• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

[不同基因型地中海贫血患儿铁代谢指标的变化]

[Changes of iron metabolism indices in children with various genotypes of thalassema].

作者信息

Huang Yu-Jun, Wu Shao-Guo, Ou Xiao-Bing, Zhang Li

机构信息

Guangzhou Women and Children's Medical Center, Guangzhou 510120, China.

出版信息

Zhongguo Dang Dai Er Ke Za Zhi. 2010 Feb;12(2):85-8.

PMID:20199717
Abstract

OBJECTIVE

To study the value of iron metabolism indices, serum iron (SI), total iron blinding capacity (TIBC) and transferring (Tf), in thalassema.

METHODS

The serum samples from 9 children with silent alpha thalassema, 56 with standard alpha thalassema, 26 with HbH disease, 40 with beta+ thalassema, 56 with beta0 thalassema, 45 with iron deficiency anemia (IDA) and 70 healthy children were detected for SI, TIBC and Tf levels.

RESULTS

The SI level increased (p<0.01), while the TIBC level decreased significantly in the beta0 thalassema group compared with those in the other groups (p<0.05 or 0.01), but the Tf level was not different. The Tf level of both the silent alpha thalassema and the standard alpha thalassema groups was statistically lower than that of the healthy group (p<0.01), but the levels of SI and TIBC were similar to the healthy group. Though the SI level of the HbH disease group was similar to the healthy group, the TIBC and Tf levels were statistically lower (p<0.01).

CONCLUSIONS

Compared with Tf, SI and TIBC are better indices for monitoring iron loading in children with thalassema. The increased SI level and decreased TIBC level are two indices for the diagnosis of beta(0) thalassema in children with cellule anaemia.

摘要

目的

研究铁代谢指标血清铁(SI)、总铁结合力(TIBC)和转铁蛋白(Tf)在地中海贫血中的价值。

方法

检测9例静止型α地中海贫血患儿、56例标准型α地中海贫血患儿、26例血红蛋白H病患儿、40例β+地中海贫血患儿、56例β0地中海贫血患儿、45例缺铁性贫血(IDA)患儿及70例健康儿童的血清SI、TIBC和Tf水平。

结果

与其他组相比,β0地中海贫血组SI水平升高(p<0.01),TIBC水平显著降低(p<0.05或0.01),但Tf水平无差异。静止型α地中海贫血组和标准型α地中海贫血组的Tf水平均低于健康组(p<0.01),但SI和TIBC水平与健康组相似。血红蛋白H病组SI水平与健康组相似,但TIBC和Tf水平低于健康组(p<0.01)。

结论

与Tf相比,SI和TIBC是监测地中海贫血患儿铁负荷的更好指标。SI水平升高和TIBC水平降低是诊断细胞贫血患儿β(0)地中海贫血的两个指标。

相似文献

1
[Changes of iron metabolism indices in children with various genotypes of thalassema].[不同基因型地中海贫血患儿铁代谢指标的变化]
Zhongguo Dang Dai Er Ke Za Zhi. 2010 Feb;12(2):85-8.
2
[Status of iron metabolism and erythropoietic proliferation in children with various genotypes of thalassemia].[不同基因型地中海贫血患儿铁代谢及红细胞生成增殖状况]
Zhongguo Dang Dai Er Ke Za Zhi. 2010 Aug;12(8):602-4.
3
Evaluation of soluble transferring receptor levels in children with iron deficiency and beta thalassemia trait, and in newborns and their mothers.缺铁性贫血和β地中海贫血特质儿童以及新生儿及其母亲血清可溶性转铁蛋白受体水平的评估
Turk J Pediatr. 2002 Oct-Dec;44(4):289-93.
4
High serum transferrin receptor level in anemia of chronic disorders indicates coexistent iron deficiency.慢性病性贫血患者血清转铁蛋白受体水平升高表明存在合并缺铁。
Am J Hematol. 2003 Mar;72(3):158-61. doi: 10.1002/ajh.10260.
5
Absorption of iron from grape-molasses and ferrous sulfate: a comparative study in normal subjects and subjects with iron deficiency anemia.葡萄糖浆和硫酸亚铁中铁的吸收:正常受试者与缺铁性贫血受试者的对比研究
Turk J Pediatr. 1997 Oct-Dec;39(4):465-71.
6
[Comparison of indirect and direct measurement of transferrin in healthy and sick children (author's transl)].健康与患病儿童中转铁蛋白间接与直接测量的比较(作者译)
Monatsschr Kinderheilkd. 1980 Sep;128(9):598-601.
7
Hemoglobinization and functional availability of iron for erythropoiesis in case of thalassemia and iron deficiency anemia.地中海贫血和缺铁性贫血时红细胞生成中铁的血红蛋白化及功能可用性
Clin Lab. 2006;52(3-4):107-14.
8
Total iron binding capacity or transferrin concentration alone outperforms iron and saturation indices in predicting iron deficiency.单独的总铁结合力或转铁蛋白浓度在预测缺铁方面比铁和饱和度指标表现更优。
Clin Chim Acta. 2007 May 1;380(1-2):203-7. doi: 10.1016/j.cca.2007.02.032. Epub 2007 Feb 23.
9
α-Thalassemia frequency and mutations in children with hypochromic microcytic anemias and relation with β-thalassemia, iron deficiency anemia.低色素小细胞性贫血患儿中α地中海贫血的频率和突变及其与β地中海贫血、缺铁性贫血的关系
Pediatr Hematol Oncol. 2012 Apr;29(3):241-6. doi: 10.3109/08880018.2012.661831.
10
The correlation of transferrin saturation and ferritin in non-splenectomized thalassemic children.非脾切除的地中海贫血患儿中转铁蛋白饱和度与铁蛋白的相关性
J Med Assoc Thai. 1999 Nov;82 Suppl 1:S74-6.