MétaCan
Menu
Back to cohort
Record W4385477459 · doi:10.1002/mds.29559

As Frequent as Polyglutamine Spinocerebellar Ataxias: <scp>SCA27B</scp> in a Large German Autosomal Dominant Ataxia Cohort

2023· letter· en· W4385477459 on OpenAlexafffundabout
Holger Hengel, David Pellerin, Carlo Wilke, Zofia Fleszar, Bernard Brais, Tobias B. Haack, Andreas Traschütz, Lüdger Schöls, Matthis Synofzik

Bibliographic record

VenueMovement Disorders · 2023
Typeletter
Languageen
FieldNeuroscience
TopicGenetic Neurodegenerative Diseases
Canadian institutionsMcGill UniversityMontreal Neurological Institute and Hospital
FundersElse Kröner-Fresenius-StiftungDeutsche ForschungsgemeinschaftGénome Québec
KeywordsSpinocerebellar ataxiaTrinucleotide repeat expansionAtaxiaCohortPopulationGeneticsBiologyMedicineInternal medicineNeuroscienceGeneAllele

Abstract

fetched live from OpenAlex

German Autosomal Dominant Ataxia CohortIntronic GAA repeat expansions in the fibroblast growth factor 14 gene (FGF14) have recently been shown to be a common cause of adult-onset degenerative ataxia (spinocerebellar ataxia 27B [SCA27B], MIM: 620174), 1,2 but frequencies in strictly consecutive SCA cohorts are unknown.Here we studied the relative frequencies of SCA27B in a cohort of genetically undetermined autosomal dominant cerebellar ataxia (ADCAs) and relative to other forms of genetically confirmed SCAs. ADCA ScreeningWe screened a consecutive cohort of 79 German patients from 51 families with genetically undetermined ADCA for the intronic FGF14 GAA repeat expansion.All index patients were negative for SCA types 1, 2, 3, 6, 7, and 17 and negative on either exome or short-read genome sequencing.Detailed inclusion criteria and methods are outlined in the Supporting Information.Twenty-Six of 51 families (26/79 patients) were found to carry a FGF14 (GAA) ≥250 expansion, thus accounting for 31% of patients with ADCA (Fig. 1A).Although only expansions of at least 250 GAA repeat units were considered pathogenic 1,2 and used for the current frequency analysis, we identified one family with late-onset largely pure cerebellar ataxia, and thus compatible with SCA27B, 3 in which the index patient had a repeat count of 256 GAA units, whereas her affected mother had a repeat count of 234 repeat units (Supporting Information Fig. S2).This indicates that the pathogenic threshold might be even be lower than the previously established cutoff of 250 repeat units.This hypothesis warrants further confirmation in future larger segregation and population studies.Moreover, a (GAAGGA) n repeat expansion was found in three index patients.This hexanucleotide expansion did not segregate with disease in all three families (Supporting Information Fig. S1).This provides further evidence for previous observations suggesting that non-GAA repeat expansions are unlikely pathogenic 1 and warrants caution on recent discussions of its pathogenicity.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.001
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.006
Threshold uncertainty score0.011

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.001
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.001
Science and technology studies0.0010.000
Scholarly communication0.0010.000
Open science0.0000.001
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0020.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.014
GPT teacher head0.266
Teacher spread0.252 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations65
Published2023
Admission routes3
Has abstractyes

Explore more

Same venueMovement DisordersSame topicGenetic Neurodegenerative DiseasesFrench-language works237,207