Statistical Modeling of Atrioventricular Nodal Function
during Atrial Fibrillation
An Update
Valentina D. A. Corino
1
, Frida Sandberg
2
, Federico Lombardi
3
, Luca T. Mainardi
1
and Leif S
¨
ornmo
2
1
Department of Bioengineering, Politecnico di Milano, Milan, Italy
2
Department of Electrical and Information Technology and Center for Integrative Electrocardiology (CIEL),
Lund University, Lund, Sweden
3
Cardiologia, Dipartimento di Medicina, Chirurgia e Odontoiatria, Ospedale San Paolo, University of Milan, Milan, Italy
Keywords:
Atrial Fibrillation, Atrioventricular Node, Statistical Modeling, Maximum Likelihood Estimation.
Abstract:
This paper introduces a number of advancements of our recently proposed model of atrioventricular (AV)
node function during atrial fibrillation (AF). The model is defined by parameters characterizing the arrival
rate of atrial impulses, the probability of an impulse choosing either one of the two AV nodal pathways, the
refractory periods of these pathways, and their prolongation. In the updated model, the characterization of AV
nodal pathways is made more detailed and the number of pathways is determined by the Bayesian information
criterion. The performance is evaluated on ECG data acquired from twenty-five AF patients during rest and
head-up tilt test. The results show that the refined AV node model provides significantly better fit than did the
original model. During tilt, the AF frequency increased (6.25 ± 0.58 Hz vs. 6.32 ± 0.61 Hz, p < 0.05, rest vs.
tilt) and the prolongation of the refractory periods decreased for both pathways (slow pathway: 0.23 ± 0.20 s
vs. 0.11 ± 0.10 s, p < 0.001, rest vs. tilt; fast pathway: 0.24 ± 0.31 s vs. 0.16 ±0.19 s, p < 0.05, rest vs. tilt).
These results show that AV node characteristics can be assessed noninvasively for the purpose of quantifying
changes induced by autonomic stimulation.
1 INTRODUCTION
The atrioventricular (AV) node is subjected to the
impact of atrial impulses during atrial fibrillation
(AF) which leads to summation and/or cancellation
of wavefronts in the AV node and, accordingly, a high
level of disorganization of the penetrating impulses.
As a result, the ventricular rhythm becomes much
more irregular than during normal sinus rhythm. Dif-
ferent properties such as intrinsic refractoriness of
the AV node and concealed conduction determine
the characteristics of the ventricular response (Fuster
et al., 2006), but they are not routinely evaluated in
clinical practice mainly because of the lack of nonin-
vasive methodology.
Statistical model-based analysis of essential AV
nodal characteristics constitutes a powerful method
to assess AV node properties during AF. A statisti-
cal model suitable for parameter estimation was at an
early stage described in (Cohen et al., 1983): the AV
node was treated as a lumped structure whose behav-
ior represented the temporal and spatial summation
of the cellular electrical activity. The atrial impulses
were assumed to arrive randomly to the AV node ac-
cording to a Poisson process. When the AV node
was not refractory, its transmembrane potential was
assumed to increase with the contribution of each ar-
riving atrial impulse as well as to increase sponta-
neously. When the transmembrane potential reached
a certain threshold, a new action potential initiated a
ventricular beat. Despite the fact that the model was
statistical in nature, the model parameters were de-
termined from the RR series using an ad hoc proce-
dure. A serious limitation of that procedure was that
the resulting parameter estimates could assume non-
physiological values. An extension of this model was
proposed (Lian et al., 2006), however, the proposed
model was suitable for simulation purposes only.
Other AV node models have been proposed, mainly
based on the analysis of atrial electrograms recorded
during electrophysiological studies (Jørgensen et al.,
2002; Mangin et al., 2005); None of those models
25
D. A. Corino V., Sandberg F., Lombardi F., T. Mainardi L. and Sörnmo L..
Statistical Modeling of Atrioventricular Nodal Function during Atrial Fibrillation - An Update.
DOI: 10.5220/0004194100250029
In Proceedings of the International Conference on Bio-inspired Systems and Signal Processing (BIOSIGNALS-2013), pages 25-29
ISBN: 978-989-8565-36-5
Copyright
c
2013 SCITEPRESS (Science and Technology Publications, Lda.)
were accompanied by a statistical estimation proce-
dure.
In a recent paper, we proposed a statistical model
of the AV nodal function during AF w hich lends itself
to ECG-based parameter estimation (Corino et al.,
2011). The model is defined by a small set of pa-
rameters which characterizes the arrival rate of atrial
impulses, the probability of an impulse choosing ei-
ther one of the dual AV nodal pathways, the refractory
periods of the pathways, and the prolongation of re-
fractory periods. The parameters were estimated from
the RR series using maximum likelihood (ML) esti-
mation, except for the shorter refractory period which
was estimated from the Poincar
´
e plot of successive
RR intervals, and the mean arrival rate of atrial im-
pulses which was estimated by the AF frequency de-
rived from the f-waves of the ECG (Sandberg et al.,
2008).
Subsequent application of our AV node model
suggests that certain model properties should be ex-
tended and the estimation performance improved with
respect to robustness. Therefore, this paper introduces
a more detailed characterization of the dual pathways.
In particular, the effect of tilting on the refractory pe-
riods of the AV node was assessed by means of the
model parameters.
2 METHODS
2.1 Existing AV Node Model
In the present model, the AV node is treated as a
lumped structure which accounts for concealed con-
duction, relative refractoriness, and dual AV nodal
pathways. Atrial impulses are assumed to arrive to the
AV node according to a Poisson process with mean ar-
rival rate λ. Each arriving impulse is suprathreshold,
i.e., the impulse results in ventricular activation un-
less blocked by a refractory AV node. The probability
of an atrial impulse passing through the AV node de-
pends on the time elapsed since the previous ventric-
ular activation t. The length of the refractory period is
defined by a deterministic part τ and a stochastic part
τ
p
. The latter part models prolongation due to con-
cealed conduction and/or relative refractoriness, and
is assumed to be uniformly distributed in the inter-
val [0; τ
p
]. Hence, all atrial impulses arriving to the
AV node before the end of the refractory period τ are
blocked. Then follows an interval [τ, τ + τ
p
] with lin-
early increasing likelihood of penetration into the AV
node. Finally, no impulses can be blocked if they ar-
rive after the end of the maximally prolonged refrac-
tory period τ + τ
p
. The mathematical characterization
of refractoriness of the i:th pathway (i = 1,2) is thus
defined by the positive-valued function β
i
(t),
β
i
(t) =
0, 0 < t < τ
i
t τ
i
τ
p
, τ
i
t < τ
i
+ τ
p
1, t τ
i
+ τ
p
,
(1)
where t denotes the time elapsed since the preceding
ventricular activation.
The probability of an atrial impulse to take the
pathway with the shorter refractory period τ
1
is equal
to α, and accordingly the other pathway is taken with
probability (1 α). For this model, the time intervals
x
i
between consecutive ventricular activations, i.e.,
corresponding to the RR intervals, are independent.
It can be shown that the joint PDF is given by (Corino
et al., 2011)
p
x
(x
1
, x
2
, . . . , x
M
) =
M
m=1
(αp
x,1
(x
m
) + (1 α)p
x,2
(x
m
)),
(2)
where M is the total number of intervals, and
p
x,i
(x
m
), i = 1, 2, is given by
p
x,i
(x) =
0, x < τ
i
λy
i
τ
p
exp
{
λy
2
i
2τ
p
}
, τ
i
x < τ
i
+ τ
p
λexp
{
λτ
p
2
λ(y
i
τ
p
)
}
, x τ
i
+ τ
p
.
(3)
where y
i
= x τ
i
.
2.2 Model Parameter Estimation
2.2.1 Estimation of τ
min
1
Since the property of statistical independence is not
fully valid for observed RR intervals, a simple func-
tional dependence of the refractory periods related to
the previous RR interval is explored. The interdepen-
dence of consecutive RR intervals can be reduced by
preprocessing the original RR interval series, denoted
x
m
, with the linear transformation,
x
m
= x
m
ˆs
τ
x
m1
. (4)
where ˆs
τ
, together with an estimate of the minimal
refractory period τ
min
1
, is found from the line that de-
fines the lower envelope of the Poincar
´
e plot using the
Hough transform, see (Corino et al., 2012) for details
on how to determine this line. The interval series x
m
that results from (4) constitutes the data used for ML
estimation.
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An estimate of the refractory period τ
m,1
of the
slow pathway and the m:th activation may be obtained
from the linear relationship
τ
m,1
= τ
min
1
+ s
τ
x
m1
. (5)
Assuming that s
τ
applies to both τ
m,1
and τ
m,2
, the
problem of estimating τ
m,2
is identical to the problem
of estimating a fixed duration ∆τ since
τ
m,2
= ∆τ +τ
m,1
. (6)
2.2.2 Maximum Likelihood Estimation of Dual
Pathway Parameters
The model parameters related to the dual AV nodal
pathways and the refractory period prolongation are
estimated by maximizing the log-likelihood function
Λ(θ) with respect to θ, i.e.,
ˆ
θ = argmax
θ
Λ(θ) (7)
= arg max
θ
log p
x
(x
1
, x
2
, . . . , x
M
|θ;
ˆ
λ,
ˆ
τ
min
1
),
where θ = [α ∆τ τ
p,i
]
T
. Since no closed-form so-
lution could be found for
ˆ
θ, combined with the fact
that the gradient is discontinuous, simulated anneal-
ing was employed for maximization. The optimiza-
tion algorithm was initiated with 10 different, ran-
domly chosen values for each estimation. The opti-
mal
ˆ
θ was then chosen as that value for which Λ(
ˆ
θ)
is maximum, almost invariably being the dominant
value.
2.3 AV Node Model Update
2.3.1 Dual Pathways
To date, no evidence has been presented which sug-
gests that refractory period prolongation is identical
for the dual AV nodal pathways. Rather, it has been
found that the input regions of the atrial impulses play
an important role in determining the properties of AV
nodal conduction and refractoriness (Mazgalev et al.,
1984). Inspired by the work in (Climent et al., 2011),
our original model is here extended to account for
pathway-dependent prolongation of the refractory pe-
riod. Hence, prolongation is described by the two pa-
rameters τ
p,1
and τ
p,2
, implying that the PDF p(x
i
) in
(3) is modified so that τ
p,i
replaces τ
p
.
2.3.2 Estimation of λ
In the original AV node model, the atrial impulses
were assumed to arrive to the AV node according to a
Poisson process at a rate λ. An estimate of λ was ob-
tained by first estimating the dominant AF frequency
λ
AF
from the ECG, independently of the AV node pa-
rameters, and then assuming that
λ = λ
AF
. (8)
The details of the procedure for estimating λ
AF
are de-
scribed in (Corino et al., 2011). A disadvantage with
such an approach is that it does not account for the
fact that there is a minimum time interval δ between
successive impulses arriving to the AV node. Such an
interval was included in the simulation model in (Lian
et al., 2006), where it was assumed that the atria de-
polarize again after δ = 50 ms.
Evidently, the Poisson model does not impose
a minimum time interval δ between successive im-
pulses arriving to the AV node, but they can ar-
rive immediately upon each other. Therefore, the
use of (8) produces an underestimated value of λ.
For Poisson-distributed impulses not arriving closer
to each other than a minimum interval δ, the arrival
rate λ
AF
should be modified according to (Larsen and
Kostinski, 2009)
λ =
λ
AF
1 δλ
AF
, (9)
2.3.3 Selection of Single or Dual Pathways
The selection of single or dual pathway model is de-
termined by the Bayesian information criterion (BIC),
defined by
C
BIC
(k) = 2Λ(
ˆ
θ
k
) + n
k
log(M), k = 1, 2, (10)
where the parameter estimate is either equal to
ˆ
θ
1
=
τ
p,1
for a single pathway or
ˆ
θ
2
= [α ∆τ τ
p,1
τ
p,2
]
T
for dual pathways. The number of parameters n
k
is
thus equal to 1 or 4. The number of pathways is
given by that index k which produces the lowest value
of C
BIC
(k). The original use of simulated anneal-
ing for maximization of the log-likelihood function is
here replaced with a genetic algorithm because it was
found to offer much faster maximization.
3 DATA
We analyzed 25 consecutive patients with persistent
AF (67 ± 7 years, 16 females) who underwent elec-
trical cardioversion, according to the international
guidelines, at the Cardiology department of San Paolo
Hospital, Milan, Italy. Recordings were acquired at
rest and during a passive orthostatic stimulus (75
tilt-
ing). One patient was excluded from analysis due to
poor ECG quality preventing the estimation of AF fre-
quency. Hence, the results presented below are based
on 24 patients.
StatisticalModelingofAtrioventricularNodalFunctionduringAtrialFibrillation-AnUpdate
27
The ECG was recorded at rest for 10 min and,
when applicable, followed by tilting, using three or-
thogonal leads and a sampling rate of 1 kHz. All
recordings were performed in the morning in a quiet
environment following 15 min of adaptation. The
study was approved by the Ethics Committee, and all
patients gave their written informed consent to partic-
ipate.
4 RESULTS
To assess if the present model could provide a better
fit of the data, an index taking the underlying PDF
into account is preferable. However, since the under-
lying PDF is unknown for ECG-derived RR intervals,
an empirical PDF, denoted ˜p
x
(x), was determined by
wavelet-based density estimation (Corino et al., 2011;
Ogden, 1997). The capability to model different RR
series was evaluated in terms of a percentage measure
of fit U, defined by
U = 100 ·
(
1
2
0
p
x
(x|
ˆ
θ
k
;
ˆ
λ,
ˆ
τ
min
1
) ˜p
x
(x)
dx
)
,
(11)
where the upper integration limit reflects the fact that
very few RR intervals are longer than 2 s during AF.
The reason for using wavelet-based density estima-
tion rather than comparing p
x
(x|
ˆ
θ
k
;
ˆ
λ,
ˆ
τ
min
1
) to the RR
interval histogram is the poor statistical properties of
the histogram (Ogden, 1997).
Figure 1 indicates that the model fit, as described
by U, was significantly better with the present model,
both for rest and tilt data. Figure 2 shows an exam-
ple of histogram of the transformed RR intervals and
the estimated model PDF from the same patient using
the original and the present model. The latter model
fits the histogram much better than does the original
one, U increasing from 84% to 89%. It can be noted
that the histograms of transformed RR intervals are
not exactly the same because the transformation de-
pends on
ˆ
τ
1
which is different in the two models. In
the following, the presented results are obtained using
the present model.
To assess whether the model parameters can cap-
ture changes occurring due to increased sympathetic
tone, such as during a tilt test, parameters during rest
were compared to those during tilt. Table 1 com-
pares the model parameter estimates obtained at rest
and during tilt, with significant changes due to sym-
pathetic activation in
ˆ
τ
p,1
and
ˆ
τ
p,2
. The AF frequency
was found to increase significantly during tilt. The
probability of an atrial impulse of choosing either
pathway is almost equal during rest and tilt (α = 0.5),
70
80
90
100
original new
(a)
U %
70
80
90
100
original new
(b)
U %
Figure 1: Boxplots of U for data during rest and tilt, com-
paring the original and the updated AV node model.
* p<0.05, ** p<0.01.
0 0.5 1 1.5 2
0
5
10
15
20
25
30
35
40
transformed RR interval (s)
# transformed RR intervals
(a)
0 0.5 1 1.5 2
0
5
10
15
20
25
30
35
transformed RR interval (s)
# transformed RR intervals
(b)
Figure 2: Histogram of transformed RR intervals and the es-
timated model PDF from the same patient during rest using
(a) the original and (b) the new AV node model.
although α spans the range from 0.05 to 1, thus mak-
ing the involvement of the pathway with slower re-
fractory period (α < 0.5) in about half of all record-
ings. The refractory periods of both pathways remain
almost unchanged during tilt, whereas their prolonga-
tion, due to concealed conduction, relative refractori-
ness etc., are significantly shortened during tilt.
Both the mean and standard deviation of RR in-
tervals are significantly shortened during tilt due to
sympathetic activation. The mean RR interval length
was 743 ± 146 ms vs. 680 ± 125 ms (rest vs. tilt,
p < 0.0001), and the related standard deviation was
156 ± 51 vs. 137 ± 29 ms (rest vs. tilt, p < 0.0001).
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Table 1: Comparison of rest and tilt parameters. *p<0.05,
**p<0.001.
Rest Tilt
ˆ
α 0.52 ± 0.24 0.51 ± 0.30
ˆ
τ
min
1
(s) 0.37 ± 0.09 0.38 ± 0.10
ˆ
τ
min
2
(s) 0.46 ± 0.12 0.47 ± 0.09
ˆ
τ
p,1
(s) 0.23 ± 0.20 0.11 ± 0.10 **
ˆ
τ
p,2
(s) 0.24 ± 0.31 0.16 ± 0.19 *
ˆ
λ (Hz) 6.25 ± 0.58 6.32 ± 0.61 *
5 CONCLUSIONS
We have proposed an updated AV node model in
which i) the characterization of the AV nodal path-
ways is made more detailed using two different pa-
rameters representing the prolongation of related re-
fractory periods, ii) the number of pathways is deter-
mined by the BIC, and iii) the arrival rate is corrected
to take into account there is a minimum time inter-
val between successive impulses arriving to the AV
node. The updated model leads to better estimation
of the PDF when two peaks with different width are
to be modeled, and also the most parsimonious model
is selected (choosing between single or dual pathway
model). Considering physiological aspects, our re-
sults indicate that tilting is associated with significant
changes in AV conduction that are well-described by
the model and reflected by shortening of both τ
p,1
and
τ
p,2
during adrenergic activation. Thus, the present
AV node model is adequate for studying and describ-
ing the functional characteristics of AV conduction in
AF patients.
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