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Volumn 18, Issue 3, 2012, Pages 320-323

Prevalence of factor v Leiden G1691A, MTHFR C677T, and prothrombin G20210A among Asian Indian sickle cell patients

Author keywords

factor V Leiden; MTHFR; polymorphism; prothrombin; SCD

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); BLOOD CLOTTING FACTOR 5 LEIDEN; BLOOD CLOTTING FACTOR V LEIDEIN G1691A; PROTHROMBIN; PROTHROMBIN G20210A; UNCLASSIFIED DRUG;

EID: 84860714984     PISSN: 10760296     EISSN: 19382723     Source Type: Journal    
DOI: 10.1177/1076029611425830     Document Type: Article
Times cited : (11)

References (39)
  • 1
    • 33846610962 scopus 로고    scopus 로고
    • The case for dedicated sickle cell centres
    • Serjeant GR.. The case for dedicated sickle cell centres. Indian J Hum Genet. 2006 ; 12 (3). 148-151 (Pubitemid 46183414)
    • (2006) Indian Journal of Human Genetics , vol.12 , Issue.3 , pp. 148-151
    • Serjeant, G.R.1
  • 3
    • 0025756644 scopus 로고
    • ßs Gene cluster haplotypes in sickle cell anemia. Clinical and hematologic features
    • ßs Gene cluster haplotypes in sickle cell anemia. Clinical and hematologic features. Hematol Oncol Clin North Am. 1991 ; 5 (3). 475-493
    • (1991) Hematol Oncol Clin North Am , vol.5 , Issue.3 , pp. 475-493
  • 4
    • 0025963843 scopus 로고
    • Effect of beta-globin gene cluster haplotype on the hematological and clinical features of sickle cell anemia
    • Rieder RF, Safaya S, Gillette P, et al. Effect of beta-globin gene cluster haplotype on the hematological and clinical features of sickle cell anemia. Am J Hematol. 1991 ; 36 (3). 184-189
    • (1991) Am J Hematol , vol.36 , Issue.3 , pp. 184-189
    • Rieder, R.F.1    Safaya, S.2    Gillette, P.3
  • 6
    • 0024837758 scopus 로고
    • Estimation of plasma kallikrein in sickle-cell anemia, and its relation to the coagulation and fibrinolytic systems
    • Lourenço D, Sampaio MU, Kerbauy J, Sampaio CA.. Estimation of plasma kallikrein in sickle-cell anemia, and its relation to the coagulation and fibrinolytic systems. Adv Exp Med Biol. 1989 ; 247B: 553-557
    • (1989) Adv Exp Med Biol , vol.247 , pp. 553-557
    • Lourenço, D.1    Sampaio, M.U.2    Kerbauy, J.3    Sampaio, C.A.4
  • 9
    • 0035170948 scopus 로고    scopus 로고
    • Natural coagulation inhibitors (protein C, protein S, antithrombin) in patients with sickle cell anemia in a steady state
    • DOI 10.1046/j.1442-200X.2001.01476.x
    • Bayazit AK, Kilinc Y.. Natural coagulation inhibitors (protein C, protein S, antithrombin) in patients with sickle cell anemia in a steady state. Pediatr Int. 2001 ; 43 (6). 592-596 (Pubitemid 33071122)
    • (2001) Pediatrics International , vol.43 , Issue.6 , pp. 592-596
    • Bayazit, A.K.1    Kilinc, Y.2
  • 10
    • 0035761409 scopus 로고    scopus 로고
    • Thrombophilia in sickle cell disease: The red cell connection
    • Setty BN, Rao AK, Stuart MJ.. Thrombophilia in sickle cell disease: the red cell connection. Blood. 2001 ; 98 (12). 3228-3233
    • (2001) Blood , vol.98 , Issue.12 , pp. 3228-3233
    • Setty, B.N.1    Rao, A.K.2    Stuart, M.J.3
  • 11
    • 0035370375 scopus 로고    scopus 로고
    • Thrombogenesis or thrombogenic risk?
    • DOI 10.1067/mlc.2001.115453
    • Hebbel RP.. Thrombogenesis or thrombogenic risk?. J Lab Clin Med. 2001 ; 137 (6). 381-382 (Pubitemid 32473617)
    • (2001) Journal of Laboratory and Clinical Medicine , vol.137 , Issue.6 , pp. 381-382
    • Hebbel, R.P.1
  • 13
    • 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 30-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood. 1996 ; 88 (10). 3698-3703 (Pubitemid 26383091)
    • (1996) Blood , vol.88 , Issue.10 , pp. 3698-3703
    • Poort, S.R.1    Rosendaal, F.R.2    Reitsma, P.H.3    Bertina, R.M.4
  • 14
    • 0035057410 scopus 로고    scopus 로고
    • C677T and A1298C polymorphisms of the methylenetetrahydrofolate reductase gene: Incidence and effect of combined genotypes on plasma fasting and post-methionine load homocysteine in vascular disease
    • Hanson NQ, Aras O, Yang F, Tsai MY.. C677T and A1298C polymorphisms of the methylenetetrahydrofolate reductase gene: incidence and effect of combined genotypes on plasma fasting and post-methionine load homocysteine in vascular disease. Clin Chem. 2001 ; 47 (4). 661-666 (Pubitemid 32275808)
    • (2001) Clinical Chemistry , vol.47 , Issue.4 , pp. 661-666
    • Hanson, N.Q.1    Aras, O.2    Yang, F.3    Tsai, M.Y.4
  • 15
    • 0031724415 scopus 로고    scopus 로고
    • Inherited DNA mutations contributing to thrombotic complications in patients with sickle cell disease
    • DOI 10.1002/(SICI)1096-8652(199812)59:4<267::AID-AJH1>3.0.CO;2-W
    • Zimmerman SA, Ware RE.. Inherited DNA mutations contributing to thrombotic complications in patients with sickle cell disease. Am J Hematol. 1998 ; 59 (4). 267-272 (Pubitemid 28543614)
    • (1998) American Journal of Hematology , vol.59 , Issue.4 , pp. 267-272
    • Zimmerman, S.A.1    Ware, R.E.2
  • 16
    • 0031825212 scopus 로고    scopus 로고
    • Prothrombin mutant, factor V leiden, and thermolabile variant of methylenetetrahidrofolate reductase among patients with sickle cell disease in Brazil
    • DOI 10.1002/(SICI)1096-8652(199809)59:1<46::AID-AJH9>3.0.CO;2-#
    • Andrade FL, Annichino-Bizzacchi JM, Saad ST, Costa FF, Arruda VR.. Prothrombin mutant, factor V Leiden, and thermolabile variant of methylenetetrahydrofolate reductase among patients with sickle cell disease in Brazil. Am J Hematol. 1998 ; 59 (1). 46-50 (Pubitemid 28395006)
    • (1998) American Journal of Hematology , vol.59 , Issue.1 , pp. 46-50
    • Andrade, F.L.1    Annichino-Bizzacchi, J.M.2    Saad, S.T.O.3    Costa, F.F.4    Arruda, V.R.5
  • 18
    • 0025756673 scopus 로고
    • Hyperhomocysteinemia: An independent risk factor for vascular disease
    • Clarke R, Daly L, Robinson K, et al. Hyperhomocysteinemia: an independent risk factor for vascular disease. N Engl J Med. 1991 ; 324 (17). 1149-1155
    • (1991) N Engl J Med , vol.324 , Issue.17 , pp. 1149-1155
    • Clarke, R.1    Daly, L.2    Robinson, K.3
  • 19
    • 0029049553 scopus 로고
    • A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
    • Frosst P, Blom HJ, Milos R, et al. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nature Genet. 1995 ; 10 (1). 111-113
    • (1995) Nature Genet , vol.10 , Issue.1 , pp. 111-113
    • Frosst, P.1    Blom, H.J.2    Milos, R.3
  • 21
    • 4243621156 scopus 로고    scopus 로고
    • Frequency of a common thermolabile MTHFR (5,10-methylenetetrahydrofolate reductase) mutant among patients with sickle cell disease
    • Kutlar F, Holley L, McKie BC, McKie KM, Woods KF, Kutlar A.. Frequency of a common thermolabile MTHFR (5,10-methylenetetrahydrofolate reductase) mutant among patients with sickle cell disease. Blood. 1997 ; 90 (10 suppl 1). 28b
    • (1997) Blood , vol.90 , Issue.10 SUPPL. 1
    • Kutlar, F.1    Holley, L.2    McKie, B.C.3    McKie, K.M.4    Woods, K.F.5    Kutlar, A.6
  • 22
    • 0006866822 scopus 로고    scopus 로고
    • MTHFR (5,10-methylenetetrahydrofolare reductase) 677 C-T mutation as a candidate risk factor for avascular necrosis (AVN) in patients with sickle cell disease
    • Kutlar F, Tural C, Park D, Markkowitz RB, Woods KF, Kutlar A.. MTHFR (5,10-methylenetetrahydrofolare reductase) 677 C-T mutation as a candidate risk factor for avascular necrosis (AVN) in patients with sickle cell disease. Blood. 1998 ; 82 (10 suppl 1). 695a
    • (1998) Blood , vol.82 , Issue.10 SUPPL. 1
    • Kutlar, F.1    Tural, C.2    Park, D.3    Markkowitz, R.B.4    Woods, K.F.5    Kutlar, A.6
  • 23
    • 3042646355 scopus 로고    scopus 로고
    • Factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations among patients with sickle cell disease in Eastern Saudi Arabia
    • DOI 10.1002/ajh.20087
    • Fawaz NA, Bashawery L, Al-Sheikh I, Qatari A, Al-Othman SS, Almawi WY.. Factor V-Leiden, Prothrombin G20210A, and MTHFR C677T mutations among patients with sickle cell disease in Eastern Saudi Arabia. Am J Hematol. 2004 ; 76 (3). 307-309 (Pubitemid 38828860)
    • (2004) American Journal of Hematology , vol.76 , Issue.3 , pp. 307-309
    • Fawaz, N.A.1    Bashawery, L.2    Al-Sheikh, I.3    Qatari, A.4    Al-Othman, S.S.5    Almawi, W.Y.6
  • 24
    • 0038304845 scopus 로고    scopus 로고
    • Primary thrombophilia in Saudi Arabia
    • Al-Jaouni SK.. Primary thrombophilia in Saudi Arabia. Saudi Med J. 2003 ; 24 (6). 614-616 (Pubitemid 36833552)
    • (2003) Saudi Medical Journal , vol.24 , Issue.6 , pp. 614-616
    • Al-Jaouni, S.K.1
  • 25
    • 0035869387 scopus 로고    scopus 로고
    • Endothelial dysfunction in patients with sickle cell disease is related to selective impairment of shear stress-mediated vasodilation
    • DOI 10.1182/blood.V97.6.1584
    • Belhassen L, Pelle G, Sediame S, et al. Endothelial dysfunction in patients with sickle cell disease is related to selective impairment of shear stress-mediated vasodilation. Blood. 2001 ; 97 (6). 1584-1589 (Pubitemid 32217221)
    • (2001) Blood , vol.97 , Issue.6 , pp. 1584-1589
    • Belhassen, L.1    Pelle, G.2    Sediame, S.3    Bachir, D.4    Carville, C.5    Bucherer, C.6    Lacombe, C.7    Galacteros, F.8    Adnot, S.9
  • 26
    • 0032752359 scopus 로고    scopus 로고
    • The methylenetetrahydrofolate reductase gene C677T polymorphism in patients with homozygous sickle cell disease and stroke
    • Cumming AM, Olujohungbe A, Keeney S, Singh H, Hay CR, Serjeant GR.. The methylenetetrahydrofolate reductase gene C677T polymorphism in patients with homozygous sickle cell disease and stroke. Br J Haematol. 1999 ; 107 (3). 569-571
    • (1999) Br J Haematol , vol.107 , Issue.3 , pp. 569-571
    • Cumming, A.M.1    Olujohungbe, A.2    Keeney, S.3    Singh, H.4    Hay, C.R.5    Serjeant, G.R.6
  • 27
    • 0036062012 scopus 로고    scopus 로고
    • Hyperhomocysteinemia is associated with low plasma pyridoxine levels in children with sickle cell disease
    • DOI 10.1097/00043426-200206000-00010
    • Balasa VV, Kalinyak KA, Bean JA, Stroop D, Gruppo RA.. Hyperhomocysteinemia is associated with low plasma pyridoxine levels in children with sickle cell disease. J Pediatr Hematol Oncol. 2002 ; 24 (5). 374-379 (Pubitemid 34774008)
    • (2002) Journal of Pediatric Hematology/Oncology , vol.24 , Issue.5 , pp. 374-379
    • Balasa, V.V.1    Kalinyak, K.A.2    Bean, J.A.3    Stroop, D.4    Gruppo, R.A.5
  • 28
    • 0036172543 scopus 로고    scopus 로고
    • Thrombosis-associated gene variants in sickle cell anemia
    • Romana M, Muralitharan S, Ramasawmy R, Nagel RL, Krishnamoorthy R.. Thrombosis-associated gene variants in sickle cell anemia. Thromb Haemost. 2002 ; 87 (2). 356-358 (Pubitemid 34139887)
    • (2002) Thrombosis and Haemostasis , vol.87 , Issue.2 , pp. 356-358
    • Romana, M.1
  • 29
    • 0033398399 scopus 로고    scopus 로고
    • The 677T genotype of the common MTHFR thermolabile variant and fasting homocysteine in childhood venous thrombosis
    • Koch HG, Nabel P, Junker R, et al. The 677T genotype of the common MTHFR thermolabile variant and fasting homocysteine in childhood venous thrombosis. Eur J Pediatr. 1999 ; 158 (suppl 3). S113 - S116
    • (1999) Eur J Pediatr , vol.158 , Issue.SUPPL. 3
    • Koch, H.G.1    Nabel, P.2    Junker, R.3
  • 30
    • 0031713550 scopus 로고    scopus 로고
    • Effect of the MTHFRC677T variant on risk of venous thromboembolism: Interaction with factor V leiden and prothrombin (F2G20210A) mutations
    • DOI 10.1046/j.1365-2141.1998.00935.x
    • Brown K, Luddington R, Baglin T.. Effect of the MTHFRC677T variant on risk of venous thromboembolism: interaction with factor VLeiden and prothrombin (F2G20210A) mutations. Br J Haematol. 1998 ; 103 (1). 42-44 (Pubitemid 28470797)
    • (1998) British Journal of Haematology , vol.103 , Issue.1 , pp. 42-44
    • Brown, K.1    Luddington, R.2    Baglin, T.3
  • 35
    • 0036526239 scopus 로고    scopus 로고
    • Hyperhomocysteinemia increases the risk of venous thrombosis independent of the C677T mutation of the methylenetetrahydrofolate reductase gene in selected Brazilian patients
    • DOI 10.1097/00001721-200204000-00014
    • Morelli VM, Lourenço DM, D'Almeida V, et al. Hyperhomocysteinemia increases the risk of venous thrombosis independent of the C677T mutation of the methylenetetrahydrofolate reductase gene in selected Brazilian patients. Blood Coagul Fibrinolysis. 2002 ; 13: 271-275 (Pubitemid 35001894)
    • (2002) Blood Coagulation and Fibrinolysis , vol.13 , Issue.3 , pp. 271-275
    • Morelli, V.M.1    Lourenco, D.M.2    D'Almeida, V.3    Franco, R.F.4    Miranda, F.5    Zago, M.A.6    Noguti, M.A.E.7    Cruz, E.8    Kerbauy, J.9
  • 38
    • 4544305476 scopus 로고    scopus 로고
    • A C677T methylenetetrahydrofolate reductase (MTHFR) polymorphism and G20210A mutation in the prothrombin gene of sickle cell anemia patients from Northeast Brazil
    • DOI 10.1081/HEM-120040308
    • Couto FD, Vilas Boas W, Lyra I, et al. AC677T methylenetetrahydrofolate reductase (MTHFR)polymorphisms and G20210A mutation in the prothrombin gene of sickle cell anemia patients from Northeast Brazil. Hemoglobin. 2004 ; 28 (3). 237-241 (Pubitemid 39238146)
    • (2004) Hemoglobin , vol.28 , Issue.3 , pp. 237-241
    • Couto, F.D.1    Vilas Boas, W.2    Lyra, I.3    Zanette, A.4    Dupuit, M.F.5    Tavares Almeida, M.N.6    Galvao Reis, M.7    Souza Goncalves, M.8
  • 39
    • 2642701740 scopus 로고    scopus 로고
    • Analysis of the 677 C→T mutation of the methylenetetrahydrofolate reductase gene in different ethnic groups
    • Franco RF, Araujo AG, Guerreiro JF, Elion J, Zago MA.. Analysis of the 677 C→T mutation of the methylenetetrahydrofolate reductase gene in different ethnic groups. Thromb Haemostasis. 1998 ; 79 (1). 119-121 (Pubitemid 28037069)
    • (1998) Thrombosis and Haemostasis , vol.79 , Issue.1 , pp. 119-121
    • Franco, R.F.1    Araujo, A.G.2    Guerreiro, J.F.3    Elion, J.4    Zago, M.A.5


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