Literature DB >> 18675996

[123I]-FP-CIT and [99mTc]-HMPAO single photon emission computed tomography in a new sporadic case of rapid-onset dystonia-parkinsonism.

Paolo Zanotti-Fregonara1, Marie Vidailhet, Aurélie Kas, Laurie J Ozelius, Fabienne Clot, Elif Hindié, Laura Ravasi, Jean-Yves Devaux, Emmanuel Roze.   

Abstract

UNLABELLED: Rapid-onset dystonia-parkinsonism (RDP) is a rare, autosomal-dominantly inherited syndrome characterized by abrupt onset, over hours to days, of dystonic and parkinsonian symptoms. To date, RDP has been described in a small number of families, and in only four sporadic cases.
METHODS: We here report a new sporadic case of RDP who has a novel de novo mutation in the ATP1A3 gene. Striatal dopamine transporters have been assessed quantitatively using [123I]-FP-CIT SPECT. A volume of interest (VOI) was drawn within the occipital cortex to obtain non-specific activity and specific to non-specific binding ratios (BR) were calculated. A single template of predefined VOI 3D-drawn on right and left caudate nucleus and putamen was applied to the spatially normalized BR images. BR values were compared to those obtained from an age-matched control group and from a group of patients suffering from Parkinson's disease (Hoehn and Yahr score 2 or 3). A [99mTc]-HMPAO cerebral blood flow study was also performed.
RESULTS: In the control group, BR values (mean+/-Standard Deviation) were 3.5+/-0.4 for the left striatum and 3.3+/-0.3 for the right one. RDP patient's values were 3 and 2.7, respectively. In the Parkinson group, values were 1.6+/-0.3 and 1.7+/-0.4, respectively. [99mTc]-HMPAO scan showed homogeneous cortical and sub-cortical perfusion.
CONCLUSION: Quantification of striatal [123I]-FP-CIT uptake in a new sporadic case of RDP with a novel mutation in the ATP1A3 gene showed values just within the range of normality. [99mTc]-HMPAO scan was normal.

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Year:  2008        PMID: 18675996     DOI: 10.1016/j.jns.2008.06.033

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  20 in total

1.  The rapid-onset dystonia parkinsonism mutation D923N of the Na+, K+-ATPase alpha3 isoform disrupts Na+ interaction at the third Na+ site.

Authors:  Anja Pernille Einholm; Mads S Toustrup-Jensen; Rikke Holm; Jens Peter Andersen; Bente Vilsen
Journal:  J Biol Chem       Date:  2010-06-24       Impact factor: 5.157

2.  Neurological disease mutations compromise a C-terminal ion pathway in the Na(+)/K(+)-ATPase.

Authors:  Hanne Poulsen; Himanshu Khandelia; J Preben Morth; Maike Bublitz; Ole G Mouritsen; Jan Egebjerg; Poul Nissen
Journal:  Nature       Date:  2010-08-15       Impact factor: 49.962

3.  Factors in the disease severity of ATP1A3 mutations: Impairment, misfolding, and allele competition.

Authors:  Elena Arystarkhova; Ihtsham U Haq; Timothy Luebbert; Fanny Mochel; Rachel Saunders-Pullman; Susan B Bressman; Polina Feschenko; Cynthia Salazar; Jared F Cook; Scott Demarest; Allison Brashear; Laurie J Ozelius; Kathleen J Sweadner
Journal:  Neurobiol Dis       Date:  2019-08-16       Impact factor: 5.996

4.  Rapid-onset dystonia-parkinsonism: case report.

Authors:  Marina Svetel; Laurie J Ozelius; Amber Buckley; Katja Lohmann; Lela Brajković; Christine Klein; Vladimir S Kostić
Journal:  J Neurol       Date:  2010-03       Impact factor: 4.849

5.  Molecular diversity of combined and complex dystonia: insights from diagnostic exome sequencing.

Authors:  Michael Zech; Robert Jech; Matias Wagner; Tobias Mantel; Sylvia Boesch; Michael Nocker; Angela Jochim; Riccardo Berutti; Petra Havránková; Anna Fečíková; David Kemlink; Jan Roth; Tim M Strom; Werner Poewe; Evžen Růžička; Bernhard Haslinger; Juliane Winkelmann
Journal:  Neurogenetics       Date:  2017-08-28       Impact factor: 2.660

6.  Characterization of Atp1a3 mutant mice as a model of rapid-onset dystonia with parkinsonism.

Authors:  Mark P DeAndrade; Fumiaki Yokoi; Thomas van Groen; Jerry B Lingrel; Yuqing Li
Journal:  Behav Brain Res       Date:  2010-09-17       Impact factor: 3.332

Review 7.  ATP1A3 mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia.

Authors:  Allison Brashear; Jonathan W Mink; Deborah F Hill; Niki Boggs; W Vaughn McCall; Mark A Stacy; Beverly Snively; Laney S Light; Kathleen J Sweadner; Laurie J Ozelius; Leslie Morrison
Journal:  Dev Med Child Neurol       Date:  2012-08-28       Impact factor: 5.449

Review 8.  Distinct neurological disorders with ATP1A3 mutations.

Authors:  Erin L Heinzen; Alexis Arzimanoglou; Allison Brashear; Steven J Clapcote; Fiorella Gurrieri; David B Goldstein; Sigurður H Jóhannesson; Mohamad A Mikati; Brian Neville; Sophie Nicole; Laurie J Ozelius; Hanne Poulsen; Tsveta Schyns; Kathleen J Sweadner; Arn van den Maagdenberg; Bente Vilsen
Journal:  Lancet Neurol       Date:  2014-05       Impact factor: 44.182

9.  Novel mutations affecting the Na, K ATPase alpha model complex neurological diseases and implicate the sodium pump in increased longevity.

Authors:  Lesley J Ashmore; Stacy L Hrizo; Sarah M Paul; Wayne A Van Voorhies; Greg J Beitel; Michael J Palladino
Journal:  Hum Genet       Date:  2009-05-12       Impact factor: 4.132

Review 10.  The genetics of dystonia: new twists in an old tale.

Authors:  Gavin Charlesworth; Kailash P Bhatia; Nicholas W Wood
Journal:  Brain       Date:  2013-06-17       Impact factor: 13.501

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