首页> 美国卫生研究院文献>Advances in Hematology >The Iron Status of Sickle Cell Anaemia Patients in Ilorin North Central Nigeria
【2h】

The Iron Status of Sickle Cell Anaemia Patients in Ilorin North Central Nigeria

机译:尼日利亚中北部伊洛林镰刀状细胞贫血患者的铁状况

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Objectives. Sickle cell anaemia (SCA) is one of the commonest genetic disorders in the world. It is characterized by anaemia, periodic attacks of thrombotic pain, and chronic systemic organ damage. Recent studies have suggested that individuals with SCA especially from developing countries are more likely to be iron deficient rather than have iron overload. The study aims to determine the iron status of SCA patients in Ilorin, Nigeria. Methods. A cross-sectional study of 45 SCA patients in steady state and 45 non-SCA controls was undertaken. FBC, blood film, sFC, sTfR, and sTfR/log sFC index were done on all subjects. Results. The mean patients' serum ferritin (589.33 ± 427.61 ng/mL) was significantly higher than the mean serum ferritin of the controls (184.53 ± 119.74 ng/mL). The mean serum transferrin receptor of the patients (4.24 ± 0.17 μg/mL) was higher than that of the controls (3.96 ± 0.17 μg/mL) (p = 0.290). The mean serum transferrin receptor (sTfR)/log serum ferritin index of the patients (1.65 ± 0.27 μg/mL) was significantly lower than that of the control (1.82 ± 0.18 μg/mL) (p = 0.031). Conclusion. Iron deficiency is uncommon in SCA patients and periodic monitoring of the haematological, biochemical, and clinical features for iron status in SCA patients is advised.
机译:目标。镰状细胞性贫血(SCA)是世界上最常见的遗传性疾病之一。它的特点是贫血,血栓性疼痛的定期发作和慢性全身器官损害。最近的研究表明,尤其是来自发展中国家的患有SCA的人更容易缺铁而不是铁过载。这项研究旨在确定尼日利亚伊洛林的SCA患者的铁状况。方法。进行了一项横断面研究,包括45位处于稳态的SCA患者和45位非SCA对照。对所有受试者进行FBC,血膜,sFC,sTfR和sTfR / log sFC指数。结果。患者的平均血清铁蛋白(589.33±427.61 ng / mL)显着高于对照组的平均血清铁蛋白(184.53±119.74ng / mL)。患者的平均血清转铁蛋白受体(4.24±0.17μg/ mL)高于对照组(3.96±0.17μg/ mL)(p = 0.290)。患者的平均血清转铁蛋白受体(sTfR)/ log铁蛋白指数(1.65±0.27μg/ mL)显着低于对照组(1.82±0.18μg/ mL)(p = 0.031)。结论。铁缺乏症在SCA患者中很少见,建议定期监测SCA患者铁的血液学,生化和临床特征。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号