Literature DB >> 23216540

Increased leucocyte apoptosis in transfused β-thalassaemia patients.

Patrick B Walter1, John Porter, Patricia Evans, Janet L Kwiatkowski, Ellis J Neufeld, Thomas Coates, Patricia J Giardina, Robert W Grady, Elliott Vichinsky, Nancy Olivieri, Felicia Trachtenberg, Daniele Alberti, Ellen Fung, Bruce Ames, Annie Higa, Paul Harmatz.   

Abstract

This exploratory study assessed apoptosis in peripheral blood leucocytes (PBL) from β-thalassaemia patients receiving chronic transfusions and chelation therapy (deferasirox or deferoxamine) at baseline, 1, 6, and 12 months. At baseline, thalassaemic PBLs presented 50% greater levels of Bax (BAX), 75% higher caspase-3/7, 48% higher caspase-8 and 88% higher caspase-9 activities and 428% more nucleosomal DNA fragmentation than control subjects. Only neutrophils correlated significantly with apoptotic markers. Previously, we showed that over the treatment year, hepatic iron declined; we now show that the ratio of Bax/Bcl-2 (BCL2), (-27·3%/year), and caspase-9 activity (-13·3%/year) declined in both treatment groups, suggesting that chelation decreases body iron and indicators of PBL apoptosis.
© 2012 Blackwell Publishing Ltd.

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Year:  2012        PMID: 23216540      PMCID: PMC4597914          DOI: 10.1111/bjh.12076

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  15 in total

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  2 in total

Review 1.  Deferasirox for managing iron overload in people with thalassaemia.

Authors:  Claudia Bollig; Lisa K Schell; Gerta Rücker; Roman Allert; Edith Motschall; Charlotte M Niemeyer; Dirk Bassler; Joerg J Meerpohl
Journal:  Cochrane Database Syst Rev       Date:  2017-08-15

2.  Leukocytes apoptosis and adipocytokines in children with beta thalassemia major.

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  2 in total

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