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Published on: August 22, 2018
Finding a constrained number of predictor phenotypes for multiple outcome prediction
Jenna M Reps1,2, Jenna Wong3, Egill A Fridgeirsson2
1Johnson & Johnson LLC, Raritan, New Jersey, USA jreps@its.jnj.com.
Insights
Researchers identified a core set of 67 predictors, plus age and sex, that can be used to build multiple prognostic models. This approach simplifies clinical decision-making by enabling many prediction models on a single website form.
Area of Science:
- Medical informatics
- Clinical prediction modeling
- Biostatistics
Background:
- Prognostic models are crucial for medical decision-making but often predict single outcomes.
- Existing models require unique predictors, limiting their integrated use.
- A need exists for a unified clinical tool predicting multiple outcomes from common predictors.
Purpose of the Study:
- To identify a constrained, outcome-agnostic set of predictors.
- To develop a method for creating versatile prognostic models.
Main Methods:
- A novel technique aggregated standardized mean differences across numerous outcomes.
- This method identified a constrained set of predictors relevant to multiple outcomes.
- Model performance was evaluated on eight prediction tasks against various benchmarks.
Main Results:
- A constrained set of 67 predictors, plus age and sex, was identified.
- These predictors encompass cardiovascular, kidney/liver, mental health, gastrointestinal, infectious, and oncologic conditions.
- Models using the constrained set showed comparable or slightly lower discrimination than models with extensive predictors, outperforming existing clinical models.
Conclusions:
- A small, common set of predictors can support models for numerous outcomes.
- This facilitates the implementation of multiple prediction models via a single interface.
- The identified predictor set serves as a foundation for future prognostic model research.
Background:
Prognostic models help aid medical decision-making. Various prognostic models are available via websites such as MDCalc, but these models typically predict one outcome, for example, stroke risk. Each model requires individual predictors, for example, age, lab results and comorbidities. There is no clinical tool available to predict multiple outcomes from a list of common medical predictors.
Objective:
Identify a constrained set of outcome-agnostic predictors.
Methods:
We proposed a novel technique aggregating the standardised mean difference across hundreds of outcomes to learn a constrained set of predictors that appear to be predictive of many outcomes. Model performance was evaluated using the constrained set of predictors across eight prediction tasks. We compared against existing models, models using only age/sex predictors and models without any predictor constraints.
Results:
We identified 67 predictors in our constrained set, plus age/sex. Our predictors included illnesses in the following categories: cardiovascular, kidney/liver, mental health, gastrointestinal, infectious and oncologic. Models developed using the constrained set of predictors achieved comparable discrimination compared with models using hundreds or thousands of predictors for five of the eight prediction tasks and slightly lower discrimination for three of the eight tasks. The constrained predictor models performed as good or better than all existing clinical models.
Conclusions:
It is possible to develop models for hundreds or thousands of outcomes that use the same small set of predictors. This makes it feasible to implement many prediction models via a single website form. Our set of predictors can also be used for future models and prognostic model research.
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