메뉴 건너뛰기




Volumn 45, Issue 4, 2010, Pages 289-292

Strong association between a new marker of hemolysis and glomerulopathy in sickle cell anemia

Author keywords

Glomerulopathy; Hemolysis; Red blood cells; Sickle cell anemia

Indexed keywords

ALPHA GLOBIN; BILIRUBIN; BIOCHEMICAL MARKER; HEMOGLOBIN; LACTATE DEHYDROGENASE;

EID: 78649444537     PISSN: 10799796     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bcmd.2010.08.001     Document Type: Article
Times cited : (37)

References (31)
  • 1
    • 27944496081 scopus 로고    scopus 로고
    • Outcome of sickle cell anemia: a 4-decade observational study of 1056 patients
    • Powars D.R., Chan L.S., Hiti A., Ramicone E., Johnson C. Outcome of sickle cell anemia: a 4-decade observational study of 1056 patients. Medicine 2005, 84:363-376.
    • (2005) Medicine , vol.84 , pp. 363-376
    • Powars, D.R.1    Chan, L.S.2    Hiti, A.3    Ramicone, E.4    Johnson, C.5
  • 2
    • 0025355908 scopus 로고
    • Renal abnormalities in sickle cell disease
    • Allon M. Renal abnormalities in sickle cell disease. Arch Intern Med 1990, 150:501-504.
    • (1990) Arch Intern Med , vol.150 , pp. 501-504
    • Allon, M.1
  • 3
    • 33846881560 scopus 로고    scopus 로고
    • Elderly survivors with homozygous sickle cell disease
    • Serjeant G.R., Higgs D.R., Hambleton I.R. Elderly survivors with homozygous sickle cell disease. N Engl J Med 2007, 356:642-643.
    • (2007) N Engl J Med , vol.356 , pp. 642-643
    • Serjeant, G.R.1    Higgs, D.R.2    Hambleton, I.R.3
  • 4
    • 33846279380 scopus 로고    scopus 로고
    • Deconstructing sickle cell disease: reappraisal of the role of hemolysis in the development of clinical subphenotypes
    • Kato G.J., Gladwin M.T., Steinberg M.H. Deconstructing sickle cell disease: reappraisal of the role of hemolysis in the development of clinical subphenotypes. Blood Reviews 2007, 21:37-47.
    • (2007) Blood Reviews , vol.21 , pp. 37-47
    • Kato, G.J.1    Gladwin, M.T.2    Steinberg, M.H.3
  • 5
    • 65349087881 scopus 로고    scopus 로고
    • Endogenous nitric oxide synthase inhibitors in sickle cell disease: abnormal levels and correlations with pulmonary hypertension, desaturation, haemolysis, organ dysfunction and death
    • Kato G.J., Wang Z., Machado R.F., Blackwelder W.C., Taylor J.G., Hazen S.L. Endogenous nitric oxide synthase inhibitors in sickle cell disease: abnormal levels and correlations with pulmonary hypertension, desaturation, haemolysis, organ dysfunction and death. Br J Haematol 2009, 145:506-513.
    • (2009) Br J Haematol , vol.145 , pp. 506-513
    • Kato, G.J.1    Wang, Z.2    Machado, R.F.3    Blackwelder, W.C.4    Taylor, J.G.5    Hazen, S.L.6
  • 6
    • 33644775612 scopus 로고    scopus 로고
    • Lactate dehydrogenase as a biomarker of hemolysis-associated nitric oxide resistance, priapism, leg ulceration, pulmonary hypertension, and death in patients with sickle cell disease
    • Kato G.J., McGowan V., Machado R.F., Little J.A., Taylor J., Morris C.R., Nichols J.S., Wang X., Poljakovic M., Morris S.M., Gladwin M.T. Lactate dehydrogenase as a biomarker of hemolysis-associated nitric oxide resistance, priapism, leg ulceration, pulmonary hypertension, and death in patients with sickle cell disease. Blood 2006, 107:2279-2285.
    • (2006) Blood , vol.107 , pp. 2279-2285
    • Kato, G.J.1    McGowan, V.2    Machado, R.F.3    Little, J.A.4    Taylor, J.5    Morris, C.R.6    Nichols, J.S.7    Wang, X.8    Poljakovic, M.9    Morris, S.M.10    Gladwin, M.T.11
  • 7
    • 27644535417 scopus 로고    scopus 로고
    • Hemolysis-associated priapism in sickle cell disease
    • Nolan V.G., Wyszynski D.F., Farrer L.A., Steinberg M.H. Hemolysis-associated priapism in sickle cell disease. Blood 2005, 106:3264-3267.
    • (2005) Blood , vol.106 , pp. 3264-3267
    • Nolan, V.G.1    Wyszynski, D.F.2    Farrer, L.A.3    Steinberg, M.H.4
  • 9
    • 65949124657 scopus 로고    scopus 로고
    • Mechanisms of vasculopathy in sickle cell disease and thalassemia
    • Morris C.R. Mechanisms of vasculopathy in sickle cell disease and thalassemia. Hematology Am Soc Hematol Educ Program 2008, 177-185.
    • (2008) Hematology Am Soc Hematol Educ Program , pp. 177-185
    • Morris, C.R.1
  • 12
    • 77956229673 scopus 로고    scopus 로고
    • Lactate dehydrogenase as a predictor of kidney involvement in patients with sickle cell anemia
    • [Epub ahead of print], Jun
    • Gurkan S., Scarponi K.J., Hotchkiss H., Savage B., Drachtman R. Lactate dehydrogenase as a predictor of kidney involvement in patients with sickle cell anemia. Pediatr Nephrol Jun 2 2010, [Epub ahead of print].
    • (2010) Pediatr Nephrol
    • Gurkan, S.1    Scarponi, K.J.2    Hotchkiss, H.3    Savage, B.4    Drachtman, R.5
  • 13
    • 33746530641 scopus 로고    scopus 로고
    • Glomerular involvement in adults with sickle cell hemoglobinopathies: prevalence and clinical correlates of progressive renal failure
    • Guasch A., Navarrete J., Nass K., Zayas C.F. Glomerular involvement in adults with sickle cell hemoglobinopathies: prevalence and clinical correlates of progressive renal failure. J Am Soc Nephrol 2006, 17:2228-2235.
    • (2006) J Am Soc Nephrol , vol.17 , pp. 2228-2235
    • Guasch, A.1    Navarrete, J.2    Nass, K.3    Zayas, C.F.4
  • 16
    • 78649446982 scopus 로고    scopus 로고
    • Performing a blood count
    • Blackwell Publishing Asia Pty Ltd, Australia, B. Bain (Ed.)
    • Bain B. Performing a blood count. Blood Cells: A Practical Guide 2006, 20-60. Blackwell Publishing Asia Pty Ltd, Australia. B. Bain (Ed.).
    • (2006) Blood Cells: A Practical Guide , pp. 20-60
    • Bain, B.1
  • 18
    • 47749090563 scopus 로고    scopus 로고
    • Chronic hyper-hemolysis in sickle cell anemia: association of vascular complications and mortality with less frequent vasoocclusive pain
    • Taylor J.G., Nolan V.G., Mendelsohn L., Kato G.J., Gladwin M.T., Steinberg M.H. Chronic hyper-hemolysis in sickle cell anemia: association of vascular complications and mortality with less frequent vasoocclusive pain. PLoS ONE 2008, 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
  • 20
    • 0042241869 scopus 로고    scopus 로고
    • General pathophysiology of sickle cell anemia
    • Cambridge University Press, M.H. Steinberg, B.G. Forget, D.R. Higgs, R.L. Nagel (Eds.)
    • Nagel R.L., Platt O.S. General pathophysiology of sickle cell anemia. Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management 2001, 494-526. Cambridge University Press. M.H. Steinberg, B.G. Forget, D.R. Higgs, R.L. Nagel (Eds.).
    • (2001) Disorders of Hemoglobin: Genetics, Pathophysiology, and Clinical Management , pp. 494-526
    • Nagel, R.L.1    Platt, O.S.2
  • 21
    • 0030853520 scopus 로고    scopus 로고
    • Reticulocyte hemoglobin, an integrated parameter for evaluation of erythropoietic activity
    • Brugnara C., Zelmanovic D., Sorette M., Ballas S.K., Platt O. Reticulocyte hemoglobin, an integrated parameter for evaluation of erythropoietic activity. Am J Clin Pathol 1997, 108:133-142.
    • (1997) Am J Clin Pathol , vol.108 , pp. 133-142
    • Brugnara, C.1    Zelmanovic, D.2    Sorette, M.3    Ballas, S.K.4    Platt, O.5
  • 22
    • 0001362338 scopus 로고
    • Rapid analysis of α3.7 triplication by enzymatic amplification analysis
    • Dode C., Krishnamoorthy R., Lamb J., Rochette J. Rapid analysis of α3.7 triplication by enzymatic amplification analysis. Br J Haematol 1992, 82:105-111.
    • (1992) Br J Haematol , vol.82 , pp. 105-111
    • Dode, C.1    Krishnamoorthy, R.2    Lamb, J.3    Rochette, J.4
  • 23
    • 1642299543 scopus 로고    scopus 로고
    • The new reticulocyte parameter (RET-Y) of the Sysmex XE 2100. Its use in the diagnosis and monitoring of posttreatment sideropenic anemia
    • Buttarello M., Temporin V., Ceravolo R., Farina G., Bulian P. The new reticulocyte parameter (RET-Y) of the Sysmex XE 2100. Its use in the diagnosis and monitoring of posttreatment sideropenic anemia. Am J Clin Pathol 2004, 121:489-495.
    • (2004) Am J Clin Pathol , vol.121 , pp. 489-495
    • Buttarello, M.1    Temporin, V.2    Ceravolo, R.3    Farina, G.4    Bulian, P.5
  • 24
    • 48249141136 scopus 로고    scopus 로고
    • Automated blood cell counts, state of the art
    • Buttarello M., Plebani M. Automated blood cell counts, state of the art. Am J Clin Pathol 2008, 130:104-116.
    • (2008) Am J Clin Pathol , vol.130 , pp. 104-116
    • Buttarello, M.1    Plebani, M.2
  • 25
    • 3042514131 scopus 로고    scopus 로고
    • Potential utility of Ret-Y in the diagnosis of iron-restricted erythropoiesis
    • Franck S., Linssen J., Messinger M., Thomas L. Potential utility of Ret-Y in the diagnosis of iron-restricted erythropoiesis. Clin Chem 2004, 50:1240-1242.
    • (2004) Clin Chem , vol.50 , pp. 1240-1242
    • Franck, S.1    Linssen, J.2    Messinger, M.3    Thomas, L.4
  • 26
    • 33748997056 scopus 로고    scopus 로고
    • Reticulocyte hemoglobin equivalent (Ret He) and assessment of iron-deficient states
    • Brugnara C., Schiller B., Moran J. Reticulocyte hemoglobin equivalent (Ret He) and assessment of iron-deficient states. Clin Lab Haem 2006, 28:303-308.
    • (2006) Clin Lab Haem , vol.28 , pp. 303-308
    • Brugnara, C.1    Schiller, B.2    Moran, J.3
  • 28
  • 29
    • 44649092159 scopus 로고    scopus 로고
    • Venous incompetence, poverty and lactate dehydrogenase in Jamaica are important predictors of leg ulceration in sickle cell anaemia
    • Cumming V., King L., Fraser R., Serjeant G., Reid M. Venous incompetence, poverty and lactate dehydrogenase in Jamaica are important predictors of leg ulceration in sickle cell anaemia. Br J Haematol 2008, 142:119-125.
    • (2008) Br J Haematol , vol.142 , pp. 119-125
    • Cumming, V.1    King, L.2    Fraser, R.3    Serjeant, G.4    Reid, M.5
  • 30
    • 0032913410 scopus 로고    scopus 로고
    • Evidence that microdeletions in the α globin gene protect against the development of sickle cell glomerulopathy in humans
    • Guasch A., Zayas C.F., Eckman J.R., Muralidharan K., Zhang W., Elsas L.J. Evidence that microdeletions in the α globin gene protect against the development of sickle cell glomerulopathy in humans. J Am Soc Nephrol 1999, 10:1014-1019.
    • (1999) J Am Soc Nephrol , vol.10 , pp. 1014-1019
    • Guasch, A.1    Zayas, C.F.2    Eckman, J.R.3    Muralidharan, K.4    Zhang, W.5    Elsas, L.J.6
  • 31
    • 77955282543 scopus 로고    scopus 로고
    • Alpha-thalassemia is associated with a decreased occurrence and a delayed age-at-onset of albuminuria in sickle cell anemia patients
    • [Epub ahead of print], Jul
    • Nebor D., Broquere C., Brudey K., Mougenel D., Tarer V., Connes P., Elion J., Romana M. Alpha-thalassemia is associated with a decreased occurrence and a delayed age-at-onset of albuminuria in sickle cell anemia patients. Blood Cells Mol Dis Jul 1 2010, [Epub ahead of print].
    • (2010) Blood Cells Mol Dis
    • Nebor, D.1    Broquere, C.2    Brudey, K.3    Mougenel, D.4    Tarer, V.5    Connes, P.6    Elion, J.7    Romana, M.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.