Literature DB >> 34773506

Fracture prevalence in thalassemia: a systematic review and meta-analysis.

Nipith Charoenngam1,2,3, Thanitsara Rittiphairoj4, Ben Ponvilawan5.   

Abstract

BACKGROUND: Multiple observational studies have reported high prevalence of fracture in patients with thalassemia. However, most of these studies have included limited number of patients, and only few of them have reported prevalence of fracture among patients with different types and severity of thalassemia.
OBJECTIVE: This systematic review and meta-analysis was conducted to summarize all available data of fracture prevalence among patients with thalassemia.
METHODS: A systematic review was conducted using EMBASE and MEDLINE databases from inception to June 2021 to determine studies that reported prevalence of fracture in thalassemia patients. The pooled prevalence with 95% confidence interval (95%CI) of fracture across studies was determined using a random-effect, generic inverse variance method.
RESULTS: After two rounds of systematic review, a total of 25 studies with 4934 patients were included in the meta-analysis. The pooled prevalence of fracture among patients with thalassemia was 16% (95%CI, 15-17%, I2 = 94.3%). The subgroup analyses showed that the pooled prevalence of fracture was 4% (95%CI, 2-6%; I2 = 70.4%) among patients with alpha thalassemia, 17% (95%CI, 16-19%; I2 = 93.2%) among patients with beta thalassemia, 18% (95%CI, 16-19%; I2 = 89.0%) among patients with transfusion-dependent thalassemia, and 7% (95%CI, 4-10%; I2 = 94.2%) among patients with non-transfusion-dependent thalassemia.
CONCLUSION: Fracture is common in patients with thalassemia, and may be more prevalent in beta thalassemia and transfusion-dependent thalassemia than in alpha thalassemia and non-transfusion-dependent thalassemia.
© 2021. International Osteoporosis Foundation and National Osteoporosis Foundation.

Entities:  

Keywords:  Fracture; Meta-analysis; Systematic review; Thalassemia

Mesh:

Year:  2021        PMID: 34773506     DOI: 10.1007/s11657-021-01026-0

Source DB:  PubMed          Journal:  Arch Osteoporos            Impact factor:   2.617


  35 in total

1.  Spectrum of α-thalassemia mutations in transfusion-dependent β-thalassemia patients from the Eastern Province of Saudi Arabia.

Authors:  Mohammed Shakil Akhtar; Fuad Qaw; J Francis Borgio; Waleed Albuali; Ahmed Suliman; Zaki Nasserullah; Sana Al-Jarrash; Amein Al-Ali
Journal:  Hemoglobin       Date:  2013       Impact factor: 0.849

2.  Spine bone texture assessed by trabecular bone score (TBS) to evaluate bone health in thalassemia major.

Authors:  M Baldini; F M Ulivieri; S Forti; S Serafino; S Seghezzi; A Marcon; F Giarda; C Messina; E Cassinerio; B Aubry-Rozier; D Hans; M D Cappellini
Journal:  Calcif Tissue Int       Date:  2014-10-28       Impact factor: 4.333

3.  Assessment of bone quality by quantitative ultrasound of proximal phalanges of the hand and fracture rate in children and adolescents with bone and mineral disorders.

Authors:  Giampiero I G L I Baroncelli; Giovanni Federico; Silvano Bertelloni; Federica Sodini; Francesca De Terlizzi; Ruggero Cadossi; Giuseppe Saggese
Journal:  Pediatr Res       Date:  2003-04-16       Impact factor: 3.756

4.  Bone metabolism and mineral density in patients with beta-thalassemia major.

Authors:  Umit Dundar; Alphan Kupesiz; Sebahat Ozdem; Erdal Gilgil; Tiraje Tuncer; Akif Yesilipek; Meral Gultekin
Journal:  Saudi Med J       Date:  2007-09       Impact factor: 1.484

5.  Increased prevalence of fractures in inadequately transfused and chelated Indian children and young adults with beta thalassemia major.

Authors:  Veena Ekbote; Raja Padidela; Vaman Khadilkar; Vijay Ramanan; Ankita Maheshwari; Zulf Mughal; Eleni P Kariki; Nicola Crabtree; Anuradha Khadilkar
Journal:  Bone       Date:  2020-09-18       Impact factor: 4.398

Review 6.  Morbidities in non-transfusion-dependent thalassemia.

Authors:  Antoine N Saliba; Ali T Taher
Journal:  Ann N Y Acad Sci       Date:  2016-03       Impact factor: 5.691

7.  Effects of calcitonin therapy on osteoporosis in patients with thalassemia.

Authors:  D Canatan; N Akar; A Arcasoy
Journal:  Acta Haematol       Date:  1995       Impact factor: 2.195

8.  The ability of lumbar spine DXA and phalanx QUS to detect previous fractures in young thalassemic patients with hypogonadism, hypothyroidism, diabetes, and hepatitis-B: A 2-year subgroup analysis from the Taranto Area of Apulia Region.

Authors:  Alberto Argentiero; Cosimo Neglia; Angelo Peluso; Salvatore di Rosa; Antonio Ferrarese; Gianluca Di Tanna; Vincenzo Caiaffa; Marco Benvenuto; Alexandru Cozma; Giovanna Chitano; Nadia Agnello; Daniele Paladini; Nicola Baldi; Alessandro Distante; Prisco Piscitelli
Journal:  J Pediatr Hematol Oncol       Date:  2013-08       Impact factor: 1.289

Review 9.  Beta-thalassemia.

Authors:  Antonio Cao; Renzo Galanello
Journal:  Genet Med       Date:  2010-02       Impact factor: 8.822

10.  Comparison of Bone Mineral Density in Thalassemia Major Patients with Healthy Controls.

Authors:  Mahesh Chand Meena; Alok Hemal; Mukul Satija; Shilpa Khanna Arora; Shahina Bano
Journal:  Adv Hematol       Date:  2015-12-31
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  2 in total

1.  Analysis of circRNAs and circRNA-associated competing endogenous RNA networks in β-thalassemia.

Authors:  Fang Yang; Heyun Ruan; Shuquan Li; Wei Hou; Yuling Qiu; Lingjie Deng; Sha Su; Ping Chen; Lihong Pang; Ketong Lai
Journal:  Sci Rep       Date:  2022-05-16       Impact factor: 4.996

Review 2.  New Entity-Thalassemic Endocrine Disease: Major Beta-Thalassemia and Endocrine Involvement.

Authors:  Mara Carsote; Cristina Vasiliu; Alexandra Ioana Trandafir; Simona Elena Albu; Mihai-Cristian Dumitrascu; Adelina Popa; Claudia Mehedintu; Razvan-Cosmin Petca; Aida Petca; Florica Sandru
Journal:  Diagnostics (Basel)       Date:  2022-08-09
  2 in total

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