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P0183 DIAGNOSIS AND OUTCOME OF WILSON DISEASE IN A PAEDIATRIC COHORT

2004· article· en· W4390568260 on OpenAlexaff
E A Roberts, Catherine O’Connor, D W Cox

Bibliographic record

VenueJournal of Pediatric Gastroenterology and Nutrition · 2004
Typearticle
Languageen
FieldNursing
TopicTrace Elements in Health
Canadian institutionsSeagen (Canada)University of AlbertaHospital for Sick Children
Fundersnot available
KeywordsMedicineSick childCohortPediatric gastroenterologyInternal medicineAssociate editorCohort studyPediatricsFamily medicineProportional hazards modelDiseaseGastroenterologyLibrary science

Abstract

fetched live from OpenAlex

Introduction: Wilson disease (WD) is highly variable clinically. It may present as hepatic, neurological or psychiatric disease. Classic features include: age at presentation between 5 and 35 years-old, Kayser-Fleischer (K-F) rings evident, and serum ceruloplasmin <50 mg/L. In non-classic cases diagnosis is difficult. With >250 mutations of the ATP7B gene identified and high prevalence of compound heterozygotes, genetic diagnosis—though definitive—may be elusive. The aim of this study was to review our clinical experience with WD at the Hospital for Sick Children in the past 20 years. Methods: 35 patients were reviewed who have been diagnosed or treated at the Hospital for Sick Children; adult and correspondence-only referral patients were excluded. Results: 5 patients presented with fulminant hepatic failure (FHF): 4 (3 female) had typical Wilsonian FHF and all required liver transplant (OLT). One male patient who had WD and coincidental viral FHF survived without OLT. Of the other 30 patients (15 F, 15 M), 22 presented with clinical disease (21 hepatic) and 8 were identified by sib screening. These 30 patients were young (mean age 10.8 ± 3.4 [SD] yrs). K-F rings were identified in 14 of 28 patients (50%); no statistically significant difference in age was found between those with or without K-F rings. Mean serum Cu concentration was 9.0 micromol/L (within normal range in 25%). Serum ceruloplasmin was <50 mg/L in 12 of 28 patients and >150 mg/L in 8 of 28 patients. Mean basal 24-hr urinary Cu (BUrCu; n=23) was 11.5 micromol/d. All but one patient (96%) had BUrCu >0.6 micromol/d; 7 patients had BUrCu 0.6–3 micromol/d. After pencillamine challenge, 9 of 16 patients had urinary Cu excretion of at least 25 micromol/d. Notably, 7 patients (44%) did not achieve this benchmark, but diagnosis was secure or genetically proven in all 7. In subset analysis (n= at least 15), liver biopsy rarely showed copper histochemically (positive in 24%) but often showed typical changes in mitochondria by electron microscopy (in 93%). The Nazer index (Gut 1986;27:1377) used in 14 patients was inaccurate in predicting outcome of 2 patients. Genotype determination frequently revealed Arg778Leu. Currently 29 of 35 patients are alive without OLT and 68% are taking either trientine or zinc. Conclusion: K-F rings are infrequently found in children with WD. Serum ceruloplasmin is often not informative. Basal 24-hr urinary Cu excretion is nearly always >0.6 micromol/d. Some WD patients may not have a “diagnostic” penicillamine challenge.

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)0.003
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 score0.003
Threshold uncertainty score0.007

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.003
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.001
Science and technology studies0.0010.001
Scholarly communication0.0010.001
Open science0.0000.001
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0020.000

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 head0.014
GPT teacher head0.285
Teacher spread0.271 · 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".

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Citations0
Published2004
Admission routes1
Has abstractyes

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