Evaluation of Ischaemia Modified Albumin as a Marker of Oxidative Stress in Beta Thalassemia Major Children

نویسندگان

چکیده


 Introduction: Iron overload in thalassemia catalyses the production of a variety reactive oxygen species leading to cumulative cell damage. Ischemia modified albumin (IMA) is an end product oxidative stress. It imperative pick up stress early order prevent organ damage thalassemia. Therefore this study was undertaken estimate IMA levels and see correlation between ferritin establish whether can be proxy marker for stress.
 Methods: A total 76 children were included out which 46 diagnosed cases β- Thalassemia major 30 formed healthy controls. Pre transfusion haemoglobin, AST, ALT, estimated compared with control children. Correlation drawn IMA.
 Results: There significant elevation level as controls (p = < 0.001). positive negative haemoglobin % IMA. Regression relationship established that (ng/ mL) 246.118 + 0.829 (Ferritin ng/dL).
 Conclusions: significantly elevated correlated positively levels. By establishing regression levels, we fairly Hence, utilise instead

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

Evaluation of ischaemia-modified albumin as a marker of myocardial ischaemia in end-stage renal disease.

The early diagnosis of myocardial ischaemia is problematic in patients with ESRD (end-stage renal disease). The aim of the present study was to determine whether IMA (ischaemia-modified albumin) increases during dobutamine stress and detects myocardial ischaemia in patients with ESRD. A total of 114 renal transplant candidates were studied prospectively, and all received DSE (dobutamine stress ...

متن کامل

Predicting Factors of Atherosclerosis in Children with Beta-Thalassemia Major

Background: Atherosclerosis is an important cardiovascular disorder in beta-thalassemia major patients. The present study aimed to predict factors of atherosclerosis in children with beta-thalassemia major. Materials and Methods: This cross-sectional study was conducted on 36 patients with beta-thalassemia major and 36 healthy children as the control group. The carotid intima-media thickness ...

متن کامل

Frequency of Celiac Disease in Children with Beta Thalassemia major

Background We aimed to investigate the frequency of celiac disease in children with β-thalassemia major (B-TM) in Shiraz, southern Iran. Materials and Methods In this study, the prevalence of celiac disease in children with B-TM was evaluated. Children with BTM were screened for celiac disease by ant-tissue transglutaminase (anti-tTG) IgA antibody, IgA level and anti-tTG IgG. A total o...

متن کامل

Serum Antioxidant Levels in Children with Beta-Thalassemia Major

Background: Thalassemia represents a serious health problem in Iran because of its heterogeneous frequency and the existing endogamy system. It is an inherited blood disease characterized by the under production of normal hemoglobin, the oxygen-carrying protein in red blood cells. Materials and Methods: In this study, serum antioxidants including selenium (Se), zinc (Zn) and copper (Cu) were m...

متن کامل

Assessment of Hypothyroidism in Children with Beta-Thalassemia Major in North Eastern Iran

Abstract Background Hypothyroidism usually appears in the second decade of life and is thought to be associated with iron overload in patients with thalassemia major. This study aimed to evaluate thyroid dysfunctions in patients with beta-thalassemia major. Materials and Methods This research is a descriptive – cross sectional study, carried out in 2009 to assess thyroid function in 100 p...

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 Nepal Paediatric Society

سال: 2021

ISSN: ['1990-7982', '1990-7974']

DOI: https://doi.org/10.3126/jnps.v41i1.29931