The invention relates to a system and method for modifying the circadian cycle of a subject. Particular embodiments of the invention involve providing stimulus to controllably adjust a subject's circadian cycle to track a reference trajectory.
Biological organisms of many kinds exhibit cycles which manifest themselves in a variety of physiological and behavioral characteristics. The cycles may have periods of hours (ultradian), days (circadian), or longer intervals (infradian). Circadian cycles are commonly observed in humans, as is evidenced by fluctuations in core body temperature, hormone levels, alertness and cognitive performance, for example. Of particular interest are alertness and cognitive performance, as these characteristics are correlated to health, safety and productivity.
There are circumstances where it may be desirable to alter or otherwise control a circadian cycle of a subject. For example, it may be desirable to maximize the alertness or cognitive performance of a subject for particular periods of time during which they are required to perform important or dangerous tasks, such as when they are flying an aircraft or performing an operation.
The biological basis of circadian cycles in humans is believed to be an endogenous circadian pacemaker: a self-oscillating chemical process in the suprachiasmatic nucleus region of the brain with a period very near to 24 hours (see, for example, C. A. Czeisler, J. F. Duffy, T. L. Shanahan, E. N. Brown, J. F. Mitchell D. W. Rimmer, J. M. Ronda, E. J. Silva, J. S. Allan, J. S. Emens, D. J., Dijk, and R. E. Kronauer., “Stability, precision, and near-24-hour period of the human circadian pacemaker.” Science, Vol. 284, No.5423 (1999), pp. 2177-2181). External stimuli influence the endogenous circadian pacemaker cycle, and in turn, the various circadian cycles that it regulates. Light is a particularly effective stimulus for modifying the circadian pacemaker cycle of a human subject (see, for example, C. A. Czeisler, J. S. Allan, S. H. Strogatz, J. M. Ronda, R. Sanchez, C. D. Rios, W. O. Freitag, G. S. Richardson, and R. E. Kronauer, “Bright light resets the human circadian pacemaker independent of the timing of the sleep-wake cycle.” Science, Vol. 233, No. 4764, (August 1986), pp.667-671).
The effect of external stimuli (such as light) on the human circadian pacemaker cycle has led to a number of patents, including: U.S. Pat. Nos. 5,163,426; 5,167,228; 5,176,133; 5,304,212; and 5,545,192 (to Czeisler et al.); U.S. Pat. Nos. 5,343,121; and 5,589,741 (to Terman et al.); U.S. Pat. No. 6,350,275 (to Vreman). The techniques proposed by these patents have a variety of limitations which include, inter alia: slow or otherwise non-optimal shifting of the subject's circadian pacemaker cycle; lack of feedback based on measurement of parameter(s) indicative of the state of the subject's circadian pacemaker cycle; lack of mechanisms for incorporating limitations on available stimuli; lack of mechanisms for incorporating differences between individual subjects, modeling errors, unknown initial conditions and/or the introduction of disturbances, and lack of a continuous connection or dependence between assessment of the subject's circadian state and the modification of the subject's circadian pacemaker cycle.
There is a general desire to provide systems and methods for controllably adjusting a circadian cycle of a subject which overcome or ameliorate some of the aforementioned disadvantages of the prior art.
A first aspect of the invention provides a method for controllably adjusting the circadian cycle of a subject using light (or other stimulus) through application of model-based predictive control techniques. This approach allows the use of closed-loop feedback to compensate for modeling errors, unknown initial conditions and disturbances. It also allows an optimal level of light (or other stimulus) to be generated based on minimization of a cost function. The cost function may incorporate a term associated with tracking errors and a term associated with the amount of light used. The tracking function may be minimized subject to one or more constraints which may include a minimum and maximum amount of light (or other stimulus) for example.
Another aspect of the invention provides a method for controllably adjusting a circadian cycle of a subject to track a reference trajectory. The method involves providing at least one model representative of a response of a circadian state of the subject to a stimulus control signal and generating an optimal stimulus control signal using model predictive control based on the model. Generating the optimal stimulus control signal comprises minimizing a cost function which may comprise a cost term which is a function of a tracking error and a cost term related to an amplitude of the stimulus control signal. Minimizing the cost function is subject to constraints which comprise minimum and maximum stimulus control signal levels.
Generating the optimal stimulus control signal may be based, at least in part, on a circadian state feedback signal. The circadian state feedback signal may be determined by modeling the response of the circadian state of the subject to the stimulus control signal. Modeling the response of the subject to the stimulus control signal may comprise using a mathematical model based on a Jewett-Kronauer model. The mathematical model may comprise a linearized version of the Jewett-Kronauer model. The circadian state feedback signal may be determined by estimating the circadian state of the subject based, at least in part, on one or more sensed parameters which relate to the physiology of the subject. The sensed parameters may include: heart rate, core body temperature, respiration, endocrine function levels, physical activity levels, blood pressure, blood oxygen concentration and/or skin temperature.
The stimulus control signal may comprises a light control signal and the method may comprise applying the light control signal to determine an intensity of one or more light sources.
The at least one model may comprise a response predictor subject model. Generating the optimal stimulus control signal may comprise predicting a free response of the circadian state of the subject starting at a current time and extending out to a control horizon time using the response predictor subject model. Predicting the free response may comprise assuming that a current value of the circadian state feedback signal represents an initial condition and that the light control signal remains constant between the current time and the control horizon time.
The at least one model may comprise a controller subject model. Generating the optimal stimulus control signal may comprise determining an optimal series of control moves starting at the current time and extending out to the control horizon time using the controller subject model. Determining the optimal series of control moves may be based, at least in part, on the free response of the circadian state of the subject, the reference trajectory and the circadian state feedback signal.
The response predictor subject model and/or the controller subject model may comprise a mathematical model defined by a plurality of differential equations. The mathematical model may be based on a Jewett-Kronauer model. The mathematical model may comprise a linearized version of the Jewett-Kronauer model.
Predicting the free response may be based, at least in part, on a light estimate signal representative of a light intensity experienced by the subject. Determining the optimal series of control moves may be based, at least in part, on the light estimate signal. The method may involve estimating the light intensity experienced by the subject using a model to obtain the light estimate signal. The method may involve sensing the light intensity experienced by the subject using at least one light sensor to obtain the light estimate signal.
The stimulus control signal may be provided in a domain of a driving input B of the Jewett-Kronauer model. The method may comprise converting the stimulus control signal from the domain of the driving input B to the light control signal in a light intensity domain I. The method may also comprise converting the minimum and maximum stimulus control signal levels from a light intensity domain I to a domain of a driving input B of the Jewett-Kronauer model.
The cost function may comprise a first weighting factor associated with the tracking error cost term and a second weighting factor associated with the stimulus control signal cost term. The first and second weighting factors may vary over a duration of the circadian cycle of the subject.
Another aspect of the invention provides a method for controllably adjusting a circadian cycle of a subject to track a reference trajectory. The method involves obtaining input information which comprises a signal representative of the reference trajectory, a feedback signal representative of a circadian state of the subject and one or more stimulus level constraints. The method also involves predicting a free response of the circadian state of the subject starting at a current time and extending out to a first future time using a response predictor subject model representative of a response of the circadian state of the subject to a stimulus. An optimal series of control moves is determined starting at the current time and extending out to second future time using a controller subject model representative of a response of the circadian state of the subject to a stimulus. The optimal series of control moves is based, at least in part, on the free response of the circadian state of the subject, the reference trajectory signal and the current circadian state feedback signal. The method also involves outputting a stimulus control signal comprising a current one of the series of control moves to one or more stimulus sources and applying the stimulus control signal to one or more stimulus sources to determine an intensity thereof.
Another aspect of the invention comprises a system for controllably adjusting a circadian cycle of a subject to track a reference trajectory. The system comprises one or more inputs for receiving the reference trajectory and for receiving constraints which comprise minimum and maximum stimulus control signal levels. A response predictor is connected to receive a feedback signal representative of a circadian state of the subject and is configured to predict a free response of the circadian state of the subject starting at a current time and extending out to a first future time using a response predictor subject model representative of a response of the circadian state of the subject to a stimulus. A control sequence generator is connected to receive the reference trajectory, the constraints, the feedback signal and the free response of the circadian state of the subject. The control sequence generator is configured to determine an optimal series of control moves starting at the current time and extending out to a second future time using a controller subject model representative of a response of the circadian state of the subject to a stimulus. The control sequence generator is connected to output a stimulus control signal to at least one stimulus source. The stimulus control signal comprises a current control move in the optimal series of control moves and the stimulus control signal determines an intensity of the at least one stimulus source.
Yet another aspect of the invention provides a system for controllably adjusting a circadian cycle of a subject to track a reference trajectory. The system comprises one or more inputs for receiving the reference trajectory and for receiving constraints which comprise minimum and maximum stimulus control signal levels. The system also comprises means for predicting a free response of a circadian state of the subject starting at a current time and extending out to a first future time based, at least in part, on a feedback signal representative of the circadian state of the subject and means for determining an optimal series of control moves starting at the current time and extending out to a second future time based, at least in part, on the reference trajectory, the constraints, the feedback signal and the free response of the circadian state of the subject. Means for applying a stimulus control signal to at least one stimulus source are also provided. The stimulus control signal comprises at least a portion of the optimal series of control moves and the stimulus control signal determines an intensity of the at least one stimulus source.
Still another aspect of the invention provides a method for altering a phase of a circadian cycle of a subject. The method comprises providing a controller subject model representing a response of a circadian state of the subject to a stimulus, receiving a reference circadian trajectory, which is phase shifted from a current circadian cycle of the subject, determining a series of stimulus control moves predicted by the controller subject model to result in the circadian cycle of the subject changing to track the reference circadian trajectory and applying at least a portion of the series of stimulus control moves to one or more stimulus sources. The one or more stimulus sources provide stimulus which is received by the subject. Determining the series of stimulus control moves comprises applying an optimization process using the controller subject model.
Further features and applications of specific embodiments of the invention are described below.
In drawings which depict non-limiting embodiments of the invention:
Throughout the following description, specific details are set forth in order to provide a more thorough understanding of the invention. However, the invention may be practiced without these particulars. In other instances, well known elements have not been shown or described in detail to avoid unnecessarily obscuring the invention. Accordingly, the specification and drawings are to be regarded in an illustrative, rather than a restrictive, sense.
Aspects of the present invention provide systems and methods for controlling the circadian pacemaker cycle of a subject to track a reference trajectory. Controlled amounts of light (or other stimulus) are provided to the subject in such a manner that the subject's circadian pacemaker cycle is caused to track the reference trajectory. In some embodiments, the control systems and methods make use of one or more models. Such models may empirically describe the response of a typical subject's circadian state to light or other stimulus. Feedback may be used to compensate for differences between individuals, modeling errors, unknown initial conditions and other disturbances.
The control systems and methods may incorporate one or more physiological sensors, which sense one or more parameters that are correlated to or otherwise indicate the subject's circadian state. Such parameter(s) may be used as feedback. In some embodiments, the control systems and methods comprise one or more stimulus sensors, which sense the amount light (or other stimulus) applied to the subject and which feed this information back to the controller.
In some embodiments, the systems and methods determine an “optimum” application of light (or other stimulus) to adjust the subject's circadian cycle to the desired reference trajectory. The “optimum” application of light may be achieved by substantially minimizing a cost function. In some embodiments, the cost function incorporates a term related to the tracking error and a term related to the amount of stimulus required. The optimization cost function may be minimized subject to physical constraints inherent in the system. Such constraints may include a minimum and maximum amount of light (or other stimulus).
In some embodiments, the models used to predict the subject's circadian state comprise nonlinear models. The systems and methods may comprise a variety of approximation techniques for transforming or otherwise reducing such nonlinear models to linear models.
In some embodiments, the reference trajectory is selected so that the subject is more alert in certain desired time periods.
Some embodiments of the invention make use of mathematical models which describe the response of a human circadian pacemaker state to light (or other stimulus). Such models may be empirically determined. In some embodiments, such models comprise a system of differential equations derived from the well known van der Pol equations. Particular embodiments of the invention make use of the model described in M. E. Jewett, D. B. Forger, and R. E. Kronauer, “Revised Limit Cycle Oscillator Model of Human Circadian Pacemaker.” Journal of Biological Rhythms, Vol. 14, No. 6 (1999), pp. 493-499, which is hereby incorporated herein by reference.
The Jewett-Kronauer model comprises a set of differential equations which describe the nonlinear effects of light on the circadian pacemaker cycle. In accordance with the Jewett-Kronauer model, the circadian state of a subject is described by a pair of circadian state variables (x, xc). The circadian state variables (x, xc) are mathematical constructs which represent the circadian state of a subject. According to the Jewett-Kronauer model, the response of the circadian state variables (x, xc) to a driving input B is given by:
where μ, q and k are constants, which may be empirically determined, and τx is the intrinsic period of oscillation of the circadian cycle (in hours). The driving input B is related to light intensity I as will be described further below. In one particular embodiment, μ=0.13, q=1/3, k=0.55 and τx=24.2 hours.
The parameter B is the driving input for the Jewett-Kronauer model equations (1) and (2). Accordingly, given any value of the driving input B and historical information about the circadian state variables (x, xc) (i.e. initial conditions), equations (1) and (2) may be used to predict future values of the circadian state variables (x, xc). As can be seen by examining equations (1) and (2), the circadian state variables (x, xc) comprise oscillating functions which may be approximately sinusoidal in nature and which are approximately 90° (or ¼ period) out of phase with each another.
The Jewett-Kronauer model also comprises another state variable n which is not specifically related to the individual's circadian state, but rather is related to the individual's dynamic response to light. In accordance with the Jewett-Kronauer model, the state variable n is related to a parameter a which is an indication of an individual's perception of a given light intensity I. It will be appreciated that the human eye and brain have a nonlinear response to light intensity. For example, the introduction of a single candle into an otherwise dark room causes a dramatic increase in an individual's ability to perceive his or her environment, whereas the addition of one extra flourescent tube into a room already lit with five such tubes makes comparatively little difference. The response α of the human eye to light with an intensity I may be modeled by:
where I is measured in lux and αo and p are constants which may be empirically determined. In one particular embodiment, αo=0.16 and p=0.6.
The third state variable n of the Jewett-Kronauer model may then be expressed in terms of α, the driving input B and the circadian state variables (x, xc):
{dot over (n)}=60[α(1−n)−βn] (4)
B=Gα(1−n)(1−mx)(1−mxc) (5)
where β and G are constants which may be empirically determined. In one particular embodiment, β=0.013 and G=19.875.
The driving input B is related to light intensity I. It is useful for the purpose of employing the Jewett-Kronauer model in real world applications to provide transformations back and forth between the domain of driving input B and the domain of light intensity I. Such transformations allow systems which make use of the Jewett-Kronauer model to work in either the driving input domain B or in the light intensity domain I. Transformations back and forth between the driving input domain B and the light intensity domain I may involve one or more simplifying approximations.
Some embodiments of the invention make use of a particular transformation between the driving input domain B of the Jewett-Kronauer model and the light intensity domain I, the derivation of which is presented below. Equation (5) may be rearranged as:
As can be appreciated by analyzing equation (4), the state variable n has a nonlinear dependence on the value of α. In some embodiments of the present invention, light pulses are applied to individuals to controllably alter their circadian cycles. In particular applications of the invention, light pulses of interest typically have durations greater than two hours. In these circumstances, it can assumed that the decaying exponential dependence of n on α (as described by equation (4)) will reach a steady state within a period of time significantly less than the duration of the light pulses. Accordingly, in such applications, the time derivative of n can be approximated as zero, such that equation (4) may be solved for an approximate value of n:
Substituting this approximate value of n from equation (7) into equation (6) yields:
In addition, equation (3) may be rearranged as:
and substituting equation (8) into equation (9) yields:
Equation (10) represents a transformation function of the form I=f(x, xc, B) which can be used in conjunction with the circadian state variables (x, xc) to transform a value in the driving input domain B into a corresponding value in the light intensity domain I.
Using the same approximation for n from equation (7) and substituting it into equation (5) yields:
Then, substituting equation (3) into equation (10A) yields:
Equation (10B) represents a transformation function of the form B=g(x, xc, I) which can be used in conjunction with the circadian state variables (x, xc) to transform a value in the light intensity domain I into a corresponding value in the driving input domain B.
The direction of the phase shift caused by light pulse 40 on circadian state variables (x, xc) depends on the actual phase of these circadian state variables (x, xc) in relation to the timing of light pulse 40. In the example graphs of
The Jewett-Kronauer model represented by equations (1)-(10B) is a nonlinear model. In particular, equations (1) and (2), which describe the circadian state variables (x, xc), comprise a pair of nonlinear equations expressed in terms of the driving variable B and the circadian state variables (x, xc). Some embodiments of the present invention make use of linearizing transformations or manipulations which allow a nonlinear model to be approximated by a linear model. Such manipulations may involve nonlinear state feedback compensation and/or various linearizing approximations.
Particular embodiments of the invention employ linearizing approximations to provide linearized versions of equations (1) and (2) of the Jewett-Kronauer model. With respect to equation (1), it may be observed that there are two higher order (i.e. nonlinear) terms of the circadian state variable x, both of which are scaled by the factor μ. It may also be observed that equation (1) is an odd function of x, which has an integral of zero over the range of x (xε[−1,1]). Because these higher order terms introduce relatively small contributions that average to zero over the range of x, one possible approximation for equation (1) involves setting μ=0. With regard to equation (2), there are two higher order terms which are functions of Bxc and Bx and which are scaled by scaling factors q and k respectively. As with the approximation for equation (1), one possible approximation for equation (2) involves setting the scaling factors q and k to zero. These approximations to equations (1) and (2) (i.e. setting scaling factors μ, q and k equal to zero) result in the following linearized state space equations:
In the
In one particular embodiment, model 11 comprises the Jewett-Kronauer model described above in equations (10)-(10B). In another particular embodiment, model 11 comprises the Jewett-Kronauer model described above in equations (1)-(10B), except that linearized equation (11) replaces nonlinear equations (1) and (2). In such embodiments, model 11 predicts one or more of the circadian state variables (x, xc) and feeds this information back to controller 10 as circadian state feedback signal 14. Those skilled in the art will appreciate that model 11 may make use of transformations between the intensity domain I of light control signal 13 and the driving input domain B of the Jewett-Kronauer model.
Reference trajectory input 15 is preferably representative of a target time varying circadian pacemaker cycle. System 12 controllably adjusts the circadian pacemaker cycle of subject 17 to track reference trajectory input 15. In some embodiments, reference trajectory input 15 comprises desired values of one or more of the circadian state variables (x, xc) of the Jewett-Kronauer model described above. Light constraint inputs 16 may comprise minimum and/or maximum light intensity levels which may be applied to subject 17. Such minimum and maximum levels may be related to actual physical constraints of light source(s) 18 or to other levels, such as levels designed to promote the comfort of subject 17 for example. Light estimate input 21 is an optional input which comprises an estimate of light 19 experienced by subject 17. Light estimate input 21 may be in the intensity domain I and may be measured in lux. Light estimate input 21 comes from light estimator 20. In some embodiments, light estimator 20 comprises one or more sensors for measuring light 19. In other embodiments, light estimator 20 comprises a model which generates a signal representative of the light experienced by subject 17 and feeds this signal back to controller 10 as light estimate input 21. Such a model may take into account the current light signal 13, other sources of light (not shown), such as sunlight, ambient light, background artificial light, and other factors, such as time of day, date, location, activity patterns, and amount of light that will be incident on the retinas of subject 17.
In the
Control system 10 comprises response predictor 32 which comprises a response predictor subject model 36. Response predictor 32 receives light estimate input 21 and circadian state feedback signal 14 and generates free response information 38. In preferred embodiments, free response information 38 comprises a prediction of the future circadian state of individual 17 under the assumptions that the initial circadian state of individual 17 is indicated by circadian state feedback signal 14 and the current light level I indicated by light estimate input 21 remains constant. Response predictor 32 calculates the free response future circadian state of individual 17 (i.e. free response information 38) out to a control horizon H.
In particular embodiments, response predictor 32 calculates a plurality of future free response values of the circadian state of individual 17 after each of a number p of discrete sampling intervals between the current time and the control horizon H. In general, the control horizon H and the sampling interval may be of any duration depending on the application, processor resources, etc. In some preferred embodiments, the sampling interval is in a range of 1 minute to 1 hour. In particularly preferred embodiments, each sampling interval is in a range of 10-30 minutes. In some preferred embodiments, the length of the control horizon H is in a range of 12-72 hours. In particularly preferred embodiments, the length of the control horizon H is in a range of 24-36 hours.
In the
Controller 10 also comprises a control sequence generator 40 which comprises a controller subject model 44. In one particular embodiment, controller subject model 44 comprises the Jewett-Kronauer model described above in equations (1)-(10B). In a preferred embodiment, controller subject model 44 comprises the Jewett-Kronauer model described above in equations (1)-(10B), except that linearized equation (11) replaces nonlinear equations (1) and (2).
Control sequence generator 40 receives B domain constraints 42 (i.e. light constraints 16 converted from the intensity domain I to the B domain by I to B converter 34), free response information 38, light estimate input 21 and circadian state feedback signal 14 and uses these inputs to generate a series of control moves in the B domain (not shown). In preferred embodiments, control sequence generator 40 determines a series of “optimal” control moves in the B domain (not shown) which extend over a time period beginning at the current time and extending out to the control horizon H. As explained further below, this series of control moves is “optimized” by minimizing a cost function over the time period between the current time and the control horizon H. At each sampling interval, control sequence generator 40 outputs the first control move of this series as B domain control signal 46. B domain control signal 46 is converted by B to I converter 48 into light control signal 13 in the intensity domain I. As discussed above, light control signal 13 controls the operation of light source(s) 18 and the amount of light 19 experienced by subject 17.
In some embodiments, the cost function used by control sequence generator 40 is a least squares cost function. In one particular embodiment, the cost function used by control sequence generator 40 is expressed as:
where p is the number of samples between the current time t and the control horizon H, δ(k) is a weighting factor associated with the tracking error (i.e. the difference between the circadian state {circumflex over (x)} predicted by controller subject model 44 and the reference circadian state r described by reference trajectory 15), λ(k) is a weighting factor associated with the cost of the driving input B and k is an index variable that indexes a particular sampling interval within the control horizon H. In some embodiments, weighting factors δ(k) and λ(k) are constant. In other embodiments, however, weighting factors δ(k) and λ(k) are functions of k, such that additional weight may be applied to tracking particular points on the reference trajectory 15, such as the maxima and minima of reference trajectory 15 or the zero crossing points of reference trajectory 15 for example.
Control sequence generator 40 may make use of controller subject model 44 and the inputs described above to determine the “optimal” control moves (in the B domain) which will minimize the cost function of equation (13) over the control horizon H. Such control moves may comprise a series of B values (i.e. at each sampling time) from the current time and extended out to the control horizon H. After each sample interval, the control horizon H is extended by the time of one sampling interval and the control sequence generator 40 recalculates the “optimal” moves.
In practical situations, there will be light constraints 16 on the light intensity I. Such light constraints 16 may comprise minimum and maximum light intensity levels which may be related to actual physical constraints of light source(s) 18 or to other levels, such as levels designed to promote the comfort of subject 17 or the sleep/wake schedule of subject 17 for example. Light constraints 16 in the intensity domain I are converted to B domain constraints 42 by I to B converter 34 and are provided to control sequence generator 40. Preferably, light constraints 16 (and corresponding B domain constraints 42) comprise light constraint values for times extending out to the control horizon H. In some embodiments, light constraints 16 (and corresponding B domain constraints 42) may be constant.
As discussed above, I to B converter 34 may make use of a transformation of the form of equation (10B) to transform light constraints 16 in the intensity domain into corresponding B domain constraints 42. However, calculation of future B domain constraints 42 from future I domain constraints 16 in accordance with equation (10B) requires information about the future values of circadian state variables (x, xc). This creates an iterative problem, because future values of the circadian state variables (x, xc) depend in turn on the future B domain constraints 42.
In the
As discussed above, intensity domain light constraints 16 preferably comprise maximum and minimum light intensity levels. These maximum and minimum light intensity levels correspond with maximum and minimum B domain levels, Bmax and Bmin. Once the current and future B domain constraints 42 are determined by I to B converter 34, control sequence generator 40 determines the “optimal” control moves by minimizing a cost function in subject to the constraints:
Bmin(k)≦B(k)≦Bmax(k) for k=1 . . . p (14)
In embodiments where the cost function is given by equation (13), control sequence generator 40 selects B values for each sampling interval between the current time and extending out to the control horizon H (i.e. where k=p) which minimize the cost function of equation (13) within the constraints given by equation (14). Those skilled in the art of control systems and model-based predictive control are familiar with various techniques and algorithms for numerically or otherwise solving this minimization problem. Typically, such techniques involve constrained quadratic programming methods.
For the purposes of the examples illustrated in
In the example depicted in
In the example illustrated in
Curve 70 represents the circadian state variable xc as a function of time. In the example of
Physiological sensors 124 sense one or more physiological parameters from subject 117. Preferably, the physiological parameters sensed by sensors 124 are correlated to or otherwise related to the circadian state of subject 117. Preferably, the physiological parameters sensed by sensors 124 vary periodically in a manner that is related to the periodic variation of the circadian cycle of subject 17. Examples of physiological parameters include, without limitation: heart rate, core body temperature, respiration, endocrine function levels, physical activity levels, blood pressure, blood oxygen concentration and/or skin temperature.
The sensed values 126 of the physiological sensors 124 are provided to circadian state estimator 127. In some embodiments, the sensed values 126 of the physiological sensors 124 are communicated to circadian state estimator 127 via a wireless communication means (not shown). This allows subject 117 to be mobile. In other embodiments, the sensed values 126 of the physiological sensors 124 are communicated to circadian state estimator 127 via one or more corresponding wires. Noise 125 may appear parasitically in the sensed values 126 of the physiological sensors 124 prior to their reaching circadian state estimator 127. Noise 125 may be modeled as part of circadian state estimator 127 and/or in the model(s) associated with light controller 110. In some embodiments, noise 125 is modeled stochastically.
Circadian state estimator 127 receives the sensed values 126 of the physiological sensors 124 and uses this information to determine an estimate of the circadian pacemaker state of subject 117. This estimate of the circadian pacemaker state of subject 117 is provided to controller 110 as circadian state feedback signal 114. Preferably, circadian state feedback signal 114 generated by circadian state estimator 127 comprises one or more of the circadian state variables (x, xc) of the Jewett-Kronauer model. In some embodiments, circadian state estimator 127 comprises a model (not shown) which relates the values of one or more physiological parameters to the circadian state of subject 117. Such a model may be empirically determined and may use the sensed values 126 from physiological sensors 124.
Circadian state estimator 127 may receive other information 128 which it uses to help determine an estimate of the circadian state of subject 117. Information 128 may include one or more parameters that may be entered by subject 117, such as the sleep/wake schedule of subject 117 for example. Information 128 may include one or more parameters that are particular to subject 117, such as an indicator of the responsiveness of subject 117 to light (or other stimulus) for example. Information 128 may include one or more parameters associated with the environment in which subject 117 spends his or her time, such as temperature, time of day, time zone and background stimulus level for example.
As with system 12 of
In other respects, system 112 is substantially similar to system 12 of
In some embodiments, determining the initial conditions in block 202 involves arbitrarily assigning initial conditions. In other embodiments, determining the initial conditions in block 202 involves estimating the circadian state of the subject based on measurement of one or more physiological parameters. Such estimation may be substantially similar to the estimation performed by circadian state estimator 127 described above and may incorporate other information similar to information 128 described above. In still other embodiments, determining the initial conditions in block 202 may comprise determining an initial time and using a population average circadian state for the initial time.
Method 200 then proceeds to block 204 where input information is obtained. As shown best in
Block 206 of method 200 involves determining the free response of the subject out to a control horizon H. As discussed above in the description of
In block 208, method 200 involves determining the optimal control moves out to the control horizon H. As discussed above in the description of
Model based predictive control techniques of the type employed in blocks 206 and 208 of method 200 are well known to those skilled in the art and are described comprehensively in “Predictive Control with Constraints”, Jan Maciejowski, 2002 (Pearson Education POD), which is hereby incorporated herein by reference.
Once the optimal control moves are determined in block 208, method 200 proceeds to block 210 which involves outputting a control stimulus signal. As discussed above, the control stimulus signal may comprise a light control signal 13. Preferably, the control stimulus signal comprises the first control move of the optimal series of control moves determined in block 208.
After outputting a control stimulus signal in block 210, method 200 loops back to block 204 and then repeats itself. Preferably, the loop which comprises blocks 204, 206, 208 and 210 is performed at least once every sampling interval.
The systems and methods of the current invention have useful application in a variety of fields including, without limitation: controlling workplace lighting to maintain maximum employee performance; synchronizing multiple subjects to a common circadian cycle to improve operational efficiency; modifying circadian cycles of individuals undergoing medical therapy to improve their response to pharmaceutical drugs; modifying circadian cycles of athletes to allow peak performance at certain times; controlling lighting in the home to help make the daily processes of waking and falling asleep more comfortable, and providing invidualized light recommendations or control for personal advisory systems.
Controlling workplace lighting by providing additional light or restricting the level of light as appropriate can create benefits for various types of employees. Example applications include workers in windowless or underground rooms, submarine personnel and miners who receive no natural light; hospital employees, utility employees and other types of shift workers who may receive some natural light at times that may be inappropriate to the workers' circadian pacemaker cycle; and workers (or other travelers) aboard aircraft or spacecraft, who experience abnormal natural light levels due to the speed of their travel in relation to the sun. The systems and methods of the invention could be applied to control the levels of light stimulus to help advantageously regulate the circadian cycles of these types of subjects.
Another application of the systems and methods of the invention comprises synchronization of the circadian cycles of multiple subjects. Scientific research often requires the performance of experiments such as controlled tests of a new technology, drug, method or product on a given sample group of animals. The sample group may consist of rats, mice, primates and other animals, or human subjects. In many instances, the response of each test subject in the sample group will vary depending on the state of the test subject's circadian cycle. It would be advantageous, therefore, to normalize the initial conditions of each test subject in a sample group by providing a means for synchronizing the circadian pacemaker cycle of each member of the sample group before conducting the experiment. The particular pattern of light exposure could be customized for each member of the sample group in order to most efficiently entrain their circadian pacemaker cycle to a desired common cycle.
In addition to improving the accuracy of scientific experimentation, synchronization of the circadian cycles of multiple human subjects may be beneficial in certain kinds of military operations. In particular, when a given military operation requires the simultaneous action of many individuals, the probability of success of the operation may be higher if the individual members of the force are all operating at maximum alertness and cognitive performance.
Another application of the systems and methods of the present invention relates to adjusting the circadian pacemaker cycle of individuals who compete in athletic events. In some circumstances, such athletes have to travel relatively long distances to compete and after traveling such a distance, it may be advantageous to control the circadian pacemaker cycle of such athletes to achieve maximum performance during the athletic event.
Another application of the systems and methods of the present invention is in the area of medical therapy. It is well understood by medical professionals that a patient undergoing pharmaceutical drug treatment responds differently to prescribed drugs at different states of her endogenous circadian pacemaker cycle. The methods and systems of the present invention could be used to control the patient's circadian pacemaker cycle such that the drugs could be administered at optimum times to have a desired effect.
Yet another area in which the systems and methods of the present invention may be useful is generally known as home automation. Basic lighting and sound systems used in homes require manual control to adjust the levels of intensity. Before during, and immediately after waking, and also in the evening immediately before and after falling asleep, such manual control may be inconvenient and uncomfortable. The systems and methods of the invention may be employed to control lighting and/or sound systems to turn them on or off at specific times or to increase/decrease their intensity at specific rates of change. Such systems could function as part of a waking alarm, generating a gradually increasing level of light (and/or other stimulus) at a specific time over a given interval of time, so as to beneficially modify the subject's circadian pacemaker cycle towards a cycle consistent with experiencing wakefulness at desired times.
Still another field of application of the systems and methods of the present invention relates to a personal ambient light advisory system, to assist with adjusting an individual's circadian pacemaker cycle. The invention could be applied as an off-line system that uses models to generate recommended light levels for a given set of constraints and objectives. The advisory system could optionally also incorporate real-time sensor input regarding light levels, activity patterns, or physiological parameters. The controller could then update its advice on light levels in real-time. Systems of these types could be implemented on personal digital assistants (PDA's), cellular telephones, personal computers or other portable devices with computational capability for example. Such an advisory system could comprise or otherwise be coupled with a light delivery apparatus such as a portable high-intensity light source, where it could provide recommendations for use or directly control the light output. Potential users of such systems include transmeridian airline travelers and shift work professionals.
Certain implementations of the invention comprise computer processors which execute software instructions which cause the processors to perform a method of the invention. The invention may also be provided in the form of a program product. The program product may comprise any medium which carries a set of computer-readable signals comprising instructions which, when executed by a data processor, cause the data processor to execute a method of the invention. The program product may be in any of a wide variety of forms. The program product may comprise, for example, physical media such as magnetic data storage media including floppy diskettes, hard disk drives, optical data storage media including CD ROMs, DVDs, electronic data storage media including ROMs, flash RAM, or the like or transmission-type media such as digital or analog communication links. The program product may also comprise data, databases or other information which may be accessible to, but not necessarily executed by, a processor.
Where a component (e.g. a controller, model, assembly, device, etc.) is referred to above, unless otherwise indicated, reference to that component (including a reference to a “means”) should be interpreted as including as equivalents of that component any component which performs the function of the described component (i.e., that is functionally equivalent), including components which are not structurally equivalent to the disclosed structure which performs the function in the illustrated exemplary embodiments of the invention.
As will be apparent to those skilled in the art in the light of the foregoing disclosure, many alterations and modifications are possible in the practice of this invention without departing from the spirit or scope thereof. For example:
This application claims the benefit of the filing date of U.S. Patent Application No. 60/475529 filed 3 Jun. 2003.
Number | Date | Country | |
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60475529 | Jun 2003 | US |