Literature DB >> 27055046

New insights into sickle cell disease: mechanisms and investigational therapies.

Gregory J Kato1.   

Abstract

PURPOSE OF REVIEW: Sickle cell disease (SCD) afflicts millions worldwide. The simplicity of its single nucleotide mutation belies the biological and psychosocial complexity of the disease. Despite only a single approved drug specifically for the treatment of SCD, new findings reviewed from 2015 provide the direction forward. RECENT
FINDINGS: The last year has provided a wealth of support for mechanisms affecting the red cell, hemolysis and vasculopathy, the innate immune system activation, blood cell and endothelial adhesiveness, central sensitization to pain, and chronic brain injury. The evidence supporting expanded use of hydroxyurea continues to mount. Many promising therapies are reaching clinical trial, including curative therapies, with more on the horizon.
SUMMARY: Evidence is compelling that the use of hydroxyurea must be expanded by clinicians to gain the full pleiotropic benefits of this approved drug. Clinicians must become aware that severe acute and chronic pain has a biological and neurologic basis, and the understanding of this basis is growing. Researchers are testing investigational therapies at an unprecedented pace in SCD, and partnership between patients, researchers, and the private sector provides the most rapid and productive way forward.

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Year:  2016        PMID: 27055046      PMCID: PMC4969007          DOI: 10.1097/MOH.0000000000000241

Source DB:  PubMed          Journal:  Curr Opin Hematol        ISSN: 1065-6251            Impact factor:   3.284


  55 in total

1.  Brain venular pattern by 7T MRI correlates with memory and haemoglobin in sickle cell anaemia.

Authors:  Enrico M Novelli; C Elizabeth Sarles; Howard Jay Aizenstein; Tamer S Ibrahim; Meryl A Butters; Anne Connelly Ritter; Kirk I Erickson; Caterina Rosano
Journal:  Psychiatry Res       Date:  2015-04-25       Impact factor: 3.222

2.  Chronic transfusion therapy improves but does not normalize systemic and pulmonary vasculopathy in sickle cell disease.

Authors:  Jon A Detterich; Roberta M Kato; Miklos Rabai; Herbert J Meiselman; Thomas D Coates; John C Wood
Journal:  Blood       Date:  2015-06-02       Impact factor: 22.113

Review 3.  Estimated pulmonary artery systolic pressure and sickle cell disease: a meta-analysis and systematic review.

Authors:  Melissa C Caughey; Charles Poole; Kenneth I Ataga; Alan L Hinderliter
Journal:  Br J Haematol       Date:  2015-04-09       Impact factor: 6.998

4.  Oscillatory haematopoiesis in adults with sickle cell disease treated with hydroxycarbamide.

Authors:  John H Baird; Caterina P Minniti; Jung-Min Lee; Xin Tian; Colin Wu; Mary Jackson; Shoaib Alam; James G Taylor; Gregory J Kato
Journal:  Br J Haematol       Date:  2014-11-06       Impact factor: 6.998

5.  Heart rate recovery is impaired after maximal exercise testing in children with sickle cell anemia.

Authors:  Anthony M Alvarado; Kendra M Ward; Devin S Muntz; Alexis A Thompson; Mark Rodeghier; Bo Fernhall; Robert I Liem
Journal:  J Pediatr       Date:  2014-12-02       Impact factor: 4.406

6.  2p15-p16.1 microdeletions encompassing and proximal to BCL11A are associated with elevated HbF in addition to neurologic impairment.

Authors:  Alister P W Funnell; Paolo Prontera; Valentina Ottaviani; Maria Piccione; Antonino Giambona; Aurelio Maggio; Fiorella Ciaffoni; Sandra Stehling-Sun; Manuela Marra; Francesca Masiello; Lilian Varricchio; John A Stamatoyannopoulos; Anna R Migliaccio; Thalia Papayannopoulou
Journal:  Blood       Date:  2015-05-27       Impact factor: 22.113

7.  Risk factor analysis of cerebral white matter hyperintensities in children with sickle cell disease.

Authors:  Veronica van der Land; Henri J M M Mutsaerts; Marc Engelen; Harriët Heijboer; Mark Roest; Martine J Hollestelle; Taco W Kuijpers; Paul J Nederkoorn; Marjon H Cnossen; Charles B L M Majoie; Aart J Nederveen; Karin Fijnvandraat
Journal:  Br J Haematol       Date:  2015-10-22       Impact factor: 6.998

8.  Revisiting the hyperhemolysis paradigm.

Authors:  Mark T Gladwin
Journal:  Blood       Date:  2015-08-06       Impact factor: 22.113

9.  Activation of the erythroid K-Cl cotransporter Kcc1 enhances sickle cell disease pathology in a humanized mouse model.

Authors:  Fiona C Brown; Ashlee J Conway; Loretta Cerruti; Janelle E Collinge; Catriona McLean; James S Wiley; Ben T Kile; Stephen M Jane; David J Curtis
Journal:  Blood       Date:  2015-10-08       Impact factor: 22.113

10.  Role of innate immunity-triggered pathways in the pathogenesis of Sickle Cell Disease: a meta-analysis of gene expression studies.

Authors:  Bidossessi Wilfried Hounkpe; Maiara Marx Luz Fiusa; Marina Pereira Colella; Loredana Nilkenes Gomes da Costa; Rafaela de Oliveira Benatti; Sara T Olalla Saad; Fernando Ferreira Costa; Magnun Nueldo Nunes dos Santos; Erich Vinicius De Paula
Journal:  Sci Rep       Date:  2015-12-09       Impact factor: 4.379

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  12 in total

Review 1.  Treating sickle cell disease by targeting HbS polymerization.

Authors:  William A Eaton; H Franklin Bunn
Journal:  Blood       Date:  2017-04-06       Impact factor: 22.113

2.  Kinetic assay shows that increasing red cell volume could be a treatment for sickle cell disease.

Authors:  Quan Li; Eric R Henry; James Hofrichter; Jeffrey F Smith; Troy Cellmer; Emily B Dunkelberger; Belhu B Metaferia; Stacy Jones-Straehle; Sarah Boutom; Garrott W Christoph; Terri H Wakefield; Mary E Link; Dwayne Staton; Erica R Vass; Jeffery L Miller; Matthew M Hsieh; John F Tisdale; William A Eaton
Journal:  Proc Natl Acad Sci U S A       Date:  2017-01-17       Impact factor: 11.205

3.  Testosterone replacement in transgenic sickle cell mice controls priapic activity and upregulates PDE5 expression and eNOS activity in the penis.

Authors:  B Musicki; S Karakus; W Akakpo; F H Silva; J Liu; H Chen; B R Zirkin; A L Burnett
Journal:  Andrology       Date:  2017-11-16       Impact factor: 3.842

Review 4.  Oxidative pathways in the sickle cell and beyond.

Authors:  Abdu I Alayash
Journal:  Blood Cells Mol Dis       Date:  2017-05-20       Impact factor: 3.039

Review 5.  Sickle Cell Disease: Advances in Treatment.

Authors:  Renée V Gardner
Journal:  Ochsner J       Date:  2018

Review 6.  Gene Therapy with Hematopoietic Stem Cells: The Diseased Bone Marrow's Point of View.

Authors:  Marina Cavazzana; Jean-Antoine Ribeil; Chantal Lagresle-Peyrou; Isabelle André-Schmutz
Journal:  Stem Cells Dev       Date:  2016-10-16       Impact factor: 3.272

7.  Bivalent ligand MCC22 potently attenuates nociception in a murine model of sickle cell disease.

Authors:  Giuseppe Cataldo; Mary M Lunzer; Julie K Olson; Eyup Akgün; John D Belcher; Gregory M Vercellotti; Philip S Portoghese; Donald A Simone
Journal:  Pain       Date:  2018-07       Impact factor: 7.926

8.  Hydroxyurea: Pattern of Use, Patient Adherence, and Safety Profile in Patients with Sickle Cell Disease in Oman.

Authors:  Jimmy Jose; Refaat Abdullah Elsadek; Beena Jimmy; Prasad George
Journal:  Oman Med J       Date:  2019-07

9.  All-Cause Mortality and Incidence of Major Adverse Cardiac Events in Sickle Cell Nephropathy: A Comparative Study.

Authors:  Kunjan Udani; Nayda Parisio-Poldiak; Julia Campbell; Victor Collier; Pooja Patel
Journal:  Cureus       Date:  2021-05-16

10.  Whole blood viscosity and red blood cell adhesion: Potential biomarkers for targeted and curative therapies in sickle cell disease.

Authors:  Erdem Kucukal; Yuncheng Man; Ailis Hill; Shichen Liu; Allison Bode; Ran An; Jaikrishnan Kadambi; Jane A Little; Umut A Gurkan
Journal:  Am J Hematol       Date:  2020-08-10       Impact factor: 10.047

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