| Literature DB >> 35528954 |
Fan Yi Khong1, Tee Connie1, Michael Kah Ong Goh1, Li Pei Wong2, Pin Shen Teh3, Ai Ling Choo4.
Abstract
Background: The unprecedented development of Artificial Intelligence has revolutionised the healthcare industry. In the next generation of healthcare systems, self-diagnosis will be pivotal to personalised healthcare services. During the COVID-19 pandemic, new screening and diagnostic approaches like mobile health are well-positioned to reduce disease spread and overcome geographical barriers. This paper presents a non-invasive screening approach to predict the health of a person from visually observable features using machine learning techniques. Images like face and skin surface of the patients are acquired using camera or mobile devices and analysed to derive clinical reasoning and prediction of the person's health.Entities:
Keywords: Health prediction; Machine learning; Remote screening and diagnosis
Mesh:
Year: 2021 PMID: 35528954 PMCID: PMC9039370 DOI: 10.12688/f1000research.72894.2
Source DB: PubMed Journal: F1000Res ISSN: 2046-1402
A summary of works related to this study.
| Author | Method | Database | Classes | Recognition Rate | Pros | Cons |
|---|---|---|---|---|---|---|
| Zhao, Q., Rosenbaum, K., Sze, R., Zand, D., Summar, M., & Linguraru, M. G.
|
Geometric + SVM Texture + SVM Combined + SVM | Self-collected dataset | Down syndrome + Normal | 97.92% | 1. Contourlets preserve important wavelet features and provide a high level of anisotropy and directionality
| Facial anatomical landmarks and texture features need to be defined manually, requires more time and effort |
| Saraydemir, Ş., Taşpınar, N., Eroğul, O., Kayserili, H., & Dinçkan, N.
|
GWT + PCA & LDA + SVM GWT + PCA & LDA + k-NN |
University Medicine Faculty Department of Medical Genetics Down Syndrome Association of Turkey and Istanbul | Down syndrome + Healthy | 97.34% | 1. Dataset is small to produce robust results
| Manual normalization requires more effort and time than automated approaches |
| Ferry, Q., Steinberg, J., Webber, C., FitzPatrick, D. R., Ponting, C. P., Zisserman, A., & Nellåker, C.
| PCA + AAM + k-NN |
Publicly available resources Scientifically published pictures of patients | Eight genetic disorders + Healthy | 99.5% | 1. Robust to artificial variations such as lighting, pose, and image quality
| 1. AAMs involve complex texture mapping and image warping operations which are susceptible to errors
|
| Zhao, Q., Okada, K., Rosenbaum, K., Kehoe, L., Zand, D. J., Sze, R., Summar, M., & Linguraru, M. G.
| Features:
Geometric LBP Geometric + LBP GWT Geometric + GWT
SVM-RBF Linear SVM k-NN RF LDA | Self-collected dataset | Down syndrome + Healthy | 96.7% | 1. CLMs are more generative and discriminative on unseen appearance
| 1. ICA requires large datasets to train to produce good results
|
| Mixed syndromes + Healthy | 97% | |||||
| Kong, X., Gong, S., Su, L., Howard, N., & Kong, Y.
|
k-NN SVM RF |
SCUT-FBP dataset Neurosurgery inpatient departments of hospitals in China Self-collected dataset | Acromegaly + Normal | 95% | SVM performs well on extracted facial features | 1. A possibility of bias caused by the selection of samples may occur
|
Figure 1. Proposed framework.
Number of images for each class and subclass.
| Class | Subclass | Number of images |
|---|---|---|
|
| - | 500 |
|
| Fever | 78 |
| Sore throat | 80 | |
| Running nose | 75 |
Experimental results of SVM variants.
| Methods | 1 st Level classification testing | 2 nd Level classification testing |
|---|---|---|
| LBP + SVM | 80.88 | 73.32 |
| PCA + SVM | 85.85 | 64.05 |
| LDS + SVM | 85.37 | 63.01 |
| GABOR FILTER + SVM | 81.29 | 63.45 |
Experimental results of RF variants.
The best results are highlighted in bold.
| Methods | 1 st Level classification testing | 2 nd Level classification testing |
|---|---|---|
| LBP + RF | 83.61 | 67.95 |
| PCA + RF |
|
|
| LDA + RF | 85.31 | 64.15 |
| GABOR FILTER + RF | 87.89 | 62.41 |
Experimental results of KNN variants.
The best results are highlighted in bold.
| Methods | 1 st Level classification testing | 2 nd Level classification testing |
|---|---|---|
| LBP + NN | 83.54 | 65.33 |
| PCA + KNN |
|
|
| LDA + KNN | 86.53 | 63.78 |
| GABOR FILTER + KNN | 72.26 | 63.02 |
Figure 2. Confusion matrix of PCA+KNN at first-level classification.
Figure 3. Confusion matrix of PCA+RF at second-level classification.
A comparison with state-of-the-art methods.
| Methods | 1 st Level classification testing |
|---|---|
| LBP + NN (First level classification) | 86.87 |
| PCA + RF (First level classification) | 88.57 |
| CNN
| 92.71 |
| VGGFace
| 96.25 |
Experimental results of NN variants.
The best results are highlighted in bold.
| Methods | 1 st Level classification testing | 2 nd Level classification testing |
|---|---|---|
| LBP + NN | 86.87 |
|
| PCA + NN |
| 66.96 |
| LDA + NN | 86.87 | 63.19 |
| GABOR FILTER + NN | 86.05 | 66.93 |