Urinary copper/zinc ratio: a promising parameter for replacement of 24-hour urinary copper excretion for diagnosis of Wilson's disease in children
- PMID: 20127216
- DOI: 10.1007/s12519-010-0023-4
Urinary copper/zinc ratio: a promising parameter for replacement of 24-hour urinary copper excretion for diagnosis of Wilson's disease in children
Abstract
Background: Although 24-hour urinary copper excretion is valuable for diagnosis of Wilson's disease, accurate, timed collection entails practical difficulties. This study aimed to investigate the feasibility of morning urinary copper/creatinine or copper/zinc ratio as replacement parameter for diagnosing Wilson's disease.
Methods: Five random urinary samples collected during 24 hours from two inpatients were used to estimate the consistency of urinary copper/creatinine and copper/zinc ratios. The correlation of the ratios with 24-hour urinary copper excretion was studied in 15 patients with liver diseases. The diagnostic value of morning urinary copper/zinc ratio was further studied in 9 children with Wilson's disease and 22 children with other liver diseases.
Results: The coefficients of variation of urinary copper/creatinine and copper/zinc ratios during 24 hours were 12.5% and 9.3% respectively. The morning urinary copper/creatinine ratio, copper/zinc ratio, and 24-hour urinary copper excretion were correlated well. The area under receiver-operating characteristic curve was comparable between the morning urinary copper/zinc ratio and 24-hour urinary copper excretion (0.983 vs. 0.977).
Conclusion: Morning urinary copper/zinc ratio seems to be a promising parameter in replacement of 24-hour urinary copper excretion for diagnosis of Wilson's disease.
Similar articles
-
[The reassessment of the diagnostic value of 24-hour urinary copper excretion in children with Wilson's disease].Zhonghua Gan Zang Bing Za Zhi. 2010 Jan;18(1):49-53. doi: 10.3760/cma.j.issn.1007-3418.2010.01.012. Zhonghua Gan Zang Bing Za Zhi. 2010. PMID: 20128970 Chinese.
-
Urinary 24-hour copper excretion at the time of diagnosis in children with Wilson's disease.Acta Gastroenterol Belg. 2018 Jul-Sep;81(3):410-414. Acta Gastroenterol Belg. 2018. PMID: 30350530
-
Value of urinary copper excretion after penicillamine challenge in the diagnosis of Wilson's disease.Hepatology. 1992 Apr;15(4):609-15. doi: 10.1002/hep.1840150410. Hepatology. 1992. PMID: 1551638
-
Practical recommendations and new therapies for Wilson's disease.Drugs. 1995 Aug;50(2):240-9. doi: 10.2165/00003495-199550020-00004. Drugs. 1995. PMID: 8521757 Review.
-
Wilson's disease: current status.Am J Med. 1992 Jun;92(6):643-54. doi: 10.1016/0002-9343(92)90783-8. Am J Med. 1992. PMID: 1605146 Review.
Cited by
-
Functional Characterization of Novel ATP7B Variants for Diagnosis of Wilson Disease.Front Pediatr. 2018 Apr 30;6:106. doi: 10.3389/fped.2018.00106. eCollection 2018. Front Pediatr. 2018. PMID: 29761093 Free PMC article.
-
Wilson disease in children and young adults - State of the art.Saudi J Gastroenterol. 2022 Jan-Feb;28(1):21-31. doi: 10.4103/sjg.sjg_501_21. Saudi J Gastroenterol. 2022. PMID: 35042319 Free PMC article. Review.
-
Urinary Levels of 14 Metal Elements in General Population: A Region-Based Exploratory Study in China.Toxics. 2023 May 27;11(6):488. doi: 10.3390/toxics11060488. Toxics. 2023. PMID: 37368588 Free PMC article.
-
Could Urinary Copper/Zinc Ratio Be a Newer Tool to Replace 24-Hour Urinary Copper Excretion for Diagnosing Wilson Disease in Children?Pediatr Gastroenterol Hepatol Nutr. 2024 Jan;27(1):53-61. doi: 10.5223/pghn.2024.27.1.53. Epub 2024 Jan 9. Pediatr Gastroenterol Hepatol Nutr. 2024. PMID: 38249640 Free PMC article.
-
Ideal serum non-ceruloplasmin bound copper prediction for long-term treated patients with Wilson disease: a nomogram model.Front Med (Lausanne). 2023 Nov 3;10:1275242. doi: 10.3389/fmed.2023.1275242. eCollection 2023. Front Med (Lausanne). 2023. PMID: 38020085 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical