Evidence map›Paper›PMID 39198325›Full record

SynthesisCerebellum (London, England)2024

Polyneuropathy in Patients with Spinocerebellar Ataxias Types 2, 3, and 10: A Systematic Review.

André Eduardo de Almeida Franzoi, Gustavo Figueiredo da Silva, Eduardo de Souza Somensi, Marcelo Henrique de Moura Campos, Giulia Murillo Wollmann, Otto Jesus Hernandez Fustes, Gustavo Lenci Marques, Helio Afonso Ghizoni Teive

Abstract readSystematic Review
PubMed Publisher
In one paragraph

Synthesis in Cerebellum (London, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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.

André Eduardo de Almeida FranzoiDepartment of Internal Medicine, Neurology Service, Hospital de Clínicas, Federal University of Paraná, Curitiba, Paraná, Brazil. andrefranzoi@hotmail.com.
Gustavo Figueiredo da SilvaDepartment of Internal Medicine, Neurology Service, Hospital de Clínicas, Federal University of Paraná, Curitiba, Paraná, Brazil.
Eduardo de Souza SomensiDepartment of Internal Medicine, Hospital de Clínicas, Federal University of Paraná, Curitiba, Paraná, Brazil.
Marcelo Henrique de Moura CamposDepartment of Internal Medicine, Joinville Regional University, UNIVILLE, Joinville, Santa Catarina, Brazil.
Giulia Murillo WollmannDepartment of Neurology, Hospital Mãe de Deus, Porto Alegre, Rio Grande do Sul, Brazil.
Otto Jesus Hernandez FustesDepartment of Internal Medicine, Neurology Service, Hospital de Clínicas, Federal University of Paraná, Curitiba, Paraná, Brazil.
Gustavo Lenci MarquesDepartment of Internal Medicine, Cardiology Service, Hospital de Clínicas, Federal University of Paraná, Curitiba, Paraná, Brazil.
Helio Afonso Ghizoni TeiveDepartment of Internal Medicine, Neurology Service, Hospital de Clínicas, Federal University of Paraná, Curitiba, Paraná, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spinocerebellar ataxia (SCA) is an autosomal dominant hereditary disease with a low prevalence, for which more than 50 types have been described. This group of neurodegenerative diseases can present as different phenotypes with varying progression rates and clinical manifestations of different severities. Herein, we systematically reviewed existing medical literature to describe the main characteristics of polyneuropathy in patients with SCA types 2, 3, and 10. Using relevant keywords, 16,972 articles were identified from the databases. Of these, 5,329 duplicate studies were excluded before screening. Subsequently, 11,643 studies underwent title and abstract review, of which only 49 were selected for full-text review. Among these, 24 studies were included. The medical literature suggests peripheral neuropathy - probably in a polyneuropathy phenotype - in SCA types 2 and 3. It is not possible to determine whether there is peripheral neuropathy in patients with SCA type 10, as there is only one case series in Mexico that described peripheral neuropathy in this group. Further studies are required to investigate peripheral neuropathy in patients with SCA types 2, 3, and 10. The study and description of a possible statistical association between CAG repeats and SARA scale scores with the presence of peripheral neuropathy are important points requiring assessment in future research.

Indexed as

PolyneuropathiesSpinocerebellar AtaxiasHumansMachado-Joseph DiseaseElectroneuromyographyPeripheral neuropathyPolyneuropathySpinocerebellar ataxia

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.