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Record W4248029586 · doi:10.1002/hep.28186

Parallel 17: Hepatitis B: Prevention, Natural History, and Outcomes

2015· article· en· W4248029586 on OpenAlexaffabout
Adrian M. Di Bisceglie, M. Lombardero, Jeffrey Teckman, Lewis R. Roberts, Harry L.A. Janssen, Steven H. Belle, Jay Hoof- Nagle, Jay H. Hoofnagle, Gina Choi, Marina Serper, David E. Kaplan, Kimberly A. Forde, Gregory J. Gores, Conatus Lewis, Richard B. Roberts

Bibliographic record

VenueHepatology · 2015
Typearticle
Languageen
FieldMedicine
TopicHepatitis B Virus Studies
Canadian institutionsUniversity of Toronto
Fundersnot available
KeywordsNatural historyMedicineNatural (archaeology)HepatitisVirologyInternal medicineHistory

Abstract

fetched live from OpenAlex

Background: HBV infection is frequent world-wide and may result in progressive liver disease or HCC.Effective therapies are available but treatment is usually reserved for patients (pts) with selected biochemical and serological profiles (phenotypes).Currently, criteria for defining HBV phenotype are not standardized and are based upon expert opinion rather than medical evidence.Aim: To determine the distribution of phenotypes in a large cohort of North American pts with chronic HBV infection using standardized definitions and calculation.Methods: Epidemiologic, demographic, biochemical and virologic features of pts enrolled into the HBRN Cohort Study at 19 US and 1 Canadian site were analyzed, assigning pts into 1 of 4 phenotypes: immune tolerant (IT), chronic hepatitis B with (CHB e+) or without HBeAg (CHB e-) or inactive carrier (IC) based upon baseline HBV DNA and ALTs.Cut-off HBV DNA values used to define phenotypes were 10 4 IU/ml for e-negative and 10 5 for e-positive pts.ALT cut-offs were analyzed using either fixed values (30 U/L for men, 20 U/L for women) or using each local lab ULN.Pts not fitting into a phenotype were designated "Indeterminant".Independently, local investigators assigned a phenotype at baseline based on available laboratory values and clinical impression.Results: 1398 adults (51% male, 71% Asian) had data needed to determine phenotype.The table shows the distribution of phenotypes calculated by two methods of assessing ALT and physician assessment.Only moderate agreement was found between clinician-determined and calculated phenotype using fixed ALTs (Kappa 0.39, 95% CI 0.36-0.42).Of note, only 13% of pts were designated Indeterminant by clinicians compared to 20-40% by computer calculation.Using the Fixed ALT groups for comparison, IT was most distinct, being generally younger, more frequently Asian and female.The most frequent clinical phenotype identified was Indeterminant, the majority of whom (83%) had elevated ALT values despite low levels of HBV DNA, not apparently associated with higher BMI, alcohol consumption or HBV genotype.Clinician estimates often differed from the calculated phenotype.Conclusions: The clinical significance of HBV phenotypes using these standardized definitions requires further study based on long term follow up of these patient cohorts but there is clearly a need to re-examine categorization of pts with chronic HBV infection to more accurately predict their outcomes and need for therapy.

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)0.002
metaresearch head score (Gemma)0.005
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 score0.064

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0020.005
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0000.001
Bibliometrics0.0010.002
Science and technology studies0.0000.000
Scholarly communication0.0010.001
Open science0.0010.001
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0190.002

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 head0.047
GPT teacher head0.308
Teacher spread0.261 · 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
Published2015
Admission routes2
Has abstractyes

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