Monitoring the effects of sleep deprivation using neuronal avalanches
Abstract
The present invention is directed to a method of continuously monitoring neuronal avalanches in a subject comprising (a) determining a deviation in avalanche exponent (α) or branching parameter (σ) from a predetermined value at rest, wherein the pre-determined value of a is a slope of a size distribution of the synchronized neuronal activity and the predetermined value is −3/2 and the pre-determined value of 6 is a ratio of successively propagated synchronized neuronal activity and the predetermined value is 1; and (b) repeating step (a) one or more times to continuously monitor neuronal avalanches in a subject. The invention also features methods of determining or monitoring the degree of sleep deprivation in a subject, methods of identifying subjects that are susceptible to a sleep disorder and methods of diagnosing a sleep disorder in a subject.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method of identifying a subject that is susceptible to a sleep disorder comprising:
(a) performing an EEG using sensors provided on the subject; (b) determining, by at least one processing device, an avalanche exponent a or a branching parameter σ from signals output by the sensors, wherein α is a slope of a size distribution of a synchronized neuronal activity and σ is a ratio of successively propagated synchronized neuronal activity; (c) determining, by the at least one processing device, a deviation in α or σ as determined from a pre-determined value of α or σ at rest, wherein:
the pre-determined value of α is −3/2, and
the pre-determined value of σ is 1;
(d) repeating steps (a)-(c) one or more times; (e) identifying, by the at least one processing devices, the subject as being susceptible to a sleeping disorder when it is determined there is a deviation in α or σ from the pre-determined value of α or σ; (f) providing, by the at least one processing devices, a notification that the subject is identified as being susceptible to the sleeping disorder; and (g) providing intervention or guidance of treatment to the subject in response to identification of the subject as being susceptible to the sleeping disorder.
2 . The method of claim 1 , further comprising:
(h) identifying the time when α and σ are determined to deviate from their pre-determined values at rest.
3 . The method of claim 1 , wherein step (a) further comprises:
(i) filtering the signals output from the sensors; (ii) the sensors include multiple EEG electrodes, and positive/negative threshold crossings at each EEG electrode are detected; (iii) clustering threshold crossings on the EEG electrodes on a pre-determined time scale; and (iv) calculating the cluster size distribution for determining α or calculating a ratio of successive threshold crossings for determining σ.
4 . The method of claim 3 , wherein the EEG is continuously recorded at more than one site.
5 . The method of claim 3 , wherein the EEG is filtered between 1-100 Hz or wherein the time scale is 1-50 ms.
6 . The method of claim 1 , wherein the subject with the deviation in α or σ from the pre-determined value of α or σ performs a psychomotor vigilance task.
7 . The method of claim 1 , further comprising determining, by the at least one processing device, a magnitude and spatial distribution of theta power in the signals output by the sensors.
8 . The method of claim 1 , further comprising gathering data from other physiological sensors.
9 . The method of claim 1 , wherein the method is operational with hardware or software or a combination thereof.
10 . The method of claim 1 , wherein the sensors include multiple dry electrodes of a headset, wherein the dry electrodes are individually isolated and amplified, wherein the headset is wearable in a non-laboratory setting.
11 . A method of diagnosing a sleep disorder in a subject comprising:
(a) performing an EEG using sensors provided on the subject (b) determining, by at least one processing device, an avalanche exponent α or a branching parameter σ from signals output by the sensors, wherein α is a slope of a size distribution of a synchronized neuronal activity and σ is a ratio of successively propagated synchronized neuronal activity; (c) determining, by the at least one processing device, a deviation in α or σ as determined from a pre-determined value of α or σ at rest, wherein: the pre-determined value of α is −3/2, and the pre-determined value of δ is 1; (d) repeating step (a)-(c) one or more times; (e) diagnosing, by the at least one processing device, the subject as having a sleeping disorder when it is determined there is a deviation in α or σ from the pre-determined value of α or σ; (f) providing, by the at least one processing devices, a notification that the subject is diagnosed as having the sleeping disorder; and (g) providing intervention or guidance of treatment to the subject in response to diagnosing the subject as having the sleeping disorder.
12 . The method of claim 11 , further comprising:
(h) identifying the time when α and σ are determined to deviate from their pre-determined values at rest.
13 . The method of claim 11 , wherein step (a) further comprises:
(i) filtering the signals output from the sensors; (ii) the sensors include multiple EEG electrodes, and positive/negative threshold crossings at each EEG electrode are detected; (iii) clustering threshold crossings on the EEG electrodes on a pre-determined time scale; and (iv) calculating the cluster size distribution for determining a or calculating a ratio of successive threshold crossings for determining σ.
14 . The method of claim 13 , wherein the EEG is continuously recorded at more than one site.
15 . The method of claim 13 , wherein the EEG is filtered between 1-100 Hz or wherein the time scale is 1-50 ms.
16 . The method of claim 11 , wherein the subject with the deviation in α or σ from the pre-determined value of α or σ performs a psychomotor vigilance task.
17 . The method of claim 11 , further comprising determining, by the at least one processing device, a magnitude and spatial distribution of theta power in the signals output by the sensors.
18 . The method of claim 11 , further comprising gathering data from other physiological sensors.
19 . The method of claim 11 , wherein the method is operational with hardware or software or a combination thereof.
20 . The method of claim 11 , wherein the sensors include multiple dry electrodes of a headset, wherein the dry electrodes are individually isolated and amplified, wherein the headset is wearable in a non-laboratory setting.Join the waitlist — get patent alerts
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