Could Urinary Copper/Zinc Ratio Be a Newer Tool to Replace 24-Hour Urinary Copper Excretion for Diagnosing Wilson Disease in Children?
1
조회
0
다운로드
0
인용
0
참고문헌
키워드
초록
Purpose: Although the 24-hours urinary copper excretion is useful for the diagnosis of Wilson disease (WD), there are practical difficulties in the accurate and timed collection of urine samples. The purpose of this study was to verify if the spot morning urinary Copper/ Zinc (Cu/Zn) ratio could be used as a replacement parameter of 24-hours urinary copper excretion in the diagnosis of WD. Methods: A cross-sectional study was conducted at the Department of Pediatric Gastroenterology and Nutrition, Bangabandhu Sheikh Mujib Medical University (BSMMU), Dhaka, Bangladesh, from June 2019 to May 2021 on 67 children over three years of age who presented with liver disease. Twenty-seven children who fulfilled the inclusion criteria for WD were categorized into the test group, and the remaining forty children were considered to have non-Wilsonian liver disease and were categorized into the control group. Along with other laboratory investigations, spot morning urinary samples were estimated for the urinary Cu/Zn ratio in all patients and were compared to the 24-hour urinary copper excretion. The diagnostic value of the Cu/Zn ratio was then analyzed. Results: Correlation of spot morning urinary Cu/Zn ratio with 24-hours urinary copper excretion was found to be significant (r=0.60). The area under ROC curve with 95% confidence interval of morning urinary Cu/Zn ratio measured using 24-hours urine sample was 0.84 (standard error, 0.05; p<0.001). Conclusion: Spot morning urinary Cu/Zn ratio seems to be a promising parameter for the replacement of 24-hours urinary copper excretion in the diagnosis of WD.
Abstract
Purpose: Although the 24-hours urinary copper excretion is useful for the diagnosis of Wilson disease (WD), there are practical difficulties in the accurate and timed collection of urine samples. The purpose of this study was to verify if the spot morning urinary Copper/ Zinc (Cu/Zn) ratio could be used as a replacement parameter of 24-hours urinary copper excretion in the diagnosis of WD. Methods: A cross-sectional study was conducted at the Department of Pediatric Gastroenterology and Nutrition, Bangabandhu Sheikh Mujib Medical University (BSMMU), Dhaka, Bangladesh, from June 2019 to May 2021 on 67 children over three years of age who presented with liver disease. Twenty-seven children who fulfilled the inclusion criteria for WD were categorized into the test group, and the remaining forty children were considered to have non-Wilsonian liver disease and were categorized into the control group. Along with other laboratory investigations, spot morning urinary samples were estimated for the urinary Cu/Zn ratio in all patients and were compared to the 24-hour urinary copper excretion. The diagnostic value of the Cu/Zn ratio was then analyzed. Results: Correlation of spot morning urinary Cu/Zn ratio with 24-hours urinary copper excretion was found to be significant (r=0.60). The area under ROC curve with 95% confidence interval of morning urinary Cu/Zn ratio measured using 24-hours urine sample was 0.84 (standard error, 0.05; p<0.001). Conclusion: Spot morning urinary Cu/Zn ratio seems to be a promising parameter for the replacement of 24-hours urinary copper excretion in the diagnosis of WD.
참고문헌 (28)
- Hui J, "Inherited metabolic diseases in the Southern Chinese population : Spectrum of diseases and estimated incidence from recurrent mutations", Pathology, 46, pp.375~382 (2014)
- Seo GH, "Biochemical and molecular characterisation of neurological Wilson disease", J Med Genet, 55, pp.587~593 (2018)
- Członkowska A, "Wilson disease", Nat Rev Dis Primers, 4, pp.21~ (2018)
- Riordan SM, "The Wilson’s disease gene and phenotypic diversity", J Hepatol, 34, pp.165~171 (2001)
- Roberts EA, "Update on the diagnosis and management of Wilson disease", Curr Gastroenterol Rep, 20, pp.56~ (2018)
- Wiernicka A, "Early onset of Wilson disease : Diagnostic challenges", J Pediatr Gastroenterol Nutr, 65, pp.555~560 (2017)
- Piotr S, "Wilson's disease in children : a position paper by the Hepatology Committee of the European Society for Paediatric Gastroenterology, Hepatology and Nutrition", J Pediatr Gastroenterol Nutr, 66, pp.334~344 (2018)
- Gow PJ, "Diagnosis of Wilson’s disease : an experience over three decades", Gut, 46, pp.415~419 (2000)
- Mak CM, "Diagnosis of Wilson’s disease : a comprehensive review", Crit Rev Clin Lab Sci, 45, pp.263~290 (2008)
- Yüce A, "Evaluation of diagnostic parameters of Wilson’s disease in childhood", Indian J Gastroenterol, 22, pp.4~6 (2003)
- Ala A, "Wilson’s disease", Lancet, 369, pp.397~408 (2007)
- Pang Y, "Effects of dietary copper supplementation and copper source on digesta pH, calcium, zinc, and copper complex size in the gastrointestinal tract of the broiler chicken", Poult Sci, 86, pp.531~537 (2007)
- Gao L, "Simultaneous spectrophotometric determination of four metals by two kinds of partial least squares methods", Spectrochim Acta A Mol Biomol Spectrosc, 61, pp.3013~3019 (2005)
- Fieten H, "Urinary excretion of copper, zinc and iron with and without D-penicillamine administration in relation to hepatic copper concentration in dogs", Vet J, 197, pp.468~473 (2013)
- Wang JS, "Urinary copper", zinc ratio : a promising parameter for replacement of 24-hour urinary copper excretion for diagnosis of Wilson’s disease in children, 2010, pp.6, 148~153
- Moore RET, "Determination of major and trace element variability in healthy human urine by ICP-QMS and specific gravity normalization", RSC Adv, 8, pp.38022~38035 (2018)
- Nagral A, "Wilson’s disease : Clinical Practice Guidelines of the Indian National Association for Study of the Liver, the Indian Society of Pediatric Gastroenterology, Hepatology and Nutrition, and the Movement Disorders Society of India", J Clin Exp Hepatol, 9, pp.74~98 (2019)
- Afridi HI, "Determination of copper and iron in biological samples of viral hepatitis(A-E)female patients", Biol Trace Elem Res, 129, pp.78~87 (2009)
- Kalkan A, "Trace elements in viral hepatitis", J Trace Elem Med Biol, 16, pp.227~230 (2002)
- Araki S, "Circadian rhythms in the urinary excretion of metals and organic substances in"Healthy"men", Arch Environ Health, 38, pp.360~366 (1983)
- Fernando M, "Wilson disease in children and adolescents", Arch Dis Child, 105, pp.499~505 (2020)
- Kiio J, "Bioequivalence of micronutrient powders to Corn-soy Blend on serum zinc concentration of children(6-36 months)with Moderate Acute Malnutrition in Thika urban slums, Kenya : a cluster-randomized controlled trial", PLoS One, 17, pp.e0274870~ (2022)
- Alonso EM, "Liver Ddisease in Cchildren", pp.71~96 (2007), Cambridge University Press
- Roberts EA, "Schilsky ML A practice guideline on Wilson disease", Hepatology, 37, pp.1475~1492 (2003)
- Schilsky ML, "Non-invasive testing for Wilson disease : revisiting the d-penicillamine challenge test", J Hepatol, 47, pp.172~173 (2007)
- Müller T, "Re-evaluation of the penicillamine challenge test in the diagnosis of Wilson’s disease in children", J Hepatol, 47, pp.270~276 (2007)
- Morales JV, "Is morning urinary protein", creatinine ratio a reliable estimator of 24-hour proteinuria in patients with glomerulonephritis and different levels of renal function?, 2004, pp.17, 666~672
- Stamoulis I, "Zinc and the liver : an active interaction", Dig Dis Sci, 52, pp.1595~1612 (2007)
