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Authors:
Víctor Gimeno, Teresa Sagales, Luchi Miguel,
Mercedes Ballarin
Servei de
Neurofisiologia,
I-Iospital
Universitari Vall d'Hebron, Barcelona, Spain
Pharrnacoelectroencephalography
Original
Paper
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Key Words
Sleep,
Actigraphy,
Series
of events,
Statistical
distribution functions
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Abstract
The
purpose of this work was to describe the basic statistical properties of the
process of production of movements measured with a wrist actimeter, along a
complete sleep period in normal human subjects. Two distinct types of random
magnitudes were considered to analyze the data, the times between successive
groups of movements and the number of movements at each fixed time (1 min)
measurement epoch. Suitable probabilistic models for the two variates were
chosen, fitting theoretical distribution functions to the observed data. It is
concluded that interval data fit a one-parameter exponential distribution,
while the number of movements fit a two-parameter negative binomial
distribution. The estimated values of these parameters, besides being necessary to perform further statistical analysis, are a measure of the
intensity
and frequency of the movements. Finally the relationship between polysomnography measures and the elicited parameters was studied.
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Introduction
Measurement
of motility by wrist actigraphy has become a popular method in the study of
human sleep ( 1 - 1 0), for it employs an inexpensive, easily wearable device,
which is simple to use and allows ambulatory recordings to be taken. Actigraphic
records consist of raw data usually presented as a comprehensible plot of
number of movements versus time. However there is a lack of uniformity in the
approach to the analysis of this data in the literature, which is mainly
focused on the production of automatic sleep-wake scoring algorithms [l 1 ].
In fact, a precise characterization of the basic statistical properties of
these series of events has yet to be done.
When
measuring random data its basic properties are described in terms of statistical
parameters, as the well known mean value and standard deviation pair in the case
of random variables following the classical Gaussian distribution.
Movements
can be considered as a series of random point events occurring on a time axis,
but besides their position in time they are distinguished by an additional
random quantity which is the number of movements appearing at each f́xed time
measurement epoch. There are therefore two different types of magnitudes whose
distributions must be considered, the times between successive appearances
of movements and the number of movements. Properties of both descriptors, time
intervals and counts, serve to characterize the process of production of
movements. A joint analysis of these two different types of random variables is
also necessary to elicit the possible association between both variates.
In this work, plausible theoretical distribution forms were fitted to the
actimetric experimental data, estimating their parameters and testing their adequacy. Any
further analysis of the actimetric data should take these results into
account.
Subjects
and Methods
Twenty-three healthy
volunteers, 11 female, 12 male,
between the ages of 24 and 47, were submitted to a polysomnography (PSG) during 2 consecutive nights. Subjects also wore an
actimeter (Mini-Logger Series
2000), placed on their nondominant wrist, set to collect the number of
movements in 1-min consecutive intervals. Actimeter and polygraphic recorder
clocks were carefully synchronized to achieve a precise timing in both
recordings. Stored actimeter data were read by a computer through a serial
interface and stored in a disk file for further processing. After a first
accommodation night, actigraphic records were analyzed during the second night,
using data from only deep period time, i.e. discarding data prior to sleep onset
and the epochs awake after the end of the sleep, as detected by the PSG. Extreme
care was taken to minimize the presence of artifacts in the records, continuously
checking the position of the device through a video camera to make sure that
the influence from either breathing movements or the blocking of the arm for
any postural reason produced no important artifacts [7, 12]. Hypnogram and
actigraphic data were also jointly inspected to discard gross discrepancies between
both records. Subjects presented no periodic limb movements and no sleep
apneas. Three evident cases of irregular awakening and activity, two as a
result of getting up to go to the toilet and another with breathing problems due
to a cold were withdrawn from the study. PSG and actigraphic recordings of the
remaining subjects were considered of good quality. Therefore the definite size
of the sample was n = 20. Observing actigraphic recordings, an evident clustering
of the movements can be clearly seen in most of them. Clustered distributions of
this type (also called 'contagious' in statistics) present a variance substantially larger than the mean which precludes the
possibility of a single
Poisson process as the generating mechanism of the series [ 1 3], but clusters
themselves can arise from a completely random (i.e. Poisson) process. In
other words, times between the appearance of clusters are independent. This
was the first hypothesis tested, regarding these intervals, or immobility
periods,
as the variate to analyze. If the distribution of clusters is consistent with a
Poisson process, these periods will follow an exponential (continuous) distribution [ 1 4]. The
parameter 'b' of this distribution (its estimated value will
be denoted as'b') is easily estimated by the arithmetic mean of the intervals,
i.e. the mean duration of immobility periods. Departures from this distribution
for the interval data can then be used to reject this first hypothesis. A c2 test
for the goodness of fit was used in this work [see 14 for a thorough discussion
about tests for Poisson and for more general renewal processes]. With respect to
the number of movements produced at each measurement epoch, i.e. every minute, a
natural choice to model its distribution is to use a negative binomial (NB)
distribution function [15], which is a two-parameter (m, k) distribution with its
mode usually near the origin and with a long tail (the definitions of this distribution vary slightly from one author to another). Clustered
distributions
frequently arise in various fields and in most instances an NB(m,k) form appears
as an adeguate model. This was therefore the second hypothesis tested. Estimation of its two
parameters can be made using several methods [ I 6]. The parameter 'm' is
estimated by the mean, i.e. it is the average rate of occurrence of movements.
Tbc other parameter, 'k', varies according to the proportion of time without
movements, and its values were estimated in this work by the method of maximum
likelihood. cgoodness-of-fit methods were also used to test this second hypothesis.
To gain a better insight into the meaning of these two
parameters, Spearman's correlation coefficients between the obtained values of 'm'
and the proportion of time with presence of movements as well as between the
values of 'k' and the average length of the intervals were calculated.
Finally, the relation between position and magnitude
(i.e. number of activity counts in a cluster) of the movements was investigated by the estimation of
the proportion of movements that were
directly associated with the time of occurrence. Standard regression techniques were used for
the analysis, considering the time of origin of each
cluster as the independent variable and the number of movements in the cluster
as the dependent variable.
A study of the relationship between
the structure of
sleep as assessed from PSG and the elicited parameters 'b', 'm', 'k', was also
carried out. Sleep efficiency (Eff%) and accumulated time awake after sleep
onset (WASO) are the parameters that can be most closely estimated by present
actigraphic methods [5, 17-19]. In this work these two parameters and the number
of awakenings (AW) during the sleep period time were taken as sleep descriptors.
Entering 'b', 'm', 'k', as independent variables, multiple linear regression analyses
were performed for these PSG measures to test the hypothesis that there is a
significant relationsbip between PSG descriptors and actigraphic parameters.
Results
The
pattern of a typical actigraphic recording presents random production times
combined with random number of movements. We used a graphic presentation that
includes both cumulative (fig. 1a) and individual (fig. 1 b) number of
movements versus time. It is worth noting that the departure of the cumulative plot from a straight line measures the lack of uniformity in the appearance of
movements, as the slope of the line between any two points represents the mean
number of movements per unit time for that interval.
Goodness-of-fit tests for the exponential distribution, fitted to the
interval data, lead to the conclusion that this model can be considered adeguate
in all but 2 cases. However, in those cases, coefficients of variation had
sample values near unity and serial correlation coefficients were calculated
giving values which were also compatible with the hypothesis of independence of
the intervals [14]. Regarding the number of movements produced at each point, it
was also possible to fit the sample data to a negative binomial distribution
by an appropriate choice of its two parameters, 'm', 'k'. This was checked by c2
analysis.
Only in 1 subject presenting a very low sleep
efficiency was the fit rejected.
The elicited Spearman's correlation coefficients yielded high
values, significantly different from zero: r = 0.8303 between 'm'
and the proportion of time with movements and a negative correlation of r =
-0.7829 between 'k' and the average length of the intervals. This correlation
was improved considering reciprocal 'k' values (r = 0.9482).
Regression
analysis for the different series showed that the number of movements appearing
at each cluster is not related to its time value, i.e. the number of movements
does not depend on the time of observation (coefficients of determination were
as low as 0.1578). Having examined scatter diagrams (fig. 2) of the
number of movements in each cluster against the time interval between the
beginning of the cluster and the end of the previous one, it was also found that
there is no apparent relationship.
Variability in our numerical findings is summarized in
table
1.
The results of the regression analyses are presented in
table 2. They show that there is a significant dependence (p < 0.05) of each PSG deseriptor on the three statistical
parameters.
Tbc proportions of variance in PSG data attributable to
the dependence of PSG on 'b', 'm', 'k', are 64, 44 and 66% for Eff%, AW and WASO,
respectively. Standard partial
regression coefficients were used as indications of relative importance of the
parameters 'b', Gm', 'k', in determining the value of PSG deseriptors. It was
found that 'm' is the most irnportant parameter in determining the value of
Eff% and WASO, and 'b' is the most impor- tant parameter in determining the
value of AW.
Although the parameter 'k' has a low relative
importance, separate simple correlation analyses between PSG descriptors and 'k'
indicate that there is a signifícant relationship between them. Results are
shown in table 3.
Discussion
There
are currently a number of automatic scoring algorithms of the actimetric data to
estimate several sleep parameters [2, 10, 20-22]. However, there has been little
work on the investigation of actigraphic data throug, mathematical models
carried out to date, although it is of great statistical importance to have
reliable models that serve to describe the experimental measurements [23] Wallner
[24] was able to estimate sleep efficiency and total sleep time analysing the
body movement density function, and perfomed spectral analysis of data from
sequence
of several days to study circadian and ultradian rhythms. Home et al [25] used a
filtered version of the actigram to convert it into a binary signal to study the effect of noise on
sleep.
In
our work, although other distribution functions could have been chosen to fit
actimetric data, e.g. a more general gamma form for the intervals, the chosen
models were simple and it was shown that they were also adequate. The
estimated parameters are easily related to natural descriptors of actigraphic
records. The parameter 'b' of the exponential distribution represents the mean
duration of the immobility periods, its reciprocal value therefore giving
information about the frequency of the process. As far as the NB distribution
is concerned, its parameter 'm' (the average rate of occurrence of movements)
was found to be highly correlated with the proportion of time with presence of
movements, thus being a measure
of
the average intensity of the process. The other parameter,'k', was found to
be closely related to the inverse of the average length of the intervals between
movements, therefore it is also a measure of the frequency of the process. In
fact, similar parameters can be found among the large number of variables that
are used in the literature [26]. However, our different approach, based on the
statistical analysis of the data, leads us to conclude that the triplet 'b',
'm', 'k', must be considered as a natural necessary minimum set of activity
descriptors to be elicited as the first step in the analysis of nocturnal
actigraphic data.
Moreover,
the finding that the clusters of movements appeared randomly in time, added to
the fact that the number
of movements did not depend on the time of observation, makes the hypothesis of
two different underlying processes as the generating mechanisms of the series
of movements feasible. One would drive the timing of the series or, in other
words, its frequency, and the other its intensity. However, it is not
possible to draw reliable conclusions on the role of these processes in the
regulation of movements during sleep and this question has yet to be studied.
Underlying
mechanisms for motor activity are not completely understood to date. Although the
investigation of the relationship between movements and other
underlying
processes determining sleep stages, stage sbifts, etc., is out of the scope of
this paper, these movement processes are likely to be related to sleep
structure. As it could be expected, our regression analyses show that Eff% is
positively related to 'b' and negatively related to 'm' and'k'. Conversely,
WASO is negatively related to'b' and positively related to 'm' and 'k'. As it
could also be expected, AW is negatively related to 'b', but the negative
relationship between AW and 'm' cannot be clearly ex plained.
When calculating a simple correlation between AW and 'm', wc found a
nonsignificant value (r = 0.05 1). This could suggest that these two variables
are in fact independent.
We
have also measured the density of movements (number of movements per unit time)
for each sleep stage and found that there is a decrease in activity in the
sequence of stages W > 1 > 2 > R > 314 in 45% of the
subjectsandw> 1 >R>2>314 in 35% other subjects. In 80% of the subjects
the lowest density of movements was found in stare 314. These results agree with
those of Conradt [27], showing that there is some degree of correlation
between sleep structure and movements, albeit limited.
Our
findings point to a multiple origin of the movement processes, not only to an
intrinsie sleep origin. The analysis of other underlying mechanisms in the
production of night movements need further investigation but the general description of the distribution of these
movements should take into account
the parameters found in this paper.

Fig. I. Number of movements versus time. a = Cumulative
number of movements. b = Number of movements in 1-min epochs.

Fig. 2. Example of scatter diagram for a particular
subject showing the number of movements in eacb cluster against the time
interval from the previous cluster.

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