Literature DB >> 19940469

Hypercoagulable state and methylenetetrahydrofolate reductase (MTHFR) C677T mutation in patients with beta-thalassemia major in Kuwait.

Nada Y Mustafa1, Rajaa Marouf, Salah Al-Humood, Suad M Al-Fadhli, Olusegun Mojiminiyi.   

Abstract

INTRODUCTION: Patients with thalassemia major often present with a hypercoagulable state, the pathogenesis of which is still not understood.
MATERIALS AND METHODS: This study evaluates the risk factors for hypercoagulability in 50 beta-thalassemia major patients and 50 healthy controls. Fasting total homocysteine, protein C (PC), protein S (PS), antithrombin (AT), activated protein C resistance (APCR) and lupus anticoagulant (LA) were assessed. MTHFR C677T mutation was determined.
RESULTS: Significant reductions in PC, PS and AT were noted in patients. Only 4% of the patients had hyperhomocysteinemia. Thirty-two percent of the patients were heterozygous and 4% were homozygous for MTHFR C677T mutation.
CONCLUSION: The natural coagulation inhibitors PC, PS and AT were significantly reduced in patients with beta-thalassemia major and were thus important risk factors for the hypercoagulable state, but hyperhomocysteinemia and MTHFR mutation do not seem to be significant risk factors for thromboembolic events. Copyright (c) 2009 S. Karger AG, Basel.

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Year:  2009        PMID: 19940469     DOI: 10.1159/000260069

Source DB:  PubMed          Journal:  Acta Haematol        ISSN: 0001-5792            Impact factor:   2.195


  5 in total

Review 1.  Pulmonary hypertension associated with thalassemia syndromes.

Authors:  Dustin R Fraidenburg; Roberto F Machado
Journal:  Ann N Y Acad Sci       Date:  2016-03-23       Impact factor: 5.691

2.  Prevalence and Determinants of Anemia and Iron Deficiency in Kuwait.

Authors:  Sameer Al Zenki; Husam Alomirah; Suad Al Hooti; Nawal Al Hamad; Robert T Jackson; Aravinda Rao; Nasser Al Jahmah; Ina'am Al Obaid; Jameela Al Ghanim; Mona Al Somaie; Sahar Zaghloul; Amani Al Othman
Journal:  Int J Environ Res Public Health       Date:  2015-07-31       Impact factor: 3.390

3.  Protein C and Anti-Thrombin-III Deficiency in Children With Beta-Thalassemia.

Authors:  Suzy Abd El Mabood; Doaa Moawad Fahmy; Ahmed Akef; Shadia El Sallab
Journal:  J Hematol       Date:  2018-05-10

4.  Unusual causes of papilledema: Two illustrative cases.

Authors:  Ha Son Nguyen; Kathryn M Haider; Laurie L Ackerman
Journal:  Surg Neurol Int       Date:  2013-04-18

5.  Impact of Genetic Polymorphism of methylenetetrahydrofolate reductase C677T on Development of Hyperhomocysteinemia and Related Oxidative Changes in Egyptian β-Thalassemia Major Patients.

Authors:  Mai A Abd-Elmawla; Sherine M Rizk; Ilham Youssry; Amira A Shaheen
Journal:  PLoS One       Date:  2016-05-17       Impact factor: 3.240

  5 in total

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