Literature DB >> 11970927

Liver disease in transfusion dependent thalassaemia major.

C K Li1, K W Chik, C W K Lam, K F To, S C H Yu, V Lee, M M K Shing, A Y K Cheung, P M P Yuen.   

Abstract

AIMS: To study the prevalence and severity of liver diseases of transfusion dependent thalassaemia major patients, and correlate the histological and biochemical changes of iron overload in liver with the peripheral blood markers.
METHOD: Liver biopsy was performed to assess the histological changes and liver iron content (LIC).
RESULTS: One hundred patients were evaluated (median age 11.7 years, range 1.5-27). A total of 81 liver biopsies were performed in 73 patients; 43 samples were analysed for LIC. Grade 3-4 haemosiderosis and hepatic fibrosis was found in 44% and 30% of patients respectively; both were significantly associated with higher serum ferritin, liver enzymes, and LIC. Very high LIC (>15 mg/g dry weight) was present in 16.3% of patients.
CONCLUSION: Severe haemosiderosis and hepatic fibrosis were common in patients with thalassaemia major despite the use of chelation therapy. Liver biopsy provided information on fibrosis and LIC which could not be accurately predicted from peripheral blood markers.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 11970927      PMCID: PMC1751092          DOI: 10.1136/adc.86.5.344

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN: 0003-9888            Impact factor:   3.791


  20 in total

1.  A prospective evaluation of iron chelation therapy in children with severe beta-thalassemia. A six-year study.

Authors:  H S Maurer; J D Lloyd-Still; C Ingrisano; F Gonzalez-Crussi; G R Honig
Journal:  Am J Dis Child       Date:  1988-03

2.  Long-term outcome of continuous 24-hour deferoxamine infusion via indwelling intravenous catheters in high-risk beta-thalassemia.

Authors:  B A Davis; J B Porter
Journal:  Blood       Date:  2000-02-15       Impact factor: 22.113

3.  Survival and causes of death in thalassaemia major.

Authors:  M G Zurlo; P De Stefano; C Borgna-Pignatti; A Di Palma; A Piga; C Melevendi; F Di Gregorio; M G Burattini; S Terzoli
Journal:  Lancet       Date:  1989-07-01       Impact factor: 79.321

4.  Desferrioxamine ototoxicity: evaluation of risk factors in thalassaemic patients and guidelines for safe dosage.

Authors:  J B Porter; M S Jaswon; E R Huehns; C A East; J W Hazell
Journal:  Br J Haematol       Date:  1989-11       Impact factor: 6.998

5.  Evaluation of a prenatal screening procedure for beta-thalassaemia carriers in a Chinese population based on the mean corpuscular volume (MCV).

Authors:  A Ghosh; J S Woo; C W Wan; C Machenry; V Wong; H K Ma; V Chan; T K Chan
Journal:  Prenat Diagn       Date:  1985 Jan-Feb       Impact factor: 3.050

6.  Cirrhosis associated with multiple transfusions in thalassaemia.

Authors:  G Jean; S Terzoli; R Mauri; L Borghetti; A Di Palma; A Piga; M Magliano; M Melevendi; M Cattaneo
Journal:  Arch Dis Child       Date:  1984-01       Impact factor: 3.791

7.  Hereditary hemochromatosis. Phenotypic expression of the disease.

Authors:  G E Cartwright; C Q Edwards; K Kravitz; M Skolnick; D B Amos; A Johnson; L Buskjaer
Journal:  N Engl J Med       Date:  1979-07-26       Impact factor: 91.245

8.  Visual and auditory neurotoxicity in patients receiving subcutaneous deferoxamine infusions.

Authors:  N F Olivieri; J R Buncic; E Chew; T Gallant; R V Harrison; N Keenan; W Logan; D Mitchell; G Ricci; B Skarf
Journal:  N Engl J Med       Date:  1986-04-03       Impact factor: 91.245

9.  Survival and disease complications in thalassemia major.

Authors:  C Borgna-Pignatti; S Rugolotto; P De Stefano; A Piga; F Di Gregorio; M R Gamberini; V Sabato; C Melevendi; M D Cappellini; G Verlato
Journal:  Ann N Y Acad Sci       Date:  1998-06-30       Impact factor: 5.691

10.  Iron state and hepatic disease in patients with thalassaemia major, treated with long term subcutaneous desferrioxamine.

Authors:  M A Aldouri; B Wonke; A V Hoffbrand; D M Flynn; M Laulicht; L A Fenton; P J Scheuer; C C Kibbler; C A Allwood; D Brown
Journal:  J Clin Pathol       Date:  1987-11       Impact factor: 3.411

View more
  14 in total

1.  Modification of CYP2E1 and CYP3A4 activities in haemoglobin E-beta thalassemia patients.

Authors:  Nuntiya Somparn; Upa Kukongviriyapan; Wichittra Tassaneeyakul; Arunee Jetsrisuparb; Veerapol Kukongviriyapan
Journal:  Eur J Clin Pharmacol       Date:  2006-11-21       Impact factor: 2.953

2.  Iron overload correlates with serum liver fibrotic markers and liver dysfunction: Potential new methods to predict iron overload-related liver fibrosis in thalassemia patients.

Authors:  Man Wang; Rongrong Liu; Yuzhen Liang; Gaohui Yang; Yumei Huang; Chunlan Yu; Kaiqi Sun; Yongrong Lai; Yang Xia
Journal:  United European Gastroenterol J       Date:  2016-06-23       Impact factor: 4.623

3.  Hepatic iron quantitation and its relationship with disease measures and histologically assessed iron content.

Authors:  Shabbar Sajjad; Moises Garcia; Ahmed Malik; David H Van Thiel
Journal:  Dig Dis Sci       Date:  2007-10-13       Impact factor: 3.199

4.  Major causes of hospital admission in Beta thalassemia major patients in southern iran.

Authors:  Mehran Karimi; Vahid Emadmarvasti; Jacob Hoseini; Lotfolah Shoja
Journal:  Iran J Pediatr       Date:  2011-12       Impact factor: 0.364

5.  Infections in thalassemia and hemoglobinopathies: focus on therapy-related complications.

Authors:  Bianca Maria Ricerca; Arturo Di Girolamo; Deborah Rund
Journal:  Mediterr J Hematol Infect Dis       Date:  2009-12-28       Impact factor: 2.576

6.  Serum or plasma ferritin concentration as an index of iron deficiency and overload.

Authors:  Maria Nieves Garcia-Casal; Sant-Rayn Pasricha; Ricardo X Martinez; Lucero Lopez-Perez; Juan Pablo Peña-Rosas
Journal:  Cochrane Database Syst Rev       Date:  2021-05-24

7.  Liver Iron Concentration and Liver Impairment in Relation to Serum IGF-1 Levels in Thalassaemia Major Patients: A Retrospective Study.

Authors:  Vincenzo De Sanctis; Ashraf T Soliman; Giancarlo Candini; Christos Kattamis; Giuseppe Raiola; Heba Elsedfy
Journal:  Mediterr J Hematol Infect Dis       Date:  2015-02-20       Impact factor: 2.576

8.  Liver Enzymes in Children with beta-Thalassemia Major: Correlation with Iron Overload and Viral Hepatitis.

Authors:  Khaled M Salama; Ola M Ibrahim; Ahmed M Kaddah; Samia Boseila; Leila Abu Ismail; May M Abdel Hamid
Journal:  Open Access Maced J Med Sci       Date:  2015-05-28

9.  Hematological and biochemical evaluation of β-thalassemia major (βTM) patients in Gaza Strip: A cross-sectional study.

Authors:  Hani Ayyash; Mahmoud Sirdah
Journal:  Int J Health Sci (Qassim)       Date:  2018 Nov-Dec

10.  Longitudinal Study on Liver Functions in Patients with Thalassemia Major before and after Deferasirox (DFX) Therapy.

Authors:  Ashraf Soliman; Mohamed Yassin; Fawzia Al Yafei; Lolwa Al-Naimi; Noora Almarri; Aml Sabt; Vincenzo De Sanctis
Journal:  Mediterr J Hematol Infect Dis       Date:  2014-04-07       Impact factor: 2.576

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.