg.39.7.478.
  18. Mellor RH, Brice G, Stanton AW, French J, Smith A, Jeffery S, Levick JR, Burnand KG, Mortimer PS. Mutations in FOXC2 are strongly associated with primary valve failure in veins of the lower limb. Circulation. 2007;115(14):1912-1920. doi: 10.1161/CIRCULATIONAHA.106.675348.
  19. Zamboni P, Tognazzo S, Izzo M, Pancaldi F, Scapoli GL, Liboni A, Gemmati D. Hemochromatosis C282Y gene mutation increases the risk of venous leg ulceration. Journal of vascular surgery. 2005;42(2):309-314.  doi: 10.1016/j.jvs.2005.04.003.
  20. Surendran S, Girijamma A, Nair R, Ramegowda KS, Nair DH, Thulaseedharan JV, Lakkappa RB, Kamalapurkar G, Kartha CC. Forkhead box C2 promoter variant c.512C>T is associated with increased susceptibility to chronic venous diseases. PLoS One. 2014;9(3):e90682. doi:10.1371/journal.pone.0090682.

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