Evidence map›Paper›PMID 32997296›Full record

ArticleJournal of neurology2021

Unusual electrophysiological findings in a Chinese ALS 4 family with SETX-L389S mutation: a three-year follow-up.

Lin Lei, Hai Chen, Yan Lu, Wenjia Zhu, Yasheng Ouyang, Jianying Duo, Zhiguo Chen, Yuwei Da

Abstract read
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In one paragraph

Article in Journal of neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
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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

8 authors at 1 institution in 1 country.

Lin Lei *Department of NEUROLOGY, Xuanwu Hospital, Capital Medical University, Changchun Street, Beijing, 100053, China.
Hai Chen *Department of NEUROLOGY, Xuanwu Hospital, Capital Medical University, Changchun Street, Beijing, 100053, China.
Yan Lu *Department of NEUROLOGY, Xuanwu Hospital, Capital Medical University, Changchun Street, Beijing, 100053, China.
Wenjia ZhuDepartment of NEUROLOGY, Xuanwu Hospital, Capital Medical University, Changchun Street, Beijing, 100053, China.
Yasheng OuyangDepartment of NEUROLOGY, Xuanwu Hospital, Capital Medical University, Changchun Street, Beijing, 100053, China.
Jianying DuoDepartment of NEUROLOGY, Xuanwu Hospital, Capital Medical University, Changchun Street, Beijing, 100053, China.
Zhiguo ChenKey Laboratory of Neurodegenerative Diseases, Ministry of Education, Cell Therapy Center, National Clinical Research Center for Geriatric Diseases, Beijing Institute of Geriatrics, Xuanwu Hospital, Capital Medical University, Beijing, China. chenzhiguo@gmail.com.
Yuwei DaDepartment of NEUROLOGY, Xuanwu Hospital, Capital Medical University, Changchun Street, Beijing, 100053, China. dayuwei100@hotmail.com.ORCID http://orcid.org/0000-0002-0318-148X
Capital Medical University · CN

Funding

National Key R&D Program of China, Precision Medicine Program No. 2017YFC0907700
6 · The paper itself

Abstract

Amyotrophic lateral sclerosis type 4 (ALS4) is a familial form of ALS caused by mutations in the SETX gene. To date, there are seven unrelated ALS4 families with four missense mutations (L389S, T31I, R2136H, and M386T) in SETX. ALS4 is characterized by early onset, distal muscle weakness and atrophy, pyramidal signs, and the absence of sensory deficits. Motor conduction studies often present normality or reduced amplitudes of compound muscle action potential (CMAP). The conduction blocks (CBs) are rare and only observed in one male of an Italian ALS4 family. Our study showed that seven symptomatic patients presented the classical ALS4 phenotype with two asymptomatic females in a Chinese family spanning three generations. Sequencing analysis revealed a heterozygous c.1166T > C/p.L389S mutation in SETX that co-segregated with disease phenotype in the family. The same mutation has been identified previously in three ALS4 families from the United States and Italy, respectively. Specifically, three young males presented multiple CBs and abnormal temporal dispersions (TD) in the median, ulnar and tibial nerves over the three-year follow-up period. Moreover, for the first time, we found that senataxin was also expressed in the myelin sheath of peripheral nerves besides axons. The study indicates that CBs and abnormal TD are the characteristics in the ALS4 family, providing pivotal familial evidence of CBs and TD of motor nerves in ALS4. The unusual electrophysiological features may be associated with the expression of senataxin in peripheral nerves.

Indexed as

Amyotrophic Lateral SclerosisChinaDNA HelicasesFemaleFollow-Up StudiesHumansItalyMaleMultifunctional EnzymesMutationRNA HelicasesDNA HelicasesMultifunctional EnzymesRNA HelicasesSETX protein, humanAmyotrophicConduction blockElectrophysiologyFamilialLateral sclerosis (ALS)SETXTemporal dispersion

Identifiers

PMID32997296
OpenAlexW3091720810

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Registered trials

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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.