Literature DB >> 33432439

The effect of curcumin on serum copper, zinc, and zinc/copper ratio in patients with β-thalassemia intermedia: a randomized double-blind clinical trial.

Mohammadreza Saeidnia1, Peyman Nowrouzi-Sohrabi2,3, Mehran Erfani4, Pooria Fazeli5, Gholamhossein Tamaddon6, Mehran Karimi7.   

Abstract

Thalassemia intermedia is a subgroup of β-thalassemia which originates from mutations in the beta-globin gene. Zinc and copper play important roles in the metabolism. Due to its significant therapeutic effects, curcumin has led many studies to focus on curcumin. In a double-blind clinical trial study, 30 patients with beta-thalassemia intermedia with an age range of 20 to 35 years were randomly selected 1:1 to receive either curcumin or placebo for 3 months. Before and after the intervention period, 5 ml of blood was taken to determine the serum levels of zinc and copper. The laboratory tests were checked at baseline and at the end of the treatment. While the serum levels of zinc and zinc/copper significantly increased, the serum levels of copper decreased after 3 months of curcumin intake. In addition, on the basis of baseline characteristics, a negative correlation was found between zinc and body mass index and positive correlations were identified between copper with triglyceride and high-density lipoprotein. Also, the level of ferritin protein in the curcumin group compared to the placebo group showed a significant decrease after 3 months of curcumin use. Therefore, it could be concluded that curcumin might exert a net protective effect on copper toxicity in thalassemia intermedia patients. The investigation also implicated that curcumin represents an approach to regulating zinc homeostasis and may be useful as a complementary treatment of patients with thalassemia intermedia, especially in patients with zinc deficiency or low serum zinc/copper ratio. Clinical Trial Registration Number: IRCT20190902044668N1.

Entities:  

Keywords:  Copper; Curcumin; Thalassemia intermedia; Zinc

Mesh:

Substances:

Year:  2021        PMID: 33432439     DOI: 10.1007/s00277-021-04397-z

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


  7 in total

1.  Analysis of serum lipid profiles, metal ions and thyroid hormones levels abnormalities in beta-thalassaemic children of Bangladesh.

Authors:  Mohammed Zubaerul Ferdaus; A K M Mahbub Hasan; Hossain Uddin Shekhar
Journal:  J Pak Med Assoc       Date:  2010-05       Impact factor: 0.781

Review 2.  Thalassemia intermedia.

Authors:  C Camaschella; M D Cappellini
Journal:  Haematologica       Date:  1995 Jan-Feb       Impact factor: 9.941

3.  Evaluation of some essential element levels in thalassemia major patients in Mosul district, Iraq.

Authors:  Abdulmunaim H Al-Samarrai; Mohaisen H Adaay; Khudhair A Al-Tikriti; Muayed M Al-Anzy
Journal:  Saudi Med J       Date:  2008-01       Impact factor: 1.484

4.  Zinc and copper status of thalassemic children.

Authors:  S Kajanachumpol; T Tatu; W Sasanakul; A Chuansumrit; P Hathirat
Journal:  Southeast Asian J Trop Med Public Health       Date:  1997-12       Impact factor: 0.267

5.  Serum copper, zinc, ceruloplasmin and superoxide dismutase in Thai overweight and obese.

Authors:  Rungsunn Tungtrongchitr; Praneet Pongpaew; Benjaluck Phonrat; Anchalee Tungtrongchitr; Duangkamol Viroonudomphol; Niyomsri Vudhivai; Frank Peter Schelp
Journal:  J Med Assoc Thai       Date:  2003-06

6.  Zinc and copper status in children with Beta-thalassemia major.

Authors:  Abolfazl Mahyar; Parviz Ayazi; Ali-Asghar Pahlevan; Hoshyar Mojabi; Mohammad-Reza Sehhat; Amir Javadi
Journal:  Iran J Pediatr       Date:  2010-09       Impact factor: 0.364

7.  Copper status in patients with thalassemia major in zahedan, iran.

Authors:  Mohamad Ali Mashhadi
Journal:  Int J Hematol Oncol Stem Cell Res       Date:  2013
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.