TY - JOUR
T1 - A transition-constrained discrete hidden Markov model for automatic sleep staging
AU - Pan, Shing Tai
AU - Kuo, Chih En
AU - Zeng, Jian Hong
AU - Liang, Sheng Fu
N1 - Funding Information:
The authors would like to thank Prof. Fu-Zen Shaw of the Department of Psychology, National Cheng Kung University, Taiwan, for providing the PSG recording data to develop and evaluate our methods. This work was supported by the National Science Council of Taiwan under Grants NSC 98-2221-E-006 -161-MY3, 100-2221-E-390-025-MY2 and 101-2220-E-006 -010.
PY - 2012/8/21
Y1 - 2012/8/21
N2 - Background: Approximately one-third of the human lifespan is spent sleeping. To diagnose sleep problems, all-night polysomnographic (PSG) recordings including electroencephalograms (EEGs), electrooculograms (EOGs) and electromyograms (EMGs), are usually acquired from the patient and scored by a well-trained expert according to Rechtschaffen & Kales (R&K) rules. Visual sleep scoring is a time-consuming and subjective process. Therefore, the development of an automatic sleep scoring method is desirable.Method: The EEG, EOG and EMG signals from twenty subjects were measured. In addition to selecting sleep characteristics based on the 1968 R&K rules, features utilized in other research were collected. Thirteen features were utilized including temporal and spectrum analyses of the EEG, EOG and EMG signals, and a total of 158 hours of sleep data were recorded. Ten subjects were used to train the Discrete Hidden Markov Model (DHMM), and the remaining ten were tested by the trained DHMM for recognition. Furthermore, the 2-fold cross validation was performed during this experiment.Results: Overall agreement between the expert and the results presented is 85.29%. With the exception of S1, the sensitivities of each stage were more than 81%. The most accurate stage was SWS (94.9%), and the least-accurately classified stage was S1 (<34%). In the majority of cases, S1 was classified as Wake (21%), S2 (33%) or REM sleep (12%), consistent with previous studies. However, the total time of S1 in the 20 all-night sleep recordings was less than 4%.Conclusion: The results of the experiments demonstrate that the proposed method significantly enhances the recognition rate when compared with prior studies.
AB - Background: Approximately one-third of the human lifespan is spent sleeping. To diagnose sleep problems, all-night polysomnographic (PSG) recordings including electroencephalograms (EEGs), electrooculograms (EOGs) and electromyograms (EMGs), are usually acquired from the patient and scored by a well-trained expert according to Rechtschaffen & Kales (R&K) rules. Visual sleep scoring is a time-consuming and subjective process. Therefore, the development of an automatic sleep scoring method is desirable.Method: The EEG, EOG and EMG signals from twenty subjects were measured. In addition to selecting sleep characteristics based on the 1968 R&K rules, features utilized in other research were collected. Thirteen features were utilized including temporal and spectrum analyses of the EEG, EOG and EMG signals, and a total of 158 hours of sleep data were recorded. Ten subjects were used to train the Discrete Hidden Markov Model (DHMM), and the remaining ten were tested by the trained DHMM for recognition. Furthermore, the 2-fold cross validation was performed during this experiment.Results: Overall agreement between the expert and the results presented is 85.29%. With the exception of S1, the sensitivities of each stage were more than 81%. The most accurate stage was SWS (94.9%), and the least-accurately classified stage was S1 (<34%). In the majority of cases, S1 was classified as Wake (21%), S2 (33%) or REM sleep (12%), consistent with previous studies. However, the total time of S1 in the 20 all-night sleep recordings was less than 4%.Conclusion: The results of the experiments demonstrate that the proposed method significantly enhances the recognition rate when compared with prior studies.
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U2 - 10.1186/1475-925X-11-52
DO - 10.1186/1475-925X-11-52
M3 - Article
C2 - 22908930
AN - SCOPUS:84865072705
SN - 1475-925X
VL - 11
JO - BioMedical Engineering Online
JF - BioMedical Engineering Online
M1 - 52
ER -