Evidence map›Paper›PMID 25684666›Full record

Trial reportHepatology (Baltimore, Md.)2015

Improvement of predictive models of risk of disease progression in chronic hepatitis C by incorporating longitudinal data.

Monica A Konerman, Yiwei Zhang, Ji Zhu, Peter D R Higgins, Anna S F Lok, Akbar K Waljee

Open access · greenAbstract readClinical Trial
In one paragraph

Trial report in Hepatology (Baltimore, Md.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

32 citing papers in PubMed, 1 synthesis or guideline pooled it, 65 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
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  5. Review
  6. The role of artificial intelligence in the management of liver diseases.The Kaohsiung journal of medical sciences · 2024
    Review
  7. Review
  8. Article
  9. Machine learning prediction model for treatment responders in patients with primary biliary cholangitis.JGH open : an open access journal of gastroenterology and hepatology · 2023
    Article
  10. Review
  11. Article
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  13. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Monica A KonermanDivision of Gastroenterology, Department of Internal Medicine, University of Michigan Health System, Ann Arbor, MI.
Yiwei ZhangDivision of Gastroenterology, Department of Internal Medicine, University of Michigan Health System, Ann Arbor, MI.
Ji ZhuDivision of Gastroenterology, Department of Internal Medicine, University of Michigan Health System, Ann Arbor, MI.
Peter D R HigginsDivision of Gastroenterology, Department of Internal Medicine, University of Michigan Health System, Ann Arbor, MI.
Anna S F LokDivision of Gastroenterology, Department of Internal Medicine, University of Michigan Health System, Ann Arbor, MI.
Akbar K WaljeeDivision of Gastroenterology, Department of Internal Medicine, University of Michigan Health System, Ann Arbor, MI.
Michigan Medicine · US

Funding

University of Michigan Center for Gastrointestinal ResearchP30DK034933 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WILEY, JOHN W · 1986 to 2021
$22.5M
Training Program in Gastrointestinal EpidemiologyT32DK062708 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Peter D.R. Higgins, Elliot Tapper · 2003 to 2026
$3.9M
Application of Machine Learning Algorithms to Thiopurine Monitoring in IBDR01GM097117 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HIGGINS, PETER D.R. · 2012 to 2016
$1.9M
Risk Stratification and Targeted Therapy for HELP Diseases in VeteransIK2HX000775 · VA · VETERANS HEALTH ADMINISTRATION · PI WALJEE, AKBAR K · 2014 to 2014
–
HSRD VA IK2 HX000775NIDDK NIH HHS P30 DK034933NIDDK NIH HHS T32 DK062708NIDDK NIH HHS T32DK062708NIGMS NIH HHS R01 GM097117
6 · The paper itself

Abstract

unlabelledExisting predictive models of risk of disease progression in chronic hepatitis C have limited accuracy. The aim of this study was to improve upon existing models by applying novel statistical methods that incorporate longitudinal data. Patients in the Hepatitis C Antiviral Long-term Treatment Against Cirrhosis trial were analyzed. Outcomes of interest were (1) fibrosis progression (increase of two or more Ishak stages) and (2) liver-related clinical outcomes (liver-related death, hepatic decompensation, hepatocellular carcinoma, liver transplant, or increase in Child-Turcotte-Pugh score to ≥7). Predictors included longitudinal clinical, laboratory, and histologic data. Models were constructed using logistic regression and two machine learning methods (random forest and boosting) to predict an outcome in the next 12 months. The control arm was used as the training data set (n = 349 clinical, n = 184 fibrosis) and the interferon arm, for internal validation. The area under the receiver operating characteristic curve for longitudinal models of fibrosis progression was 0.78 (95% confidence interval [CI] 0.74-0.83) using logistic regression, 0.79 (95% CI 0.77-0.81) using random forest, and 0.79 (95% CI 0.77-0.82) using boosting. The area under the receiver operating characteristic curve for longitudinal models of clinical progression was 0.79 (95% CI 0.77-0.82) using logistic regression, 0.86 (95% CI 0.85-0.87) using random forest, and 0.84 (95% CI 0.82-0.86) using boosting. Longitudinal models outperformed baseline models for both outcomes (P < 0.0001). Longitudinal machine learning models had negative predictive values of 94% for both outcomes.

conclusionsPrediction models that incorporate longitudinal data can capture nonlinear disease progression in chronic hepatitis C and thus outperform baseline models. Machine learning methods can capture complex relationships between predictors and outcomes, yielding more accurate predictions; our models can help target costly therapies to patients with the most urgent need, guide the intensity of clinical monitoring required, and provide prognostic information to patients.

Indexed as

Disease ProgressionModels, BiologicalArtificial IntelligenceFemaleFibrosisHepatitis C, ChronicHumansLiverMaleMiddle AgedRisk AssessmentStatistics as Topic

Identifiers

PMID25684666
PMCPMC4480773
OpenAlexW1724747758

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.