Literature DB >> 21705977

The multifactorial origin of growth failure in thalassaemia.

Nicos Skordis1, Andreas Kyriakou.   

Abstract

Growth failure in thalassaemia major (TM) has been recognised for many years, and has persisted despite major therapeutic advances. The child with TM has a particular growth pattern, which is relatively normal until age 9-10 years; after this age a slowing down of growth velocity and reduced or absent pubertal growth spurt are observed. The pathogenesis of growth failure is multifactorial. The fundamental problem is the free iron and hemosiderosis-induced damage of the endocrine glands. Additional factors may contribute to the aetiology of growth delay including chronic anaemia and hypoxia, chronic liver disease, zinc and folic acid and nutritional deficiencies, intensive use of chelating agents, emotional factors, endocrinopathies (hypogonadism, delayed puberty, hypothyroidism, disturbed calcium homeostasis and bone disease) and last but not least dysregulation of the GH-IGF-1 axis.Three phases of growth disturbances according to age of presentation are well recognised, and have different aetiologies: in the first phase growth disturbance is mainly due to hypoxia, anaemia, ineffective erythropoiesis and nutritional factors. During late childhood (second phase), growth retardation is mainly due to iron overload affecting GH-IGF-1 axis and other potential endocrine complications. Although appropriate iron chelation therapy can improve growth and development, TM children and adolescents treated intensively with desferrioxamine remain short as well, showing body disproportion between the upper and lower body segment. After the age of 10-11 years (third phase), delayed or arrested puberty is an important contributing factor to growth failure in adolescent thalassaemics, who do not exhibit a normal growth spurt. During the last decades therapeutic progress and bone marrow transplantation resulted in a prolonged life expectancy in TM patients. Growth retardation, however, continues to be a significant challenge in these individuals, often affecting their social adjustment and quality of life.

Entities:  

Mesh:

Year:  2011        PMID: 21705977

Source DB:  PubMed          Journal:  Pediatr Endocrinol Rev        ISSN: 1565-4753


  10 in total

Review 1.  An international registry of survivors with Hb Bart's hydrops fetalis syndrome.

Authors:  Duantida Songdej; Christian Babbs; Douglas R Higgs
Journal:  Blood       Date:  2017-01-05       Impact factor: 22.113

Review 2.  Chronic Kidney Disease and Dietary Measures to Improve Outcomes.

Authors:  Oleh M Akchurin
Journal:  Pediatr Clin North Am       Date:  2019-02       Impact factor: 3.278

Review 3.  Impact of bone disease and pain in thalassemia.

Authors:  Antonio Piga
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2017-12-08

4.  Evaluation of electrocardiography, echocardiography and cardiac T2* for cardiac complications in beta thalassemia major.

Authors:  Fadime Ersoy Dursun; Gönül Açıksarı; Serçin Özkök; Onur İncealtın
Journal:  Int J Cardiovasc Imaging       Date:  2021-10-08       Impact factor: 2.357

5.  Insulin-like Growth Factor-1 (IGF-1): Demographic, Clinical and Laboratory Data in 120 Consecutive Adult Patients with Thalassaemia Major.

Authors:  Vincenzo De Sanctis; Ashraf T Soliman; Giancarlo Candini; Mohamed Yassin; Giuseppe Raiola; Maria Concetta Galati; Rania Elalaily; Heba Elsedfy; Nicos Skordis; Piernicola Garofalo; Salvatore Anastasi; Saveria Campisi; Mehran Karimi; Christos Kattamis; Duran Canatan; Yurdanur Kilinc; Praveen Sobti; Bernadette Fiscina; Mohamed El Kholy
Journal:  Mediterr J Hematol Infect Dis       Date:  2014-11-01       Impact factor: 2.576

6.  2021 Thalassaemia International Federation Guidelines for the Management of Transfusion-dependent Thalassemia.

Authors:  Dimitrios Farmakis; John Porter; Ali Taher; Maria Domenica Cappellini; Michael Angastiniotis; Androulla Eleftheriou
Journal:  Hemasphere       Date:  2022-07-29

7.  Erythropoiesis-independent effects of iron in chronic kidney disease.

Authors:  Edwin Patino; Oleh Akchurin
Journal:  Pediatr Nephrol       Date:  2021-07-09       Impact factor: 3.651

8.  Frequency of Celiac Disease in Children with Beta Thalassemia major.

Authors:  N Honar; S Kamali; M Karimi
Journal:  Iran J Ped Hematol Oncol       Date:  2014-04-20

9.  Growth and Endocrine Function in Tunisian Thalassemia Major Patients.

Authors:  Naouel Guirat Dhouib; Monia Ben Khaled; Monia Ouederni; Habib Besbes; Ridha Kouki; Fethi Mellouli; Mohamed Bejaoui
Journal:  Mediterr J Hematol Infect Dis       Date:  2018-05-01       Impact factor: 2.576

10.  Malnutrition, Its Attributes, and Impact on Quality of Life: An Epidemiological Study among β-Thalassemia Major Children.

Authors:  Bijit Biswas; Narendra Nath Naskar; Keya Basu; Aparajita Dasgupta; Rivu Basu; Bobby Paul
Journal:  Korean J Fam Med       Date:  2020-01-20
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.