Consumption of a green tea extract–curcumin drink decreases blood urea nitrogen and redox iron in β-thalassemia patients-Reference-Cited by-同舟云学术

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Consumption of a green tea extract–curcumin drink decreases blood urea nitrogen and redox iron in β-thalassemia patients

Published:2020 Issue:1 Volume:11 Page:932-943
ISSN:2042-6496
Container-title:Food & Function
language:en
Short-container-title:Food Funct.

Author:

Koonyosying Pimpisid¹²³⁴⁵^ORCID,Tantiworawit Adisak⁶²³⁴⁵^ORCID,Hantrakool Sasinee⁶²³⁴⁵^ORCID,Utama-ang Niramon⁷⁸³⁴⁵,Cresswell Michael¹²³⁴⁵,Fucharoen Suthat⁹¹⁰¹¹¹²⁵^ORCID,Porter John B.¹³¹⁴¹⁵¹⁶^ORCID,Srichairatanakool Somdet¹²³⁴⁵^ORCID

Affiliation:

1. Department of Biochemistry

2. Faculty of Medicine

3. Chiang Mai University

4. Chiang Mai 50200

5. Thailand

6. Department of Internal Medicine

7. Department of Product Development Technology

8. Faculty of Agro-Industry

9. Thalassemia Research Center

10. Institute of Molecular Bioscience

11. Mahidol University Salaya Campus

12. Nakornpathom 73170

13. Department of Haematology

14. University College London

15. London WC1E 6BT

16. UK

Abstract

The most important cause of death in β-thalassemia major patients is organ dysfunction due to iron deposits.

Funder

Royal Golden Jubilee (RGJ) Ph.D. Programme

National Research Council of Thailand

Chiang Mai University

National Science and Technology Development Agency

Publisher

Royal Society of Chemistry (RSC)

Subject

General Medicine,Food Science

Link

http://pubs.rsc.org/en/content/articlepdf/2020/FO/C9FO02424G

Reference68 articles.

1. Body iron metabolism and pathophysiology of iron overload

2. Renal function in pediatric patients with β-thalassemia major

3. Efficacy and safety of iron-chelation therapy with deferoxamine, deferiprone, and deferasirox for the treatment of iron-loaded patients with nontransfusion-dependent thalassemia syndromes

4. Optimizing iron chelation strategies in β-thalassaemia major

5. A randomized, controlled study evaluating effects of amlodipine addition to chelators to reduce iron loading in patients with thalassemia major

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