Evidence map›Paper›PMID 32501971›Full record

Observational studyMedicine2020

Genetic mutation analysis of hereditary spastic paraplegia: A retrospective study.

Fang Cui, LiuQing Sun, Jie Qiao, JianYong Li, Mao Li, SiYu Chen, Bo Sun, XuSheng Huang

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 33% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. NovelFrontiers in genetics · 2024
    Article
  4. Article
  5. Review
  6. Article
  7. Article
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.

Fang CuiDepartment of Neurology, Hainan Branch of Chinese PLA General Hospital.
LiuQing SunDepartment of Neurology, Hainan Branch of Chinese PLA General Hospital.
Jie QiaoDepartment of Neurology, Chinese PLA General Hospital, Beijing, China.
JianYong LiDepartment of Neurology, Hainan Branch of Chinese PLA General Hospital.
Mao LiDepartment of Neurology, Chinese PLA General Hospital, Beijing, China.
SiYu ChenDepartment of Neurology, Chinese PLA General Hospital, Beijing, China.
Bo SunDepartment of Neurology, Chinese PLA General Hospital, Beijing, China.
XuSheng HuangDepartment of Neurology, Chinese PLA General Hospital, Beijing, China.ORCID 0000-0002-2451-0254
Chinese PLA General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hereditary spastic paraplegias are heterogeneous disorders with diversified clinical manifestations, and genetic testing is important for the diagnosis and typing of hereditary spastic paraplegias.Gene panel sequencing containing 55 hereditary spastic paraplegias-related genes was performed to screen the pathogenic genes for hereditary spastic paraplegias. Sanger sequencing was adopted to validate if the family member carried the same pathogenic gene as the proband.Fifteen out of 53 patients carried mutation(s) in the screened hereditary spastic paraplegias-related genes. Among the 23 identified mutations, only one mutation had been previously reported as a pathogenic mutation. In the pedigree of case 6, the proband, his mother and uncle all carried the same novel deletion mutation (c.1459delA) at SPAST gene. Based on the pedigree, the disease was inherited in an AD pattern. In the pedigree of case 53, the family disease may be in an X-linked recessive inheritance pattern. The proband (case 53) carried two novel mutations in ALT1 gene and L1CAM gene (c.2511C>A), respectively. The L1CAM gene is the causative gene for the SPG1 X-linked recessive-hereditary spastic paraplegias.Our data confirm the genetic heterogeneity of hereditary spastic paraplegias, and SPG4/SPAST were the most frequent forms. The pathogenicity of the novel mutations is worth to be further investigated.

Indexed as

DNA Mutational AnalysisFemaleHumansMalePedigreeRetrospective StudiesSequence DeletionSpastic Paraplegia, Hereditary

Identifiers

PMID32501971
PMCPMC7306340
OpenAlexW3034086518

What OpenQuestion holds

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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.