| Literature DB >> 30800255 |
Alberto Ferrari1, Luca Bergamini2, Giorgio Guerzoni2, Simone Calderara2, Nicola Bicocchi2, Giorgio Vitetta2, Corrado Borghi3, Rita Neviani3, Adriano Ferrari3,4.
Abstract
Diplegia is a specific subcategory of the wide spectrum of motion disorders gathered under the name of cerebral palsy. Recent works proposed to use gait analysis for diplegia classification paving the way for automated analysis. A clinically established gait-based classification system divides diplegic patients into 4 main forms, each one associated with a peculiar walking pattern. In this work, we apply two different deep learning techniques, namely, multilayer perceptron and recurrent neural networks, to automatically classify children into the 4 clinical forms. For the analysis, we used a dataset comprising gait data of 174 patients collected by means of an optoelectronic system. The measurements describing walking patterns have been processed to extract 27 angular parameters and then used to train both kinds of neural networks. Classification results are comparable with those provided by experts in 3 out of 4 forms.Entities:
Year: 2019 PMID: 30800255 PMCID: PMC6360037 DOI: 10.1155/2019/3796898
Source DB: PubMed Journal: J Healthc Eng ISSN: 2040-2295 Impact factor: 2.682
Diplegia forms defined by Ferrari et al. [4].
| Form | Main traits |
|---|---|
| Form I | Antepulsion of trunk, toe balancing. Constant support from canes |
| Form II | Pronounced knee flexion in midstance, loaded knee behavior, short steps |
| Form III | Frontal trunk swinging and use of upper limbs to keep balance, presence of dysperceptive disorders (fear of falling and of open spaces) |
| Form IV | Mainly a motor deficit. Increased talipes equinus at the start of walking. Difficulty to stop immediately the walking |
Equipment commonly employed for gait analysis.
| Device | Description |
|---|---|
| Optoelectronic system | Reflecting markers attached to patients in specific anatomical landmarks allowing to acquire 3D motion of human segments |
| Force plate | Force plate placed on the ground to measure the intensity and direction of the reaction force to body weight |
| Electromyography | Skin electrodes capable of acquiring the electrical signals generated by the contraction of muscles |
| Video system | Cameras and other devices employed to record the movements of a patient in a walking trial |
Distribution of patients, trials, and sequences among the four classes (or forms) of Table 1 before and after data augmentation (in parentheses); the adopted partitioning for training and test phases is also shown.
| Form | Train | Test | ||||
|---|---|---|---|---|---|---|
| Patients | Trials | Seq. | Patients | Trials | Seq. | |
| 1 | 9 | 47 (94) | 1404 (2808) | 4 | 16 | 664 |
| 2 | 36 | 183 | 2720 | 13 | 83 | 1354 |
| 3 | 25 | 174 | 1894 | 9 | 49 | 712 |
| 4 | 58 | 372 | 3676 | 20 | 114 | 927 |
Body marker IDs and their description.
| Identifier | Marker position |
|---|---|
| C7 | 7th cervical vertebrae |
| LA | Left acromioclavicular joint |
| RA | Right acromioclavicular joint |
| REP | Right lateral elbow epicondyle |
| LEP | Left lateral elbow epicondyle |
| RUL | Right lateral prominence of the ulna |
| LUL | Left lateral prominence of the ulna |
| RASIS | Right anterior superior iliac spine |
| LASIS | Left anterior superior iliac spine |
| RPSIS | Right posterior superior iliac spine |
| LPSIS | Left posterior superior iliac spine |
| RGT | Right prominence of the greater trochanter |
| LGT | Left prominence of the greater trochanter |
| RLE | Right lateral knee epicondyle |
| LLE | Left lateral knee epicondyle |
| RCA | Right upper ridge of the calcaneus posterior surface |
| LCA | Left upper ridge of the calcaneus posterior surface |
| RFM | Right dorsal aspect of first metatarsal head |
| LFM | Left dorsal aspect of first metatarsal head |
Absolute 3D coordinates have been transformed into 27 three-dimensional angles, as most of the clinical signs of diplegia are strongly related to angular information.
| Marker I | Marker II | Marker III |
|---|---|---|
| LGT | LPSIS | LLE |
| LLE | LGT | LCA |
| LCA | LLE | LFM |
| LEP | LA | LUL |
| LEP | C7 | LUL |
| LLE | LASIS | LFM |
| LA | C7 | LEP |
| RGT | RPSIS | RLE |
| RLE | RGT | RCA |
| RCA | RLE | RFM |
| REP | RA | RUL |
| REP | C7 | RUL |
| RLE | RASIS | RFM |
| RA | C7 | REP |
| LPSIS | LGT | RGT |
| LASIS | LGT | RGT |
| LPSIS | LLE | RLE |
| C7 | LA | RA |
| C7 | LEP | REP |
| RPSIS | LGT | RGT |
| RASIS | LGT | RGT |
| RPSIS | LLE | RLE |
| C7 | LUL | RUL |
| LASIS | C7 | LPSIS |
| RASIS | C7 | RPSIS |
| LA | LASIS | RASIS |
| RA | LASIS | RASIS |
Figure 1Proposed MLP network. Every cell is fully connected with the output of the previous layer through a set of weights (plus a bias) which are used to compute the new output.
Figure 2Architecture of the proposed RNN network. The network uses a many-to-many layer with L1 < L2 < 1 and a single LSTM layer.
Top one accuracy scores (train set).
| Form | MLP | LSTM | SVM |
|---|---|---|---|
| Top one | Top one | Top one | |
| 1 | 0.98 | 0.97 | 0.98 |
| 2 | 0.985 | 0.97 | 0.99 |
| 3 | 0.8 | 0.96 | 0.95 |
| 4 | 0.965 | 0.965 | 0.965 |
| Overall | 0.941 | 0.967 | 0.986 |
Accuracy scores on the test set, where T1 stands for top one and T2 stands for top two.
| Form | MLP | LSTM | SVM | |||
|---|---|---|---|---|---|---|
| T1 | T2 | T1 | T2 | T1 | T2 | |
| 1 | 0.75 | 0.75 | 1.0 | 1.0 | 0.0 | 0.15 |
| 2 | 0.846 | 1.0 | 0.692 | 0.923 | 0.461 | 0.615 |
| 3 | 0.111 | 0.333 | 0.333 | 0.555 | 0.0 | 0.777 |
| 4 | 0.6 | 0.9 | 0.75 | 0.95 | 0.9 | 0.95 |
| Overall | 0.587 | 0.804 | 0.674 |
| 0.522 | 0.7519 |
Confusion matrices for the considered patients; both LSTM (left) and MLP (right) networks are considered.
| Predicted | Predicted | ||||||||
|---|---|---|---|---|---|---|---|---|---|
| Ground truth | 4 | 0 | 0 | 0 | Ground truth | 3 | 1 | 0 | 0 |
| 0 | 9 | 3 | 1 | 0 | 11 | 2 | 0 | ||
| 0 | 1 | 3 | 5 | 0 | 4 | 1 | 4 | ||
| 0 | 2 | 3 | 15 | 0 | 7 | 1 | 12 | ||