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Conductive heterogeneity (gregion)

Author: Patrick Boyle pmjboyle@gmail.com

Problem Setup

This example will run one simulations using a 2D sheet model (1 cm x 1 cm) that has been divided into four regions (striped horizontally from top to bottom, each occupying 1/4 of the total mesh). Test parameters can be modified to explore the consequences of setting conductivity different values, adjusting anisotropy ratio (i.e., longitudinal:transverse), adjusting whether the different regions are electrically coupled to each other or isolated, and choose the electrical stimulus type.

Usage

The following optional arguments are available (default values are indicated):

./run.py
  --reg0_giL          = 2.00000  # conductivity along fibre direction (i.e., :math:`\sigma_{iL}`) in region 0
  (bottom slice)

           --reg1_giL          =
  0.50000  # as above, but for second region

           --reg2_giL          =
  0.12500  # as above, but for third region

           --reg3_giL          =
  0.03125  # as above, but for fourth region

           --anisotropy_factor
  = 4        # factor by which transverse conductivities are smaller than longitudinal
  (i.e., :math:`\sigma_{iL}`::math:`\sigma_{iT}` = [factor]:1)

           --split             =
  0        # flag that can be asserted to electrically isolate regions instead of
  having them coupled to each other

           --non_planar_stim   =
  0        # flag that can be asserted to use one point stimuli in each region instead
  of a planar stimulus

If the program is run with the --visualize option, meshalyzer will automatically load a map showing the activation sequence in response to electrical stimulation.

./run.py
  --visualize

Interpreting Results

By default, the activation sequence in response to simulation will be as below:

There are several noteworthy observations:

• As expected, the conduction velocity in the bottom region (which has the highest conductivity value assigned) is faster than in the regions above.
• Since the stimulus is applied to the left-hand side of the sheet, the resulting wavefronts in each region are all approximately planar. As such, the effect of tissue anisotropy is relatively minimal in this example.
• The conduction velocity (CV) values in the different regions can be (very roughly) approximated by taking the activation times along the righthand side of the sheet and dividing the width of the mesh (1 cm) by those values:

To get a better idea of the exact relationship between conductivity values and CV, re-run the example with the --split option:

Now that the individual regions are electrically isolated from each other, we can observe the "native" relationship between conductivity and CV. Here, we see that the approximate CV values in the four regions are, from top to bottom:

• 0: 102.7 cm/s (\(\sigma_{iL}\) = 2.00000 mS/mm)
• 1: 77.7 cm/s (\(\sigma_{iL}\) = 0.50000 mS/mm)
• 2: 47.5 cm/s (\(\sigma_{iL}\) = 0.12500 mS/mm)
• 3: 25.6 cm/s (\(\sigma_{iL}\) = 0.03125 mS/mm)

Since the conductivity values in adjacent regions are separated by a factor of 4, this serves as a reminder that the approximation \(\Delta\,CV\propto\sqrt{\Delta\,\sigma}\), derived from the linear core conductor model of bioelectric propagation, does not generally hold up very well in the context of mondomain simulations of cardiac tissue.

Finally, to get a ckear idea of how the anisotropy ratio affects the properties of impulse propagation, re-run the example with the --non_planar_stim option:

Note that wavefronts now emanate from four point sources along the left-hand side of the sheet and the activation isolines are clearly ellipsoidal, with propagation in the Y-axis direction slower than that in the X-axis direction. This behaviour arises from the fact that the fibre orientations in this sheet are uniformly from left to right (i.e., all entries in the .lon file are <1 0 0>.

This example highlights the effect of reduced transverse conductivity (\(\sigma_{iT}\)), in this case by a factor of 4. The --anisotropy_factor argument can be adjusted to explore the effect of different magnitudes of adjustment.

One final interesting observation from the last simulation discussed above, note that although the CV in the bottom-most stripe is the fastest of the four regions (as expected), the wavefront actually arrives at the right side of the sheet later than for the stripe above. This is because the source-sink dynamics at the stimulation site vary between regions. In this case, we observe that the dramatically increased coupling in the bottom-most stripe mean that excitation dissipates more quickly from the stimulus site (i.e., the tissue is more "sink-ey", meaning that we are closer to the critical threshold below which the stimulus will not elicit a propagating response.

What''s Going On Under The Hood?

The relevant part of the .par file for this example is shown below:

#############################################################

  num_gregions             =
  4

  #############################################################

  gregion[0].g_il          =
  2.0

  gregion[0].g_it          =
  2.0

  gregion[0].g_in          =
  2.0

  gregion[0].num_IDs       =
  1

  gregion[0].ID[0]         =
  0

  

  gregion[1].g_il          =
  0.5

  gregion[1].g_it          =
  0.5

  gregion[1].g_in          =
  0.5

  gregion[1].num_IDs       =
  1

  gregion[1].ID[0]         =
  1

  

  gregion[2].g_il          =
  0.125

  gregion[2].g_it          =
  0.125

  gregion[2].g_in          =
  0.125

  gregion[2].num_IDs       =
  1

  gregion[2].ID[0]         =
  2

  

  gregion[3].g_il          =
  0.03125

  gregion[3].g_it          =
  0.03125

  gregion[3].g_in          =
  0.03125

  gregion[3].num_IDs       =
  1

  gregion[3].ID[0]         =
  3

Each gregion[] structure contains information about a different stripe in the mesh. The number of gregion[] entries is controlled by the num_gregions variable. For the purposes of this exercise, the main variables changed by the command-line arguments are the .g_il and .g_it entries, which control the conductivity values (\(\sigma_{iL}\) and \(\sigma_{iT}\), respectively) in the relevant tagged regions. Although the fibres in this example are uniformly oriented from left to right, this is frequently not the case in organ-scale simulations, due to the laminar structure of cardiac tissue. In general, for each element in a region, the "longitudinal" direction is defined by the corresponding vector entry in the .lon file. Also note, the .g_in entries are not used except when simulations are conducted using meshes that have two vectors defined for each element instead of just one (i.e., longitudinal instead of transverse) -- otherwise, the assumption is that \(\sigma_{iL} = \sigma_{iT}\). Example .lon file headers are shown below:

The relevant part of the .par file for this example is shown below:

#
  .lon file with one set of vectors

  1

  0.6
  0.4 0

  0.4
  0.6 0

  # ...
  (one line per element in .elem file)

  

  # .lon
  file with one set of vectors

  2

  1
  0 0 0 1 0

  1
  0 0 0 1 0

  # ...
  (one entry per element in .elem file)

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05A_Regions_vs_Gradients 05C_Cellular_Dynamics_Heterogeneity