메뉴 건너뛰기




Volumn 19, Issue 3, 2010, Pages 180-183

High prevalence of activated protein C resistance and factor v Leiden mutation in an Arab population and patients with venous thrombosis in Kuwait

Author keywords

activated protein C resistance; Arabs; factor V Leiden mutation; Kuwait; PCR; RFLP

Indexed keywords

BLOOD CLOTTING FACTOR 5 LEIDEN;

EID: 77951739149     PISSN: 10529551     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019606-201009000-00009     Document Type: Article
Times cited : (11)

References (40)
  • 1
    • 0029086642 scopus 로고
    • Biochemical and molecular aspects of the coagulation cascade
    • Davie EW. Biochemical and molecular aspects of the coagulation cascade. Thromb Haemost. 1995;74:1-6.
    • (1995) Thromb Haemost , vol.74 , pp. 1-6
    • Davie, E.W.1
  • 2
    • 0023918199 scopus 로고    scopus 로고
    • Blood coagulation factor v and VIII: Structural and functional similarities and their relationship to haemorrhegic and thrombotic disorders
    • Kane WH, Davie EW. Blood coagulation factor V and VIII: structural and functional similarities and their relationship to haemorrhegic and thrombotic disorders. Blood. 1998;71:539-555.
    • (1998) Blood , vol.71 , pp. 539-555
    • Kane, W.H.1    Davie, E.W.2
  • 3
    • 0028110027 scopus 로고
    • The mechanism of inactivation of human factor v and human factor Va by activated protein C
    • Kalafatis M, Rand MD, Mann KG. The mechanism of inactivation of human factor V and human factor Va by activated protein C. J Biol Chem. 1994;269:31869-31880.
    • (1994) J Biol Chem , vol.269 , pp. 31869-31880
    • Kalafatis, M.1    Rand, M.D.2    Mann, K.G.3
  • 4
    • 0028314865 scopus 로고
    • Mutation in blood coagulation factor v associated with resistance to activated protein C
    • Bertina RM, Koeleman BPC, Koster T, et al. Mutation in blood coagulation factor V associated with resistance to activated protein C. Nature. 1994;369:64-67.
    • (1994) Nature , vol.369 , pp. 64-67
    • Bertina, R.M.1    Bpc, K.2    Koster, T.3
  • 5
    • 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 USA. 1993;90: 1004-1008.
    • (1993) Proc Natl Acad Sci USA , vol.90 , pp. 1004-1008
    • Dahlback, B.1    Carlsson, M.2    Svensson, P.J.3
  • 6
    • 0029061441 scopus 로고
    • Resistance to activated protein C, the Arg506 to Gln mutation in the factor v gene, and venous thrombosis. Functional tests and DNA-based assays
    • Dahlback B. Resistance to activated protein C, the Arg506 to Gln mutation in the factor V gene, and venous thrombosis. Functional tests and DNA-based assays. Pros and Cons. Thromb Haemost. 1995;73:739-742.
    • (1995) Pros and Cons. Thromb Haemost , vol.73 , pp. 739-742
    • Dahlback, B.1
  • 7
    • 0030955080 scopus 로고    scopus 로고
    • Ethnic distribution of Factor v Leiden in 4047 men and women. Implications for venous thrmoboembolism screening
    • Ridker PM, Miletich JP, Hennekens CH, et al. Ethnic distribution of Factor V Leiden in 4047 men and women. Implications for venous thrmoboembolism screening. JAMA. 1997;277:1305-1307.
    • (1997) JAMA , vol.277 , pp. 1305-1307
    • Ridker, P.M.1    Miletich, J.P.2    Hennekens, C.H.3
  • 8
    • 1842290346 scopus 로고    scopus 로고
    • Resistance to activated protein C caused by the factor v R506Q mutation is a common risk factor for venous thrombosis
    • Dahlback B. Resistance to activated protein C caused by the factor V R506Q mutation is a common risk factor for venous thrombosis. Thromb Haemost. 1997;78:483-488.
    • (1997) Thromb Haemost , vol.78 , pp. 483-488
    • Dahlback, B.1
  • 9
    • 0030746710 scopus 로고    scopus 로고
    • Resistance to activated protein C in unselected patients with arterial and venous thrombo sis
    • Faioni EM, Razzari C, Martinelli I, et al. Resistance to activated protein C in unselected patients with arterial and venous thrombo sis. Am J Hematol. 1997;55:59-64.
    • (1997) Am J Hematol , vol.55 , pp. 59-64
    • Faioni, E.M.1    Razzari, C.2    Martinelli, I.3
  • 10
    • 0028810738 scopus 로고
    • World distribution of factor v Leiden
    • Rees DC, Cox M, Clegg JB. World distribution of factor V Leiden. Lancet. 1995;346:1133-1134.
    • (1995) Lancet , vol.346 , pp. 1133-1134
    • Rees, D.C.1    Cox, M.2    Clegg, J.B.3
  • 11
    • 0031023757 scopus 로고    scopus 로고
    • A single genetic origin for a common Caucasian risk factor for venous thrombosis
    • Zivelin A, Griffin JH, Xu X, et al. A single genetic origin for a common Caucasian risk factor for venous thrombosis. Blood. 1997; 89:397-402.
    • (1997) Blood , vol.89 , pp. 397-402
    • Zivelin, A.1    Griffin, J.H.2    Xu, X.3
  • 12
    • 0030249040 scopus 로고    scopus 로고
    • APC-resistnace as measured by a Textarin time assay: Comparison to the APTT-based method
    • Hoagland LE, Triplett DA, Peng F, et al. APC-resistnace as measured by a Textarin time assay: comparison to the APTT-based method. Thromb Res. 1996;83:363-373.
    • (1996) Thromb Res , vol.83 , pp. 363-373
    • Hoagland, L.E.1    Triplett, D.A.2    Peng, F.3
  • 13
    • 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, et al. 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
  • 14
    • 0030907104 scopus 로고    scopus 로고
    • Venous thrombosis: Factor v G1691A genotyping related to APC resistance measured by 2 methods
    • Alderborn A, Siegbahn A, Wadelius C. Venous thrombosis: factor V G1691A genotyping related to APC resistance measured by 2 methods. Eur J Haematol. 1997;58:229-232.
    • (1997) Eur J Haematol , vol.58 , pp. 229-232
    • Alderborn, A.1    Siegbahn, A.2    Wadelius, C.3
  • 15
    • 0031041270 scopus 로고    scopus 로고
    • The factor v Leiden mutation: Spectrum of thrombotic events and laboratory evaluation
    • Bontempo FA, Hassett AC, Faruki H, et al. The factor V Leiden mutation: spectrum of thrombotic events and laboratory evaluation. J Vasc Surg. 1997;25:271-275.
    • (1997) J Vasc Surg , vol.25 , pp. 271-275
    • Bontempo, F.A.1    Hassett, A.C.2    Faruki, H.3
  • 16
    • 0031012256 scopus 로고    scopus 로고
    • Inherited thrombotic disorders: An update
    • Florell SR, Rodgers GM. Inherited thrombotic disorders: an update. Am J Hematol. 1997;54:53-60.
    • (1997) Am J Hematol , vol.54 , pp. 53-60
    • Florell, S.R.1    Rodgers, G.M.2
  • 17
    • 0029908647 scopus 로고    scopus 로고
    • Diagnosis and clinical characteristics of inherited activated protein C resistance
    • Samama MM, Simon D, Horellou MH, et al. Diagnosis and clinical characteristics of inherited activated protein C resistance. Haemo-stasis. 1996;26:315-330.
    • (1996) Haemo-stasis , vol.26 , pp. 315-330
    • Samama, M.M.1    Simon, D.2    Horellou, M.H.3
  • 18
    • 0029864822 scopus 로고    scopus 로고
    • Resistance to activated protein C, the FV: Q506 allele, and the venous thrombosis
    • Dahlback B, Hillarp A, Rosen S, et al. Resistance to activated protein C, the FV: Q506 allele, and the venous thrombosis. Ann Hematol. 1996;72:166-176.
    • (1996) Ann Hematol , vol.72 , pp. 166-176
    • Dahlback, B.1    Hillarp, A.2    Rosen, S.3
  • 19
    • 0030793389 scopus 로고    scopus 로고
    • Familial thrombophilia: A complex genetic disorder
    • Koeleman BPC, Reitsma PH, Bertina RM. Familial thrombophilia: a complex genetic disorder. Semin Hematol. 1997;34:256-264.
    • (1997) Semin Hematol , vol.34 , pp. 256-264
    • Bpc, K.1    Reitsma, P.H.2    Bertina, R.M.3
  • 20
    • 0029940597 scopus 로고    scopus 로고
    • Evidence of a single origin of factor v Leiden
    • Cox MJ, Rees DC, Martinson JJ, et al. Evidence of a single origin of factor V Leiden. Br J Haematol. 1996;92:1022-1025.
    • (1996) Br J Haematol , vol.92 , pp. 1022-1025
    • Cox, M.J.1    Rees, D.C.2    Martinson, J.J.3
  • 21
    • 0031056991 scopus 로고    scopus 로고
    • The risk of recurrent venous thromboembolism in patients with an Arg506-G mutation in the gene for factor v (factor v Leiden)
    • Simioni P, Prandoni P, Lensing AW, et al. The risk of recurrent venous thromboembolism in patients with an Arg506-G mutation in the gene for factor V (factor V Leiden). N Engl J Med. 1997; 336:399-403.
    • (1997) N Engl J Med , vol.336 , pp. 399-403
    • Simioni, P.1    Prandoni, P.2    Lensing, A.W.3
  • 22
    • 0030954466 scopus 로고    scopus 로고
    • Factor v Leiden prevalence in venous thromboembolism patients
    • Leroyer C, Mercier B, Escoffre M, et al. Factor V Leiden prevalence in venous thromboembolism patients. Chest. 1997;111:1603-1606.
    • (1997) Chest , vol.111 , pp. 1603-1606
    • Leroyer, C.1    Mercier, B.2    Escoffre, M.3
  • 23
    • 0035654205 scopus 로고    scopus 로고
    • Prevalence of factor v Leiden and prothrombin 20210A mutations in indigenous Australians
    • Bennett JA, Palmer LJ, Musk AW, et al. Prevalence of factor V Leiden and prothrombin 20210A mutations in indigenous Australians. Thromb Haemost. 2001;86:1592-1593.
    • (2001) Thromb Haemost , vol.86 , pp. 1592-1593
    • Bennett, J.A.1    Palmer, L.J.2    Musk, A.W.3
  • 24
    • 0029039978 scopus 로고
    • Factor v Leiden (FVQ 506) is common in a Brazilian population
    • Arruda VR, Annichino-Bizzacchi JM, Costa FF, et al. Factor V Leiden (FVQ 506) is common in a Brazilian population. Am J Hematol. 1995;49:242-243.
    • (1995) Am J Hematol , vol.49 , pp. 242-243
    • Arruda, V.R.1    Annichino-Bizzacchi, J.M.2    Costa, F.F.3
  • 25
    • 0030560928 scopus 로고    scopus 로고
    • Low prevalence of activated protein C resistance and coagulation factor v Arg506 to Gln mutation among Japanese patients with various forms of thrombosis, and normal individuals
    • Zama T, Murata M, Ono F, et al. Low prevalence of activated protein C resistance and coagulation factor V Arg506 to Gln mutation among Japanese patients with various forms of thrombosis, and normal individuals. Int J Hematol. 1996;65:71-78.
    • (1996) Int J Hematol , vol.65 , pp. 71-78
    • Zama, T.1    Murata, M.2    Ono, F.3
  • 26
    • 0031059758 scopus 로고    scopus 로고
    • Prevalence of factor v Leiden mutation in non-European populations
    • Pepe G, Rickards O, Vanegas OC, et al. Prevalence of factor V Leiden mutation in non-European populations. Thromb Haemost. 1997;77:329-331.
    • (1997) Thromb Haemost , vol.77 , pp. 329-331
    • Pepe, G.1    Rickards, O.2    Vanegas, O.C.3
  • 27
    • 0033391093 scopus 로고    scopus 로고
    • Prevalence of factor v Leiden in the Chinese population
    • Ho CH, Chau WK, Hsu HC, et al. Prevalence of factor V Leiden in the Chinese population. Zhonghua Yi Xue Za Zhi. 62:875-878.
    • Zhonghua Yi Xue Za Zhi. , vol.62 , pp. 875-878
    • Ho, C.H.1    Chau, W.K.2    Hsu, H.C.3
  • 28
    • 0030031847 scopus 로고    scopus 로고
    • World distribution of factor v Leiden mutation
    • De Maat MPM, Kluft C, Jespersen J, et al. World distribution of factor V Leiden mutation. Lancet. 1996;347:58.
    • (1996) Lancet , vol.347 , pp. 58
    • De Maat Mpm1    Kluft, C.2    Jespersen, J.3
  • 29
    • 0032723944 scopus 로고    scopus 로고
    • High frequency of factor v Leiden in a population of Israeli Arabs
    • Rosen E, Renbaum P, Heyd J, et al. High frequency of factor V Leiden in a population of Israeli Arabs. Thromb Haemost. 1999; 82:1768.
    • (1999) Thromb Haemost , vol.82 , pp. 1768
    • Rosen, E.1    Renbaum, P.2    Heyd, J.3
  • 30
    • 23844551772 scopus 로고    scopus 로고
    • A case control study on the contribution of factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations to the genetic susceptibility of deep venous thrombosis
    • Almawi WY, Tamim H, Kreidy R, et al. A case control study on the contribution of factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations to the genetic susceptibility of deep venous thrombosis. J Thromb Thrombolysis. 2005;19:189-196.
    • (2005) J Thromb Thrombolysis , vol.19 , pp. 189-196
    • Almawi, W.Y.1    Tamim, H.2    Kreidy, R.3
  • 31
    • 0030059030 scopus 로고    scopus 로고
    • World distribution of factor v Leiden
    • Dzimiri N, Meyer B. World distribution of factor V Leiden. Lancet. 1996;347:481-482.
    • (1996) Lancet , vol.347 , pp. 481-482
    • Dzimiri, N.1    Meyer, B.2
  • 32
    • 0033976404 scopus 로고    scopus 로고
    • High prevalence of factor v mutation (Leiden) in the Eastern Mediterranean
    • Irani-Hakime N, Tamim H, Elias G, et al. High prevalence of factor V mutation (Leiden) in the Eastern Mediterranean. Clin Chem. 2000;46:134-136.
    • (2000) Clin Chem , vol.46 , pp. 134-136
    • Irani-Hakime, N.1    Tamim, H.2    Elias, G.3
  • 33
    • 0034898551 scopus 로고    scopus 로고
    • High prevalence of Factor v Leiden mutation among healthy individuals and patients with deep venous thrombosis in Lebanon: Is the eastern Mediterranean region the area of origin of this mutation?
    • Taher A, Khalil I, Shamseddine A, et al. High prevalence of Factor V Leiden mutation among healthy individuals and patients with deep venous thrombosis in Lebanon: is the eastern Mediterranean region the area of origin of this mutation? Thromb Haemost. 2001;86:723-724.
    • (2001) Thromb Haemost , vol.86 , pp. 723-724
    • Taher, A.1    Khalil, I.2    Shamseddine, A.3
  • 34
    • 24044478750 scopus 로고    scopus 로고
    • Prevalence of Factor v Leiden, prothrombin G20210A, and MTHFR G677A among 594 thrombotic Jordanian patients
    • Eid SS, Shubeilat T. Prevalence of Factor V Leiden, prothrombin G20210A, and MTHFR G677A among 594 thrombotic Jordanian patients. Blood Coagul Fibrinolysis. 2005;16:417-421.
    • (2005) Blood Coagul Fibrinolysis , vol.16 , pp. 417-421
    • Eid, S.S.1    Shubeilat, T.2
  • 35
    • 7444249002 scopus 로고    scopus 로고
    • Prevalence of factor v Leiden mutation and other hereditary thrombophilic factors in Egyptian children with portal vein thrombosis: Results of a single-center case-control study
    • El-Karaksy H, El-Koofy N, El-Hawary M, et al. Prevalence of factor V Leiden mutation and other hereditary thrombophilic factors in Egyptian children with portal vein thrombosis: results of a single-center case-control study. Ann Hematol. 2004;83:712-715.
    • (2004) Ann Hematol , vol.83 , pp. 712-715
    • El-Karaksy, H.1    El-Koofy, N.2    El-Hawary, M.3
  • 36
    • 32144432660 scopus 로고    scopus 로고
    • Hereditary thrombophilia in ethnic Omani patients
    • Pathare A, Al Kindi S, Al Haddabi H, et al. Hereditary thrombophilia in ethnic Omani patients. Am J Hematol. 2006;81:101-106.
    • (2006) Am J Hematol , vol.81 , pp. 101-106
    • Pathare, A.1    Al Kindi, S.2    Al Haddabi, H.3
  • 37
    • 55849112244 scopus 로고    scopus 로고
    • Frequency of factor v Leiden mutation in Egyptian cases with myocardial infarction
    • Settin A, Dowaidar M, El-Baz R, et al. Frequency of factor V Leiden mutation in Egyptian cases with myocardial infarction. Hematology. 2008;13:170-174.
    • (2008) Hematology , vol.13 , pp. 170-174
    • Settin, A.1    Dowaidar, M.2    El-Baz, R.3
  • 38
    • 0035654949 scopus 로고    scopus 로고
    • How old is Factor v Leiden mutation?
    • Pawar AR, Shetty S, Ghosh K, et al. How old is Factor V Leiden mutation? Thromb Haemost. 2001;86:1591-1592.
    • (2001) Thromb Haemost , vol.86 , pp. 1591-1592
    • Pawar, A.R.1    Shetty, S.2    Ghosh, K.3
  • 40
    • 70350341972 scopus 로고    scopus 로고
    • The prevalence of factor v Leiden, prothrombin G20210A and methylenetetrahydro-folate reductase polymorphism C677T among G6PD deficient individuals from Western Iran
    • Mozafari H, Rahimi Z, Heidarpour A, et al. The prevalence of factor V Leiden, prothrombin G20210A and methylenetetrahydro-folate reductase polymorphism C677T among G6PD deficient individuals from Western Iran. Mol Biol Rep. 2009;36:2361-2364.
    • (2009) Mol Biol Rep , vol.36 , pp. 2361-2364
    • Mozafari, H.1    Rahimi, Z.2    Heidarpour, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.