메뉴 건너뛰기




Volumn 54, Issue 77, 2007, Pages 1438-1442

Factor V Leiden G1691A, prothrombin G20210A, and MTHFR C677T mutations in Turkish inflammatory bowel disease patients

Author keywords

Factor V Leiden G1691A; Gene mutation; Inflammatory bowel disease; Methylene tetrahydrofolate reductase C677T; Prothrombin G20210A

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); ANTIBIOTIC AGENT; AZATHIOPRINE; BLOOD CLOTTING FACTOR 5; CYCLOSPORIN; IMMUNOSUPPRESSIVE AGENT; MESALAZINE; PROTHROMBIN; STEROID;

EID: 34547633637     PISSN: 01726390     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (16)

References (41)
  • 2
    • 0033855472 scopus 로고    scopus 로고
    • Prevalence of factor V Leiden and the G20210A prothrombin-gene mutation in inflammatory bowel disease
    • Papa A, Stefano VD, Gasbarrini P, Chiusolo R, Cianci I, Casorelli K, et al: Prevalence of factor V Leiden and the G20210A prothrombin-gene mutation in inflammatory bowel disease. Blood Coag Fibrinol 2000; 11:599-603.
    • (2000) Blood Coag Fibrinol , vol.11 , pp. 599-603
    • Papa, A.1    Stefano, V.D.2    Gasbarrini, P.3    Chiusolo, R.4    Cianci, I.5    Casorelli, K.6
  • 7
    • 0030895756 scopus 로고    scopus 로고
    • Thrombosis in inflammatory bowel disease: Clinical setting, procoagulant profile and factor V Leiden
    • Jackson LM, O'Gorman PJ, O'Connell J, Cronin CC, Cotter KP, Shanahan F: Thrombosis in inflammatory bowel disease: Clinical setting, procoagulant profile and factor V Leiden. QJM 1997; 90:183-188.
    • (1997) QJM , vol.90 , pp. 183-188
    • Jackson, L.M.1    O'Gorman, P.J.2    O'Connell, J.3    Cronin, C.C.4    Cotter, K.P.5    Shanahan, F.6
  • 8
    • 0032810850 scopus 로고    scopus 로고
    • Increased prevalence of methylenetetrahydrafolate reductase in patients with inflammatory bowel disease, and its clinical implications
    • Mahmut N, Molloy A, McPartlin J, Corbally R, Whitehead AS, Scott JM, et al: Increased prevalence of methylenetetrahydrafolate reductase in patients with inflammatory bowel disease, and its clinical implications. Gut 1999; 45:389-394.
    • (1999) Gut , vol.45 , pp. 389-394
    • Mahmut, N.1    Molloy, A.2    McPartlin, J.3    Corbally, R.4    Whitehead, A.S.5    Scott, J.M.6
  • 10
    • 0027446268 scopus 로고
    • Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: Prediction of a cofactor to activated protein C
    • Dahlback B, Carlsson M, Svensson PJ: Familial thrombophilia due to a previously unrecognized mechanism characterized by poor anticoagulant response to activated protein C: prediction of a cofactor to activated protein C. Proc Natl Acad Sci 1993; 90:1004-1008.
    • (1993) Proc Natl Acad Sci , vol.90 , pp. 1004-1008
    • Dahlback, B.1    Carlsson, M.2    Svensson, P.J.3
  • 11
    • 0028098210 scopus 로고
    • Resistance to Activated Protein C as a Basis for Venous Thrombosis
    • Svensson PJ, Dahlback B: Resistance to Activated Protein C as a Basis for Venous Thrombosis. N Engl J Med 1994; 330:517-522.
    • (1994) N Engl J Med , vol.330 , pp. 517-522
    • Svensson, P.J.1    Dahlback, B.2
  • 12
    • 0035912152 scopus 로고    scopus 로고
    • Genetic susceptibility to venous thrombosis
    • Seligsohn U, Libertsky A: Genetic susceptibility to venous thrombosis. N Engl J Med 2001; 344:1222-1231.
    • (2001) N Engl J Med , vol.344 , pp. 1222-1231
    • Seligsohn, U.1    Libertsky, A.2
  • 13
    • 0031680257 scopus 로고    scopus 로고
    • Leiden mutation increases the risk of venous thrombosis in patients with inflammatory bowel disease
    • Liebman HA, Kashani N, Sutherland D, McGehee W, Kam AL: The factor V Leiden mutation increases the risk of venous thrombosis in patients with inflammatory bowel disease. Gastroenterology 1998; 115:830-834.
    • (1998) Gastroenterology , vol.115 , pp. 830-834
    • Liebman, H.A.1    Kashani, N.2    Sutherland, D.3    McGehee, W.4    Kam, A.L.5    The factor, V.6
  • 14
  • 15
    • 0033869354 scopus 로고    scopus 로고
    • Inflammatory bowel diseases are not associated with major hereditary conditions predisposing to thrombosis
    • Vecchi M, Sacchi E, Saibeni S, Meucci G, Tagliabue L, Duca F, et al: Inflammatory bowel diseases are not associated with major hereditary conditions predisposing to thrombosis. Dig Dis Sci 2000; 45:1465-1469.
    • (2000) Dig Dis Sci , vol.45 , pp. 1465-1469
    • Vecchi, M.1    Sacchi, E.2    Saibeni, S.3    Meucci, G.4    Tagliabue, L.5    Duca, F.6
  • 16
    • 0029850530 scopus 로고    scopus 로고
    • A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
    • Poort SR, Rosendaal FR, Reitsma PH, Bertina RM: A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood 1996; 88:3698-3703.
    • (1996) Blood , vol.88 , pp. 3698-3703
    • Poort, S.R.1    Rosendaal, F.R.2    Reitsma, P.H.3    Bertina, R.M.4
  • 19
    • 0037499810 scopus 로고    scopus 로고
    • Prevalence of factor V Leiden, FII G20210A, FXIII Val34Leu and MTHFR C677T polymorphisms in cancer patients with and without venous thrombosis
    • Ramacciotti E, Wolosker N, Puech-Leao P, Zeratti EA, Gusson PR, delGiglio A, et al: Prevalence of factor V Leiden, FII G20210A, FXIII Val34Leu and MTHFR C677T polymorphisms in cancer patients with and without venous thrombosis. Thrombos Res 2003; 109:171-174.
    • (2003) Thrombos Res , vol.109 , pp. 171-174
    • Ramacciotti, E.1    Wolosker, N.2    Puech-Leao, P.3    Zeratti, E.A.4    Gusson, P.R.5    delGiglio, A.6
  • 21
    • 0014277999 scopus 로고
    • Life histories of patients with chronic ulcerative colitis: A review of 2,000 cases
    • Sloan WP, Bargen Ja, Gage RB: Life histories of patients with chronic ulcerative colitis: A review of 2,000 cases. Gastroenterology 1968; 54:819-822.
    • (1968) Gastroenterology , vol.54 , pp. 819-822
    • Sloan, W.P.1    Bargen, J.2    Gage, R.B.3
  • 22
    • 84941818179 scopus 로고
    • Venous thrombosis occurring in non-specific ulcerative colitis. A necropsy study
    • Graef V, Baggenstoss AH, Sauer WG, Spittel J: Venous thrombosis occurring in non-specific ulcerative colitis. A necropsy study. Arch Intern Med 1966; 117:377-382.
    • (1966) Arch Intern Med , vol.117 , pp. 377-382
    • Graef, V.1    Baggenstoss, A.H.2    Sauer, W.G.3    Spittel, J.4
  • 24
    • 0028949781 scopus 로고
    • Inherited disorders of coagulation appear to protect against inflammatory bowel disease
    • Thompson NP, Wakefield AJ, Pounder RE: Inherited disorders of coagulation appear to protect against inflammatory bowel disease. Gastroenterology 1995; 108:110-115.
    • (1995) Gastroenterology , vol.108 , pp. 110-115
    • Thompson, N.P.1    Wakefield, A.J.2    Pounder, R.E.3
  • 25
    • 0028037137 scopus 로고
    • Identification of the same factor V gene mutation in 47 out of 50 thrombosis-prone families with inherited resistance to activated protein C
    • Zoller B, Svensson PJ, He X, Dahlback B: Identification of the same factor V gene mutation in 47 out of 50 thrombosis-prone families with inherited resistance to activated protein C. J Clin Invest 1994; 94:2521-2524.
    • (1994) J Clin Invest , vol.94 , pp. 2521-2524
    • Zoller, B.1    Svensson, P.J.2    He, X.3    Dahlback, B.4
  • 26
    • 0028931717 scopus 로고
    • High-risk of thrombosis in patients homozygous factor V Leiden (acquired protein C resistance)
    • Rosendal FR, Koster T, Vonderbraucke JP, Reitsma PH: High-risk of thrombosis in patients homozygous factor V Leiden (acquired protein C resistance). Blood 1995; 85:1504-1511.
    • (1995) Blood , vol.85 , pp. 1504-1511
    • Rosendal, F.R.1    Koster, T.2    Vonderbraucke, J.P.3    Reitsma, P.H.4
  • 27
    • 0034161456 scopus 로고    scopus 로고
    • Role of hemostatic gene polymorphism in venous and arterial thrombotic disease
    • Lane DA and Grant PJ: Role of hemostatic gene polymorphism in venous and arterial thrombotic disease. Blood 2000; 95:1517-1532.
    • (2000) Blood , vol.95 , pp. 1517-1532
    • Lane, D.A.1    Grant, P.J.2
  • 28
    • 0033539096 scopus 로고    scopus 로고
    • The risk of recurrent deep venous thrombosis among heterozygous carriers of both factor V Leiden and G20210A prothrombin mutation
    • De Stefano V, Martinelli I, Mannucci PM, Paciaruni K, Chiusolo P, Casonelli I, et al: The risk of recurrent deep venous thrombosis among heterozygous carriers of both factor V Leiden and G20210A prothrombin mutation. N Engl J Med 1999; 341:801-806.
    • (1999) N Engl J Med , vol.341 , pp. 801-806
    • De Stefano, V.1    Martinelli, I.2    Mannucci, P.M.3    Paciaruni, K.4    Chiusolo, P.5    Casonelli, I.6
  • 29
    • 0033938933 scopus 로고    scopus 로고
    • Inflammatory bowel disease promotes venous thrombosis earlier in life
    • Grip O, Svensson PJ, Lindgren S: Inflammatory bowel disease promotes venous thrombosis earlier in life. Scand J Gastroenterol 2000; 35:619-623.
    • (2000) Scand J Gastroenterol , vol.35 , pp. 619-623
    • Grip, O.1    Svensson, P.J.2    Lindgren, S.3
  • 31
    • 0034771941 scopus 로고    scopus 로고
    • Factor V Leiden and prothrombin gene mutation in inflammatory bowel disease in a Mediterranean area
    • Turri D, Rosselli M, Simioni P, Tormene D, Grimaudo S, Martorana G, et al: Factor V Leiden and prothrombin gene mutation in inflammatory bowel disease in a Mediterranean area. Dig Liv Dis 2001; 33:559-562.
    • (2001) Dig Liv Dis , vol.33 , pp. 559-562
    • Turri, D.1    Rosselli, M.2    Simioni, P.3    Tormene, D.4    Grimaudo, S.5    Martorana, G.6
  • 32
    • 0033869354 scopus 로고    scopus 로고
    • Inflammatory bowel diseases are not associated with major hereditary conditions predisposing to thrombosis
    • Vecchi M, Sacchi E, Saibeni S, Meucci G, Tagliabue L, Duca F, et al: Inflammatory bowel diseases are not associated with major hereditary conditions predisposing to thrombosis. Dig Dis Sci 2000; 45:1465-1469.
    • (2000) Dig Dis Sci , vol.45 , pp. 1465-1469
    • Vecchi, M.1    Sacchi, E.2    Saibeni, S.3    Meucci, G.4    Tagliabue, L.5    Duca, F.6
  • 33
    • 0033028676 scopus 로고    scopus 로고
    • Arg506Gln factor V mutation and Val34Leu factor XIII polymorphism in Finnish patients with inflammatory bowel disease
    • Helio T, Wartiovaara U, Halme L, Turunen UM, Mikkola H, Palotie A, et al: Arg506Gln factor V mutation and Val34Leu factor XIII polymorphism in Finnish patients with inflammatory bowel disease. Scand J Gastroenterol 1999; 34:170-174.
    • (1999) Scand J Gastroenterol , vol.34 , pp. 170-174
    • Helio, T.1    Wartiovaara, U.2    Halme, L.3    Turunen, U.M.4    Mikkola, H.5    Palotie, A.6
  • 34
    • 0343807499 scopus 로고    scopus 로고
    • Prothrombotic inherited abnormalities other than factor V Leiden mutation do not play a role in venous thrombosis in inflammatory bowel disease
    • Guedon C, Le Cam-Duchez V, Lalaude O, Menard JF, Levebours E, Borg JY: Prothrombotic inherited abnormalities other than factor V Leiden mutation do not play a role in venous thrombosis in inflammatory bowel disease. Am J Gastroenterol 2001; 96:1448-1454.
    • (2001) Am J Gastroenterol , vol.96 , pp. 1448-1454
    • Guedon, C.1    Le Cam-Duchez, V.2    Lalaude, O.3    Menard, J.F.4    Levebours, E.5    Borg, J.Y.6
  • 35
    • 0033793437 scopus 로고    scopus 로고
    • The high prevalence of the factor V Leiden mutation in central European inflammatory bowel disease patients
    • Nagy Z, Nagy A, Karadi O, Par A, Mozsik G: The high prevalence of the factor V Leiden mutation in central European inflammatory bowel disease patients. Am J Gastroenterol 2000; 95:3013-3014.
    • (2000) Am J Gastroenterol , vol.95 , pp. 3013-3014
    • Nagy, Z.1    Nagy, A.2    Karadi, O.3    Par, A.4    Mozsik, G.5
  • 36
    • 0032732001 scopus 로고    scopus 로고
    • An investigation of the association of the factor V Leiden mutation and inflammatory bowel disease
    • Haslam N, Standen GR, Probert CS: An investigation of the association of the factor V Leiden mutation and inflammatory bowel disease. Eur J Gastroenterol Hepatol 1999; 11:1289-1291.
    • (1999) Eur J Gastroenterol Hepatol , vol.11 , pp. 1289-1291
    • Haslam, N.1    Standen, G.R.2    Probert, C.S.3
  • 37
    • 0030845360 scopus 로고    scopus 로고
    • The 20210A allele the prothrombin gene is a common risk factor among Swedish outpatients with verified deep venous thrombosis
    • Hillarp A, Zoller B, Svensson P, Dahlback B: The 20210A allele the prothrombin gene is a common risk factor among Swedish outpatients with verified deep venous thrombosis. Thromb Haemost 1997; 78:990-992.
    • (1997) Thromb Haemost , vol.78 , pp. 990-992
    • Hillarp, A.1    Zoller, B.2    Svensson, P.3    Dahlback, B.4
  • 38
  • 39
    • 0034519760 scopus 로고    scopus 로고
    • C677T Mutation in the Methylene Tetrahydrofolate Reductase Gene as a Risk Factor for Venous Thrombotic Disease in Austrian Patients
    • Seinost G, Renner W, Brodmann M, Winkler M, Koppel H, Pilger E: C677T Mutation in the Methylene Tetrahydrofolate Reductase Gene as a Risk Factor for Venous Thrombotic Disease in Austrian Patients. Thrombos Res 2000; 100:405-407.
    • (2000) Thrombos Res , vol.100 , pp. 405-407
    • Seinost, G.1    Renner, W.2    Brodmann, M.3    Winkler, M.4    Koppel, H.5    Pilger, E.6
  • 40
    • 0034827834 scopus 로고    scopus 로고
    • Hyperhomocysteinemia and prevalence of polymorphisms of homocysteine metabolism-related enzymes in patients with inflammatory bowel disease
    • Papa A, De Stefano V, Danese S, Chiusolo P, Persichilli S, Casorelli I, et al: Hyperhomocysteinemia and prevalence of polymorphisms of homocysteine metabolism-related enzymes in patients with inflammatory bowel disease. Am J Gastroenterol 2001; 96:2677-2682.
    • (2001) Am J Gastroenterol , vol.96 , pp. 2677-2682
    • Papa, A.1    De Stefano, V.2    Danese, S.3    Chiusolo, P.4    Persichilli, S.5    Casorelli, I.6
  • 41
    • 0034190659 scopus 로고    scopus 로고
    • 5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalities: A HuGe review
    • Botto LD, Yang Q: 5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalities: A HuGe review. Am J Epidemiol 2000; 151:862-877.
    • (2000) Am J Epidemiol , vol.151 , pp. 862-877
    • Botto, L.D.1    Yang, Q.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.