Isotopic analysis of Cu in serum samples for diagnosis of Wilson's disease: a pilot study

被引:82
作者
Aramendia, Maite [1 ,4 ]
Rello, Luis [2 ]
Resano, Martin [3 ]
Vanhaecke, Frank [4 ]
机构
[1] Ctr Univ Def Acad Gen Mil Zaragoza, Zaragoza 50090, Spain
[2] Miguel Servet Univ Hosp, Dept Clin Biochem, Zaragoza 50009, Spain
[3] Univ Zaragoza, Fac Sci, Dept Analyt Chem, E-50009 Zaragoza, Spain
[4] Univ Ghent, Dept Analyt Chem, B-9000 Ghent, Belgium
关键词
PLASMA-MASS SPECTROMETRY; COPPER TRANSPORT; COLLECTOR; BLOOD; FRACTIONATION; SEPARATION; RATIOS; SPOTS; ZN; FE;
D O I
10.1039/c3ja30349g
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学];
摘要
Wilson's disease (WD) is a genetic disorder affecting Cu metabolism, which can lead to severe physiological and neurological symptoms, and even death if untreated. Based on the fact that WD patients show low Cu levels in serum, implementation of screening programs for diagnosis of this condition at the moment of birth, when progression of the disease can be still arrested, has been attempted in the past. These attempts, however, have been unsuccessful, as healthy new-borns often show low Cu levels in serum due to liver immaturity. In this work, the potential use of isotopic analysis of Cu in serum samples as an alternative diagnostic parameter for Wilson's disease has been investigated. For this purpose, the Cu isotopic composition of a set of serum samples from different groups showing either low (i.e. WD patients, patients who had undergone bariatric surgery, infants) or normal (supposedly healthy adults) Cu concentration levels was determined by means of multi-collector ICP-mass spectrometry (MC-ICP-MS), after chromatographic isolation of Cu. For this purpose, AG-MP-1 strong anion exchange resin was relied upon, enabling quantitative recovery of Cu in pure form from the serum samples. MC-ICP-MS measuring conditions were optimized to avoid the influence of spectral overlap, and Ni was admixed as an internal standard for correction of instrumental mass discrimination. The use of this optimized method provided delta Cu-65 for the serum samples with a typical analytical uncertainty of similar to 0.20 parts per thousand (k = 2). Our results show that, for the population considered in this study, combination of Cu concentration values and Cu isotopic information allows classification of WD patients, infants and controls into different groups, while the use of concentration values only is not sufficient for this purpose. Although further studies with a larger number of samples are needed, results are encouraging as far as the use of Cu isotopic analysis for early diagnosis of Wilson's disease is concerned.
引用
收藏
页码:675 / 681
页数:7
相关论文
共 34 条
[1]
Wilson's disease [J].
Ala, Aftab ;
Walker, Ann P. ;
Ashkan, Keyoumars ;
Dooley, James S. ;
Schilsky, Michael L. .
LANCET, 2007, 369 (9559) :397-408
[2]
Isotopic evidence of unaccounted for Fe and Cu erythropoietic pathways [J].
Albarede, Francis ;
Telouk, Philippe ;
Lamboux, Aline ;
Jaouen, Klervia ;
Balter, Vincent .
METALLOMICS, 2011, 3 (09) :926-933
[3]
Direct Trace-Elemental Analysis of Urine Samples by Laser Ablation-Inductively Coupled Plasma Mass Spectrometry after Sample Deposition on Clinical Filter Papers [J].
Aramendia, Maite ;
Rello, Luis ;
Vanhaecke, Frank ;
Resano, Martin .
ANALYTICAL CHEMISTRY, 2012, 84 (20) :8682-8690
[4]
Copper and tin isotopic analysis of ancient bronzes for archaeological investigation: development and validation of a suitable analytical methodology [J].
Balliana, Eleonora ;
Aramendia, Maite ;
Resano, Martin ;
Barbante, Carlo ;
Vanhaecke, Frank .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2013, 405 (09) :2973-2986
[5]
Revised exponential model for mass bias correction using an internal standard for isotope abundance ratio measurements by multi-collector inductively coupled plasma mass spectrometry [J].
Baxter, DC ;
Rodushkin, I ;
Engström, E ;
Malinovsky, D .
JOURNAL OF ANALYTICAL ATOMIC SPECTROMETRY, 2006, 21 (04) :427-430
[6]
Chemical separation and isotopic variations of Cu and Zn from five geological reference materials [J].
Chapman, John B. ;
Mason, Thomas F. D. ;
Weiss, Dominik J. ;
Coles, Barry J. ;
Wilkinson, Jamie J. .
GEOSTANDARDS AND GEOANALYTICAL RESEARCH, 2006, 30 (01) :5-16
[7]
EASL Clinical Practice Guidelines, 2012, J HEPATOL, V56, P671
[8]
Mechanisms underlying iron and copper ions toxicity in biological systems: Pro-oxidant activity and protein-binding effects [J].
Eugenia Letelier, Maria ;
Sanchez-Jofre, Sebastian ;
Peredo-Silva, Liliana ;
Cortes-Troncoso, Juan ;
Aracena-Parks, Paula .
CHEMICO-BIOLOGICAL INTERACTIONS, 2010, 188 (01) :220-227
[9]
Diagnosis and phenotypic classification of Wilson disease [J].
Ferenci, P ;
Caca, K ;
Loudianos, G ;
Mieli-Vergani, G ;
Tanner, S ;
Sternlieb, I ;
Schilsky, M ;
Cox, D ;
Berr, F .
LIVER INTERNATIONAL, 2003, 23 (03) :139-142
[10]
Authenticity and provenance studies of copper-bearing andesines using Cu isotope ratios and element analysis by fs-LA-MC-ICPMS and ns-LA-ICPMS [J].
Fontaine, Gisela H. ;
Hametner, Kathrin ;
Peretti, Adolf ;
Guenther, Detlef .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2010, 398 (7-8) :2915-2928