메뉴 건너뛰기




Volumn 93, Issue 7, 2014, Pages 1123-1129

Influence of the βs haplotype and α-thalassemia on stroke development in a Brazilian population with sickle cell anaemia

Author keywords

Genetic polymorphisms; Sickle cell anaemia; Stroke; Thalassemia

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); BILIRUBIN; BLOOD CLOTTING FACTOR 5 LEIDEN; ENDOTHELIAL NITRIC OXIDE SYNTHASE; GLUCOSE 6 PHOSPHATE DEHYDROGENASE; HEMOGLOBIN; HEMOGLOBIN F; LACTATE DEHYDROGENASE; PROTHROMBIN; TUMOR NECROSIS FACTOR ALPHA;

EID: 84902663035     PISSN: 09395555     EISSN: 14320584     Source Type: Journal    
DOI: 10.1007/s00277-014-2016-1     Document Type: Article
Times cited : (27)

References (55)
  • 1
    • 80053329221 scopus 로고    scopus 로고
    • TNF-alpha and IL-8: Serum levels and gene polymorphisms (-308G>A and -251A>T) are associated with classical biomarkers and medical history in children with sickle cell anemia
    • Cajado C, Cerqueira BA, Couto FD, Moura-Neto JP, Vilas-Boas W, Dorea MJ et al (2011) TNF-alpha and IL-8: serum levels and gene polymorphisms (-308G>A and -251A>T) are associated with classical biomarkers and medical history in children with sickle cell anemia. Cytokine 56:312-317
    • (2011) Cytokine , vol.56 , pp. 312-317
    • Cajado, C.1    Cerqueira, B.A.2    Couto, F.D.3    Moura-Neto, J.P.4    Vilas-Boas, W.5    Dorea, M.J.6
  • 2
    • 65549111723 scopus 로고    scopus 로고
    • Genetic etiologies for phenotypic diversity in sickle cell anemia
    • Steinberg MH (2009) Genetic etiologies for phenotypic diversity in sickle cell anemia. Sci World J 9:46-67
    • (2009) Sci World J , vol.9 , pp. 46-67
    • Steinberg, M.H.1
  • 3
    • 5044239523 scopus 로고    scopus 로고
    • Sickle-cell disease
    • DOI 10.1016/S0140-6736(04)17192-4, PII S0140673604171924
    • Stuart MJ, Nagel RL (2004) Sickle-cell disease. Lancet 364:1343-1360 (Pubitemid 39335827)
    • (2004) Lancet , vol.364 , Issue.9442 , pp. 1343-1360
    • Stuart, M.J.1    Nagel, R.L.2
  • 6
    • 47749090563 scopus 로고    scopus 로고
    • Chronic hyper-hemolysis in sickle cell anemia: Association of vascular complications andmortalitywith less frequent vasoocclusive pain
    • Taylor JG, Nolan VG, Mendelsohn L, Kato GJ, Gladwin MT, SteinbergMH (2008) Chronic hyper-hemolysis in sickle cell anemia: association of vascular complications andmortalitywith less frequent vasoocclusive pain. PLoS One 3:e2095
    • (2008) PLoS One , vol.3
    • Taylor, J.G.1    Nolan, V.G.2    Mendelsohn, L.3    Kato, G.J.4    Gladwin, M.T.5    Steinberg, M.H.6
  • 9
    • 60749094795 scopus 로고    scopus 로고
    • Newer aspects of the pathophysiology of sickle cell disease vaso-occlusion
    • Conran N, Franco-Penteado CF, Costa FF (2009) Newer aspects of the pathophysiology of sickle cell disease vaso-occlusion. Hemoglobin 33:1-16
    • (2009) Hemoglobin , vol.33 , pp. 1-16
    • Conran, N.1    Franco-Penteado, C.F.2    Costa, F.F.3
  • 12
    • 0024446352 scopus 로고
    • Mortality in children and adolescents with sickle cell disease
    • Leikin SL, Gallagher D, Kinney TR, Sloane D, Klug P, Rida W (1989) Mortality in children and adolescents with sickle cell disease. Cooperative study of sickle cell disease. Pediatrics 84:500-508 (Pubitemid 19216350)
    • (1989) Pediatrics , vol.84 , Issue.3 , pp. 500-508
    • Leikin, S.L.1    Gallagher, D.2    Kinney, T.R.3    Sloane, D.4    Klug, P.5    Rida, W.6
  • 14
    • 34548269532 scopus 로고    scopus 로고
    • Confirmation of an association between the TNF(-308) promoter polymorphism and stroke risk in children with sickle cell anemia
    • DOI 10.1161/STROKEAHA.107.483115, PII 0000767020070800000020
    • Hoppe C, KlitzW, D'Harlingue K, Cheng S, Grow M, Steiner L et al (2007) Confirmation of an association between the TNF(-308) promoter polymorphism and stroke risk in children with sickle cell anemia. Stroke 38:2241-2246 (Pubitemid 47457562)
    • (2007) Stroke , vol.38 , Issue.8 , pp. 2241-2246
    • Hoppe, C.1    Klitz, W.2    D'Harlingue, K.3    Cheng, S.4    Grow, M.5    Steiner, L.6    Noble, J.7    Adams, R.8    Styles, L.9
  • 15
    • 15844431322 scopus 로고    scopus 로고
    • TCD in sickle cell disease: An important and useful test
    • Adams RJ (2005) TCD in sickle cell disease: an important and useful test. Pediatr Radiol 35:229-234
    • (2005) Pediatr Radiol , vol.35 , pp. 229-234
    • Adams, R.J.1
  • 17
    • 16844366938 scopus 로고    scopus 로고
    • Genetic dissection and prognostic modeling of overt stroke in sickle cell anemia
    • Sebastiani P, Ramoni MF, Nolan V, Baldwin CT, Steinberg MH (2005) Genetic dissection and prognostic modeling of overt stroke in sickle cell anemia. Nat Genet 37:435-440
    • (2005) Nat Genet , vol.37 , pp. 435-440
    • Sebastiani, P.1    Ramoni, M.F.2    Nolan, V.3    Baldwin, C.T.4    Steinberg, M.H.5
  • 22
    • 0025165882 scopus 로고
    • Identification of a single base change in a new human mutant glucose-6-phosphate dehydrogenase gene by polymerase-chain-reaction amplification of the entire coding region from genomic DNA
    • Poggi V, Town M, Foulkes NS, Luzzatto L (1990) Identification of a single base change in a new human mutant glucose-6-phosphate dehydrogenase gene by polymerase-chain-reaction amplification of the entire coding region from genomic DNA. Biochem J 271:157-160 (Pubitemid 20331211)
    • (1990) Biochemical Journal , vol.271 , Issue.1 , pp. 157-160
    • Poggi, V.1    Town, M.2    Foulkes, N.S.3    Luzzatto, L.4
  • 23
    • 0025756644 scopus 로고
    • Beta s-gene-cluster haplotypes in sickle cell anemia. Clinical and hematologic features
    • Powars DR (1991) Beta s-gene-cluster haplotypes in sickle cell anemia. Clinical and hematologic features. Hematol Oncol Clin North Am 5:475-493
    • (1991) Hematol Oncol Clin North Am , vol.5 , pp. 475-493
    • Powars, D.R.1
  • 27
    • 0029049553 scopus 로고
    • A candidate genetic risk factor for vascular disease: A commonmutation in methylenetetrahydrofolate reductase
    • Frosst P, Blom HJ, Milos R, Goyette P, Sheppard CA, Matthews RG et al (1995) A candidate genetic risk factor for vascular disease: a commonmutation in methylenetetrahydrofolate reductase. Nat Genet 10:111-113
    • (1995) Nat Genet , vol.10 , pp. 111-113
    • Frosst, P.1    Blom, H.J.2    Milos, R.3    Goyette, P.4    Sheppard, C.A.5    Matthews, R.G.6
  • 28
    • 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 (1996) 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 88:3698-3703 (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
  • 29
    • 42449097982 scopus 로고    scopus 로고
    • Family screening for HBB*S gene and detection of new cases of sickle cell trait in Northeastern Brazil
    • Bandeira FM, Santos MN, Bezerra MA, Gomes YM, Araujo AS, Braga MC et al (2008) Family screening for HBB*S gene and detection of new cases of sickle cell trait in Northeastern Brazil. Rev Saude Publica 42:234-241
    • (2008) Rev Saude Publica , vol.42 , pp. 234-241
    • Bandeira, F.M.1    Santos, M.N.2    Bezerra, M.A.3    Gomes, Y.M.4    Araujo, A.S.5    Braga, M.C.6
  • 30
    • 33847015229 scopus 로고    scopus 로고
    • Molecular variations linked to the grouping of beta- and alpha-globin genes in neonatal patients with sickle cell disease in the state of Pernambuco, Brazil
    • Bezerra MA, Santos MN, Araujo AS, Gomes YM, Abath FG, Bandeira FM (2007) Molecular variations linked to the grouping of beta- and alpha-globin genes in neonatal patients with sickle cell disease in the state of Pernambuco, Brazil. Hemoglobin 31:83-88
    • (2007) Hemoglobin , vol.31 , pp. 83-88
    • Bezerra, M.A.1    Santos, M.N.2    Araujo, A.S.3    Gomes, Y.M.4    Abath, F.G.5    Bandeira, F.M.6
  • 31
    • 33644828167 scopus 로고    scopus 로고
    • Clinical, hematological, and molecular characterization of sickle cell anemia pediatric patients fromtwo different cities in Brazil
    • Lyra IM, GoncalvesMS, Braga JA,GesteiraMF, CarvalhoMH, Saad ST et al (2005) Clinical, hematological, and molecular characterization of sickle cell anemia pediatric patients fromtwo different cities in Brazil. Cad Saude Publica 21:1287-1290
    • (2005) Cad Saude Publica , vol.21 , pp. 1287-1290
    • Lyra, I.M.1    Goncalves, M.S.2    Braga, J.A.3    Gesteira, M.F.4    Carvalho, M.H.5    Saad, S.T.6
  • 32
    • 0034969365 scopus 로고    scopus 로고
    • Molecular characteristics of pediatric patients with sickle cell anemia and stroke
    • DOI 10.1002/ajh.1103
    • Sarnaik SA, Ballas SK (2001) Molecular characteristics of pediatric patients with sickle cell anemia and stroke. Am J Hematol 67:179-182 (Pubitemid 32538616)
    • (2001) American Journal of Hematology , vol.67 , Issue.3 , pp. 179-182
    • Sarnaik, S.A.1    Ballas, S.K.2
  • 33
    • 74049109698 scopus 로고    scopus 로고
    • Geneticmodifiers of the severity of sickle cell anemia identified through a genome-wide association study
    • Sebastiani P, Solovieff N, Hartley SW, Milton JN, Riva A, Dworkis DA et al (2010) Geneticmodifiers of the severity of sickle cell anemia identified through a genome-wide association study. Am J Hematol 85:29-35
    • (2010) Am J Hematol , vol.85 , pp. 29-35
    • Sebastiani, P.1    Solovieff, N.2    Hartley, S.W.3    Milton, J.N.4    Riva, A.5    Dworkis, D.A.6
  • 35
    • 79952158856 scopus 로고    scopus 로고
    • Coinheritance of alpha-thalassemia decreases the risk of cerebrovascular disease in a cohort of children with sickle cell anemia
    • Belisario AR, Rodrigues CV, Martins ML, Silva CM, Viana MB (2010) Coinheritance of alpha-thalassemia decreases the risk of cerebrovascular disease in a cohort of children with sickle cell anemia. Hemoglobin 34:516-529
    • (2010) Hemoglobin , vol.34 , pp. 516-529
    • Belisario, A.R.1    Rodrigues, C.V.2    Martins, M.L.3    Silva, C.M.4    Viana, M.B.5
  • 42
    • 20044367676 scopus 로고    scopus 로고
    • Predicting clinical severity in sickle cell anaemia
    • Steinberg MH (2005) Predicting clinical severity in sickle cell anaemia. Br J Haematol 129:465-481
    • (2005) Br J Haematol , vol.129 , pp. 465-481
    • Steinberg, M.H.1
  • 43
    • 33745141905 scopus 로고    scopus 로고
    • Regular transfusion lowers plasma free hemoglobin in children with sickle-cell disease at risk for stroke
    • DOI 10.1161/01.STR.0000221173.97108.01, PII 0000767020060600000026
    • Lezcano NE, Odo N, Kutlar A, Brambilla D, Adams RJ (2006) Regular transfusion lowers plasma free hemoglobin in children with sickle-cell disease at risk for stroke. Stroke 37:1424-1426 (Pubitemid 44305720)
    • (2006) Stroke , vol.37 , Issue.6 , pp. 1424-1426
    • Lezcano, N.E.1    Odo, N.2    Kutlar, A.3    Brambilla, D.4    Adams, R.J.5
  • 44
    • 77953057530 scopus 로고    scopus 로고
    • The risks and benefits of long-term use of hydroxyurea in sickle cell anemia: A 17.5-year follow-up
    • Steinberg MH, McCarthy WF, Castro O, Ballas SK, Armstrong FD, Smith W et al (2010) The risks and benefits of long-term use of hydroxyurea in sickle cell anemia: a 17.5-year follow-up. Am J Hematol 85:403-408
    • (2010) Am J Hematol , vol.85 , pp. 403-408
    • Steinberg, M.H.1    McCarthy, W.F.2    Castro, O.3    Ballas, S.K.4    Armstrong, F.D.5    Smith, W.6
  • 45
    • 34247480919 scopus 로고    scopus 로고
    • Genetics of ischaemic stroke among persons of non-European descent: A meta-analysis of eight genes involving approximately 32,500 individuals
    • Ariyaratnam R, Casas JP, Whittaker J, Smeeth L, Hingorani AD, Sharma P (2007) Genetics of ischaemic stroke among persons of non-European descent: a meta-analysis of eight genes involving approximately 32,500 individuals. PLoS Med 4:e131
    • (2007) PLoS Med , vol.4
    • Ariyaratnam, R.1    Casas, J.P.2    Whittaker, J.3    Smeeth, L.4    Hingorani, A.D.5    Sharma, P.6
  • 46
    • 33847335941 scopus 로고    scopus 로고
    • Association of gene polymorphism with genetic susceptibility to stroke in Asian populations: A meta-analysis
    • Banerjee I, Gupta V, Ganesh S (2007) Association of gene polymorphism with genetic susceptibility to stroke in Asian populations: a meta-analysis. J Hum Genet 52:205-219
    • (2007) J Hum Genet , vol.52 , pp. 205-219
    • Banerjee, I.1    Gupta, V.2    Ganesh, S.3
  • 47
    • 7744222619 scopus 로고    scopus 로고
    • Meta-analysis of genetic studies in ischemic stroke: Thirty-two genes involving approximately 18 000 cases and 58 000 controls
    • DOI 10.1001/archneur.61.11.1652
    • Casas JP, Hingorani AD, Bautista LE, Sharma P (2004) Meta-analysis of genetic studies in ischemic stroke: thirty-two genes involving approximately 18,000 cases and 58,000 controls. Arch Neurol 61:1652-1661 (Pubitemid 39463422)
    • (2004) Archives of Neurology , vol.61 , Issue.11 , pp. 1652-1661
    • Casas, J.P.1    Hingorani, A.D.2    Bautista, L.E.3    Sharma, P.4
  • 48
    • 58149143300 scopus 로고    scopus 로고
    • G6PD deficiency, absence of alpha-thalassemia, and hemolytic rate at baseline are significant independent risk factors for abnormally high cerebral velocities in patients with sickle cell anemia
    • Bernaudin F, Verlhac S, Chevret S, TorresM, Coic L, Arnaud C et al (2008) G6PD deficiency, absence of alpha-thalassemia, and hemolytic rate at baseline are significant independent risk factors for abnormally high cerebral velocities in patients with sickle cell anemia. Blood 112:4314-4317
    • (2008) Blood , vol.112 , pp. 4314-4317
    • Bernaudin, F.1    Verlhac, S.2    Chevret, S.3    Torres, M.4    Coic, L.5    Arnaud, C.6
  • 49
    • 34247130850 scopus 로고    scopus 로고
    • Effect of the G-308A polymorphism of the tumor necrosis factor alpha gene on the risk of ischemic heart disease and ischemic stroke: A meta-analysis
    • DOI 10.1016/j.ahj.2007.02.031, PII S0002870307001664
    • Pereira TV, Rudnicki M, Franco RF, Pereira AC, Krieger JE (2007) Effect of the G-308A polymorphism of the tumor necrosis factor alpha gene on the risk of ischemic heart disease and ischemic stroke: a meta-analysis. Am Heart J 153:821-830 (Pubitemid 46602156)
    • (2007) American Heart Journal , vol.153 , Issue.5 , pp. 821-830
    • Pereira, T.V.1    Rudnicki, M.2    Franco, R.F.3    Pereira, A.C.4    Krieger, J.E.5
  • 51
    • 84881664862 scopus 로고    scopus 로고
    • Relationship between endothelial nitric oxide synthase gene polymorphisms and ischemic stroke: A meta-analysis
    • Niu PP,YangG, Zheng BK,Guo ZN, Jin H,YangY(2013) Relationship between endothelial nitric oxide synthase gene polymorphisms and ischemic stroke: a meta-analysis. Acta Neurol Scand 128:202-212
    • (2013) Acta Neurol Scand , vol.128 , pp. 202-212
    • Niu, P.P.1    Yang, G.2    Zheng, B.K.3    Guo, Z.N.4    Jin, H.5    Yang, Y.6
  • 52
    • 84891049130 scopus 로고    scopus 로고
    • Methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms and susceptibility to ischemic stroke: A meta-analysis
    • Li P, Qin C (2013) Methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms and susceptibility to ischemic stroke: a meta-analysis. Gene 535:359-64
    • (2013) Gene , vol.535 , pp. 359-364
    • Li, P.1    Qin, C.2
  • 53
    • 84875447601 scopus 로고    scopus 로고
    • Endothelial NO synthase gene polymorphisms and risk of ischemic stroke in Asian population: A meta-analysis
    • Wang M, Jiang X,Wu W, Zhang D (2013) Endothelial NO synthase gene polymorphisms and risk of ischemic stroke in Asian population: a meta-analysis. PLoS One 8:e60472
    • (2013) PLoS One , vol.8
    • Wang, M.1    Jiang, X.2    Wu, W.3    Zhang, D.4
  • 54
    • 84898849858 scopus 로고    scopus 로고
    • Endothelial nitric oxide: Protector of a healthy mind
    • in press
    • Katusic ZS, Austin SA (2014) Endothelial nitric oxide: protector of a healthy mind. Eur Heart J (in press)
    • (2014) Eur Heart J
    • Katusic, Z.S.1    Austin, S.A.2
  • 55
    • 33846279380 scopus 로고    scopus 로고
    • Deconstructing sickle cell disease: Reappraisal of the role of hemolysis in the development of clinical subphenotypes
    • DOI 10.1016/j.blre.2006.07.001, PII S0268960X06000415
    • Kato GJ, Gladwin MT, Steinberg MH (2007) Deconstructing sickle cell disease: reappraisal of the role of hemolysis in the development of clinical subphenotypes. Blood Rev 21:37-47 (Pubitemid 46110926)
    • (2007) Blood Reviews , vol.21 , Issue.1 , pp. 37-47
    • Kato, G.J.1    Gladwin, M.T.2    Steinberg, M.H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.