Literature DB >> 18403823

A rare cause of heart failure in iron-overload thalassaemic patients-primary hypoparathyroidism.

V De Sanctis1, G Borsari, S Brachi, E Gubellini, M R Gamberini, G Carandina.   

Abstract

Hypocalcemia due to hypoparathyroidism (HPT) is a late complication of iron-overloaded patients with b-thalassaemia major (TM). The majority of patients have mild disease with parasthesias, while in the more severe form tetany, seizures or cardiac failure may occur. In the last 20 years we observed heart failure in 2 out of 38 (5.2%) TM patients (aged 18 and 22 years) with hypocalcemia secondary to HPT associated to iron overload. Calcium supplementation and vitamin D induced correction of hypocalcemia and resulted in an improvement of cardiac function. Calcium plays a key role in the maintenance and regulation of normal cardiac function. Extra-cellular calcium is indispensable for the contractile process since the sarcoplasmatic reticulum is unable to maintain a sufficient amount of calcium to trigger myocardial contraction. In conclusion, our observations stress the importance of a regular iron chelation therapy, adherence to treatment of endocrine complication and regular follow-up of TM patients with hypocalcemia.

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Year:  2008        PMID: 18403823

Source DB:  PubMed          Journal:  Georgian Med News        ISSN: 1512-0112


  3 in total

Review 1.  Reversible cardiac dysfunction associated with hypocalcemia: a systematic review and meta-analysis of individual patient data.

Authors:  Darrell B Newman; Salman S Fidahussein; Deanne T Kashiwagi; Kurt A Kennel; Kianoush B Kashani; Zhen Wang; Osama Altayar; Mohammad H Murad
Journal:  Heart Fail Rev       Date:  2014-03       Impact factor: 4.214

2.  Vitamin D Receptor (VDR) Gene Polymorphisms (FokI, BsmI) and their Relation to Vitamin D Status in Pediatrics βeta Thalassemia Major.

Authors:  Shereen Mohamed Elhoseiny; Dalia Saber Morgan; Asmaa Mohamed Rabie; Samer Tharwat Bishay
Journal:  Indian J Hematol Blood Transfus       Date:  2015-05-19       Impact factor: 0.900

3.  Growth and endocrine disorders in thalassemia: The international network on endocrine complications in thalassemia (I-CET) position statement and guidelines.

Authors:  Vincenzo De Sanctis; Ashraf T Soliman; Heba Elsedfy; Nicos Skordis; Christos Kattamis; Michael Angastiniotis; Mehran Karimi; Mohd Abdel Daem Mohd Yassin; Ahmed El Awwa; Iva Stoeva; Giuseppe Raiola; Maria Concetta Galati; Elsaid M Bedair; Bernadette Fiscina; Mohamed El Kholy
Journal:  Indian J Endocrinol Metab       Date:  2013-01
  3 in total

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