Relationships Of Vitamin D And Vitamin B12 With Malonaldehyde In Patients With Beta Thalassemia Major

نویسندگان

چکیده

Background: Beta thalassemia major (Cooley's anemia) is a congenital genetic blood disorder resulting from deficiency of β-globin chains due to severe anemia that depends on continuous transfusions for survival. Patients suffer hemoglobinopathy, infection, diabetes mellitus, growth retardation, enlargement and damage the liver spleen, bone marrow aplasia delayed sexual maturity. This complication arises accumulation iron, impairment antioxidants vitamins, an increase in lipid peroxides (MDA).Objectives: The study aimed evaluate vitamin D B12 levels their relationship with MDA, enzymes (AST, ALT, ALP), iron (Total Billirubin, Direct Indirect Billirubin).Materials methods: samples BTM patients under were (100 samples), (50 samples) both males females. Patients' ages ranged (2-30 years). While control sample was (40), (20 each two sexes. Their disease confirmed by tests, hemoglobin electrophoresis, DNA analysis, elevated ferritin levels. Vitamin assessed immunoassay. (MDA, Fe, AST, ALP) Billirubin) evaluated colorimetric methods.Results: decreased significantly (p≤0.05). increased at (p≤0.05) compared group. Where effect according results clear age.
 conclusion: Our indicate weakness antioxidant systems (vitamin B12) oxidative factors complications led exacerbation overload, causing blood, damaging spleen.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

The Comparison of Serum Vitamin D Level in Patients with Iron Deficiency Anemia and Minor Thalassemia

Abstract Background and Objective: Of the most common hypochromic microcytic anemia are iron deficiency anemia and minor thalassemia, which are common in Iran and their differential diagnosis is extremely important. The level of 25-hydroxy vitamin D is the indication of vitamin D blood status. The aim of this study was to compare serum levels of vitamin D in people with minor thalassemi...

متن کامل

Prevalence of HCVAb and HBsAg in Patients with Beta-thalassemia Major in Amirkola Thalassemia Center

Background and purpose: Beta-thalassemia major is a genetic disorder with known globin defect that leads to chronic hemolytic anemia. Due to the need for recurrent blood transfusion, the risk of infectious diseases such as hepatitis is higher in these patients. Materials and methods: This cross-sectional study recruited 518 patients with thalassemia major in Amirkola Thalassemia Center, 2013-2...

متن کامل

Cytokine Gene Polymorphisms in Iranian Patients with Beta-Thalassemia Major

Background: β-thalassemia as a hereditary disease is defined as defective synthesis of   β-globin chains, resulting in erythropoiesis abnormalities and severe anemia. Different studies have shown that cytokines and cytokine gene polymorphisms play a major role in the pathogenesis of   β-thalassemia. Single nucleotide polymorphisms (SNPs) within the promoter region or other regulatory sequences ...

متن کامل

Quality of Life and Some Related Factors in Patients With Beta Thalassemia Major in Southwest Iran

Background: Thalassemia is one of the most common genetic disorders in the world, especially in Iran. The study of various aspects affecting the physical and mental health of patients with beta thalassemia major has become more important. The aim of this study was to evaluate the Quality of life and some related factors in patients with beta-thalassemia major in Southwest Iran. Methods: In thi...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Journal of Namibian Studies : History Politics Culture

سال: 2023

ISSN: ['1863-5954']

DOI: https://doi.org/10.59670/jns.v33i.1093