Evidence map›Paper›PMID 40067487›Full record

ArticleJournal of neurology2025

The impact of interrupted ATXN10 expansions on clinical findings of spinocerebellar ataxia type 10.

Ali Hasan, Gabriel Vasata Furtado, Elaine Miglorini, Rafaella Mergener, Breno Massuyama, Orlando Barsottini, José Luiz Pedroso, Helio G Teive, Maria Luiza Saraiva-Pereira, Tetsuo Ashizawa and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

11 authors.

Ali Hasan *Programa de Pós-Graduação em Genética e Biologia Molecular, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Gabriel Vasata Furtado *Centros de Pesquisa Clínica e Experimental, Hospital de Clínicas de Porto Alegre, Porto Alegre, RS, Brazil.
Elaine MigloriniServiço de Neurologia, Departamento de Medicina Interna, Unidade de Distúrbios do Movimento, Hospital de Clínicas, Universidade Federal do Paraná, Curitiba, PR, Brazil.
Rafaella MergenerCentros de Pesquisa Clínica e Experimental, Hospital de Clínicas de Porto Alegre, Porto Alegre, RS, Brazil.
Breno MassuyamaHospital São Paulo, Universidade Federal do Estado de São Paulo, São Paulo, SP, Brazil.
Orlando BarsottiniHospital São Paulo, Universidade Federal do Estado de São Paulo, São Paulo, SP, Brazil.
José Luiz PedrosoHospital São Paulo, Universidade Federal do Estado de São Paulo, São Paulo, SP, Brazil.
Helio G TeiveServiço de Neurologia, Departamento de Medicina Interna, Unidade de Distúrbios do Movimento, Hospital de Clínicas, Universidade Federal do Paraná, Curitiba, PR, Brazil.
Maria Luiza Saraiva-PereiraPrograma de Pós-Graduação em Genética e Biologia Molecular, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil.
Tetsuo AshizawaMethodist Hospital and Houston Methodist Research Institute, Houston, TX, USA.
Laura Bannach JardimPrograma de Pós-Graduação em Genética e Biologia Molecular, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil. ljardim@hcpa.edu.br.ORCID http://orcid.org/0000-0001-6907-5068

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 404185/2019-3
6 · The paper itself

Abstract

backgroundSpinocerebellar ataxia type 10 (SCA10), due to an ATTCT repeat expansion in ATXN10, has variable expressivity and the role of presence (ATTCTint +) and absence (ATTCTint-) of interruptions in the repeat is not clear. We aimed to describe the relations between ATTCTint + and age at onset, seizures, and neurologic severity in ataxic and non-ataxic carriers from Brazil.

methodsFamily, age at onset (AO), and seizures data plus DNA were obtained from symptomatic carriers already diagnosed in Porto Alegre, Curitiba, and São Paulo, Brazil. Patients and their relatives were invited to be evaluated through Scale of Assessment and Rating of Ataxia (SARA) and other clinical scales; a SARA > 2.5 classified subjects as ataxic carriers. Repeat-primed PCR (RP-PCR) defined the expansions with (ATTCTint +) or without (ATTCTint-) interruptions. Comparisons were performed for a p level of 0.05.

resultsAmong 78 ataxic carriers, earlier AO (p = 0.039) and higher occurrences of epilepsy (p < 0.0001) were seen in subjects with ATTCTint + than in those with ATTCTint-. Clinical scales were worse in 34 ataxics than in 7 non-ataxics and 10 related controls (p = 0.006) and did not discriminate non-ataxics from controls. The 11 ataxic ATTCTint + carriers had higher SARA scores per year of disease duration than the 23 ATTCTint- carriers (r = 0.879, beta = 0.45, p = 0.0001). DISCUSSION: ATTCTint + carriers had worse clinical findings than ATTCTint- carriers: earlier AO, more seizures, and worse ataxia scores. Interruptions in the expanded repeat have a real impact in SCA10 phenotype.

Indexed as

Ataxin-10DNA Repeat ExpansionSpinocerebellar AtaxiasTrinucleotide Repeat ExpansionAdultAgedAge of OnsetBrazilEpilepsyFemaleHumansMaleMiddle AgedSeizuresSeverity of Illness IndexYoung AdultAtaxin-10ATXN10 protein, humanATTCT interruptionsATXN10NESSCANon-ataxic carriersSARASCA10

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.