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Record W7120445435

Clinical, genetic, radiological and retinal architectureevaluation in patients with SACS generelatedataxia.

2019· article· pt· W7120445435 on OpenAlexaboutno aff
Flavio Moura [UNIFESP] Rezende Filho

Bibliographic record

VenueUNIFESP Institutional Repository (Universidade Federal de São Paulo) · 2019
Typearticle
Languagept
FieldNeuroscience
TopicGenetic Neurodegenerative Diseases
Canadian institutionsnot available
Fundersnot available
KeywordsRetinalNerve fiber layerAtaxiaNeuroimagingRetinal DisorderCerebellar ataxia
DOInot available

Abstract

fetched live from OpenAlex

BACKGROUND: Cerebellar ataxia is characterized by loss of balance and coordination, and is found in several neurological conditions. This group of disorders is very diverse in clinical presentations and etiopathogenesis, and includes neurovascular, inflammatory, infectious, neurodegenerative and hereditary diseases. Genetic defects are an important cause of ataxia. The progress in molecular diagnosis techniques has allowed the identification of causative genes and characterization of new forms of ataxia, including the autosomal recessive spastic ataxia of CharlevoixSaguenay (ARSACS), described in 1978 in French-Canadian families. The causative gene of this disorder, SACS, was identified in 2000 and this allowed molecular confirmation in several regions of the world. Thickening in the retinal nerve fiber layer (RNFL) in optical coherence tomography (OCT) is a hallmark of ARSACS, which distinguishes it from other ataxias. Many aspects of the pathogenesis of ARSACS are not clear and large series of Brazilian patients have not been published. OBJECTIVES: This thesis is divided in two studies, with the following objectives: Study 1 - To evaluate the clinical, genetic, neuroimaging and ophthalmological profile of Brazilian patients with ARSACS. Study 2 - To analyze qualitatively the retinal architecture of 28 ARSACS cases. METHODS: In the Study 1, we included 13 consecutive cases of spastic ataxia harboring two SACS variants and performed detailed neurological assessment, neuroimage study and ophthalmological evaluation, and applied scales to quantify ataxia severity. Brazilian patients phenotype was compared to the largest series published. The Study 2 investigated the retinal architecture of 28 ARSACS cases using fundoscopy and perifoveal spectral domain OCT scans. RESULTS: Study 1 - The phenotype of Brazilian patients with ARSACS is characterized in most cases by spastic ataxia with onset in the first decade of life. Abnormalities in neuroimaging and retinal architecture occurred in the majority. Study 2 - Patients with ARSACS presented specific findings in qualitative analysis of retinal architecture. We identified peripapillary striations, a papillomacular fold, the saw-tooth sign and foveal hypoplasia in OCT. CONCLUSIONS: Study 1 is the first to evaluate systematically the phenotype of ARSACS in a large Brazilian cohort and confirmed the importance of neuroimaging and OCT in the work-up of recessive ataxias. Study 2 revealed specific signs of ARSACS in qualitative analysis of retinal architecture and demonstrated ARSACS causes foveal hypoplasia, suggesting a neurodevelopmental component in its pathogenesis.

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 distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesMeta-epidemiology (narrow)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.031
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0010.001
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0000.001
Science and technology studies0.0010.001
Scholarly communication0.0000.000
Open science0.0010.000
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0000.000

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 head0.016
GPT teacher head0.247
Teacher spread0.231 · 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 teacher head, not a consensus.

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
Published2019
Admission routes1
Has abstractyes

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