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MCLPD:Multi-view Contrastive Learning for EEG-based PD Detection Across Datasets

Created by
  • Haebom

Author

Qian Zhang, Ruilin Zhang, Jun Xiao, Yifan Liu, Zhe Wang

Outline

This paper proposes MCLPD, a novel semi-supervised learning framework based on electroencephalography (EEG) for the early diagnosis of Parkinson's disease (PD). MCLPD integrates multi-view contrastive learning pretraining and lightweight supervised fine-tuning to improve robust and generalizable PD detection performance despite dataset differences. The pretraining stage performs self-supervised learning using an unlabeled dataset (UNM) and generates contrastive pairs through dual augmentation in the time and frequency domains, naturally integrating time-frequency information. The fine-tuning stage performs supervised learning using only a small amount of labeled data from the other two datasets (UI and UC). Experimental results show that MCLPD achieves F1 scores of 0.91 on the UI dataset and 0.81 on the UC dataset using only 1% of the labeled data, further improving performance to 0.97 and 0.87, respectively, using 5% of the labeled data. Compared to existing methods, MCLPD significantly improves cross-dataset generalization while reducing labeled data dependence.

Takeaways, Limitations

Takeaways:
Presenting MCLPD, an effective EEG-based semi-supervised learning framework for the early diagnosis of Parkinson's disease.
Achieving high accuracy using limited label data
Performance enhancement through time-frequency information fusion
Improved generalization performance across datasets
Reduced dependence on cover data
Limitations:
The performance of the proposed method may depend on the dataset used. Further experiments on various datasets are needed.
There is a possibility that the features of the dataset used in the current experiment may degrade generalization performance when applied to other datasets.
Lack of detailed description of the size and characteristics of the UNM dataset used in the pre-training process of MCLPD.
Lack of comparative analysis with other Parkinson's disease diagnostic methods.
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