Evidence map›Paper›PMID 28456900›Full record

ArticleCerebellum (London, England)2017

NESSCA Validation and Responsiveness of Several Rating Scales in Spinocerebellar Ataxia Type 2.

Thais L Monte, Estela R Reckziegel, Marina C Augustin, Amanda S P Silva, Lucas D Locks-Coelho, Orlando Barsottini, José L Pedroso, Fernando R Vargas, Maria-Luiza Saraiva-Pereira, Vanessa Bielefeldt Leotti and 2 more

Abstract readValidation Study
PubMed Publisher
In one paragraph

Article in Cerebellum (London, England), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.7field-weighted citation impact, top 36% 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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Rehabilitation in patients with cerebellar ataxias.Arquivos de neuro-psiquiatria · 2022
    Article
  3. Review
  4. Article
  5. Review
  6. 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

12 authors at 4 institutions in 1 country.

Thais L MonteServiço de Neurologia, Hospital de Clínicas de Porto Alegre, Porto Alegre, Rio Grande do Sul, Brazil.
Estela R ReckziegelFaculdade de Medicina, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Marina C AugustinFaculdade de Medicina, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Amanda S P SilvaFaculdade de Medicina, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Lucas D Locks-CoelhoFaculdade de Medicina, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Orlando BarsottiniSetor de Neurologia Geral e Ataxias, Disciplina de Neurologia Clínica da UNIFESP-Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil.
José L PedrosoSetor de Neurologia Geral e Ataxias, Disciplina de Neurologia Clínica da UNIFESP-Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil.
Fernando R VargasLaboratório de Epidemiologia de Malformações Congênitas, Fundação Oswaldo Cruz, Rio de Janeiro, Brazil.
Maria-Luiza Saraiva-PereiraServiço de Genética Médica, Hospital de Clínicas de Porto Alegre, Porto Alegre, Rio Grande do Sul, Brazil.
Vanessa Bielefeldt LeottiDepartamento de Matemática e Estatística, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Laura Bannach JardimPrograma de Pós-Graduação em Ciências Médicas, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil. ljardim@hcpa.edu.br.
Rede Neurogenética
Universidade Federal do Rio Grande do Sul · BRHospital de Clínicas de Porto Alegre · BRFundação Oswaldo Cruz · BRUniversidade Federal de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Spinocerebellar ataxia type 2 (SCA2), caused by a CAG expansion (CAGexp) at ATXN2, has a complex clinical picture. While validated ataxia scales are available, comprehensive instruments to measure all SCA2 neurological manifestations are required. This study aims to validate the Neurological Examination Score for the assessment of Spinocerebellar Ataxias (NESSCA) to be used in SCA2 and to compare its responsiveness to those obtained with other instruments. NESSCA, SARA, SCAFI, and CCFS scales were applied in symptomatic SCA2 patients. Correlations were done with age at onset, disease duration, CAGexp, and between scales. Responsiveness was estimated by comparing deltas of stable to worse patients after 12 months, according to Patient Global Impression of change, and the area under the curve (AUC) of the Receiver Operating Characteristics curve of scores range. Eighty-eight evaluations (49 patients) were obtained. NESSCA had an even distribution and correlated with disease duration (r = 0.55), SARA (r = 0.63), and CAGexp (rho = 0.32): both explained 44% of NESSCA variance. Deltas (95% CI) after 1 year in stable and worse patients were only significantly different for SARA. NESSCA, SARA, SCAFI, and CCFS AUC were 0.63, 0.81, 0.49, and 0.48, respectively. NESSCA is valid to be used in SCA2. However, the only instrument that presented good responsiveness to change in 1 year was SARA. We suggest that NESSCA can be used as a secondary outcome in future trials in SCA2 due to the burden of neurological disabilities related to disease progression.

Indexed as

Neurologic ExaminationSeverity of Illness IndexAdultAgedAge of OnsetArea Under CurveDisease ProgressionFemaleFollow-Up StudiesHeterozygoteHumansMaleMiddle AgedROC CurveSpinocerebellar AtaxiasYoung AdultNESSCANeurological Examination Score for Spinocerebellar AtaxiaSARASCA2SCAFISpinocerebellar ataxia type 2

Identifiers

PMID28456900
OpenAlexW2608868980

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.