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Detection and Localization of Myocardial Ischemia
by Multichannel Magnetocardiography
Helena Hänninen ab), Panu Takala bc), Markku Mäkijärvi ab), Juha Montonen bc)
Katja Pesola bc), Petri Korhonen ab), Lasse Oikarinen ab), Kim Simelius bc),
Jukka Nenonen bc) Toivo Katila bc), and Lauri Toivonen ab)
a)Division of Cardiology and b)BioMag Laboratory, Helsinki University Central Hospital
c)Laboratory of Biomedical Engineering, Helsinki University of Technology, Helsinki, Finland
Correspondence: Helena Hänninen, Helsinki University Central Hospital, Division of Cardiology,
Haartmaninkatu 4, FIN 00290 Helsinki, Finland.
E-mail: hahannin@sci.fi, phone +358 9 4717 2442, fax: +358 9 4717 4574
Abstract.. Magnetocardiography
(MCG) is a novel multichannel mapping technique for recording
the cardiac magnetic fields. Comparison of multichannel MCG
and body surface potential mapping (BSPM) allows a comprehensive
study of electromagnetic field generated by the heart. In
healthy subjects, significant amplitude changes in MCG not
detected in BSPM have been reported during the repolarization
period of the cardiac cycle. Transient, exercise induced myocardial
ischemia induces a change in the polarity of the magnetic
isofield maps. This change in the field polarity has been
quantified using surface gradient method. The magnetic field
orientation and strenght during QT-interval at rest has also
separated coronary artery disease patients with normal ECGs
and patients with previous myocardial infarctions from healthy
controls. Localization of chronic myocardial ischemia using
current density estimation (CDE) is a promising clinical application
for MCG. In patients with chronic myocardial ischemia and
left ventricular dysfunction, the areas of low CDE amplitude
have been found to match with scar regions whereas a high
CDE amplitude was reported to correlate with areas of viable
ischemia cardiac tissue. Detection and localization of myocardial
ischemia is a promising application for MCG. Further studies
are needed to confirm the very first studies of MCG in ischemia
detection.
Keywords: Magnetocardiography; Coronary Artery Disease;
Myocardial Ischemia; Exercise Testing
1. Introduction
Magnetocardiography (MCG) is a novel noninvasive multichannel
mapping technique to record cardiac electromagnetic signals,
generated by the same ionic currents underlying the ECG
[Siltanen, 1989]. The MCG has similar morphological features
as the ECG, such as QRS complex, T-, P-, and U-waves, but
there are some fundamental differences. The MCG is more
sensitive to tangential currents in the heart than the ECG,
and it is also sensitive to vortex currents, which cannot
be detected by the ECG [Siltanen, 1989]. In normal heart,
the main direction of the activation wavefront is radial,
from endocardium to epicardium. For these reasons, MCG may
show ischemia-induced deviations from the normal direction
of depolarization and repolarization with better accuracy
than the ECG. MCG is affected less by conductivity variations
in the body (lungs, muscles, skin) than ECG [Nenonen et
al., 1994]. In addition, because MCG is a fully noncontact
method, the problems in the skin-electrode contact encountered
in ECG are avoided [Siltanen et al., 1989]. To improve signal
to noise ratio, sensitive MCG recordings are typically performed
in a magnetically shielded room [Nenonen et al., 1997].
Body surface potential mapping (BSPM) covers an extensive
area of the thorax offering better spatial scope and resolution
compared to the standard ECG due to sampling in areas of
the thoracic surface not covered by the conventional six
precordial leads. It has been reported to be more sensitive
in the detection of myocardial infarction than the 12-lead
ECG [Kornreich et al., 1993]. In acute myocardial infarction
the optimal electrode positions for recognition of different
types of myocardial infarction have been found to be located
in positions other than the conventional ones of the 12-lead
ECG. The time consuming placement of electrodes is the major
disadvantage of body surface potential mapping.
Combining the body surface potential mapping and multichannel
magnetocardiography allows a comprehensive study of electromagnetic
fields generated by the heart in different clinical settings.
These multichannel mapping techniques have made it possible
also to look at the ischemia-induced spatial changes both
in the magnetic and electric fields over the thorax.
2. Electromagnetic Changes Caused by Ischemia
Myocardial ischemia causes changes in the electrophysiological
properties of the myocardium. The resting membrane potential
decreases and the upstroke velocity of the action potential
and its velocity is lowered [Janse et al., 1981]. The conduction
velocity decreases markedly and unhomogenously in the ischemic
areas resulting in the dispersion of the activation wavefront.
Acute transient ischemia and on the other hand infarcted
necrotic regions therefore have different electromagnetic
properties. Furthermore, in acute myocardial infarction
after experimental occlusion of a coronary artery, opposite
ST-segment and baseline shifts on direct current MCG have
been found, suggesting MCG to have an advantage over ECG
in the detection of injury currents [Cohen et al., 1975].
3. Exercise MCG in Healthy Controls
In healthy subjects, ST-T segment changes have been reported
in MCG mapping after pharmacological stress testing, not
visible in 32-lead ECG [Brockmeier et al., 1997]. These
changes included ST segment depressions, as well as T-wave
inversions with monopolar negative MCG maps after stress.
The changes in MCG were concluded to be of non-pathological
origin, and the authors suggested that they could have been
induced by circular, so-called vortex currents not detectable
by ECG. Significant amplitude changes in the MCG, not detectable
in the BSPM have also been reported in a another study [Takala
et al., 1998]. At the T-wave apex, a bending of the spatial
zero-field line from rest to the cessation of stress was
found to take place, and monopolar group-mean difference
maps at the T-wave apex as well as during the ST segment
were detected.
Due to these physiological changes reported the ischemia
detection in stress MCG cannot be based solely in similar
amplitude parameters used in standard ECG testing. Instead,
novel multichannel mapping techniques have made it possible
also to look at the ischemia-induced spatial changes in
the cardiac magnetic field.
4. Exercise Induced Ischemia in MCG
Cohen et al. reported the first stress MCG study, in which
during exercise the ST segment in the MCG became depressed
and the baseline TQ segment elevated in direct current MCG
[Cohen et al., 1983]. The baseline elevation disappeared
after termination of stress more rapidly than the ST depression.
The ischemic ST depression in the MCG was mostly due to
a steady injury current in the TQ segment, only detectable
in the direct current MCG but not in the ECG. The first
non-direct current stress MCG recording was performed to
a coronary artery disease patient [Saarinen et al., 1974,
1989]. The 12-lead ECG and single channel MCG from 3 different
locations were recorded after physical stress. The ratio
of the ischemic ST segment depression to R-wave amplitude
after stress was even greater in the MCG than in the ECG.
In another study MCG was recorded in rest 5 patients with
acute myocardial infarction and after physical stress testing
in 11 patients with coronary artery disease [Seese et al.,
1995]. Minimum norm method was used for the construction
of the current density during the ST-segment. The results
were compared with coronary angiography and myocardial scintigraphy.
Injury currents during transient exercise-induced ischemia
were in most cases directed from the ischemic area to the
non-ischemic area, whereas the injury currents in acute
infarction flew in the opposite direction.
In a very recent study 27 single vessel coronary artery
disease patients and 17 healthy controls were studied with
stress MCG [Hänninen et al., 2000]. Physical stress
was induced using a nonmagnetic stress ergometer. The ischemia
was found to induce a change in the magnetic field orientation
in the ST segment and at the T-wave apex, quantified by
using a novel surface gradient method (Figs 1 and 2). This
change in the magnetic field orientation after stress compared
to rest measurement separate the coronary artery disease
patients from controls. In the ST segment this rotation
of the magnetic field was most prominent in the subgroup
of patients with stenosis in left anterior descending coronary
artery. In the subgroup of patients with stenosis in the
left circumflex coronary artery the map became monopolar
after stress. At the T-wave apex, the changes in the field
orientation were most prominent in the subgroup of patients
with stenosis in the right coronary artery.
Figure 1. The group mean ST segment magnetic
field distribution and interpolated spatial field gradient
of 17 healthy controls and 27 coronary artery disease patients
(CAD) at rest and at cessation of exercise. Spatial distribution
of the magnetic field component Bz at rest (A) and at cessation
of exercise (C). The line connecting the magnetic field
maximum and minimum is marked by an arrow. The change in
the magnetic field orientation can be seen as a rotation
of the arrow. Interpolated gradient arrows at rest (B) and
at cessation of exercise (D). The peak gradient is marked
by a circled arrow, which is enlargened. The map direction
in A and C parallels the direction of the maximal field
gradient in B and D, respectively. Continuous line: positive
field distribution, dotted line: negative field distribution,
the step between two consecutive lines is 0.1 pT.
Figure 2. The group mean T-wave apex magnetic
field distribution and interpolated spatial field gradient
of 17 healthy controls and 8 patients with stenosis in right
coronary artery (RCA) at rest and 4 minutes postexercise.
Spatial distribution of the magnetic field component Bz
at rest (A) and 4 minutes postexercise (C). Interpolated
gradient arrows at rest (B) and 4 minutes postexercise (D).
Technical description is the same as for Figure 1 for the
ST-segment. The step between two consecutive lines is 0.5
pT.
5. Myocardial Infarction in MCG
In a study on healthy subjects and post-infarction patients
with abnormal ECG, the cardiac magnetic field during QT-interval
was characterized by the field strength, field width, and
field orientation defined as the location of the center
of gravity [van Leeuwen et al., 1999]. The MCG field orientation
could separate the postinfarction patients from healthy
controls at rest, and these MCG changes were more prominent
in patients with multivessel disease.
Lant et al. reported the MCG and the body surface potential
mapping to be complementary [Lant et al., 1990]. The most
profound abnormalities in the MCG maps in anterior myocardial
infarction were found in the QRS-complex, while abnormalities
in inferior infarction were found during the whole repolarization
period. On the contrary, the potential mapping showed significant
differences between anterior and inferior infarctions during
QRS-complex only. The repolarization abnormalities detected
in MCG maps could have been caused by prolonged ischemic
injury increasing tangential current flow through the spared
subendocardial tissue.
6. Chronic Ischemia and Myocardial Viability
The magnetic field orientation, width and strenght during
QT-interval could separate CAD patients with normal ECGs
at rest from healthy subjects [van Leeuwen et al., 1999].
The authors suggested that MCG at rest might contain relevant
additional information to ECG, possibly reflecting silent
ischemia.
Leder et al. investigated two infarction patients (one anterior
and one inferior) and two healthy controls with multichannel
magnetocardiography, magnetic resonance imaging (MRI), coronary
angiography and Tl-SPECT [Leder et al., 1997]. Current densities
were calculated for the endocardial surface of the left
ventricle using minimum norm least square criterion during
ventricular depolarization, and applied to predefined myocardial
geometry acquired from MR images. The main finding was markedly
decreased regional current densities in the areas corresponding
to the infarcted segments of the heart defined by the clinical
reference methods. The authors concluded, however, that
further studies are needed in order to define the spatial
resolution and the diagnostic performance of this method.
Current density estimation (CDE) was also tested in ischemia
localization in three different settings: in simulation
studies, in patients with single vessel coronary artery
disease (CAD), and in patients three-vessel coronary artery
disease and regional or global left ventricular dysfunction
[Pesola et al., 1999]. First, in simulation studies zero-
and second-order regularizations were tested by placing
distrubuted sources on a triangulated epicardial surface
on the left ventricle. The source locations were simulated
to represent the myocardial regions vascularized by the
three main coronary arteries, and the CDE was found to localize
extended sources regions. In the second part, CDEs were
calculated from the ST segment difference (recovery-rest)
signals of four single vessel disease patients. The injury
currents were found to match to myocardial regions supplied
by the coronary artery in question: to the anterior and
septal area for the left anterior descending coronary artery,
and to the posterior wall for the right coronary artery
stenosis patients. In the third part of the study CDE signals
were compared to 18F-2-deoxyglucose (FDG) positron emission
tomography (PET) images to differentiate between scarred
and viable myocardium in dyskinetic ventricular areas (Fig.
3). The areas of low CDE amplitude were found to match with
the scar regions, whereas high CDE amplitude was found to
correlate with areas of viable, ischemic cardiac tissue.
Figure 3. Left: The FDG-PET result of a three-vessel
disease CAD patient showing a scar in the lateral region.
Right: The current density estimation (CDE) of the same
patient corresponding to the PET result.
7. Advantages and Disadvantages of Magnetocardiography
Multichannel MCG enables simultaneous recording of the
signal over a large area without time consuming electrode
attachment. Therefore, in the MCG signal analysis, restriction
to one or few recording locations is not needed. Instead,
spatial features of MCG maps can be utilized to detect coronary
heart disease.
MCG still has of course also some disadvantages compared
to electrical mapping. With present available technology
the measurements still have to be performed in a shielded
room, which excludes the use of method as a quick bed-side
test. Furthermore, the MCG recording system is sensitive
to metal objects, which is exclusion criteria for some patients.
8. Conclusions
When developing magnetocardiographic methods for the detection
of myocardial ischemia, the precordial negative component
during repolarization detected in the studies on healthy
volunteers should be considered as a normal response to
physical exercise. In addition to ST segment amplitude changes
similar to those used in the standard 12-lead ECG analysis,
the novel multichannel mapping techniques enable to also
look at the spatial changes of cardiac magnetic field.
Transient acute myocardial ischemia causes significant
changes in the magnetocardiogram of the coronary artery
disease patients. Exercise-induced ischemia changes the
polarity of the magnetic isofield map in the ST segment
and at the T-wave. This change can be quantified with the
surface gradient method.
Localization of chronic myocardial ischemia and viable
but dyskinetic myocardial tissue using the current density
estimation (CDE) method is a promising, clinically important
application for magnetocardiography.
Further studies of magnetocardiography in the detection
of acute and chronic myocardial ischemia are still needed.
Furthermore, dynamic analysis of cardiac magnetic fields
during provoked ischemia may improve the ischemia detection
and localization in MCG.
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