期刊文献+

肝豆状核变性患者尿铜及血清铜的测定对临床诊断的意义 被引量:3

Clinical diagnosis significance of urine copper and serum copper determination on patients with hepatolenticular degeneration
原文传递
导出
摘要 目的:探讨肝豆状核变性与尿铜和血清铜的相关性及其对临床诊断及治疗的意义。方法在血清样品和尿样中加入一定量的硝酸溶液使其酸度为1%,石墨炉原子吸收光谱法测定其中的铜含量。结果尿铜和血清铜对于肝豆状核变性均不具有单独的诊断价值,但他们确是诊断肝豆状核变性的重要参考指标。该方法检出限为1.0μg/L,相对标准偏差为2.23%,方法实测加标回收率为94%~104%。结论尿铜及血清铜检测已广泛应用于临床样本的测定,对指导肝豆状核变性患者的康复有良好的辅助作用。 Objective To investigate the relationship between urine copper and serum copper in patients with hepatolenticular degeneration and their significance on clinical diagnosis and treatment. Methods A method for the determination of copper in urine and serum in hepatolenticular degeneration patient was developed,take 1% of nitric acid to nitrify the serum and urine,and use Graphite furnace a-tomic absorption to detect. Results The results showed that urine copper and serum copper contents were really important reference index for diagnosing the disease,although they did not have separate diag-nosing significance. The detection limit of copper was 1. 00 μg/L,the relative standard deviation was 2. 23%. The recovery rates was 94% -104%. Conclusions Determination of urine copper and serum copper has been applied to detect the clinical samples and played a good role for the hepatolenticular de-generation patient’s rehabilitation.
出处 《中国实用医刊》 2016年第15期42-43,共2页 Chinese Journal of Practical Medicine
关键词 肝豆状核变性 血清铜 尿铜 Hepatolenticular degeneration Serum copper Urine copper
  • 相关文献

参考文献4

二级参考文献26

  • 1阎正,孙汉文,张建申,李迎霞,朱兵.微量注射进样一阶导数火焰原子吸收分光光度法测定耳全血铜含量[J].光谱学与光谱分析,1994,14(5):63-67. 被引量:5
  • 2陈红英.肝豆状核变性病人24小时尿铜、血清铜、血清铜蓝蛋白含量测定[J].实用预防医学,2001,8:148-148.
  • 3Roberts EA, Schilsky MI. Diagnosis and treatment of Wilson disease: Anupdate [J]. Hepatology, 2008, 47 (6): 2089- 2111.
  • 4Ferenci P, Caca K, Loudianeos G, et al. Diagnosis and phenotypie classification of Wilson disease [J]. Liver Int, 2003, 23 (3): 139-142.
  • 5Roberts EA, Schilsky MI. A practice guideline on Wilson disease [J]. Hepatology, 2003, 37 (6): 1475-1492.
  • 6Bull PC, Thomas GR, Rommerns JM, et al. The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene [J]. Nat Genet, 1993, 5 (4): 327.
  • 7Bewer GJ. Chapter 3: Simple approaches to screening and definitive diagnosis [A] In Brewer GJ, Eds. Wilson disease: A clinician ' s guide to recognition, diagnosis, and management [ M ] Netherlands: Kluwer Academec Publishers, 2001.
  • 8Martins da Costa C, Baldwin D, Portmann B, et al. Value of urinary copper excretion after penicillamine challenge in the diagnosis of Wilson disease [J]. Hepatology, 1992, 15 (4) :609- 615.
  • 9Sternlieb I. Wilson's disease [J].Clin Liver Dis, 2000, 4(1 ) : 229- 239.
  • 10Steindl P, Ferenci P, Dienes HP, et al. Wilson's disease in patients presenting with liver disease: a diagnostic challenge [ J]. Gastroenterology, 1997, 113(1): 212-218.

共引文献28

同被引文献23

引证文献3

二级引证文献6

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部