2016
DOI: 10.1155/2016/3046373
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Potential Effects of Silymarin and Its Flavonolignan Components in Patients withβ-Thalassemia Major: A Comprehensive Review in 2015

Abstract: Major β-thalassemia (β-TM) is one of the most common inherited hemolytic types of anemia which is caused as a result of absent or reduced synthesis of β-globin chains of hemoglobin. This defect results in red blood cells lysis and chronic anemia that can be treated by multiple blood transfusions and iron chelation therapy. Without iron chelation therapy, iron overload will cause lots of complications in patients. Antioxidant components play an important role in the treatment of the disease. Silymarin is an ant… Show more

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Cited by 19 publications
(14 citation statements)
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“…In one review article, patients with beta thalassemia received silymarin (420 mg/day) and desferrioxamine for 9 months to reduce iron and serum ferritin levels. In this study, silymarin was safe, and no adverse reactions occurred (Darvishi Khezri et al, ). For evaluation of iron‐chelating effect of silybin, patients with hereditary haemochromatosis ingested 140‐mg silybin (Legalon® Forte) daily for 12 weeks.…”
Section: Safety and Adverse Reactions Of Oral Silymarin In Humansmentioning
confidence: 62%
“…In one review article, patients with beta thalassemia received silymarin (420 mg/day) and desferrioxamine for 9 months to reduce iron and serum ferritin levels. In this study, silymarin was safe, and no adverse reactions occurred (Darvishi Khezri et al, ). For evaluation of iron‐chelating effect of silybin, patients with hereditary haemochromatosis ingested 140‐mg silybin (Legalon® Forte) daily for 12 weeks.…”
Section: Safety and Adverse Reactions Of Oral Silymarin In Humansmentioning
confidence: 62%
“…Some of the antioxidant compounds under investigation are food products or herbal extracts, which are used as supplements or form part of the normal diet (e.g. vitamin E [784] , [786] , [787] , resveratrol [788] , curcuminoids [784] , [789] , N -acetylcysteine [785] ), CoQ10 [790] , green tea [791] , fermented papaya preparation [792] , or the thistle Silybum marianum (L.) extract silymarin [793] , [794] .…”
Section: Toxin and Bacteria-mediated Ros Formation And Antioxidant Stmentioning
confidence: 99%
“…β‐Thalassemia major (β‐TM), a hereditary haemolytic anaemia, is common in the Mediterranean region (Rund & Rachmilewitz, ). Regular and multiple blood transfusions are the main treatments for β‐TM (Darvishi Khezri et al, ). Transfusion leads to iron overload and serious complications, such as liver and cardiac impairments, immune dysfunctions, and endocrine deficiencies (Rund & Rachmilewitz, ).…”
Section: Introductionmentioning
confidence: 99%
“…Transfusion leads to iron overload and serious complications, such as liver and cardiac impairments, immune dysfunctions, and endocrine deficiencies (Rund & Rachmilewitz, ). Standard iron chelators, such as deferoxamine (DFO), deferasirox (DFX), and deferiprone (DFP), can attenuate excess iron in the body and prevent complications in patients with β‐TM (Darvishi Khezri et al, ). DFO is the standard treatment for iron overload, but regular painful subcutaneous administration of this drug prevents optimal compliance (Moayedi Esfahani, Reisi, & Mirmoghtadaei, ).…”
Section: Introductionmentioning
confidence: 99%