Literature DB >> 23338780

Various copper and iron overload patterns in the livers of patients with Wilson disease and idiopathic copper toxicosis.

Hisao Hayashi1, Ai Hattori, Yasuaki Tatsumi, Kazuhiko Hayashi, Yoshiaki Katano, Jun Ueyama, Shinya Wakusawa, Motoyoshi Yano, Hidemi Goto.   

Abstract

Wilson disease (WD) is a major type of primary copper toxicosis associated with hypoceruloplasminemia, while idiopathic copper toxicosis (ICT) is a minor type characterized by normoceruloplasminemia. Because ceruloplasmin is the major circulating ferroxidase, iron metabolism may be affected in patients with WD. Biopsied liver specimens obtained from patients with primary copper toxicosis were fixed with glutaraldehyde solution and embedded in epoxy resin. Ultrathin sections that had or had not been stained with uranyl acetate solution were examined under an electron microscope equipped with an energy dispersive X-ray analyzer. A 7-year-old boy with WD was free from any metal overloading at the pre-treatment stage. Pre-treatment liver specimens of another 16 patients showed a variety of copper and iron overload patterns, from isolated copper to evenly distributed combined overloading. A 19-year-old female patient was free from any metal overloading after 7 years of treatment. Post-treatment overloading in another 6 patients ranged between evenly distributed combined patterns and isolated iron patterns. All patients had hypoceruloplasminemia throughout treatment periods. A patient with normoceruloplasminemic ICT continued to display isolated copper overloading after 2.5 years of treatment. In conclusion, these observations support the hypothesis that iron accumulates in patients with hypoceruloplasminemia.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 23338780     DOI: 10.1007/s00795-013-0015-2

Source DB:  PubMed          Journal:  Med Mol Morphol        ISSN: 1860-1499            Impact factor:   2.309


  26 in total

1.  Global prevalence of putative haemochromatosis mutations.

Authors:  A T Merryweather-Clarke; J J Pointon; J D Shearman; K J Robson
Journal:  J Med Genet       Date:  1997-04       Impact factor: 6.318

2.  A practice guideline on Wilson disease.

Authors:  Eve A Roberts; Michael L Schilsky
Journal:  Hepatology       Date:  2003-06       Impact factor: 17.425

3.  Effect of treatment of Wilson's disease on natural history of haemochromatosis.

Authors:  J M Walshe; D W Cox
Journal:  Lancet       Date:  1998-07-11       Impact factor: 79.321

4.  Disrupted hepcidin regulation in HFE-associated haemochromatosis and the liver as a regulator of body iron homoeostasis.

Authors:  Kim R Bridle; David M Frazer; Sarah J Wilkins; Jeanette L Dixon; David M Purdie; Darrell H G Crawford; V Nathan Subramaniam; Lawrie W Powell; Gregory J Anderson; Grant A Ramm
Journal:  Lancet       Date:  2003-02-22       Impact factor: 79.321

5.  Iron chelation therapy in aceruloplasminaemia: study of a patient with a novel missense mutation.

Authors:  R Mariani; C Arosio; S Pelucchi; M Grisoli; A Piga; P Trombini; A Piperno
Journal:  Gut       Date:  2004-05       Impact factor: 23.059

6.  HFE gene mutations and iron metabolism in Wilson's disease.

Authors:  Andreas Erhardt; Arne Hoffmann; Harald Hefter; Dieter Häussinger
Journal:  Liver       Date:  2002-12

7.  Isolation and characterization of a human liver cDNA as a candidate gene for Wilson disease.

Authors:  Y Yamaguchi; M E Heiny; J D Gitlin
Journal:  Biochem Biophys Res Commun       Date:  1993-11-30       Impact factor: 3.575

8.  Is non-Indian childhood cirrhosis caused by excess dietary copper?

Authors:  I H Scheinberg; I Sternlieb
Journal:  Lancet       Date:  1994-10-08       Impact factor: 79.321

Review 9.  Hemochromatosis: an endocrine liver disease.

Authors:  Antonello Pietrangelo
Journal:  Hepatology       Date:  2007-10       Impact factor: 17.425

10.  Familial apoceruloplasmin deficiency associated with blepharospasm and retinal degeneration.

Authors:  H Miyajima; Y Nishimura; K Mizoguchi; M Sakamoto; T Shimizu; N Honda
Journal:  Neurology       Date:  1987-05       Impact factor: 9.910

View more
  7 in total

Review 1.  Determination of copper poisoning in Wilson's disease using laser ablation inductively coupled plasma mass spectrometry.

Authors:  Sabine Weiskirchen; Philipp Kim; Ralf Weiskirchen
Journal:  Ann Transl Med       Date:  2019-04

Review 2.  Molecular mediators governing iron-copper interactions.

Authors:  Sukru Gulec; James F Collins
Journal:  Annu Rev Nutr       Date:  2014-06-02       Impact factor: 11.848

3.  Lenticular nucleus hyperechogenicity in Wilson's disease reflects local copper, but not iron accumulation.

Authors:  Uwe Walter; Marta Skowrońska; Tomasz Litwin; Grażyna Maria Szpak; Katarzyna Jabłonka-Salach; David Skoloudík; Ewa Bulska; Anna Członkowska
Journal:  J Neural Transm (Vienna)       Date:  2014-03-11       Impact factor: 3.575

4.  Laser-induced breakdown spectroscopy: a new approach for nanoparticle's mapping and quantification in organ tissue.

Authors:  Lucie Sancey; Vincent Motto-Ros; Shady Kotb; Xiaochun Wang; François Lux; Gérard Panczer; Jin Yu; Olivier Tillement
Journal:  J Vis Exp       Date:  2014-06-18       Impact factor: 1.355

5.  Copper Accumulates in Hemosiderins in Livers of Patients with Iron Overload Syndromes.

Authors:  Yukiya Ono; Masatoshi Ishigami; Kazuhiko Hayashi; Shinya Wakusawa; Hisao Hayashi; Kotaro Kumagai; Natsuko Morotomi; Tetsuji Yamashita; Miwa Kawanaka; Minemori Watanabe; Hiroaki Ozawa; Mayumi Tai; Hiroaki Miyajima; Kentarou Yoshioka; Yoshiki Hirooka; Hidemi Goto
Journal:  J Clin Transl Hepatol       Date:  2015-06-15

6.  Laser ablation inductively coupled plasma mass spectrometry imaging of metals in experimental and clinical Wilson's disease.

Authors:  Sorina Georgiana Boaru; Uta Merle; Ricarda Uerlings; Astrid Zimmermann; Christa Flechtenmacher; Claudia Willheim; Elisabeth Eder; Peter Ferenci; Wolfgang Stremmel; Ralf Weiskirchen
Journal:  J Cell Mol Med       Date:  2015-02-20       Impact factor: 5.310

7.  Haemolysis and perturbations in the systemic iron metabolism of suckling, copper-deficient mosaic mutant mice - an animal model of Menkes disease.

Authors:  Małgorzata Lenartowicz; Rafał R Starzyński; Wojciech Krzeptowski; Paweł Grzmil; Aleksandra Bednarz; Mateusz Ogórek; Olga Pierzchała; Robert Staroń; Anna Gajowiak; Paweł Lipiński
Journal:  PLoS One       Date:  2014-09-23       Impact factor: 3.240

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.