Study of calcium metabolism in Beta-Talassemia major patients

نویسندگان

  • A.GH Mashhadi esmaeil
  • M GHanei Assistant professor
  • M Hekmat
چکیده مقاله:

disturbances in calcium metabolism and both impairment are some of the known complications observed in beta thalassemia major patients.although iron deposition has been recognized to be the main factor for organ dysfunction in these patients,the relatively low prevalence of hypoparathyroidism has led to giving more emphasis to Ca metabolism disturbance among others.availability of more patients compared to the previous studies was the determining facto in doing this study.in this descriptional study of 700 major thalassemic patients in seyed-al-shohada hospital in june 1995,a population of 153 patients were selected based on simple random sampling before transfusion.analusis of serum Ca,p,alkaline phosphatase,ferretin,Mg,albumine and liver function tests were performed prior to transfusion and on fasting blood.samples were taken on average a month after blood transfusion history was taken and with proper grouping.the results were analused.ten patients(6.3%) had hypocalcemia and one patient with a low serum PTH,low serum albumin in another patient rejected true hypocalcemia.all other patients had normal PTH& serum P,expect one patient who had low serum P.thus it is possible to conclude that patients with hypocalcemia,low or normal PTH, high or normal P had hypoparathyroidism.there was also a significant correlation between different age groups & ferritin,BMI:correlation between different BMI groups & age,Ca was significant,too.yet,the correlation between serum P& number of transfusion in tha last three months was significant(p<0.05).the relative prevelance of hypothroidism was about 3.6%.it seemed that calcium disturbance in these patients was due to factors other than low PTH.the correlation between Ca & number of transfusion in the last three months suggests that P increases has been the result if an increase in hemolysis.this also suggests that because of the same reason  & also due to malabsorbtion &liver dysfunction,there has been a disturbance in Ca metamolism.these rerults imply that prescribing Ca & vit D will be applicable and useful in most of the patients.

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

Endocrine Disorders in Beta thalassemia Major Patients

Background Thalassemia is the most common hereditary disorder worldwide. The patient's’ survival is dependent on lifetime blood transfusion which leads to iron overload and its toxicity on various organs including endocrine glands. The study aimed to investigate endocrine disorders in patients with Beta-thalassemia major in the Southern Khorasan province, Iran. Materials and Methods In this des...

متن کامل

A Study of Leptin Serum Concentrations in Patients with Major Beta-Thalassemia

Background The aim of this study was to evaluate leptin serum levels in patients with major beta thalassemia which was also associated with their ferritin serum levels. Materials and Methods This case-control study was performed on 90 children -6 months to 16 years old, in Zabol, Amir- al- Momenin Hospital. Patients were divided in two groups and were matched in age and sex. All Children w...

متن کامل

Prevalence of Major Depressive and Anxiety Disorders in Hemophilic and Major Beta Thalassemic Patients

Abstract Background The purpose of this study was to assess the prevalence of major depressive and anxiety disorders in hemophilic and major beta thalassemic patients related to education of their mothers as a family’s agent. Materials and Methods A case-control study was performed on 34 major beta thalassemic patients. For each patient the control group was selected and matched (with age a...

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

faculty of psychology and social sciences group of anthropology master thesis in major of anthropology

چکیده پایان نامه (شامل خلاصه، اهداف، روش های اجرا و نتایج به دست آمده): کار جمع آوری گو یش های محلی در سال های اخیر شتاب امیدوار کننده ای به خود گرفته است. شاید از بارزترین اهداف جمع آوری گویش های مختلف، ثبت و ضبط آن، جلوگیری از نابودی و مهمتر از همه حل مشکلات دستوری زبان رسمی باشد. دقت در فرآیند های زبانی گویش های محلی نوع ارتباط مردم نواحی مختلف با پیرامون نشان را به ما نشان خواهد داد. از س...

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

منابع من

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

ذخیره در منابع من قبلا به منابع من ذحیره شده

{@ msg_add @}


عنوان ژورنال

دوره 3  شماره 1

صفحات  32- 37

تاریخ انتشار 1996-12-01

با دنبال کردن یک ژورنال هنگامی که شماره جدید این ژورنال منتشر می شود به شما از طریق ایمیل اطلاع داده می شود.

میزبانی شده توسط پلتفرم ابری doprax.com

copyright © 2015-2023