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C9orf 72 repeat expansions in a Canadian provincial cohort (P2.066)

2015· article· en· W2467093286 on OpenAlexaffabout
Anil Venkitachalam, Stacey Hume, Setareh Ashtiani, Susan Christian, Oksana Suchowersky

Bibliographic record

VenueNeurology · 2015
Typearticle
Languageen
FieldMedicine
TopicAmyotrophic Lateral Sclerosis Research
Canadian institutionsUniversity of Alberta HospitalAlberta Hospital EdmontonUniversity of Alberta
Fundersnot available
KeywordsCohortMedicineFamily medicineInternal medicine

Abstract

fetched live from OpenAlex

OBJECTIVE: To determine the referral indication, family history and clinical test sensitivity of C9orf72. BACKGROUND:The Chromosome 9 open reading frame 72 (C9orf72) gene, located on chromosome 9p21 contains a hexanucleotide GGGGCC repeat located in a non-coding region. Normal range is 2 to 23 repeats, with repeats greater than 30 considered pathogenic. These are inherited in an autosomal dominant fashion. Repeats between 23 to 30 are of intermediate significance. Research has demonstrated this repeat expansion as the most common cause of familial Amyotrophic Lateral Sclerosis (ALS) and Fronto- Temporal Dementia (FTD) with a worldwide incidence of 34[percnt] and 25[percnt] respectively. Clinical testing for this expansion became available in Alberta in January 2013. All testing for C9orf72 mutations in Alberta is performed in one laboratory at the University of Alberta in Edmonton. DESIGN/METHODS: Using the Molecular Diagnostic laboratory database, we identified all requests for C9orf72 testing and reviewed patient data. RESULTS:To date, 59 patients (35 men, 24 women) have been tested, 35 for ALS, 13 FTD, 4 Atypical Parkinsonism and 4 Late onset ataxia (LOA). Family history was positive in 27 patients (14 ALS, 7 FTD, 3 Atypical Parkinsonism and 3 LOA). C9orf72 abnormalities were detected in 10 patients (7 ALS, 3 FTD); all had a positive family history. In the FTD phenotype, 1 pathogenic expansion, 1 homozygous expansion and 1 intermediate expansion were detected. In the ALS phenotype, 1 deletion and 6 pathogenic expansions were detected. No mutations were detected in the Atypical Parkinsonism, LOA phenotypes and sporadic cases. CONCLUSIONS: C9orf72 abnormalities were detected in 17[percnt] of total cases, with 23[percnt] positive in ALS and 20[percnt] positive in FTD, similar to rates seen in Western European populations. Lack of family history significantly decreases the possibility of a positive result. Study Supported by: Toupin Research Foundation, University of Alberta

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)0.001
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 score0.019
Threshold uncertainty score0.101

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.001
Meta-epidemiology (narrow)0.0010.001
Meta-epidemiology (broad)0.0000.001
Bibliometrics0.0010.003
Science and technology studies0.0050.001
Scholarly communication0.0010.000
Open science0.0010.001
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0040.001

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 head0.038
GPT teacher head0.303
Teacher spread0.265 · 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

Citations0
Published2015
Admission routes2
Has abstractyes

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