Role of free radicals in the pathogenesis of acute chest syndrome in sickle cell disease
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Acute chest syndrome (ACS) of sickle cell disease (SCD) is characterized pathologically by vaso-occlusive processes that result from abnormal interactions between sickle red blood cells (RBCs), white blood cells (WBCs) and/or platelets, and the vascular endothelium. One potential mechanism of vascular damage in ACS is by generation of oxygen-related molecules, such as superoxide (O2-), hydrogen peroxide (H2O2), peroxynitrite (ONOO-), and the hydroxyl (*OH) radical. The present review summarizes the evidence for alterations in oxidant stress during ACS of SCD, and the potential contributions of RBCs, WBCs and the vascular endothelium to this process.
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Sickle cells produce greater amounts of O2•−, H2O2, and hydroxyl radical •OH compared with healthy RBCs.
“It has been reported that sickle cells produce greater amounts of O2•−, H2O2, and hydroxyl radical •OH compared with healthy RBCs (8, 80, 100).”
From Red Blood Cell Function and Dysfunction: Redox Regulation, Nitric Oxide Metabolism, Anemia (2017) · cites this paper as [100]
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Cites
Beckman, J. S., Beckman, T. W., Chen, J., Marshall, P. A., & Freeman, B. A. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.4.1620 · Cited by 7,029 · see citing works
Mortality in sickle cell disease. Life expectancy and risk factors for early death
Platt, O. S., Brambilla, D. J., Rosse, W. F., Milner, P. F., Castro, O., Steinberg, M. H., & Klug, P. P. (1994) · New England Journal of Medicine · doi:10.1056/nejm199406093302303 · Cited by 3,320 · see citing works
Biology of disease: free radicals and tissue injury.
Freeman, B. Α., & Jd, C. (1982) · PubMed · Cited by 3,059 · see citing works
Biochemistry of nitric oxide and its redox-activated forms
Stamler, J. S., Singel, D. J., & Loscalzo, J. (1992) · Science · doi:10.1126/science.1281928 · Cited by 2,744 · see citing works
The Pecking Order of Free Radicals and Antioxidants: Lipid Peroxidation, α-Tocopherol, and Ascorbate
Buettner, G. R. (1993) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1993.1074 · Cited by 2,417 · see citing works
Superoxide anion is involved in the breakdown of endothelium-derived vascular relaxing factor
Gryglewski, R. J., Palmer, R. M. J., & Moncada, S. (1986) · Nature · doi:10.1038/320454a0 · Cited by 2,407 · see citing works
Radí, R., Beckman, J. S., Bush, K. M., & Freeman, B. Α. (1991) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(91)90224-7 · Cited by 2,196 · see citing works
Fridovich, I. (1975) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.44.070175.001051 · Cited by 1,735 · see citing works
Causes and Outcomes of the Acute Chest Syndrome in Sickle Cell Disease
Vichinsky, E. P., Neumayr, L. D., Earles, A. N., Williams, R., Lennette, E. T., Dean, D., Nickerson, B., Orringer, E., McKie, V., Bellevue, R., et al. (2000) · New England Journal of Medicine · doi:10.1056/nejm200006223422502 · Cited by 1,234 · see citing works
Marui, N., Offermann, M. K., Swerlick, R., Kunsch, C., Rosen, C. A., Ahmad, M., Alexander, R. W., & Medford, R. M. (1993) · Journal of Clinical Investigation · doi:10.1172/jci116778 · Cited by 1,072 · see citing works
Nitric oxide synthases: which, where, how, and why?
Michel, T. M., & Féron, O. (1997) · Journal of Clinical Investigation · doi:10.1172/jci119750 · Cited by 1,018 · see citing works
Status of myocardial antioxidants in ischemia–reperfusion injury
Dhalla, N. S. (2000) · Cardiovascular Research · doi:10.1016/s0008-6363(00)00078-x · Cited by 803 · see citing works
Oxidative Stress as a Regulator of Gene Expression in the Vasculature
KUNSCH, C. A., & Medford, R. M. (1999) · Circulation Research · doi:10.1161/01.res.85.8.753 · Cited by 795 · see citing works
Endogenous nitric oxide: physiology, pathology and clinical relevance
Moncada, S., & Higgs, E. A. (1991) · European Journal of Clinical Investigation · doi:10.1111/j.1365-2362.1991.tb01383.x · Cited by 760 · see citing works
Cohen, G., & Hochstein, P. (1963) · Biochemistry · doi:10.1021/bi00906a038 · Cited by 666 · see citing works
Biosynthesis and action of nitric oxide in mammalian cells
Mayer, B., & Hemmens, B. (1997) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(97)01147-x · Cited by 600 · see citing works
Spontaneous oxygen radical generation by sickle erythrocytes.
Hebbel, R. P., Eaton, J. W., Balasingam, M., & Steinberg, M. H. (1982) · Journal of Clinical Investigation · doi:10.1172/jci110724 · Cited by 441 · see citing works
Hypoxia/reoxygenation causes inflammatory response in transgenic sickle mice but not in normal mice
Kaul, D. K., & Hebbel, R. P. (2000) · Journal of Clinical Investigation · doi:10.1172/jci9225 · Cited by 413 · see citing works
Carrell, R. W., Winterbourn, C. C., & Rachmilewitz, E. A. (1975) · British Journal of Haematology · doi:10.1111/j.1365-2141.1975.tb00540.x · Cited by 282 · see citing works
Nitric Oxide Regulation of Tissue Free Radical Injury
Rubbo, H., Darley-Usmar, V. M., & Freeman, B. Α. (1996) · Chemical Research in Toxicology · doi:10.1021/tx960037q · Cited by 274 · see citing works
Reperfusion injury pathophysiology in sickle transgenic mice
Osarogiagbon, U. R., Choong, S., Belcher, J. D., Vercellotti, G. M., Paller, M. S., & Hebbel, R. P. (2000) · Blood · doi:10.1182/blood.v96.1.314 · Cited by 234 · see citing works
Morris, C. R., Kuypers, F. A., Larkin, S. K., Vichinsky, E. P., & Styles, L. A. (2000) · The American journal of pediatric hematology/oncology · doi:10.1097/00043426-200011000-00009 · Cited by 213 · see citing works
Das, S. K., & Nair, R. C. (1980) · British Journal of Haematology · doi:10.1111/j.1365-2141.1980.tb01186.x · Cited by 198 · see citing works
Endothelial cell killing by neutrophils. Synergistic interaction of oxygen products and proteases.
Varani, J., Ginsburg, I., Schuger, L. A., Gibbs, D. F., Bromberg, J., Johnson, K. J., Ryan, U. S., & Ward, P. A. (1989) · Europe PMC (PubMed Central) · Cited by 195 · see citing works
Sickle reticulocytes adhere to VCAM-1
Gee, B., & Platt, O. (1995) · Blood · doi:10.1182/blood.v85.1.268.bloodjournal851268 · Cited by 194 · see citing works
Sickle Cell Acute Chest Syndrome: Pathogenesis and Rationale for Treatment
Stuart, M. J., & Setty, Y. B. N. (1999) · Blood · doi:10.1182/blood.v94.5.1555.417k36_1555_1560 · Cited by 186 · see citing works
Sickle cell membranes and oxidative damage
Rice-Evans, C. A., Omorphos, S. C., & BAYSAL, E. (1986) · Biochemical Journal · doi:10.1042/bj2370265 · Cited by 166 · see citing works
Fadlon, E., Vordermeier, S., Pearson, T. C., Mire‐Sluis, A. R., Dumonde, D. C., Phillips, J. K., Fishlock, K., & Brown, K. A. (1998) · Blood · doi:10.1182/blood.v91.1.266 · Cited by 163 · see citing works
Neutrophil activation in sickle cell disease
Lard, L. R., Mul, E. P. J., de Haas, M., Roos, D., & Duits, A. J. (1999) · Journal of Leukocyte Biology · doi:10.1002/jlb.66.3.411 · Cited by 162 · see citing works
Kinetic Analysis of the Fate of Nitric Oxide Synthesized by Macrophages in Vitro
Lewis, R. S., Tamir, S., Tannenbaum, S. R., & Deen, W. M. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.49.29350 · Cited by 161 · see citing works
Hofstra, T., Kalra, V., Meiselman, H. J., & Coates, T. D. (1996) · Blood · doi:10.1182/blood.v87.10.4440.bloodjournal87104440 · Cited by 147 · see citing works
Methotrexate-resistant Variants of Human Dihydrofolate Reductase with Substitutions of Leucine 22
Lewis, W. S., Cody, V., Galitsky, N., Luft, J. R., Pangborn, W. A., Chunduru, S. K., Spencer, H. T., Appleman, J. R., & Blakley, R. L. (1995) · Journal of Biological Chemistry · doi:10.1074/jbc.270.10.5057 · Cited by 144 · see citing works
Reactive Species in Sickle Cell Disease
ASLAN, M., THORNLEY‐BROWN, D., & FREEMAN, B. A. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06201.x · Cited by 136 · see citing works
Sultana, C., Shen, Y. M., Rattan, V., Johnson, C. S., & Kalra, V. K. (1998) · Blood · doi:10.1182/blood.v92.10.3924 · Cited by 130 · see citing works
Chiu, D., & Lubin, B. H. (1979) · PubMed · Cited by 114 · see citing works
Endothelin-1 Production during the Acute Chest Syndrome in Sickle Cell Disease
Hammerman, S., Kourembanas, S., Conca, T. J., Tucci, M., Brauer, M. J., & Farber, H. W. (1997) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/ajrccm.156.1.9611085 · Cited by 113 · see citing works
Self-citationJain, S. K., & Shohet, S. B. (1984) · Blood · doi:10.1182/blood.v63.2.362.362 · Cited by 112 · see citing works
Oxidative hemoglobin denaturation and RBC destruction: the effect of heme on red cell membranes.
Chiu, D., & Lubin, B. H. (1989) · PubMed · Cited by 110 · see citing works
Phelan, M. W., Perrine, S. P., Brauer, M. J., & Faller, D. V. (1995) · Journal of Clinical Investigation · doi:10.1172/jci118102 · Cited by 107 · see citing works
Homocysteine in Sickle Cell Disease
Houston, P. E., RANA, S. R., Sekhsaria, S., Perlin, E., Kim, K. S., & Castro, O. L. (1997) · The American Journal of Medicine · doi:10.1016/s0002-9343(97)00129-0 · Cited by 94 · see citing works
Adaptive Responses of the Endothelium to Stress
Pohlman, T. H., & Harlan, J. M. (2000) · Journal of Surgical Research · doi:10.1006/jsre.1999.5801 · Cited by 84 · see citing works
Elevated IL‐8 levels during sickle cell crisis
Duits, A. J., Schnog, J. B., Lard, L. R., Saleh, A. W., & Rojer, R. A. (1998) · European Journal Of Haematology · doi:10.1111/j.1600-0609.1998.tb01092.x · Cited by 78 · see citing works
Dias‐da‐Motta, P. M., Arruda, V. R., Muscará, M. N., Saad, S. T. O., Nucci, G. D., Costa, F. F., & Condino‐Neto, A. (1996) · British Journal of Haematology · doi:10.1046/j.1365-2141.1996.4951036.x · Cited by 70 · see citing works
The metabolites of nitric oxide in sickle‐cell disease
Rees, D. C., Cervi, P. L., Grimwade, D. J., O'Driscoll, A., Hamilton, M. S., Parker, N. E., & Porter, J. B. (1995) · British Journal of Haematology · doi:10.1111/j.1365-2141.1995.tb05397.x · Cited by 69 · see citing works
Altered amount and activity of superoxide dismutase in sickle cell anemia
Schacter, L., Warth, J. A., Gordon, E. M., Prasad, A. S., & Klein, B. L. (1988) · The FASEB Journal · doi:10.1096/fasebj.2.3.3350236 · Cited by 64 · see citing works
French, J. A., Kenny, D. J., Scott, J. P., Hoffmann, R. G., Wood, J. D., Hudetz, A. G., & Hillery, C. A. (1997) · Blood · doi:10.1182/blood.v89.12.4591 · Cited by 64 · see citing works
A decrease in irreversibly sickled erythrocytes in sickle cell anemia patients given vitamin E
Natta, C., Machlin, L. J., & Brin, M. (1980) · American Journal of Clinical Nutrition · doi:10.1093/ajcn/33.5.968 · Cited by 63 · see citing works
Peroxynitrite formation and apoptosis in transgenic sickle cell mouse kidneys
Bank, N., Kiroycheva, M. K., Ahmed, F., Anthony, G. M., Fabry, M. E., Nagel, R. L., & Singhal, P. C. (1998) · Kidney International · doi:10.1046/j.1523-1755.1998.00148.x · Cited by 61 · see citing works
Nitric Oxide Metabolite Levels in Acute Vaso‐occlusive Sickle‐cell Crisis
Lopez, B. L., Barnett, J., Ballas, S. K., Christopher, T. A., Davis‐Moon, L., & Ma, X. (1996) · Academic Emergency Medicine · doi:10.1111/j.1553-2712.1996.tb03367.x · Cited by 56 · see citing works
An Unusual Pattern of Neutrophil Kinetics in Sickle Cell Anemia
Boggs, D. R., Hyde, F. W., & Srodes, C. H. (1973) · Blood · doi:10.1182/blood.v41.1.59.59 · Cited by 55 · see citing works
Lopez, B. L., Davis‐Moon, L., Ballas, S. K., & Ma, X.-L. (2000) · American Journal of Hematology · doi:10.1002/(sici)1096-8652(200005)64:1 · Cited by 53 · see citing works
Inhibition of endothelium-dependent vasorelaxation by sickle erythrocytes
Mosseri, M., Bartlett-Pandite, A. N., Wenc, K., Isner, J. M., & Weinstein, R. S. (1993) · American Heart Journal · doi:10.1016/0002-8703(93)91049-k · Cited by 49 · see citing works
Endothelial cell nitric oxide production in acute chest syndrome
Hammerman, S., Klings, E. S., Hendra, K. P., Upchurch, G. R., Rishikof, D. C., Loscalzo, J., & Farber, H. W. (1999) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.1999.277.4.h1579 · Cited by 49 · see citing works
Self-citationAntioxidant Status and Susceptibility of Sickle Erythrocytes to Oxidative and Osmotic Stress
Tatum, V. L., & Chow, C. K. (1996) · Free Radical Research · doi:10.3109/10715769609149918 · Cited by 44 · see citing works
Reduced antioxidant capacity in paediatric patients with homozygous sickle cell disease.
Da, A., Thurnham, D. I., & Adekile, A. D. (1989) · PubMed · Cited by 37 · see citing works
Pulmonary Complications of Sickle Cell Disease
Johnson, C., & Verdegem, T. D. (1988) · Seminars in Respiratory and Critical Care Medicine · doi:10.1055/s-2007-1012716 · Cited by 30 · see citing works
Selected indices of micronutrient status in adult patients with sickle cell anemia (SCA)
Tangney, C., Phillips, G., Bell, R., Fernandes, P., Hopkins, R. G., & WU, S. M. (1989) · American Journal of Hematology · doi:10.1002/ajh.2830320302 · Cited by 25 · see citing works
Increased In Vivo Activation of Neutrophils and Complement in Sickle Cell Disease
Mohamed, A. O., Hashim, M. S.-K., Nilsson, U. R., & Venge, P. (1993) · American Journal of Tropical Medicine and Hygiene · doi:10.4269/ajtmh.1993.49.799 · Cited by 19 · see citing works
Phillips, G., & Tangney, C. (1992) · American Journal of Hematology · doi:10.1002/ajh.2830410402 · Cited by 18 · see citing works
Plasma levels of retinol, ascorbic acid and alpha-tocopherol in sickle cell anaemia.
Eu, E. (1995) · PubMed · Cited by 17 · see citing works
Transgenic HbS Mouse Neutrophils in Increased Susceptibility to Acute Lung Injury
Hsu, L. L.-Y., McDermott, T., Brown, L., & Aguayo, S. M. (1999) · CHEST Journal · doi:10.1378/chest.116.suppl_1.92s · Cited by 11 · see citing works
Low Plasma Prealbumln and Carotenoid Levels in Sickle Cell Disease Patients
Jain, S. K., Ross, J. D., Duett, J., & Herbst, J. J. (1990) · The American Journal of the Medical Sciences · doi:10.1097/00000441-199001000-00004 · Cited by 9 · see citing works
Serum vitamin E and the sickling status in children with sickle cell anaemia.
Ndombi, I. O., & Kinoti, S. N. (1990) · PubMed · Cited by 8 · see citing works
Ascorbic acid in sickle cell disease: results of a pilot therapeutic trial.
Akinkugbe, F. M., & Ette, S. I. (1983) · PubMed · Cited by 8 · see citing works
Flagged first, then by citations
Research works printed but not linked: 4
- Carrell WR Winterbourn CC Rachmilewitz EA Activated oxygen and haemolysis. Br J Haematol 1975 30 259 264 172110
- Cohen G Hochstein P Glutathione peroxidase: the primary agent for the elimination of H2O2 in erythrocytes. Biochemistry 1963 2 1420 1430 14093920
- Chui D Lubin B Abnormal vitamin E and glutathione peroxidase levels in sickle cell anemia. J Clin Med 1979 94 542 548 479666
- Lopez BL Barnett J Ballas SK Christopher TA Davis-Moon L Ma X Nitric oxide metabolites in acute vasoocclusive crisis patients in the emergency department. Acad Emerg Med 1996 3 1098 1103 8959162
Cited by
Sorted by citations
ACCF/AHA 2009 Expert Consensus Document on Pulmonary Hypertension
McLaughlin, V. V., Archer, S. L., Badesch, D. B., Barst, R. J., Farber, H. W., Lindner, J. R., Mathier, M. A., McGoon, M. D., Park, M., Rosenson, R. S., et al. (2009) · Journal of the American College of Cardiology · doi:10.1016/j.jacc.2009.01.004 · Cited by 2,354 · see citing works
Self-citationPulmonary Arterial Hypertension
Farber, H. W., & Loscalzo, J. (2004) · New England Journal of Medicine · doi:10.1056/nejmra035488 · Cited by 1,460 · see citing works
Self-citationACCF/AHA 2009 Expert Consensus Document on Pulmonary Hypertension
McLaughlin, V. V., Archer, S. L., Badesch, D. B., Barst, R. J., Farber, H. W., Lindner, J. R., Mathier, M. A., McGoon, M. D., Park, M., Rosenson, R. S., et al. (2009) · Circulation · doi:10.1161/circulationaha.109.192230 · Cited by 1,085 · see citing works
Self-citationPulmonary Arterial Hypertension
McLaughlin, V. V., & McGoon, M. D. (2006) · Circulation · doi:10.1161/circulationaha.104.503540 · Cited by 662 · see citing works
Red Blood Cell Function and Dysfunction: Redox Regulation, Nitric Oxide Metabolism, Anemia
Kuhn, V., Diederich, L., Keller, T. C. S., Kramer, C. M., Lückstädt, W., Panknin, C., Suvorava, T., Isakson, B. E., Kelm, M., & Cortese-Krott, M. M. (2017) · Antioxidants & Redox Signaling · doi:10.1089/ars.2016.6954 · Cited by 469 · see citing works
Walter, P. B., Fung, E. B., Killilea, D. W., Jiang, Q., Hudes, M. L., Madden, J., Porter, J. B., Evans, P., Vichinsky, E. P., & Harmatz, P. (2006) · British Journal of Haematology · doi:10.1111/j.1365-2141.2006.06277.x · Cited by 288 · see citing works
Pathogenic mechanisms of pulmonary arterial hypertension
Chan, S. Y., & Loscalzo, J. (2007) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2007.09.006 · Cited by 265 · see citing works
Kamat, A. M., Flaig, T. W., Grossman, H. B., Konety, B. R., Lamm, D. L., O’Donnell, M. A., Uchio, E., Efstathiou, J. A., & Taylor, J. A. (2015) · Nature Reviews Urology · doi:10.1038/nrurol.2015.58 · Cited by 251 · see citing works
Nur, E., Biemond, B. J., Otten, H.-M. M. B., Brandjes, D. P. M., Schnog, J. B., & the CURAMA Study Group (2011) · American Journal of Hematology · doi:10.1002/ajh.22012 · Cited by 249 · see citing works
The role of blood rheology in sickle cell disease
Connes, P., Alexy, T., Detterich, J. A., Romana, M., Hardy‐Dessources, M., & Ballas, S. K. (2015) · Blood Reviews · doi:10.1016/j.blre.2015.08.005 · Cited by 228 · see citing works
Role of oxidative stress in the pathogenesis of sickle cell disease
Chirico, E. N., & Pialoux, V. (2011) · IUBMB Life · doi:10.1002/iub.584 · Cited by 226 · see citing works
Al-Tonbary, Y. A., Tricta, F., El-Beshlawy, A. M., Badr, M. A., & Mansour, A. (2013) · The Scientific World JOURNAL · doi:10.1155/2013/912913 · Cited by 221 · see citing works
Jison, M. L., Munson, P. J., Barb, J. J., Suffredini, A. F., Talwar, S., Logun, C., Raghavachari, N., Beigel, J. H., Shelhamer, J. H., Danner, R. L., et al. (2004) · Blood · doi:10.1182/blood-2003-08-2760 · Cited by 221 · see citing works
Amer, J., Ghoti, H., Rachmilewitz, E. A., Koren, A., Levin, C., & Fibach, E. (2005) · British Journal of Haematology · doi:10.1111/j.1365-2141.2005.05834.x · Cited by 219 · see citing works
Chronic unpredictable mild stress generates oxidative stress and systemic inflammation in rats
López-López, A. L., Jaime, H. B., Villanueva, M. D. C. E., Brianza-Padilla, M., Vázquez-Palacios, G., & Aguilar, F. J. A. (2016) · Physiology & Behavior · doi:10.1016/j.physbeh.2016.03.017 · Cited by 140 · see citing works
Akohoue, S. A., Shankar, S. M., Milne, G. L., Morrow, J. D., Chen, K. Y., Ajayi, W. U., & Buchowski, M. S. (2007) · Pediatric Research · doi:10.1203/pdr.0b013e31802d7754 · Cited by 129 · see citing works
Gizi, A., Papassotiriou, I., Apostolakou, F., Lazaropoulou, C., Papastamataki, M., Kanavaki, I., Kalotychou, V., Goussetis, E., Kattamis, A. C., Rombos, I., et al. (2011) · Blood Cells Molecules and Diseases · doi:10.1016/j.bcmd.2011.01.002 · Cited by 118 · see citing works
da Silva, D. G. H., Belini-Junior, E., de Almeida, E. A., & Bonini-Domingos, C. R. (2013) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2013.08.181 · Cited by 113 · see citing works
Sickle Cell Disease: Role of Oxidative Stress and Antioxidant Therapy
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Haddad, J. J. (2002) · Respiratory Research · doi:10.1186/rr190 · Cited by 107 · see citing works
N-acetylcysteine reduces oxidative stress in sickle cell patients
on behalf of the CURAMA study group, Nur, E., Brandjes, D. P. M., Teerlink, T., Otten, H.-M. M. B., Elferink, R. P. J. O., Muskiet, F. A. J., Evers, L. M., Cate, H. T., Biemond, B. J., et al. (2012) · Annals of Hematology · doi:10.1007/s00277-011-1404-z · Cited by 94 · see citing works
Effects of oxidative stress on red blood cell rheology in sickle cell patients
Hierso, R., Xavier Waltz, A., Mora, P., Romana, M., Lemonne, N., Connes, P., & Hardy‐Dessources, M. (2014) · British Journal of Haematology · doi:10.1111/bjh.12912 · Cited by 87 · see citing works
Niihara, Y., Matsui, N. M., Shen, Y. M., Akiyama, D. A., Johnson, C. S., Sunga, M. A., Magpayo, J., Embury, S. H., Kalra, V. K., Cho, S., et al. (2005) · BMC Hematology · doi:10.1186/1471-2326-5-4 · Cited by 86 · see citing works
N-acetylcysteine amide (AD4) attenuates oxidative stress in beta-thalassemia blood cells
Amer, J., Atlas, D., & Fibach, E. (2007) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2007.11.009 · Cited by 86 · see citing works
Phytomedicines and Nutraceuticals: Alternative Therapeutics for Sickle Cell Anemia
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Pulmonary arterial hypertension
Raiesdana, A., & Loscalzo, J. (2006) · Annals of Medicine · doi:10.1080/07853890600622143 · Cited by 79 · see citing works
Early markers of renal dysfunction in patients with sickle cell/β-thalassemia
Voskaridou, E., Terpos, E., Michail, S., Hantzi, E., Anagnostopoulos, A., Margeli, A. P., Simirloglou, D., Loukopoulos, D., & Papassotiriou, I. (2006) · Kidney International · doi:10.1038/sj.ki.5000248 · Cited by 79 · see citing works
Hoppe, C. C., Kuypers, F. A., Larkin, S. K., Hagar, W., Vichinsky, E. P., & Styles, L. A. (2011) · British Journal of Haematology · doi:10.1111/j.1365-2141.2010.08480.x · Cited by 77 · see citing works
Blood Antioxidant Parameters in Sickle Cell Anemia Patients in Steady State
Lazzaretti, L. L., Griebeler, I. H., Manfredini, V. A., Brandão, V. D. M., Benfato, M. S., Santin, A. P., Wagner, S. C., de Castro, S. M., & Peralba, M. D. C. R. (2008) · Journal of the National Medical Association · doi:10.1016/s0027-9684(15)31402-4 · Cited by 73 · see citing works
Pulmonary Hypertension and Right Ventricular Dysfunction: Physiology and Perioperative Management
Strumpher, J., & Jacobsohn, E. (2011) · Journal of Cardiothoracic and Vascular Anesthesia · doi:10.1053/j.jvca.2011.02.022 · Cited by 71 · see citing works
Kim, K.-J., Kim, M., & Jung, J.-H. (2008) · Archives of Pharmacal Research · doi:10.1007/s12272-001-2153-7 · Cited by 69 · see citing works
Inflammatory Mediators of Endothelial Injury in Sickle Cell Disease
Hoppe, C. C. (2014) · Hematology/Oncology Clinics of North America · doi:10.1016/j.hoc.2013.11.006 · Cited by 63 · see citing works
Biswal, S., Rizwan, H., Pal, S., Sabnam, S., Parida, P., & Pal, A. (2018) · Hematology · doi:10.1080/10245332.2018.1498441 · Cited by 61 · see citing works
Oxidative Profile of Patients with Sickle Cell Disease
Antwi‐Boasiako, C., Dankwah, G. B., Aryee, R., Hayfron-Benjamin, C. F., Donkor, E. S., & Campbell, A. (2019) · Medical Sciences · doi:10.3390/medsci7020017 · Cited by 59 · see citing works
Al-Naama, L. M., Hassan, M. K., & Mehdi, J. K. (2015) · Qatar medical journal · doi:10.5339/qmj.2015.14 · Cited by 60 · see citing works
Protein C and S and inflammation in sickle cell disease
Schnog, J. B., Gillavry, M. R. M., van Zanten, A. P., Meijers, J. C. M., Rojer, R. A., Duits, A. J., Cate, H. T., & Brandjes, D. P. M. (2004) · American Journal of Hematology · doi:10.1002/ajh.20052 · Cited by 49 · see citing works
Fermented papaya preparation as redox regulator in blood cells of β‐thalassemic mice and patients
Amer, J., Goldfarb, A. W., Rachmilewitz, E. A., & Fibach, E. (2008) · Phytotherapy Research · doi:10.1002/ptr.2379 · Cited by 48 · see citing works
Tang, X., Guo, X.-H., Geng, D., & Lian-jin, W. (2019) · Environmental Toxicology and Pharmacology · doi:10.1016/j.etap.2019.05.001 · Cited by 48 · see citing works
Nur, E., Brandjes, D. P. M., Schnog, J. B., Otten, H.-M. M. B., Fijnvandraat, K., Schalkwijk, C. G., Biemond, B. J., & the CURAMA Study Group (2010) · British Journal of Haematology · doi:10.1111/j.1365-2141.2010.08320.x · Cited by 45 · see citing works
Nur, E., Verwijs, M., de Waart, D. R., Schnog, J. B., Otten, H.-M. M. B., Brandjes, D. P. M., Biemond, B. J., & Elferink, R. P. J. O. (2011) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2011.04.011 · Cited by 45 · see citing works
Defining stroke risk in children with sickle cell anaemia
Hoppe, C. C. (2005) · British Journal of Haematology · doi:10.1111/j.1365-2141.2004.05310.x · Cited by 45 · see citing works
Air pollution and children's health: sickle cell disease
Barbosa, S. M. D. M., Farhat, S. C. L., Martins, L. C., Pereira, L. A. A., Saldiva, P. H. N., Zanobetti, A., & Braga, A. L. F. (2015) · Cadernos de Saúde Pública · doi:10.1590/0102-311x00013214 · Cited by 45 · see citing works
Antibiotics for treating acute chest syndrome in people with sickle cell disease
Martí-Carvajal, A. J., Conterno, L. D. O., & Knight‐Madden, J. (2015) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd006110.pub4 · Cited by 42 · see citing works
Differential Expression of E‐ and P‐Selectin in the Microvasculature of Sickle Cell Transgenic Mice
Wood, K., Russell, J., Hebbel, R. P., & Granger, D. N. (2004) · Microcirculation · doi:10.1080/10739680490437559 · Cited by 42 · see citing works
Polynitroxyl albumin inhibits inflammation and vasoocclusion in transgenic sickle mice
Mahaseth, H., Vercellotti, G. M., Welch, T. E., Bowlin, P. R., Sonbol, K. M., Hsia, C. J. C., Ma, L., Bischof, J. C., Hebbel, R. P., & Belcher, J. D. (2005) · Journal of Laboratory and Clinical Medicine · doi:10.1016/j.lab.2005.02.008 · Cited by 41 · see citing works
Advanced glycation end‐products in sickle cell anaemia
Somjee, S. S., Warrier, R. P., Thomson, J. L., Ory‐Ascani, J., & Hempe, J. M. (2004) · British Journal of Haematology · doi:10.1111/j.1365-2141.2004.05274.x · Cited by 39 · see citing works
Khaleel, M., Puliyel, M. M., Shah, P., Sunwoo, J., Kato, R. M., Chalacheva, P., Thuptimdang, W., Detterich, J. A., Wood, J. C., Tsao, J., et al. (2017) · American Journal of Hematology · doi:10.1002/ajh.24858 · Cited by 39 · see citing works
Sickle cell vaso-occlusive crisis induces the release of circulating serum heat shock protein-70
Adewoye, A. H., Klings, E. S., Farber, H. W., Palaima, E., Bausero, M. A., McMahon, L. C., Odhiambo, A., Safaya, S., Yoder, M. A., Steinberg, M. H., et al. (2005) · American Journal of Hematology · doi:10.1002/ajh.20292 · Cited by 37 · see citing works
Self-citationKhan, S. A., Damanhouri, G. A., Ali, A., Khan, A. U., Khan, A., Bakillah, A., Marouf, S., Harbi, G. A., Halawani, S. H., & Makki, A. (2016) · Nutrition & Metabolism · doi:10.1186/s12986-016-0109-7 · Cited by 33 · see citing works
Oxidative profile of sickle cell patients in a Cameroonian urban hospital
Moor, V. J. A., Pieme, C. A., Chemegni, B. C., Manonji, H., Nono, B. L. N., Mamiafo, C. T., Moukette, B. M., Nzufo, F. T., & Asonganyi, T. (2016) · BMC Clinical Pathology · doi:10.1186/s12907-016-0037-5 · Cited by 31 · see citing works
Elenga, N., Loko, G., Etienne‐Julan, M., Al‐Okka, R., Adel, A. M., & Yassin, M. A. (2022) · Frontiers in Medicine · doi:10.3389/fmed.2022.931925 · Cited by 30 · see citing works
Blann, A. D., Marwah, S., Serjeant, G. R., Bareford, D., & Wright, J. (2003) · Blood Coagulation & Fibrinolysis · doi:10.1097/01.mbc.0000061293.28953.8c · Cited by 30 · see citing works
Strategies to Target Mitochondria and Oxidative Stress by Antioxidants: Key Points and Perspectives
Edeas, M. A. (2011) · Pharmaceutical Research · doi:10.1007/s11095-011-0587-2 · Cited by 30 · see citing works
Potential utility of melatonin as an antioxidant therapy in the management of sickle cell anemia
da Silva, D. G. H., Ricci, O., de Almeida, E. A., & Bonini-Domingos, C. R. (2014) · Journal of Pineal Research · doi:10.1111/jpi.12204 · Cited by 29 · see citing works
Swartz, H. M., Mason, R. P., Hogg, N., Kalyanaraman, B., Sarna, T., Plonka, P. M., Zareb, M., Gutiérrez, P. L., & Berliner, L. J. (2005) · Biological magnetic resonance · doi:10.1007/0-387-26741-7_3 · Cited by 25 · see citing works
Emokpae, A. M., Uadia, P. O., & Kuliya‐Gwarzo, A. (2010) · Cited by 24 · see citing works
Endothelial dysfunction in Sickle Cell Disease: Strategies for the treatment
Pavan, A. R., Terroni, B., & dos Santos, J. L. (2024) · Nitric Oxide · doi:10.1016/j.niox.2024.05.003 · Cited by 25 · see citing works
Magnesium for treating sickle cell disease
Than, N. N., Soe, H. H. K., Palaniappan, S. K., Abas, A. L., & Franceschi, L. D. (2017) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd011358.pub2 · Cited by 23 · see citing works
Filho, R. A. D. O., Silva, G. J., Domingos, I. F., Hatzlhofer, B. L. D., Araújo, A. D. S., Filho, J. L. D. L., Bezerra, M. A. C., Martins, D. B. G., & de Araújo, R. F. F. (2013) · Blood Cells Molecules and Diseases · doi:10.1016/j.bcmd.2013.03.003 · Cited by 22 · see citing works
Hydroxycarbamide reduces eosinophil adhesion and degranulation in sickle cell anaemia patients
Pallis, F. R., Conran, N., Fertrin, K. Y., Saad, S. T. O., Costa, F. F., & Franco‐Penteado, C. F. (2013) · British Journal of Haematology · doi:10.1111/bjh.12628 · Cited by 22 · see citing works
Ellithy, H. N., Yousry, S. M., & Shahin, G. H. (2015) · Hematology · doi:10.1179/1607845415y.0000000013 · Cited by 20 · see citing works
Mohan, J. S., Lip, G. Y. H., Blann, A. D., Bareford, D., & Marshall, J. M. (2010) · European Journal of Clinical Investigation · doi:10.1111/j.1365-2362.2010.02444.x · Cited by 20 · see citing works
Emokpae, M. A., & Uadia, P. O. (2012) · Anemia · doi:10.1155/2012/767501 · Cited by 17 · see citing works
Sickle Cell Disease and Acute Chest Syndrome: Epidemiology, Diagnosis, Management, Outcomes
Sysol, J. R., & Machado, R. F. (2016) · Respiratory medicine · doi:10.1007/978-3-319-41912-1_4 · Cited by 19 · see citing works
Increased oxidative stress alters nucleosides metabolite levels in sickle cell anemia
Castilhos, L. G., de Oliveira, J. S., Adefegha, S. A., Magni, L. P., Doleski, P. H., Abdalla, F. H., de Andrade, C. M., & Leal, D. B. R. (2017) · Redox Report · doi:10.1080/13510002.2017.1288973 · Cited by 16 · see citing works
Gonzales, J., Chakraborty, T., Romero, M. J., Mraheil, M. A., Kutlar, A., Pace, B. S., & Lucas, R. (2021) · Toxins · doi:10.3390/toxins13020157 · Cited by 16 · see citing works
Antibiotics for treating acute chest syndrome in people with sickle cell disease
Martí-Carvajal, A. J., Conterno, L. D. O., & Knight‐Madden, J. (2019) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd006110.pub5 · Cited by 16 · see citing works
Diarra, B., Roudié, J., Coulibaly, A., Ehua, S. F., Miessan, J. B. K., & Franco, D. (2008) · International Journal of Surgery · doi:10.1016/j.ijsu.2008.03.009 · Cited by 15 · see citing works
Antibiotics for treating acute chest syndrome in people with sickle cell disease
Martí-Carvajal, A. J., Conterno, L. D. O., & Knight‐Madden, J. (2007) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd006110.pub2 · Cited by 14 · see citing works
Gil, G. P., Ananina, G., Oliveira, M. B., Costa, F. F., da Silva, M. J., Santos, M. N. N., Bezerra, M. A. C., Hatzlhofer, B. L. D., Araujo, A. S., & de Melo, M. B. (2013) · Hemoglobin · doi:10.3109/03630269.2013.789438 · Cited by 13 · see citing works
Biochemical assessment of Ciklavit®, a nutraceutical used in sickle cell anaemia management
Imaga, N. A., Chukwu, C. E., Blankson, A., & Gbenle, G. O. (2013) · Journal of Herbal Medicine · doi:10.1016/j.hermed.2013.05.003 · Cited by 12 · see citing works
Elias, D. B. D., Rocha, L. B. D. S., Cavalcante, M. B., Pedrosa, A. M., Bandeira, I. C. J., & Gonçalves, R. P. (2012) · Revista Brasileira de Hematologia e Hemoterapia · doi:10.5581/1516-8484.20120069 · Cited by 12 · see citing works
Plasma Ischemia Modified Albumin Levels and Dynamic Thiol / Disulfide Balance in Sickle Cell Disease
Özcan, O., Erdal, H., İlhan, G., Demir, D., Gürpınar, A. B., Neşeli̇oğlu, S., & Erel, Ö. (2018) · Turkish Journal of Hematology · doi:10.4274/tjh.2018.0119 · Cited by 12 · see citing works
Vinhaes, C. L., Teixeira, R., Monteiro-Júnior, J. A. S., Tibúrcio, R., Cubillos-Angulo, J. M., Arriaga, M. B., Sabarin, A. G., de Souza, A. J., Silva, J. J., Lyra, I. M., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-76075-5 · Cited by 11 · see citing works
Antidepressant effect of Gentiana olivieri Griseb. in male rats exposed to chronic mild stress
Ahmet, B., Yılmaz, İ., Abacıoğlu, N., Kaymaz, M., Karaaslan, M. G., & Savan, E. K. (2020) · Libyan Journal of Medicine · doi:10.1080/19932820.2020.1725991 · Cited by 11 · see citing works
Sickle cell disease mice have cerebral oxidative stress and vascular and white matter abnormalities
Khaibullina, A., Almeida, L. E. F., Kamimura, S., Zerfas, P. M., Smith, M. L., Vogel, S., Wakim, P., Vasconcelos, O. M., Quezado, M., Horkayne‐Szakaly, I., et al. (2020) · Blood Cells Molecules and Diseases · doi:10.1016/j.bcmd.2020.102493 · Cited by 11 · see citing works
Recent trends in pulmonary arterial hypertension
Natarajan, R. (2011) · Lung India · doi:10.4103/0970-2113.76300 · Cited by 10 · see citing works
Elias, D. B. D., de Freitas, R. M., Gonçalves, R. P., Magalhães, H. Y. F., de Sousa, J. H., & Magalhães, S. M. M. (2010) · Einstein (São Paulo) · doi:10.1590/s1679-45082010ao1731 · Cited by 10 · see citing works
Buccal Micronucleus Cytome Assay in Sickle Cell Disease
Naga, M. B. S. S. (2016) · JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH · doi:10.7860/jcdr/2016/19984.7998 · Cited by 9 · see citing works
Ajibola, K. A., Adedokun, K. A., Oduola, T., Oparinde, D. P., Ayelagbe, O. G., & Ojokuku, H. O. (2019) · The Kaohsiung Journal of Medical Sciences · doi:10.1002/kjm2.12062 · Cited by 9 · see citing works
Magnesium for treating sickle cell disease
Than, N. N., Soe, H. H. K., Palaniappan, S. K., Abas, A. L., & Franceschi, L. D. (2019) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd011358.pub3 · Cited by 9 · see citing works
Assessment of some indicators of oxidative stress in nigerian sickle cell anemic patients
Nwagha, T. U., Okorie, C., & Ejezie, F. E. (2018) · Annals of African Medicine · doi:10.4103/aam.aam_26_17 · Cited by 9 · see citing works
Release of Heat Shock Proteins: Passive Versus Active Release Mechanisms
Asea, A. A. A. (2007) · Springer eBooks · doi:10.1007/978-1-4020-5585-0_1 · Cited by 9 · see citing works
Antibiotics for treating acute chest syndrome in people with sickle cell disease
Martí-Carvajal, A. J., Conterno, L. D. O., & Knight‐Madden, J. (2013) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd006110.pub3 · Cited by 9 · see citing works
Reactive Oxygen Species and Antioxidant Interactions in Erythrocytes
Rajashekaraiah, V., Pallavi, M., Choudhary, A., Bhat, C., Banerjee, P., Ranjithvishal, Laavanyaa, S., & Nithindran, S. (2022) · IntechOpen eBooks · doi:10.5772/intechopen.107544 · Cited by 8 · see citing works
Maron, B. A., Machado, R. F., & Shimoda, L. A. (2016) · Pulmonary Circulation · doi:10.1086/688315 · Cited by 8 · see citing works
Shukla, N. (2016) · JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH · doi:10.7860/jcdr/2016/18080.8186 · Cited by 8 · see citing works
Aneke, C., Okocha, E. C., Manafa, O., Onwuzuruike, E., Ibeh, C., & Chukwuma, O. M. (2017) · Medical Journal of Dr D Y Patil University · doi:10.4103/mjdrdypu.mjdrdypu_90_17 · Cited by 8 · see citing works
Alves, P. M., Martins, P. R. J., Dias, F. D. L., Burbano, R. M. R., Bianchi, M. D. L. P., & Antunes, L. M. G. (2008) · Clinical and Experimental Medicine · doi:10.1007/s10238-008-0153-3 · Cited by 8 · see citing works
Xi, C., Palani, C. D., Takezaki, M., Shi, H., Horuzsko, A., Pace, B. S., & Zhu, X. (2024) · Antioxidants · doi:10.3390/antiox13030337 · Cited by 7 · see citing works
Sun, C. W., Willmon, C. L., Wu, L.-C., Knopick, P. L., Thoerner, J., Vile, R. G., Townes, T. M., & Terman, D. S. (2016) · Frontiers in Oncology · doi:10.3389/fonc.2016.00166 · Cited by 7 · see citing works
Novel Therapies Targeting the Endothelium in Sickle Cell Disease
Hoppe, C. C. (2011) · Hemoglobin · doi:10.3109/03630269.2011.606482 · Cited by 6 · see citing works
The role of oxidative stress in the pathogenesis of pulmonary emphysema
Vučević, D. B., Radosavljević, T. S., Žunić-Božinovski, S., Djordjevic-Denic, G., Pesic, B., & Radak, D. J. (2005) · Medicinski pregled · doi:10.2298/mpns0510472v · Cited by 6 · see citing works
Methemoglobin measure in adult patients with sickle-cell anemia: influence of hydroxyurea therapy
Laurentino, M. R., Carvalho, T. M. D. J. P., dos Santos, T. E. D. J., Barbosa, M. C., dos Santos, T. N., & Gonçalves, R. P. (2014) · Jornal Brasileiro de Patologia e Medicina Laboratorial · doi:10.5935/1676-2444.20140013 · Cited by 4 · see citing works
Pathophysiology of Pulmonary Arterial Hypertension
Farber, H. W. (2008) · Humana Press eBooks · doi:10.1007/978-1-60327-075-5_4 · Cited by 3 · see citing works
Self-citationRole of iloprost and bosentan in pulmonary arterial hypertension
Saleh, J.-E. A. (2008) · Nigerian Journal of Medicine · doi:10.4314/njm.v17i1.37347 · Cited by 4 · see citing works
Characterization of S-glutathionyl Hemoglobin in Homozygous Sickle Cell Disease
Thom, G. G. A., Kallanagowdar, C., Somjee, S. S., Velez, M. C., Yu, L. C., & Hempe, J. M. (2009) · Journal of Pediatric Hematology/Oncology · doi:10.1097/mph.0b013e3181bc9c9b · Cited by 4 · see citing works
Erhabor, O., Jiya, N., Abubakar, M. B., & Usman, S. (2019) · Open Journal of Blood Diseases · doi:10.4236/ojbd.2019.93007 · Cited by 3 · see citing works
Frank's Sign as a clinical marker of cardiovascular disease
Mallinson, T. E., & Brooke, D. (2017) · Journal of Paramedic Practice · doi:10.12968/jpar.2017.9.1.8 · Cited by 3 · see citing works
Superoxide dismutase activity in sickle cell anemia patients during crisis and in steady State
Uche, E. I., Olowoselu, F. O., Augustine, B., Suleiman, A., Ismail, A., Oluwole, E. O., Akinbami, A., & Onwah, L. (2020) · Journal of Applied Hematology · doi:10.4103/joah.joah_87_19 · Cited by 3 · see citing works
- Authors
- Klings, E. S., & Farber, H. W.
- Affiliations
- Boston University (US)
- Corresponding author
- Klings, Elizabeth S
- Venue
- Respiratory Research
- Published
- 2001-07-13
- Volume
- 2
- Issue
- 5
- Pages
- 280-5
- ISSN
- 1465-9921 (ISSN-L)
- 1465-993X
- DOI
- 10.1186/rr70
- PMC
- PMC59517
- OpenAlex
- W2171650346
- Cited by
- 132
- References
- 64
- Citations by year
- 2026: 1 · 2024: 3 · 2023: 1 · 2022: 3 · 2021: 3 · 2020: 5 · 2019: 7 · 2018: 5 · 2017: 7 · 2016: 10 · 2015: 7 · 2014: 8 · 2013: 9 · 2012: 4
- FWCI
- 0.82
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Respiratory Research (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- OpenBU (Boston University) (submittedVersion)
- Funders
- American Heart Association
- Topics
- Health Sciences › Medicine › Genetics › Hemoglobinopathies and Related Disorders
- Health Sciences › Medicine › Physiology › Nitric Oxide and Endothelin Effects
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Hemoglobin structure and function
- Keywords
- acute chest syndrome, sickle cell disease, free radicals, oxidative stress, superoxide, hydrogen peroxide, peroxynitrite, hydroxyl radicals, vascular occlusion, sickle red blood cells, leukocytes, platelets, vascular endothelium
- MeSH terms
- Anemia, Sickle Cell, Animals, Antioxidants, Erythrocytes, Free Radicals, Humans, Leukocytes, Thorax, Oxidants
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