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Published on: May 16, 2025
Handling missing data in a rheumatoid arthritis registry using random forest approach.
Ahmad Alsaber1, Adeeba Al-Herz2, Jiazhu Pan1
1Department of Mathematics and Statistics, University of Strathclyde, Glasgow, UK.
Sequential random forest effectively imputes missing data in rheumatoid arthritis patient records, improving accuracy and reducing bias in clinical research. This method minimizes imputation error for various data types and missingness rates.
Area of Science:
- Clinical Epidemiology
- Biostatistics
- Data Science
Background:
- Missing data in clinical research can compromise study integrity by violating the intention-to-treat principle and introducing bias.
- Accurate imputation of missing patient data is crucial for reliable statistical analysis and valid research conclusions.
Purpose of the Study:
- To estimate and impute missing values in patient records from the Kuwait Registry for Rheumatic Diseases.
- To evaluate the accuracy of different imputation methods for handling missing data in rheumatoid arthritis research.
Main Methods:
- Utilized data from 1735 rheumatoid arthritis patients.
- Implemented and compared multiple imputation techniques, selecting the best based on the lowest Root Mean Square Error (RMSE).
- Evaluated the sequential random forest method (missForest) for its imputation accuracy across various missing data rates (10%, 20%, 30%).
Main Results:
- Missing data ranged from 5% to 65.5% across patient records.
- The sequential random forest method (missForest) demonstrated high accuracy in estimating missing values.
- missForest achieved the lowest imputation error for both continuous and categorical variables, outperforming other methods.
Conclusions:
- Sequential random forest (missForest) is a highly accurate method for imputing missing data in rheumatoid arthritis patient records.
- This imputation approach minimizes prediction error, enhancing the reliability of analyses using imputed laboratory values.
- Accurate data imputation is vital for robust clinical epidemiological research.
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