Literature DB >> 33640437

Direct Measurement of ATP7B Peptides Is Highly Effective in the Diagnosis of Wilson Disease.

Christopher J Collins1, Fan Yi1, Remwilyn Dayuha1, Phi Duong1, Simon Horslen2, Michelle Camarata3, Ayse K Coskun3, Roderick H J Houwen4, Tudor L Pop5, Heinz Zoller6, Han-Wook Yoo7, Sung Won Jung8, Karl H Weiss9, Michael L Schilsky3, Peter Ferenci10, Si Houn Hahn11.   

Abstract

BACKGROUND & AIMS: Both existing clinical criteria and genetic testing have significant limitations for the diagnosis of Wilson disease (WD), often creating ambiguities in patient identification and leading to delayed diagnosis and ineffective management. ATP7B protein concentration, indicated by direct measurement of surrogate peptides from patient dried blood spot samples, could provide primary evidence of WD. ATP7B concentrations were measured in patient samples from diverse backgrounds, diagnostic potential is determined, and results are compared with biochemical and genetic results from individual patients.
METHODS: Two hundred and sixty-four samples from biorepositories at 3 international and 2 domestic academic centers and 150 normal controls were obtained after Institutional Review Board approval. Genetically or clinically confirmed WD patients with a Leipzig score >3 and obligate heterozygote (carriers) from affected family members were included. ATP7B peptide measurements were made by immunoaffinity enrichment mass spectrometry.
RESULTS: Two ATP7B peptides were used to measure ATP7B protein concentration. Receiver operating characteristics curve analysis generates an area under the curve of 0.98. ATP7B peptide analysis of the sequence ATP7B 887 was found to have a sensitivity of 91.2%, specificity of 98.1%, positive predictive value of 98.0%, and a negative predictive value of 91.5%. In patients with normal ceruloplasmin concentrations (>20 mg/dL), 14 of 16 (87.5%) were ATP7B-deficient. In patients without clear genetic results, 94% were ATP7B-deficient.
CONCLUSIONS: Quantification of ATP7B peptide effectively identified WD patients in 92.1% of presented cases and reduced ambiguities resulting from ceruloplasmin and genetic analysis. Clarity is brought to patients with ambiguous genetic results, significantly aiding in noninvasive diagnosis. A proposed diagnostic score and algorithm incorporating ATP7B peptide concentrations can be rapidly diagnostic and supplemental to current Leipzig scoring systems.
Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  ATP7B; Immuno-SRM; Leipzig Score; Wilson disease

Mesh:

Substances:

Year:  2021        PMID: 33640437      PMCID: PMC8243898          DOI: 10.1053/j.gastro.2021.02.052

Source DB:  PubMed          Journal:  Gastroenterology        ISSN: 0016-5085            Impact factor:   22.682


  34 in total

1.  Interlaboratory evaluation of automated, multiplexed peptide immunoaffinity enrichment coupled to multiple reaction monitoring mass spectrometry for quantifying proteins in plasma.

Authors:  Eric Kuhn; Jeffrey R Whiteaker; D R Mani; Angela M Jackson; Lei Zhao; Matthew E Pope; Derek Smith; Keith D Rivera; N Leigh Anderson; Steven J Skates; Terry W Pearson; Amanda G Paulovich; Steven A Carr
Journal:  Mol Cell Proteomics       Date:  2011-12-22       Impact factor: 5.911

2.  EASL Clinical Practice Guidelines: Wilson's disease.

Authors: 
Journal:  J Hepatol       Date:  2012-03       Impact factor: 25.083

3.  Serum ceruloplasmin oxidase activity is a sensitive and highly specific diagnostic marker for Wilson's disease.

Authors:  Uta Merle; Christoph Eisenbach; Karl Heinz Weiss; Sabine Tuma; Wolfgang Stremmel
Journal:  J Hepatol       Date:  2009-07-30       Impact factor: 25.083

4.  Skyline: an open source document editor for creating and analyzing targeted proteomics experiments.

Authors:  Brendan MacLean; Daniela M Tomazela; Nicholas Shulman; Matthew Chambers; Gregory L Finney; Barbara Frewen; Randall Kern; David L Tabb; Daniel C Liebler; Michael J MacCoss
Journal:  Bioinformatics       Date:  2010-02-09       Impact factor: 6.937

5.  Age and Sex but Not ATP7B Genotype Effectively Influence the Clinical Phenotype of Wilson Disease.

Authors:  Peter Ferenci; Wolfgang Stremmel; Anna Członkowska; Ferenc Szalay; André Viveiros; Albert Friedrich Stättermayer; Radan Bruha; Roderick Houwen; Tudor Lucian Pop; Rudolf Stauber; Michael Gschwantler; Jan Pfeiffenberger; Cihan Yurdaydin; Elmar Aigner; Petra Steindl-Munda; Hans-Peter Dienes; Heinz Zoller; Karl Heinz Weiss
Journal:  Hepatology       Date:  2019-03-01       Impact factor: 17.425

6.  Quantification of ATP7B Protein in Dried Blood Spots by Peptide Immuno-SRM as a Potential Screen for Wilson's Disease.

Authors:  Sunhee Jung; Jeffrey R Whiteaker; Lei Zhao; Han-Wook Yoo; Amanda G Paulovich; Si Houn Hahn
Journal:  J Proteome Res       Date:  2016-12-09       Impact factor: 4.466

7.  Prospective evaluation of the diagnostic accuracy of hepatic copper content, as determined using the entire core of a liver biopsy sample.

Authors:  Xu Yang; Xiao-peng Tang; Yong-hong Zhang; Kai-zhong Luo; Yong-fang Jiang; Hong-yu Luo; Jian-hua Lei; Wen-long Wang; Ming-ming Li; Han-chun Chen; Shi-lin Deng; Li-ying Lai; Jun Liang; Min Zhang; Yi Tian; Yun Xu
Journal:  Hepatology       Date:  2015-08-27       Impact factor: 17.425

8.  The dilemma to diagnose Wilson disease by genetic testing alone.

Authors:  Albert Friedrich Stättermayer; Andreas Entenmann; Michael Gschwantler; Heinz Zoller; Harald Hofer; Peter Ferenci
Journal:  Eur J Clin Invest       Date:  2019-06-20       Impact factor: 4.686

9.  Non-Wilson's Disease-Associated Hypoceruloplasminemia.

Authors:  Annie Gong; Samantha Leitold; Julia Uhanova; Gerald Y Minuk
Journal:  J Clin Exp Hepatol       Date:  2019-11-26

10.  Multiplexed Proteomic Analysis for Diagnosis and Screening of Five Primary Immunodeficiency Disorders From Dried Blood Spots.

Authors:  Christopher J Collins; Fan Yi; Remwilyn Dayuha; Jeffrey R Whiteaker; Hans D Ochs; Alexandra Freeman; Helen C Su; Amanda G Paulovich; Gesmar R S Segundo; Troy Torgerson; Si Houn Hahn
Journal:  Front Immunol       Date:  2020-04-01       Impact factor: 7.561

View more
  7 in total

1.  Expanding the Diagnostic Toolkit of Wilson Disease with ATP7B Peptides.

Authors:  Valentina Medici
Journal:  Gastroenterology       Date:  2021-03-19       Impact factor: 33.883

Review 2.  Wilson disease and the differential diagnosis of its hepatic manifestations: a narrative review of clinical, laboratory, and liver histological features.

Authors:  Shannon M Schroeder; Karen E Matsukuma; Valentina Medici
Journal:  Ann Transl Med       Date:  2021-09

3.  Cuproptosis-Related Gene - SLC31A1, FDX1 and ATP7B - Polymorphisms are Associated with Risk of Lung Cancer.

Authors:  Yuhui Yun; Yun Wang; Ende Yang; Xin Jing
Journal:  Pharmgenomics Pers Med       Date:  2022-07-26

4.  Comprehensive multiomics analysis of cuproptosis-related gene characteristics in hepatocellular carcinoma.

Authors:  Jie Fu; Sixue Wang; Zhenghao Li; Wei Qin; Qing Tong; Chun Liu; Zicheng Wang; Zhiqiang Liu; Xundi Xu
Journal:  Front Genet       Date:  2022-09-06       Impact factor: 4.772

Review 5.  The Role of Zinc in the Treatment of Wilson's Disease.

Authors:  Abolfazl Avan; Anna Członkowska; Susan Gaskin; Alberto Granzotto; Stefano L Sensi; Tjaard U Hoogenraad
Journal:  Int J Mol Sci       Date:  2022-08-18       Impact factor: 6.208

Review 6.  Wilson disease in children and young adults - State of the art.

Authors:  Atchariya Chanpong; Anil Dhawan
Journal:  Saudi J Gastroenterol       Date:  2022 Jan-Feb       Impact factor: 2.485

7.  Synonymous mutation in adenosine triphosphatase copper-transporting beta causes enhanced exon skipping in Wilson disease.

Authors:  Marlene Panzer; André Viveiros; Benedikt Schaefer; Nadja Baumgartner; Klaus Seppi; Atbin Djamshidian; Theodor Todorov; William J H Griffiths; Eckart Schott; Markus Schuelke; Dennis Eurich; Albert Friedrich Stättermayer; Adrian Bomford; Pierre Foskett; Julia Vodopiutz; Rudolf Stauber; Elke Pertler; Bernhard Morell; Herbert Tilg; Thomas Müller; Stefan Kiechl; Raul Jimenez-Heredia; Karl Heinz Weiss; Si Houn Hahn; Andreas Janecke; Peter Ferenci; Heinz Zoller
Journal:  Hepatol Commun       Date:  2022-03-10
  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.