Literature DB >> 20008182

Novel therapies in sickle cell disease.

Kenneth I Ataga1.   

Abstract

Despite an increased understanding of the pathophysiology of sickle cell disease (SCD), there remains a paucity of available agents for the prevention and treatment of specific SCD-related complications. Recently, there has been significant progress in the development of novel drugs for this disease. These agents, which increase the production of fetal hemoglobin, improve red blood cell hydration, increase the availability of nitric oxide and possess anti-inflammatory effects, are in varying stages of clinical development. With the complex pathophysiology of SCD, it is unlikely that a single agent will prevent or treat all the sequelae of this disease. As a result, patients may benefit from treatment with a combination of agents that possess different mechanisms of action. This overview discusses selected novel agents that appear promising in SCD.

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Year:  2009        PMID: 20008182     DOI: 10.1182/asheducation-2009.1.54

Source DB:  PubMed          Journal:  Hematology Am Soc Hematol Educ Program        ISSN: 1520-4383


  11 in total

1.  Understanding the Self-Management Practices of Young Adults with Sickle Cell Disease.

Authors:  Nadine Matthie; Coretta Jenerette
Journal:  J Sick Cell Dis Hemoglobinopathies       Date:  2017-05

2.  Sickle cell disease is associated with iron mediated hypercoagulability.

Authors:  Nirmish Shah; Ian J Welsby; Martha A Fielder; Wayne K Jacobsen; Vance G Nielsen
Journal:  J Thromb Thrombolysis       Date:  2015-08       Impact factor: 2.300

3.  Perceptions of young adults with sickle cell disease concerning their disease experience.

Authors:  Nadine Matthie; Jill Hamilton; Diana Wells; Coretta Jenerette
Journal:  J Adv Nurs       Date:  2015-09-09       Impact factor: 3.187

4.  Sickle cell disease in adults: developing an appropriate care plan.

Authors:  Nadine Matthie; Coretta Jenerette
Journal:  Clin J Oncol Nurs       Date:  2015-10       Impact factor: 1.027

5.  Current management of sickle cell anemia.

Authors:  Patrick T McGann; Alecia C Nero; Russell E Ware
Journal:  Cold Spring Harb Perspect Med       Date:  2013-08-01       Impact factor: 6.915

Review 6.  Beyond the definitions of the phenotypic complications of sickle cell disease: an update on management.

Authors:  Samir K Ballas; Muge R Kesen; Morton F Goldberg; Gerard A Lutty; Carlton Dampier; Ifeyinwa Osunkwo; Winfred C Wang; Carolyn Hoppe; Ward Hagar; Deepika S Darbari; Punam Malik
Journal:  ScientificWorldJournal       Date:  2012-08-01

Review 7.  Minireview: Prognostic factors and the response to hydroxurea treatment in sickle cell disease.

Authors:  Winfred C Wang
Journal:  Exp Biol Med (Maywood)       Date:  2016-03-29

8.  Osteoarticular involvement in sickle cell disease.

Authors:  Geraldo Bezerra da Silva Junior; Elizabeth De Francesco Daher; Francisco Airton Castro da Rocha
Journal:  Rev Bras Hematol Hemoter       Date:  2012

9.  Fetal hemoglobin reactivation and cell engineering in the treatment of sickle cell anemia.

Authors:  Sandro Eridani; Andrea Mosca
Journal:  J Blood Med       Date:  2011-02-28

Review 10.  Evaluation of Novel Fetal Hemoglobin Inducer Drugs in Treatment of β-Hemoglobinopathy Disorders.

Authors:  Ali Dehghani Fard; Seyed Ahmad Hosseini; Mohammad Shahjahani; Fatemeh Salari; Kaveh Jaseb
Journal:  Int J Hematol Oncol Stem Cell Res       Date:  2013
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