Literature DB >> 33216196

Effects of three months of treatment with vitamin E and N-acetyl cysteine on the oxidative balance in patients with transfusion-dependent β-thalassemia.

Sezaneh Haghpanah1, Nader Cohan1, Mohammadreza Bordbar1, Asghar Bazrafshan1, Mehran Karimi1, Soheila Zareifar1, Sanaz Safaei1, Azam Aramesh1, Mohamad Moghadam1, Saeid Amiri Zadeh Fard2, Omid Reza Zekavat3.   

Abstract

Oxidative stress is a major mechanism contributing to the progression of β-thalassemia. To assess the effect of vitamin E and N-acetyl cysteine (NAC) as antioxidant agents on total oxidative stress (TOS) status and total antioxidant capacity (TAC) in patients with transfusion-dependent β-thalassemia (TDT). In this open-label randomized controlled trial, from May to August 2019, 78 eligible patients with TDT over the age of 18 were enrolled. All patients were registered at the Thalassemia Clinic of Shiraz University of Medical Sciences in Southern Iran. Patients were randomly allocated to the NAC group (10 mg/kg/day, orally), vitamin E group (10 U/kg/day, orally), and control group. The duration of the study was 3 months. The mean age of the participants was 28.5 ± 5.1 (range: 18-41) years. At the end of the study, TOS significantly decreased only in the vitamin E group (mean difference (MD), 95% confidence interval (CI): 0.27 (0.03-0.50), P = 0.026). TAC significantly decreased in both supplemented groups at the 3rd month of treatment (NAC group: MD (95% CI): 0.11 (0.04-0.18), P = 0.002 and vitamin E group: 0.09 (0.01-0.16), P = 0.022 respectively). Hemoglobin did not significantly change at the end of the study in each group (P > 0.05). Mild transient adverse events occurred in 4 patients of the NAC group and 5 patients of the vitamin E group with no need to discontinue the treatment. Vitamin E can be a safe and effective supplement in improving oxidative stress in patients with TDT. Moreover, it seems that a longer duration of using antioxidant supplements needs to make clinical hematologic improvement in TDT patients.

Entities:  

Keywords:  Antioxidants; N-Acetyl cysteine; Oxidative stress; Vitamin E; β-thalassemia

Mesh:

Substances:

Year:  2020        PMID: 33216196     DOI: 10.1007/s00277-020-04346-2

Source DB:  PubMed          Journal:  Ann Hematol        ISSN: 0939-5555            Impact factor:   3.673


  4 in total

1.  Antioxidant status in children with homozygous thalassemia.

Authors:  Veena Dhawan; Kh Ratan Kumar; R K Marwaha; Nirmal K Ganguly
Journal:  Indian Pediatr       Date:  2005-11       Impact factor: 1.411

2.  Clinical safety of high oral doses of acetylcysteine.

Authors:  L F Miller; B H Rumack
Journal:  Semin Oncol       Date:  1983-03       Impact factor: 4.929

3.  Oxidative stress in patients with beta-thalassemia major.

Authors:  L E Pavlova; V M Savov; H G Petkov; I P Charova
Journal:  Prilozi       Date:  2007-07

4.  Total Antioxidant Status in Patients with Major β-Thalassemia.

Authors:  Fatemeh Bazvand; Sedigheh Shams; Mahtab Borji Esfahani; Lili Koochakzadeh; Maryam Monajemzadeh; Mohammad-Taghi Haghi Ashtiani; Nima Rezaei
Journal:  Iran J Pediatr       Date:  2011-06       Impact factor: 0.364

  4 in total
  1 in total

Review 1.  Redox Balance in β-Thalassemia and Sickle Cell Disease: A Love and Hate Relationship.

Authors:  Rayan Bou-Fakhredin; Lucia De Franceschi; Irene Motta; Assaad A Eid; Ali T Taher; Maria Domenica Cappellini
Journal:  Antioxidants (Basel)       Date:  2022-05-13
  1 in total

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