Literature DB >> 27584852

Recent advances in the genetic neuropathies.

Alexander M Rossor1, Pedro J Tomaselli, Mary M Reilly.   

Abstract

PURPOSE OF REVIEW: Charcot-Marie-Tooth disease (CMT) is one of the commonest inherited neuromuscular diseases with a population prevalence of 1 in 2500. This review will cover recent advances in the genetics and pathomechanisms of CMT and how these are leading to the development of rational therapies. RECENT
FINDINGS: Pathomechanistic and therapeutic target advances in CMT include the identification of the ErbB receptor signalling pathway as a therapeutic target in CMT1A and pharmacological modification of the unfolded protein response in CMT1B. In CMT2D, due to mutations in glycyl-tRNA synthetase, vascular endothelial growth factor-mediated stimulation of the Nrp1 receptor has been identified as a therapeutic target. Preclinical advances have been accompanied by the publication of large natural history cohorts and the identification of a sensitive biomarker of disease (muscle MRI) that is able to detect disease progression in CMT1A over 1 year.
SUMMARY: Advances in next-generation sequencing technology, cell biology and animal models of CMT are paving the way for rational treatments. The combination of robust natural history data and the identification of sensitive biomarkers mean that we are now entering an exciting therapeutic era in the field of the genetic neuropathies.

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Mesh:

Year:  2016        PMID: 27584852      PMCID: PMC5130159          DOI: 10.1097/WCO.0000000000000373

Source DB:  PubMed          Journal:  Curr Opin Neurol        ISSN: 1350-7540            Impact factor:   5.710


  46 in total

1.  Dispersed disease-causing neomorphic mutations on a single protein promote the same localized conformational opening.

Authors:  Weiwei He; Hui-Min Zhang; Yeeting E Chong; Min Guo; Alan G Marshall; Xiang-Lei Yang
Journal:  Proc Natl Acad Sci U S A       Date:  2011-07-07       Impact factor: 11.205

2.  Diagnostic algorithms in Charcot-Marie-Tooth neuropathies: experiences from a German genetic laboratory on the basis of 1206 index patients.

Authors:  S Rudnik-Schöneborn; D Tölle; J Senderek; K Eggermann; M Elbracht; U Kornak; M von der Hagen; J Kirschner; B Leube; W Müller-Felber; U Schara; K von Au; D Wieczorek; C Bußmann; K Zerres
Journal:  Clin Genet       Date:  2015-04-29       Impact factor: 4.438

3.  HDAC6 inhibitors reverse axonal loss in a mouse model of mutant HSPB1-induced Charcot-Marie-Tooth disease.

Authors:  Constantin d'Ydewalle; Jyothsna Krishnan; Driss M Chiheb; Philip Van Damme; Joy Irobi; Alan P Kozikowski; Pieter Vanden Berghe; Vincent Timmerman; Wim Robberecht; Ludo Van Den Bosch
Journal:  Nat Med       Date:  2011-07-24       Impact factor: 53.440

4.  MORC2 mutations cause axonal Charcot-Marie-Tooth disease with pyramidal signs.

Authors:  Obaid M Albulym; Marina L Kennerson; Matthew B Harms; Alexander P Drew; Anna H Siddell; Michaela Auer-Grumbach; Alan Pestronk; Anne Connolly; Robert H Baloh; Stephan Zuchner; Stephen W Reddel; Garth A Nicholson
Journal:  Ann Neurol       Date:  2016-01-13       Impact factor: 10.422

Review 5.  Dysregulation of ErbB Receptor Trafficking and Signaling in Demyelinating Charcot-Marie-Tooth Disease.

Authors:  Samuel M Lee; Lih-Shen Chin; Lian Li
Journal:  Mol Neurobiol       Date:  2016-01-05       Impact factor: 5.590

6.  Bicyclic-Capped Histone Deacetylase 6 Inhibitors with Improved Activity in a Model of Axonal Charcot-Marie-Tooth Disease.

Authors:  Sida Shen; Veronick Benoy; Joel A Bergman; Jay H Kalin; Mariana Frojuello; Giulio Vistoli; Wanda Haeck; Ludo Van Den Bosch; Alan P Kozikowski
Journal:  ACS Chem Neurosci       Date:  2015-12-07       Impact factor: 4.418

7.  Therapeutic administration of progesterone antagonist in a model of Charcot-Marie-Tooth disease (CMT-1A).

Authors:  Michael W Sereda; Gerd Meyer zu Hörste; Ueli Suter; Naureen Uzma; Klaus-Armin Nave
Journal:  Nat Med       Date:  2003-11-09       Impact factor: 53.440

8.  Expanding Phenotype of VRK1 Mutations in Motor Neuron Disease.

Authors:  Thy P Nguyen; Suur Biliciler; Wojciech Wiszniewski; Kazim Sheikh
Journal:  J Clin Neuromuscul Dis       Date:  2015-12

Review 9.  Ascorbic acid for the treatment of Charcot-Marie-Tooth disease.

Authors:  Burkhard Gess; Jonathan Baets; Peter De Jonghe; Mary M Reilly; Davide Pareyson; Peter Young
Journal:  Cochrane Database Syst Rev       Date:  2015-12-11

10.  Responsiveness of clinical outcome measures in Charcot-Marie-Tooth disease.

Authors:  G Piscosquito; M M Reilly; A Schenone; G M Fabrizi; T Cavallaro; L Santoro; F Manganelli; G Vita; A Quattrone; L Padua; F Gemignani; F Visioli; M Laurà; D Calabrese; R A C Hughes; D Radice; A Solari; D Pareyson
Journal:  Eur J Neurol       Date:  2015-07-31       Impact factor: 6.089

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  29 in total

1.  Alternative stable conformation capable of protein misinteraction links tRNA synthetase to peripheral neuropathy.

Authors:  David Blocquel; Sheng Li; Na Wei; Herwin Daub; Mathew Sajish; Maria-Luise Erfurth; Grace Kooi; Jiadong Zhou; Ge Bai; Paul Schimmel; Albena Jordanova; Xiang-Lei Yang
Journal:  Nucleic Acids Res       Date:  2017-07-27       Impact factor: 16.971

Review 2.  Intermediate Charcot-Marie-Tooth disease: an electrophysiological reappraisal and systematic review.

Authors:  José Berciano; Antonio García; Elena Gallardo; Kristien Peeters; Ana L Pelayo-Negro; Silvia Álvarez-Paradelo; José Gazulla; Miriam Martínez-Tames; Jon Infante; Albena Jordanova
Journal:  J Neurol       Date:  2017-03-31       Impact factor: 4.849

3.  Mitochondria dysfunction in Charcot Marie Tooth 2B Peripheral Sensory Neuropathy.

Authors:  Flora Guerra; Mingzheng Hu; Alexander Pope; Yingli Gu; Kijung Sung; Wanlin Yang; Simone Jetha; Thomas A Shoff; Tessanya Gunatilake; Owen Dahlkamp; Linda Zhixia Shi; Fiore Manganelli; Maria Nolano; Yue Zhou; Jianqing Ding; Cecilia Bucci; Chengbiao Wu
Journal:  Commun Biol       Date:  2022-07-18

Review 4.  Neurodegenerative Charcot-Marie-Tooth disease as a case study to decipher novel functions of aminoacyl-tRNA synthetases.

Authors:  Na Wei; Qian Zhang; Xiang-Lei Yang
Journal:  J Biol Chem       Date:  2019-01-14       Impact factor: 5.157

5.  CMT disease severity correlates with mutation-induced open conformation of histidyl-tRNA synthetase, not aminoacylation loss, in patient cells.

Authors:  David Blocquel; Litao Sun; Zaneta Matuszek; Sheng Li; Thomas Weber; Bernhard Kuhle; Grace Kooi; Na Wei; Jonathan Baets; Tao Pan; Paul Schimmel; Xiang-Lei Yang
Journal:  Proc Natl Acad Sci U S A       Date:  2019-09-09       Impact factor: 11.205

6.  Identification of a pathogenic PMP2 variant in a multi-generational family with CMT type 1: Clinical gene panels versus genome-wide approaches to molecular diagnosis.

Authors:  Jaya Punetha; Loren Mackay-Loder; Tamar Harel; Zeynep Coban-Akdemir; Shalini N Jhangiani; Richard A Gibbs; Ian Lee; Deborah Terespolsky; James R Lupski; Jennifer E Posey
Journal:  Mol Genet Metab       Date:  2018-08-24       Impact factor: 4.797

Review 7.  Genetic modifiers and non-Mendelian aspects of CMT.

Authors:  Dana M Bis-Brewer; Sarah Fazal; Stephan Züchner
Journal:  Brain Res       Date:  2019-09-13       Impact factor: 3.252

Review 8.  Next-generation sequencing in Charcot-Marie-Tooth disease: opportunities and challenges.

Authors:  Menelaos Pipis; Alexander M Rossor; Matilde Laura; Mary M Reilly
Journal:  Nat Rev Neurol       Date:  2019-10-03       Impact factor: 42.937

9.  A multicenter retrospective study of charcot-marie-tooth disease type 4B (CMT4B) associated with mutations in myotubularin-related proteins (MTMRs).

Authors:  Davide Pareyson; Tanya Stojkovic; Mary M Reilly; Sarah Leonard-Louis; Matilde Laurà; Julian Blake; Yesim Parman; Esra Battaloglu; Meriem Tazir; Mounia Bellatache; Nathalie Bonello-Palot; Nicolas Lévy; Sabrina Sacconi; Raquel Guimarães-Costa; Sharham Attarian; Philippe Latour; Guilhem Solé; André Megarbane; Rita Horvath; Giulia Ricci; Byung-Ok Choi; Angelo Schenone; Chiara Gemelli; Alessandro Geroldi; Mario Sabatelli; Marco Luigetti; Lucio Santoro; Fiore Manganelli; Aldo Quattrone; Paola Valentino; Tatsufumi Murakami; Steven S Scherer; Lois Dankwa; Michael E Shy; Chelsea J Bacon; David N Herrmann; Alberto Zambon; Irene Tramacere; Chiara Pisciotta; Stefania Magri; Stefano C Previtali; Alessandra Bolino
Journal:  Ann Neurol       Date:  2019-05-27       Impact factor: 11.274

10.  Structural insights into Charcot-Marie-Tooth disease-linked mutations in human GDAP1.

Authors:  Aleksi Sutinen; Giang Thi Tuyet Nguyen; Arne Raasakka; Gopinath Muruganandam; Remy Loris; Emil Ylikallio; Henna Tyynismaa; Luca Bartesaghi; Salla Ruskamo; Petri Kursula
Journal:  FEBS Open Bio       Date:  2022-05-20       Impact factor: 2.792

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