Evidence map›Paper›PMID 25802885›Full record

ArticleMolecular genetics & genomic medicine2015

Improved inherited peripheral neuropathy genetic diagnosis by whole-exome sequencing.

Alexander P Drew, Danqing Zhu, Aditi Kidambi, Carolyn Ly, Shelisa Tey, Megan H Brewer, Azlina Ahmad-Annuar, Garth A Nicholson, Marina L Kennerson

Open access · goldAbstract read
In one paragraph

Article in Molecular genetics & genomic medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
2.7field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

43 citing papers in PubMed, 68 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Alexander P DrewNorthcott Neuroscience Laboratory, ANZAC Research Institute Sydney, Australia.
Danqing ZhuMolecular Medicine Laboratory, Concord Hospital Sydney, Australia.
Aditi KidambiNorthcott Neuroscience Laboratory, ANZAC Research Institute Sydney, Australia.
Carolyn LyNorthcott Neuroscience Laboratory, ANZAC Research Institute Sydney, Australia.
Shelisa TeyDepartment of Biomedical Science, Faculty of Medicine, University of Malaya 50603, Kuala Lumpur, Malaysia.
Megan H BrewerNorthcott Neuroscience Laboratory, ANZAC Research Institute Sydney, Australia ; Sydney Medical School, University of Sydney Sydney, Australia.
Azlina Ahmad-AnnuarDepartment of Biomedical Science, Faculty of Medicine, University of Malaya 50603, Kuala Lumpur, Malaysia.
Garth A NicholsonNorthcott Neuroscience Laboratory, ANZAC Research Institute Sydney, Australia ; Molecular Medicine Laboratory, Concord Hospital Sydney, Australia ; Sydney Medical School, University of Sydney Sydney, Australia.
Marina L KennersonNorthcott Neuroscience Laboratory, ANZAC Research Institute Sydney, Australia ; Molecular Medicine Laboratory, Concord Hospital Sydney, Australia ; Sydney Medical School, University of Sydney Sydney, Australia.
Anzac Research Institute · AUConcord Repatriation General Hospital · AUUniversity of Malaya · MY

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inherited peripheral neuropathies (IPNs) are a group of related diseases primarily affecting the peripheral motor and sensory neurons. They include the hereditary sensory neuropathies (HSN), hereditary motor neuropathies (HMN), and Charcot-Marie-Tooth disease (CMT). Using whole-exome sequencing (WES) to achieve a genetic diagnosis is particularly suited to IPNs, where over 80 genes are involved with weak genotype-phenotype correlations beyond the most common genes. We performed WES for 110 index patients with IPN where the genetic cause was undetermined after previous screening for mutations in common genes selected by phenotype and mode of inheritance. We identified 41 missense sequence variants in the known IPN genes in our cohort of 110 index patients. Nine variants (8%), identified in the genes MFN2, GJB1, BSCL2, and SETX, are previously reported mutations and considered to be pathogenic in these families. Twelve novel variants (11%) in the genes NEFL, TRPV4, KIF1B, BICD2, and SETX are implicated in the disease but require further evidence of pathogenicity. The remaining 20 variants were confirmed as polymorphisms (not causing the disease) and are detailed here to help interpret sequence variants identified in other family studies. Validation using segregation, normal controls, and bioinformatics tools was valuable as supporting evidence for sequence variants implicated in disease. In addition, we identified one SETX sequence variant (c.7640T>C), previously reported as a putative mutation, which we have confirmed as a nonpathogenic rare polymorphism. This study highlights the advantage of using WES for genetic diagnosis in highly heterogeneous diseases such as IPNs and has been particularly powerful in this cohort where genetic diagnosis could not be achieved due to phenotype and mode of inheritance not being previously obvious. However, first tier testing for common genes in clinically well-defined cases remains important and will account for most positive results.

Indexed as

Charcot-Marie-Tooth diseasegenetic diagnosisinherited peripheral neuropathywhole-exome sequencing

Identifiers

PMID25802885
PMCPMC4367087
OpenAlexW2094381508

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.