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本文引用的文献

1
A cross-sectional study of metabolic and endocrine complications in beta-thalassemia major.重型β地中海贫血代谢与内分泌并发症的横断面研究
Ann Saudi Med. 2008 Sep-Oct;28(5):361-6. doi: 10.5144/0256-4947.2008.361.
2
Spermatogenesis in young adult patients with beta-thalassaemia major long-term treated with desferrioxamine.长期接受去铁胺治疗的成年重型β地中海贫血患者的精子发生
Georgian Med News. 2008 Mar(156):74-7.
3
Evaluation of some essential element levels in thalassemia major patients in Mosul district, Iraq.伊拉克摩苏尔地区重型地中海贫血患者某些必需元素水平的评估
Saudi Med J. 2008 Jan;29(1):94-7.
4
Prevention of overwhelming postsplenectomy infection in thalassemia patients by partial rather than total splenectomy.通过部分脾切除术而非全脾切除术预防地中海贫血患者脾切除术后暴发性感染。
Can J Surg. 2007 Oct;50(5):382-6.
5
Failure of puberty in Egyptian beta thalassemic patients: experience in north east region - Dakahlia province.埃及β地中海贫血患者青春期发育迟缓:东北地区(达卡利亚省)的经验
Hematology. 2007 Oct;12(5):449-56. doi: 10.1080/10245330701448503.
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Bone metabolism and mineral density in patients with beta-thalassemia major.重型β地中海贫血患者的骨代谢与骨密度
Saudi Med J. 2007 Sep;28(9):1425-9.
7
Growth hormone reserve in adult beta thalassemia patients.成人β地中海贫血患者的生长激素储备
Endocrine. 2007 Feb;31(1):33-7. doi: 10.1007/s12020-007-0018-7.
8
Prevalence of growth and puberty failure with respect to growth hormone and gonadotropins secretion in beta-thalassemia major.重型β地中海贫血中生长激素和促性腺激素分泌所致生长及青春期发育障碍的患病率
Arch Iran Med. 2006 Oct;9(4):329-34.
9
Seroprevalence of hepatitis C virus specific antibodies among Iraqi children with thalassaemia.伊拉克地中海贫血患儿中丙型肝炎病毒特异性抗体的血清流行率。
East Mediterr Health J. 2006 Jan-Mar;12(1-2):204-10.
10
Pubertal evaluation of adolescent boys with beta-thalassemia major and delayed puberty.对重型β地中海贫血和青春期延迟的青春期男孩进行青春期评估。
Fertil Steril. 2006 Oct;86(4):886-90. doi: 10.1016/j.fertnstert.2006.02.118.

铁过载对男性地中海贫血患者内分泌腺功能影响的研究

Study of the effect of iron overload on the function of endocrine glands in male thalassemia patients.

作者信息

Abdulzahra Mohammed Saied, Al-Hakeim Hussein Kadhem, Ridha Mahdi Muhammed

机构信息

Departments of Internal Medicine, College of Medicine, Al-Kufa University, Iraq.

出版信息

Asian J Transfus Sci. 2011 Jul;5(2):127-31. doi: 10.4103/0973-6247.83236.

DOI:10.4103/0973-6247.83236
PMID:21897589
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3159240/
Abstract

BACKGROUND

Iron overload is an important issue in the state of thalassemic patients due to the harmful effect of high concentration of iron deposited in different tissues in human body including endocrine glands. In the present work, an attempt is carried out to estimate the effect of iron overload in thalassemic patients on the function of endocrine glands through the estimation of their ability to secrete adequate amounts of certain hormones.

MATERIALS AND METHODS

Seventy eight male children with beta-thalassemia, in the age-group of 4-11 years, were enrolled for this research. These children were being treated with frequent transfusions and long-term iron chelation therapy. Thirty age and sex matched children without thalassemia constituted the control group. Ferritin and different hormones were estimated by ELISA technique.

RESULTS

The results showed a mild reduction in the function of endocrine glands through the decrease in the level of some hormones. These changes due mainly to the hypoxia and precipitation of iron in certain glands and overlapping with the synthesis or secretion of the hormones.

CONCLUSION

There is a different hormonal disturbances in beta thalassemia patients. Reduction of total body iron store is an important goal of the treatment of thalassemia and measuring the hormones concentration is necessary for the follow up of the thalassemic patients especially during puberty.

摘要

背景

由于高浓度铁沉积于人体包括内分泌腺在内的不同组织中会产生有害影响,铁过载是地中海贫血患者面临的一个重要问题。在本研究中,通过评估内分泌腺分泌适量特定激素的能力,尝试估计地中海贫血患者铁过载对内分泌腺功能的影响。

材料与方法

本研究纳入了78名4至11岁的男性β地中海贫血患儿。这些患儿接受频繁输血和长期铁螯合治疗。30名年龄和性别匹配的非地中海贫血儿童组成对照组。采用酶联免疫吸附测定(ELISA)技术测定铁蛋白和不同激素水平。

结果

结果显示,某些激素水平降低,内分泌腺功能出现轻度减退。这些变化主要归因于特定腺体中的缺氧和铁沉淀,且与激素的合成或分泌相互影响。

结论

β地中海贫血患者存在不同的激素紊乱情况。减少体内铁储存是地中海贫血治疗的一个重要目标,尤其是在青春期,测量激素浓度对于地中海贫血患者的随访是必要的。