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Record W4386886402 · doi:10.1136/gutjnl-2023-basl.17

P1 Analysis of long-term treatment effects of odevixibat on clinical outcomes in children with progressive familial intrahepatic cholestasis in odevixibat clinical studies vs external controls from the NAPPED database

2023· article· en· W4386886402 on OpenAlex

Why this work is in the frame

A frame that forgets how it found something cannot be audited. These are the routes that admitted this work.

affAt least one author lists a Canadian institution in the pinned OpenAlex snapshot.

Bibliographic record

VenuePoster presentations · 2023
Typearticle
Languageen
FieldMedicine
TopicDrug Transport and Resistance Mechanisms
Canadian institutionsSickKids FoundationHospital for Sick ChildrenUniversity of TorontoUniversity Health Network
Fundersnot available
KeywordsMedicineInternal medicineGastroenterologyLiver transplantationCholestasisProportional hazards modelClinical endpointRetrospective cohort studyPopulationProgressive familial intrahepatic cholestasisBile acidPropensity score matchingSurvival analysisSurgeryTransplantationRandomized controlled trial

Abstract

fetched live from OpenAlex

<h3>Background</h3> Progressive familial intrahepatic cholestasis (PFIC) is a group of rare cholestatic liver diseases characterised by intractable pruritus, elevated serum bile acids (sBAs), and progressive liver damage. NAPPED (NAtural course and Prognosis of PFIC and Effect of biliary Diversion) is a large retrospective database investigating the natural history of PFIC. Odevixibat, an ileal bile acid transporter inhibitor, reduced sBAs and pruritus in patients with PFIC in the phase 3 PEDFIC 1 and PEDFIC 2 studies. We compared clinical outcomes of surgical biliary diversion (SBD), liver transplantation (LT), and death in patients from NAPPED (not treated with odevixibat) with odevixibat-treated patients from the PEDFIC studies. <h3>Methods</h3> The analysis population comprised odevixibat-naive patients from NAPPED and odevixibat-treated patients from PEDFIC 1 and/or PEDFIC 2. Patients with bile salt export pump subtype 3 (BSEP3) mutations were excluded. Eligibility criteria were aligned across cohorts and included genetically proven diagnosis of PFIC1 or PFIC2, sBAs ≥100 µmol/L, alanine aminotransaminase and total bilirubin ≤10× the upper limit of normal, and no prior SBD or LT. Propensity scores, inverse probability of treatment weighting, and matching methods were used to identify and balance baseline covariates, including PFIC1, PFIC2-BSEP1, or PFIC2-BSEP2. The primary endpoint was event-free survival (EFS; time to first event of SBD, LT, or death); secondary endpoints included native liver survival (NLS), SBD-free survival (DFS), and overall survival (OS). Survival outcomes were measured from study day 1; treatment differences were evaluated by weighted log-rank tests and Cox regression. <h3>Results</h3> A cohort of 80 NAPPED patients (controls) was compared with 69 odevixibat-treated patients. Median study duration in the odevixibat cohort was 22.6 months (range: 1.9–39.2 months). Follow-up duration in the NAPPED cohort was truncated accordingly. Odevixibat-treated patients showed significantly higher EFS and DFS than controls (hazard ratio [HR] [95% CI]: 0.20 [0.09−0.45] and 0.13 [0.04−0.39], respectively); numerical improvements in NLS and OS were also observed. Results were consistent when different sensitivity analyses were performed. Additional subgroup analyses indicated that EFS was higher in odevixibat-treated patients with PFIC1 (HR [95% CI]: 0.10 [0.02−0.55]) and PFIC2 (HR [95% CI]: 0.34 [0.12−1.00]) vs controls. <h3>Conclusions</h3> Odevixibat treatment is associated with higher EFS in patients with PFIC without prior SBD upon comparison with matched non-odevixibat-treated patients from the NAPPED registry.

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.

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 categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.008
Threshold uncertainty score0.551

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0000.001
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
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 head0.067
GPT teacher head0.424
Teacher spread0.357 · 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