期刊
JOURNAL OF ALZHEIMERS DISEASE
卷 79, 期 4, 页码 1691-1700出版社
IOS PRESS
DOI: 10.3233/JAD-201254
关键词
Alzheimer's disease; blood biomarkers; machine learning; recursive feature elimination; support vector machine
资金
- National Institute on Aging of the National Institutes of Health [R01AG058537]
The study demonstrated the effectiveness of SVM-RFE-LOO algorithm in reducing the number of biomarkers in the early detection model of AD, achieving high sensitivity and specificity. SVM-RFE-LOO outperformed other methods, showing robustness in handling noisy data and improving prediction performance.
Background: There is a need for more reliable diagnostic tools for the early detection of Alzheimer's disease (AD). This can be a challenge due to a number of factors and logistics making machine learning a viable option. Objective: In this paper, we present on a Support Vector Machine Leave-One-Out Recursive Feature Elimination and Cross Validation (SVM-RFE-LOO) algorithm for use in the early detection of AD and show how the SVM-RFE-LOO method can be used for both classification and prediction of AD. Methods: Data were analyzed on n = 300 participants (n = 150 AD; n = 150 cognitively normal controls). Serum samples were assayed via a multi-plex biomarker assay platform using electrochemiluminescence (ECL). Results: The SVM-RFE-LOO method reduced the number of features in the model from 21 to 16 biomarkers and achieved an area under the curve (AUC) of 0.980 with a sensitivity of 94.0% and a specificity of 93.3%. When the classification and prediction performance of SVM-RFE-LOO was compared to that of SVM and SVM-RFE, we found similar performance across the models; however, the SVM-RFE-LOO method utilized fewer markers. Conclusion: We found that 1) the SVM-RFE-LOO is suitable for analyzing noisy high-throughput proteomic data, 2) it outperforms SVM-RFE in the robustness to noise and in the ability to recover informative features, and 3) it can improve the prediction performance. Our recursive feature elimination model can serve as a general model for biomarker discovery in other diseases.
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