Literature DB >> 27164712

Target-enrichment sequencing and copy number evaluation in inherited polyneuropathy.

Wei Wang1, Chen Wang1, D Brian Dawson1, Erik C Thorland1, Patrick A Lundquist1, Bruce W Eckloff1, Yanhong Wu1, Saurabh Baheti1, Jared M Evans1, Steven S Scherer1, Peter J Dyck1, Christopher J Klein2.   

Abstract

OBJECTIVE: To assess the efficiency of target-enrichment next-generation sequencing (NGS) with copy number assessment in inherited neuropathy diagnosis.
METHODS: A 197 polyneuropathy gene panel was designed to assess for mutations in 93 patients with inherited or idiopathic neuropathy without known genetic cause. We applied our novel copy number variation algorithm on NGS data, and validated the identified copy number mutations using CytoScan (Affymetrix). Cost and efficacy of this targeted NGS approach was compared to earlier evaluations.
RESULTS: Average coverage depth was ∼760× (median = 600, 99.4% > 100×). Among 93 patients, 18 mutations were identified in 17 cases (18%), including 3 copy number mutations: 2 PMP22 duplications and 1 MPZ duplication. The 2 patients with PMP22 duplication presented with bulbar and respiratory involvement and had absent extremity nerve conductions, leading to axonal diagnosis. Average onset age of these 17 patients was 25 years (2-61 years), vs 45 years for those without genetic discovery. Among those with onset age less than 40 years, the diagnostic yield of targeted NGS approach is high (27%) and cost savings is significant (∼20%). However, the cost savings for patients with late onset age and without family history is not demonstrated.
CONCLUSIONS: Incorporating copy number analysis in target-enrichment NGS approach improved the efficiency of mutation discovery for chronic, inherited, progressive length-dependent polyneuropathy diagnosis. The new technology is facilitating a simplified genetic diagnostic algorithm utilizing targeted NGS, clinical phenotypes, age at onset, and family history to improve diagnosis efficiency. Our findings prompt a need for updating the current practice parameters and payer guidelines.
© 2016 American Academy of Neurology.

Entities:  

Mesh:

Substances:

Year:  2016        PMID: 27164712      PMCID: PMC4862246          DOI: 10.1212/WNL.0000000000002659

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  39 in total

Review 1.  Inherited neuropathies: clinical overview and update.

Authors:  Christopher J Klein; Xiaohui Duan; Michael E Shy
Journal:  Muscle Nerve       Date:  2013-06-26       Impact factor: 3.217

2.  Tests and expenditures in the initial evaluation of peripheral neuropathy.

Authors:  Brian Callaghan; Ryan McCammon; Kevin Kerber; Xiao Xu; Kenneth M Langa; Eva Feldman
Journal:  Arch Intern Med       Date:  2012-01-23

3.  Oral L-serine supplementation reduces production of neurotoxic deoxysphingolipids in mice and humans with hereditary sensory autonomic neuropathy type 1.

Authors:  Kevin Garofalo; Anke Penno; Brian P Schmidt; Ho-Joon Lee; Matthew P Frosch; Arnold von Eckardstein; Robert H Brown; Thorsten Hornemann; Florian S Eichler
Journal:  J Clin Invest       Date:  2011-12       Impact factor: 14.808

4.  Impairments and comorbidities of polyneuropathy revealed by population-based analyses.

Authors:  E Matthew Hoffman; Nathan P Staff; Jared M Robb; Jennifer L St Sauver; Peter J Dyck; Christopher J Klein
Journal:  Neurology       Date:  2015-04-01       Impact factor: 9.910

5.  Gain-of-function mutations in sodium channel Na(v)1.9 in painful neuropathy.

Authors:  Jianying Huang; Chongyang Han; Mark Estacion; Dymtro Vasylyev; Janneke G J Hoeijmakers; Monique M Gerrits; Lynda Tyrrell; Giuseppe Lauria; Catharina G Faber; Sulayman D Dib-Hajj; Ingemar S J Merkies; Stephen G Waxman
Journal:  Brain       Date:  2014-04-27       Impact factor: 13.501

Review 6.  Practice Parameter: evaluation of distal symmetric polyneuropathy: role of laboratory and genetic testing (an evidence-based review). Report of the American Academy of Neurology, American Association of Neuromuscular and Electrodiagnostic Medicine, and American Academy of Physical Medicine and Rehabilitation.

Authors:  J D England; G S Gronseth; G Franklin; G T Carter; L J Kinsella; J A Cohen; A K Asbury; K Szigeti; J R Lupski; N Latov; R A Lewis; P A Low; M A Fisher; D N Herrmann; J F Howard; G Lauria; R G Miller; M Polydefkis; A J Sumner
Journal:  Neurology       Date:  2008-12-03       Impact factor: 9.910

Review 7.  Evaluation of distal symmetric polyneuropathy: the role of laboratory and genetic testing (an evidence-based review).

Authors:  J D England; G S Gronseth; G Franklin; G T Carter; L J Kinsella; J A Cohen; A K Asbury; K Szigeti; J R Lupski; N Latov; R A Lewis; P A Low; M A Fisher; D Herrmann; J F Howard; G Lauria; R G Miller; M Polydefkis; A J Sumner
Journal:  Muscle Nerve       Date:  2009-01       Impact factor: 3.217

8.  A controlled investigation of the cause of chronic idiopathic axonal polyneuropathy.

Authors:  R A C Hughes; T Umapathi; I A Gray; N A Gregson; M Noori; A S Pannala; A Proteggente; A V Swan
Journal:  Brain       Date:  2004-06-16       Impact factor: 13.501

9.  CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysis.

Authors:  V Fridman; B Bundy; M M Reilly; D Pareyson; C Bacon; J Burns; J Day; S Feely; R S Finkel; T Grider; C A Kirk; D N Herrmann; M Laurá; J Li; T Lloyd; C J Sumner; F Muntoni; G Piscosquito; S Ramchandren; R Shy; C E Siskind; S W Yum; I Moroni; E Pagliano; S Zuchner; S S Scherer; M E Shy
Journal:  J Neurol Neurosurg Psychiatry       Date:  2014-11-27       Impact factor: 10.154

10.  Genetics of Charcot-Marie-Tooth (CMT) Disease within the Frame of the Human Genome Project Success.

Authors:  Vincent Timmerman; Alleene V Strickland; Stephan Züchner
Journal:  Genes (Basel)       Date:  2014-01-22       Impact factor: 4.096

View more
  25 in total

1.  Progress in Recognizing and Treating Polyneuropathy.

Authors:  Bernd C Kieseier; Hans-Peter Hartung
Journal:  Dtsch Arztebl Int       Date:  2018-02-09       Impact factor: 5.594

2.  A Consensus-Based Approach for Harmonizing the OHDSI Common Data Model with HL7 FHIR.

Authors:  Guoqian Jiang; Richard C Kiefer; Deepak K Sharma; Eric Prud'hommeaux; Harold R Solbrig
Journal:  Stud Health Technol Inform       Date:  2017

3.  Genomic analysis reveals frequent TRAF7 mutations in intraneural perineuriomas.

Authors:  Christopher J Klein; Yanhong Wu; Mark E Jentoft; Georges Mer; Robert J Spinner; P James B Dyck; Peter J Dyck; Michelle L Mauermann
Journal:  Ann Neurol       Date:  2017-01-28       Impact factor: 10.422

Review 4.  Neuromuscular Diseases Due to Chaperone Mutations: A Review and Some New Results.

Authors:  Jaakko Sarparanta; Per Harald Jonson; Sabita Kawan; Bjarne Udd
Journal:  Int J Mol Sci       Date:  2020-02-19       Impact factor: 5.923

5.  Genetic test utilization and diagnostic yield in adult patients with neurological disorders.

Authors:  Tanya M Bardakjian; Ingo Helbig; Colin Quinn; Lauren B Elman; Leo F McCluskey; Steven S Scherer; Pedro Gonzalez-Alegre
Journal:  Neurogenetics       Date:  2018-03-28       Impact factor: 2.660

Review 6.  Hereditary Neuropathies.

Authors:  Katja Eggermann; Burkhard Gess; Martin Häusler; Joachim Weis; Andreas Hahn; Ingo Kurth
Journal:  Dtsch Arztebl Int       Date:  2018-02-09       Impact factor: 5.594

Review 7.  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

Review 8.  New evidence for secondary axonal degeneration in demyelinating neuropathies.

Authors:  Kathryn R Moss; Taylor S Bopp; Anna E Johnson; Ahmet Höke
Journal:  Neurosci Lett       Date:  2020-12-24       Impact factor: 3.046

Review 9.  Next-generation sequencing in neuromuscular diseases.

Authors:  Stephanie Efthymiou; Andreea Manole; Henry Houlden
Journal:  Curr Opin Neurol       Date:  2016-10       Impact factor: 5.710

Review 10.  Application of Next-Generation Sequencing in Neurodegenerative Diseases: Opportunities and Challenges.

Authors:  Cigir Biray Avci; Behrouz Shademan; Masoud Nikanfar; Alireza Nourazarian
Journal:  Neuromolecular Med       Date:  2020-05-12       Impact factor: 3.843

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.