Literature DB >> 25541601

Transition of Thalassaemia and Friedreich ataxia from fatal to chronic diseases.

Annita Kolnagou1, Christina N Kontoghiorghe1, George J Kontoghiorghes1.   

Abstract

Thalassaemia major (TM) and Friedreich's ataxia (FA) are autosomal recessive inherited diseases related to the proteins haemoglobin and frataxin respectively. In both diseases abnormalities in iron metabolism is the main cause of iron toxicity leading to increased morbidity and mortality. Major efforts are directed towards the prevention of these diseases and also in their treatment using iron chelation therapy. Both TM and FA are endemic in Cyprus, where the frequency per total population of asymptomatic heterozygote carriers and patients is the highest worldwide. Cyprus has been a pioneering nation in preventing and nearly eliminating the birth of TM and FA patients by introducing an organized health structure, including prenatal and antenatal diagnosis. Effective iron chelation therapy, improved diagnostic methods and transfusion techniques as well as supportive therapy from other clinical specializations have improved the survival and quality of life of TM patients. Despite the tiresome clinical management regimes many TM patients are successful in their professional lives, have families with children and some are now living well into their fifties. The introduction of deferiprone led to the elimination of cardiac failure induced by iron overload toxicity, which was the major cause of mortality in TM. Effective combinations of deferiprone with deferoxamine in TM patients caused the fall of body iron to normal physiological ranges. In FA different mechanisms of iron metabolism and toxicity apply to that of TM, which can be targeted with specific iron chelation protocols. Preliminary findings from the introduction of deferiprone in FA patients have increased the hopes for improved and effective therapy in this untreatable condition. New and personalised treatments are proposed in TM and FA. Overall, advances in treatments and in particular of chelation therapy using deferiprone are transforming TM and FA from fatal to chronic conditions. The paradigm of Cyprus in the prevention and treatment of TM can be used for application worldwide.

Entities:  

Keywords:  Chelation therapy; Cyprus; Deferiprone; Deferoxamine; Friedreich ataxia; Prenatal diagnosis; Survival; Thalassaemia

Year:  2014        PMID: 25541601      PMCID: PMC4274580          DOI: 10.5662/wjm.v4.i4.197

Source DB:  PubMed          Journal:  World J Methodol        ISSN: 2222-0682


  139 in total

1.  Competition studies of L1-deferiprone with copper and iron. Possible implications on efficacy, toxicity and new therapeutic applications.

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Journal:  Transfus Sci       Date:  2000-12

2.  Capillary isoelectric focusing and high-performance cation-exchange chromatography compared for qualitative and quantitative analysis of hemoglobin variants.

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Review 3.  Deferiprone for the treatment of Friedreich's ataxia.

Authors:  Massimo Pandolfo; Laura Hausmann
Journal:  J Neurochem       Date:  2013-08       Impact factor: 5.372

4.  Inherited haemoglobin disorders: an increasing global health problem.

Authors:  D J Weatherall; J B Clegg
Journal:  Bull World Health Organ       Date:  2001-10-24       Impact factor: 9.408

5.  Long-term results of survival in patients with thalassemia major treated with bone marrow transplantation.

Authors:  Paolo Di Bartolomeo; Stella Santarone; Erminia Di Bartolomeo; Paola Olioso; Pasqua Bavaro; Gabriele Papalinetti; Paolo Di Carlo; Franco Papola; Antonio Nicolucci; Marta Di Nicola; Antonio Iacone
Journal:  Am J Hematol       Date:  2008-07       Impact factor: 10.047

6.  Myocyte damage and loss of myofibers is the potential mechanism of iron overload toxicity in congestive cardiac failure in thalassemia. Complete reversal of the cardiomyopathy and normalization of iron load by deferiprone.

Authors:  Annita Kolnagou; Yiannis Michaelides; Christos Kontos; Kyriacos Kyriacou; George J Kontoghiorghes
Journal:  Hemoglobin       Date:  2008       Impact factor: 0.849

7.  Ultrastructural sequences during liver iron overload in genetic hemochromatosis.

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Journal:  J Hepatol       Date:  1997-10       Impact factor: 25.083

8.  Cell functions impaired by frataxin deficiency are restored by drug-mediated iron relocation.

Authors:  Or Kakhlon; Hila Manning; William Breuer; Naomi Melamed-Book; Chunye Lu; Gino Cortopassi; Arnold Munnich; Z Ioav Cabantchik
Journal:  Blood       Date:  2008-09-16       Impact factor: 22.113

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Journal:  Br J Haematol       Date:  1992-10       Impact factor: 6.998

10.  Effective chelation of iron in beta thalassaemia with the oral chelator 1,2-dimethyl-3-hydroxypyrid-4-one.

Authors:  G J Kontoghiorghes; M A Aldouri; A V Hoffbrand; J Barr; B Wonke; T Kourouclaris; L Sheppard
Journal:  Br Med J (Clin Res Ed)       Date:  1987-12-12
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  9 in total

1.  New developments and controversies in iron metabolism and iron chelation therapy.

Authors:  Christina N Kontoghiorghe; George J Kontoghiorghes
Journal:  World J Methodol       Date:  2016-03-26

Review 2.  Efficacy and safety of iron-chelation therapy with deferoxamine, deferiprone, and deferasirox for the treatment of iron-loaded patients with non-transfusion-dependent thalassemia syndromes.

Authors:  Christina N Kontoghiorghe; George J Kontoghiorghes
Journal:  Drug Des Devel Ther       Date:  2016-01-29       Impact factor: 4.162

3.  Efficacy and safety of iron-chelation therapy with deferoxamine, deferiprone, and deferasirox for the treatment of iron-loaded patients with nontransfusion-dependent thalassemia syndromes.

Authors:  Ali T Taher; John B Porter; Antonis Kattamis; Vip Viprakasit; M Domenica Cappellini
Journal:  Drug Des Devel Ther       Date:  2016-12-15       Impact factor: 4.162

4.  Transfusion-Related Acute Lung Injury (TRALI) in two Thalassaemia Patients Caused by the Same Multiparous Blood Donor.

Authors:  Annita Kolnagou; Christina N Kontoghiorghe; George J Kontoghiorghes
Journal:  Mediterr J Hematol Infect Dis       Date:  2017-10-18       Impact factor: 2.576

5.  Economic Burden of Thalassemia Major in Iran, 2015.

Authors:  Firooz Esmaeilzadeh; Azita Azarkeivan; Sara Emamgholipour; Ali Akbari Sari; Mehdi Yaseri; Batoul Ahmadi; Mohtasham Ghaffari
Journal:  J Res Health Sci       Date:  2016

Review 6.  The History of Deferiprone (L1) and the Paradigm of the Complete Treatment of Iron Overload in Thalassaemia.

Authors:  George J Kontoghiorghes; Marios Kleanthous; Christina N Kontoghiorghe
Journal:  Mediterr J Hematol Infect Dis       Date:  2020-01-01       Impact factor: 2.576

Review 7.  Iron and Chelation in Biochemistry and Medicine: New Approaches to Controlling Iron Metabolism and Treating Related Diseases.

Authors:  George J Kontoghiorghes; Christina N Kontoghiorghe
Journal:  Cells       Date:  2020-06-12       Impact factor: 6.600

8.  Advances on Chelation and Chelator Metal Complexes in Medicine.

Authors:  George J Kontoghiorghes
Journal:  Int J Mol Sci       Date:  2020-04-03       Impact factor: 5.923

9.  Epidemiology of Thalassemia in Gulf Cooperation Council Countries: A Systematic Review.

Authors:  Amani Abu-Shaheen; Humariya Heena; Abdullah Nofal; Doaa A Abdelmoety; Abdulrahman Almatary; Mohammed Alsheef; Isamme AlFayyad
Journal:  Biomed Res Int       Date:  2020-10-28       Impact factor: 3.411

  9 in total

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