Abstract

Results

Predictive models using baseline data predicted which patients would develop liver signals during the trials with average validation accuracy around 80%. Baseline levels of individual liver chemistry tests were most important for predicting their own elevations during the trials. High bilirubin levels at baseline were not uncommon and were associated with a high risk of developing biochemical Hy’s law cases. Baseline γ-glutamyltransferase (GGT) level appeared to have some predictive value, but did not increase predictability beyond using established liver chemistry tests.

Conclusion

It is possible to predict which patients are at a higher risk of developing liver chemistry signals using pretreatment (baseline) data. Derived knowledge from such predictions may allow proactive and targeted risk management, and the type of analysis described here could help determine whether new biomarkers offer improved performance over established ones.

Citation impact

708
total citations
FWCI
8.02
Percentile
100%
References
12
Citations per year

Authors

5

Topics & keywords

Keywords
  • Baseline (sea)
  • Clinical trial
  • Predictability
  • Medicine
  • Internal medicine
  • Demographics
  • Statistics
  • Mathematics
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