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Machine Learning Principles Can Improve Hip Fracture Prediction

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Abstract

Apply machine learning principles to predict hip fractures and estimate predictor importance in Dual-energy X-ray absorptiometry (DXA)-scanned men and women. Dual-energy X-ray absorptiometry data from two Danish regions between 1996 and 2006 were combined with national Danish patient data to comprise 4722 women and 717 men with 5 years of follow-up time (original cohort n = 6606 men and women). Twenty-four statistical models were built on 75% of data points through k-5, 5-repeat cross-validation, and then validated on the remaining 25% of data points to calculate area under the curve (AUC) and calibrate probability estimates. The best models were retrained with restricted predictor subsets to estimate the best subsets. For women, bootstrap aggregated flexible discriminant analysis (“bagFDA”) performed best with a test AUC of 0.92 [0.89; 0.94] and well-calibrated probabilities following Naïve Bayes adjustments. A “bagFDA” model limited to 11 predictors (among them bone mineral densities (BMD), biochemical glucose measurements, general practitioner and dentist use) achieved a test AUC of 0.91 [0.88; 0.93]. For men, eXtreme Gradient Boosting (“xgbTree”) performed best with a test AUC of 0.89 [0.82; 0.95], but with poor calibration in higher probabilities. A ten predictor subset (BMD, biochemical cholesterol and liver function tests, penicillin use and osteoarthritis diagnoses) achieved a test AUC of 0.86 [0.78; 0.94] using an “xgbTree” model. Machine learning can improve hip fracture prediction beyond logistic regression using ensemble models. Compiling data from international cohorts of longer follow-up and performing similar machine learning procedures has the potential to further improve discrimination and calibration.

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Acknowledgements

We acknowledge Statistics Denmark for providing data and a server platform for data analysis. The Obel Family Foundation of Aalborg, Denmark, and the Department of Clinical Medicine at Aalborg University, Denmark, are acknowledged for funding the PhD fellowship of Dr. Christian Kruse. Grant Numbers are not applicable in Denmark.

Author Contributors

Christian Kruse designed the study and performed data management, modelling, model validation, statistical analysis, graphical presentations and manuscript preparation of first draft of the paper. He is guarantor. Pia Eiken and Peter Vestergaard performed revisions and final approval of the manuscript draft. All authors revised the paper critically for intellectual content and approved the final version. All authors agree to be accountable for the work and to ensure that any questions relating to the accuracy and integrity of the paper are investigated and properly resolved.

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Correspondence to Christian Kruse.

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Conflict of interest

CK has received travel grants from Eli Lilly, Otsuka Pharmaceutical and is a speaker for Novartis and Otsuka Pharmaceutical. PE is an advisory board member with Amgen, MSD and Eli Lilly and at the speakers bureau with Amgen and Eli Lilly, stocks from Novo Nordisk A/S. PV has received unrestricted grants from MSD and Servier, and travel grants from Amgen, Eli Lilly, Novartis, Sanofi-Aventis and Servier.

Human and Animal Rights and Informed Consent

The procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1975, as revised in 2008.

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MOESM2: Supplementary material 2: Calibration plot of binned probability intervals versus actual observed percentages. A line close to the diagonal line indicates good calibration. Female subjects, bootstrap aggregated flexible discriminant analysis with Naïve Bayes calibration.

MOESM3: Supplementary material 3: Calibration plot of binned probability intervals versus actual observed percentages. A line close to the diagonal line indicates good calibration. Male subjects, eXtreme Gradient Boosting with Naïve Bayes calibration.

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Kruse, C., Eiken, P. & Vestergaard, P. Machine Learning Principles Can Improve Hip Fracture Prediction. Calcif Tissue Int 100, 348–360 (2017). https://doi.org/10.1007/s00223-017-0238-7

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