serum lipid profiles in patients with beta-thalassemia major and intermedia in southern iran

نویسندگان

sezaneh haghpanah hematology research center, shiraz university of medical sciences, shiraz, iran

maryam davani hematology research center, shiraz university of medical sciences, shiraz, iran

behrang samadi hematology research center, shiraz university of medical sciences, shiraz, iran

afsaneh ashrafi a hematology research center, shiraz university of medical sciences, shiraz, iran.

چکیده

background: beta-thalassemia is considered to be the most frequent hereditary blood disorder worldwide. lipid abnormalities have been detected in different types of beta-thalassemia . the aim of this study is to assess the lipid profiles in beta-thalassemia major (btm) and beta-thalassemia intermedia (bti) patients in southern iran. methods: the study group consisted of 55 btm patients and 50 bti patients. the control group included 130 sex- and age-matched healthy participants. serum lipids profiles (total cholesterol, triglycerides, ldl-cholesterol, and hdl-cholesterol) as well as hemoglobin (hb) and ferritin, were compared between the three groups. p value < 0.05 was considered statistically significant. results: there were no significant differences between btm and bti patients regarding age or sex. mean triglyceride concentration was not significantly different between patients and controls. total cholesterol and ldl-cholesterol were significantly lower in patients with btm and bti in comparison with controls (p < 0.001). hdl-cholesterol was significantly lower in patients with bti than in controls (p < 0.03). conclusions: in patients with btm and bti, total cholesterol and ldl-cholesterol were lower than in control participants. the mechanisms that may account for these findings are increased erythropoiesis and cholesterol consumption in bti, and iron overload and oxidative stress in btm. keywords: beta-thalassemia major, beta-thalassemia intermedia, total cholesterol, ldl-cholesterol, hdl-cholesterol, triglycerides. normal 0 false false false microsoftinternetexplorer4

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

Serum lipid profiles in patients with beta-thalassemia major and intermedia in southern Iran

BACKGROUND Beta-thalassemia is considered to be the most frequent hereditary blood disorder worldwide. Lipid abnormalities have been detected in different types of beta-thalassemia. The aim of this study is to assess the lipid profiles in beta-thalassemia major (BTM) and beta-thalassemia intermedia (BTI) patients in southern Iran. METHODS The study group consisted of 55 BTM patients and 50 BT...

متن کامل

Malignancies in patients with beta-thalassemia major and beta-thalassemia intermedia: a multicenter study in Iran.

BACKGROUND Beta thalassemia is one of the most common genetic disorders in the world. The aim of this study was to determine the frequency, characteristics, and pattern of malignancies in patients with beta thalassemia major (BTM) and beta thalassemia intermedia (BTI) in Iran. METHODS We conducted a multicenter study via a retrospective chart review of patients with BTM and BTI between 2002 a...

متن کامل

Relationship Between Serum Hepcidin and Ferritin Levels in Patients With Thalassemia Major and Intermedia in Southern Iran

BACKGROUND Hepcidin is a key regulator of iron absorption in humans. It is mainly affected by hypoxia and iron stores. OBJECTIVES The current study aimed to determine the correlation between serum hepcidin and ferritin levels in patients with Thalassemia Major (TM) and Thalassemia Intermedia (TI). PATIENTS AND METHODS The current cross-sectional study investigated 88 randomly selected patie...

متن کامل

Serum Dickkopf-1 and Correlation with Bone Mineral Density in Patients with Beta Thalassemia Major in North-Eastern of Iran

Background and Aims: Iron overload is one of the effects of frequent transfusion in beta-thalassemia major (BTM) patients. Osteopenia and osteoporosis are the secondary complications of frequent transfusion due to toxic effects of iron on osteoblasts. Dickkopf-1 (DKK-1) is a secreted protein which plays an important role in the development of osteoporosis. The aim of this study was to investiga...

متن کامل

Bone Mineral Density in β Thalassemia Major and Intermedia, Correlation with Biochemical and Hormonal Profiles

Background: Expansion of bone marrow cavity and decreased cortical and trabecular bone tissues and osteoporosis are resulted from beta-thalassemia. The aim of this study was to assess bone mineral density (BMD) in patients with β thalassemia major and intermedia, and to determine their biochemical and hormonal profiles that may affect BMD. Materials and Methods: In a cross sectional study from ...

متن کامل

Side effects of hydroxyurea in patients with Thalassemia major and thalassemia intermedia and sickle cell anemia

Background Sickle hemoglobin is the most common abnormal hemoglobin in the United States. Hemoglobin S arises as a result of a single amino acid substitution (glutamic acid to valin at position 6 of the β-globine chain). The presence of fetal hemoglobin (HbF) plays a relatively protective role since a significant amount of HbF interferes with HbS polymerization, the pathogenesis mechanism of ...

متن کامل

منابع من

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


عنوان ژورنال:
journal of research in medical sciences

جلد ۱۵، شماره ۳، صفحات ۱۵۰-۰

میزبانی شده توسط پلتفرم ابری doprax.com

copyright © 2015-2023