Frequencies of the new thrombophilic mutations of antithrombin (SERPINC1) (IVS +141G>A), glycoprotein GPVI (Ser219Pro) and cytochrome CYP4V2 (Lys259Gln) in healthy middle-aged people in Central Bohemia
Authors:
J. Kvasnička 1; J. Hájková 1; P. Bobčíková 1; T. Kvasnička 1; D. Dušková 2; Š. Poletínová 2; V. Kieferová 2
Authors‘ workplace:
Trombotické centrum a Centrální hematologické laboratoře, přednosta prof. MUDr. Jan Kvasnička, DrSc., Ústavu klinické biochemie a laboratorní diagnostiky 1. lékařské fakulty UK a VFN v Praze, přednosta prof. MUDr. Tomáš Zima, DrSc., MBA
1; Fakultní transfuzní oddělení VFN v Praze, přednostka prim. MUDr. Daniela Dušková
2
Published in:
Vnitř Lék 2012; 58(7 a 8): 146-151
Category:
60th Birthday prof. MUDr. Miroslav Penka, CSc.
Overview
Objective:
The aim of study was to determine frequencies of alleles and genotypes of new thrombophilia polymorhisms associated according to GWAS studies with venous thrombosis in Caucasian healthy people in Central Bohemia.
Methods:
Genotyping of thrombophilic mutations SERPINC1 IVS +141G>A, GP6 13254T>C and CYP4V2 (Lys259Gln) was performed in 1,527 healthy subjects using a robotic DNA isolation and subsequent PCR amplification with melting curve analysis (LightCycler480 System, Roche).
Results:
For the reference group was the frequency of risk allele A of SERPINC1 (IVS +141G>A) polymorphism 11.3% and frequencies of genotypes were GG 78.36%, GA 20.66% and AA 0.98%. Frequency of risk allele T of GP6 13254T>C polymorphism was 87.7% and frequencies of genotypes were TT 77.14%, TC 21.15% and CC 1.70%. Frequency of risk allele A of CYP4V2 polymorphism (Lys259Gln) was 65.2% and frequencies of genotypes were CC 12.25%, CA 45.12% and AA 42.63%. Those frequencies were not differ for both genders.
Conclusion:
The results confirm relatively high prevalence of other hereditary thrombophilia polymorphisms in Central Bohemia. But their clinical significance is not fully known yet.
Key words:
SERPINC1 (IVS +141G>A) – GP6 (13254T>C) – CYP4V2 (Lys259Gln) – prevalence – Central Bohemia
Sources
1. Rosendaal FR. Venous thrombosis: a multicausal disease. Lancet 1999; 353: 1167–1173.
2. Margaglione M, Grandone E. Population genetics of venous thromboembolism. A narrative review. Thromb Haemostas 2011; 105: 221–231.
3. Gohil R, Peck G, Sharma P. The genetics of venous thromboembolism. A meta-analysis involving approximately 120,000 cases and 180,000 controls. Thromb Haemost 2009; 102: 360–370.
4. Matýšková M, Paseka J, Vorlová Z et al. Prevalence of factor V Leiden mutation in healthy women. In: Scharrer I, Schramm W (eds). 29. Hämophilie Symposion Hamburg1998, Berlin--Heidelberg: Springer Verlag 1999: 309–311.
5. Hrachovinová I, Vorlová Z, Matýšková M et al. Thrombotic risk of the prothrombin gene G20210A mutation and clinical features of thrombophilia in 50 carriers of mutation. XVIIth Congress of the ISTH, Washington D.C., USA. Thromb Haemostas 1999; (Suppl): Abstract No 2060, 652.
6. Bucková D, Izakovicová-Hollá L, Vácha J. Polymorphism 4G/5G in the plasminogen activator inhibitor-1 (PAI-1) gene is associated with IgE-mediated allergic diseases and asthma in the Czech population. Allergy 2002; 57: 446–448.
7. Bezemer ID, Bare LA, Doggen CJ et al. Gene variants associated with deep vein thrombosis. JAMA 2008; 299: 1306–1314.
8. Tregouet DA, Heath S, Saut N et al. Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach. Blood 2009; 113: 5298–3303.
9. Manolio TA. Genomewide association studies and assessment of the risk of disease. N Engl J Med 2010; 363: 166–176.
10. Austin H, De Staercke C, Lally C et al. New gene variants associated with venous thrombosis: a replication study in White and Black Americans. J Thromb Haemost 2011; 9: 489–495.
11. Antón AI, Teruel R, Corral J et al. Functional consequences of the prothrombotic SERPINC1 rs2227589 polymorphism on antithrombin levels. Haematologica 2009; 94: 589–592.
12. Clemetson JM, Polgar J, Magnenat E et al. The platelet collagen receptor glycoprotein VI is a member of the immunoglobulin superfamily closely related to FcalphaR and the natural killer receptors. J Biol Chem 1999; 274: 29019–29024.
13. Watkins NA, O’Connor MN, Rankin A et al. Definition of novel GP6 polymorphisms and major difference in haplotype frequencies between populations by a combination of in-depth exon resequencing and genotyping with tag single nucleotide polymorphisms. J Thromb Haemost 2006; 4: 1197–1205.
14. Croft SA, Samani NJ, Teare MD et al. Novel platelet membrane glycoprotein VI dimorphism is a risk factor for myocardial infarction. Circulation 2001; 104: 1459–1463.
15. Ollikainen E, Mikkelsson J, Perola M et al. Platelet membrane collagen receptor glycoprotein VI polymorphism is associated with coronary thrombosis and fatal myocardial infarction in middle-aged men. Atherosclerosis 2004; 176: 95–99.
16. Takagi S, Iwai N, Baba S et al. A GPVI polymorphism is a risk factor for myocardial infarction in Japanese. Atherosclerosis 2002; 165: 397–398.
17. Motovska Z, Kvasnicka J, Widimsky P et al. Platelet glycoprotein GP VI 13254C allele is an independent risk factor of premature myocardial infarction. Thromb Res 2010; 125: e61–e64.
18. Bray PF, Howard TD, Vittinghoff E et al. Effect of genetic variations in platelet glycoproteins Ibalpha and VI on the risk for coronary heart disease events in postmenopausal women taking hormone therapy. Blood 2007; 109: 1862–1869.
19. Snoep JD, Gaussem P, Eikenboom JC et al. The minor allele of GP6 13254T>C is associated with decreased platelet activation and a reduced risk of recurrent cardiovascular events and mortality: results from the SMILE-Platelets project. J Thromb Haemost 2010; 8: 2377–2384.
20. Parguiña AF, Grigorian-Shamagian L, Agra RM et al. Variations in platelet proteins associated with ST-elevation myocardial infarction: novel clues on pathways underlying platelet activation in acute coronary syndromes. Arterioscler Thromb Vasc Biol 2011; 31: 2957–2964.
21. Joutsi-Korhonen L, Smethurst PA, Rankin A et al. The low frequency allele of the platelet collagen signalling receptor glycoprotein VI is associated with reduced functional responses and expression. Blood 2003; 101: 4372–4379.
22. Trifiro E, Williams SA, Cheli Y et al. The low--frequency isoform of platelet glycoprotein VIb attenuates ligand-mediated signal transduction but not receptor expression or ligand binding. Blood 2009; 114: 1893–1899.
23. http//: www.Genecards.org/cgi-bin/carddisp.pl?gene=CYP4V2.
24. Li A, Jiao X, Munier FL et al. Bietti crystalline corneoretinal dystrophy is caused by mutations in the novel gene CYP4V2. Am J Hum Genet 2004; 74: 817–826.
25. Bezemer A, Morange PE, Tregouet DA. Lessons from genome-wide association studies in venous thrombosis. J Thromb Haemost 2011; 9 (Suppl 1): 258–264.
26. Li Y, Bezemer ID, Rowland CM et al. Genetic variants associated with deep vein thrombosis: the F11 locus. J Thromb Haemost 2009; 7: 1802–1808.
Labels
Diabetology Endocrinology Internal medicineArticle was published in
Internal Medicine
2012 Issue 7 a 8
Most read in this issue
- Myocardial infarction the young – our results and experience
- An anaesthesiologist’s perspective on requirements for pre-surgery examinations
- Megakaryopoesis and platelet genesis
- Aldosterone antagonists in chronic heart failure treatment