Gamma‐glutamyltransferase: a predictive biomarker of cellular antioxidant inadequacy and disease risk

G Koenig, S Seneff - Disease markers, 2015 - Wiley Online Library
Gamma‐glutamyltransferase (GGT) is a well‐established serum marker for alcohol‐related
liver disease. However, GGT's predictive utility applies well beyond liver disease: elevated …

Beta‐thalassemia major and female fertility: the role of iron and iron‐induced oxidative stress

P Roussou, NJ Tsagarakis, D Kountouras, S Livadas… - Anemia, 2013 - Wiley Online Library
Endocrine complications due to haemosiderosis are present in a significant number of
patients with beta‐thalassemia major (BTM) worldwide and often become barriers in their …

Taurine supplementation reduces oxidative stress and protects the liver in an iron-overload murine model

Z Zhang, D Liu, B Yi, Z Liao… - Molecular …, 2014 - spandidos-publications.com
We previously demonstrated that iron overload induces liver damage by causing the
formation of reactive oxygen species (ROS). Taurine is a potent free radical scavenger that …

[HTML][HTML] Hematological and biochemical status of Beta-thalassemia major patients in Bangladesh: A comparative analysis

MF Karim, M Ismail, AKMM Hasan… - International journal of …, 2016 - ncbi.nlm.nih.gov
Background: Thalassemia is one of the most common hereditary disorders and Beta-
thalassemia major is its severe form. The present study is concerned with the analysis of …

Potential Effects of Silymarin and Its Flavonolignan Components in Patients with β‐Thalassemia Major: A Comprehensive Review in 2015

H Darvishi Khezri, E Salehifar… - Advances in …, 2016 - Wiley Online Library
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 …

Oxidative status and plasma lipid profile in β-thalassemia patients

N Boudrahem-Addour, M Izem-Meziane… - …, 2015 - Taylor & Francis
Abstract β-Thalassemia (β-thal) is a genetic disorder, representing a major health problem in
Algeria. It is associated with altered lipid levels and a state of oxidative stress that can lead …

Increased levels of advanced glycation end products positively correlate with iron overload and oxidative stress markers in patients with β-thalassemia major

MS Mirlohi, H Yaghooti, S Shirali, A Aminasnafi… - Annals of …, 2018 - Springer
The impaired biosynthesis of the β-globin chain in β-thalassemia leads to the accumulation
of unpaired alpha globin chains, failure in hemoglobin formation, and iron overload due to …

Iron Overload in Transfusion‐Dependent Indonesian Thalassemic Patients

PI Fianza, A Rahmawati, SH Widihastha, S Afifah… - Anemia, 2021 - Wiley Online Library
Thalassemia is a genetic disease caused by disruption of globin chain synthesis leading to
severe anemia and thus regular blood transfusion is necessary. However, there have been …

Endothelin-1 gene polymorphism (G8002A) and endothelial monocyte-activating polypeptide II: Role in vascular dysfunction in pediatric patients with β-thalassemia …

AAG Tantawy, MAR Tadros, AAM Adly, EAR Ismail… - Cytokine, 2023 - Elsevier
Abstract Background: Endothelin-1 (ET-1), a potent endogenous vasoconstrictor, stimulates
production of reactive oxygen species. Endothelial monocyte-activating polypeptide-II …

[HTML][HTML] Silibinin: an old drug for hematological disorders

H Zou, XX Zhu, GB Zhang, Y Ma, Y Wu, DS Huang - Oncotarget, 2017 - ncbi.nlm.nih.gov
ABSTRACT Introduction: Silibinin (silybin), a non-toxic natural polyphenolic flavonoid, is the
principal and the most biologically active component of silymarin. It is efficient in the …