4.2 El pensamiento de Fehn y Pietilä
4.2.1 La idea de lo irracional en Fehn y Pietilä
4.2.1.1 Pietilä y el pensamiento irracional: el lenguaje y la naturaleza
In order to connect the candidate points into complete curves, potential endpoints of (yet
unknown) sulcal curves need to be estimated. For
∀u∈U, thus, sulcal candidates points are
collected within a geodesic distance
r
defined by an indicator function:
R(u,v) =
1
ifL
u(v)≤r ,
0
otherwise,
(3.4)
where
L
uis a geodesic distance fromu
to
v∈Ω. The geodesic distance
L
ucan be computed
by the Eikonal equation (see Equation 2.14). Assignuto a source of the wavefront propagation
by letting the tensor matrix
M(v) =
I
for
∀v∈
Ω in Equation 2.14, where
I
is the 2×2
identity matrix. Thus, with a sufficient boundary condition
L
u(u) = 0, the speed function in
Figure 3.5: Maximum curvature points (top) and detected sulcal points (bottom, where sulcal
endpoints are colored in
green
and
blue). The vertices with positive curvatures are selected
for candidate sulcal points. Since the candidate vertices are spread over a large portion of the
sulcal fundic regions, they are further filtered out by the proposed method that eventually
selects sulcal points (blue). The endpoints (green) are then selected from the selected sulcal
points.
Equation 2.15 becomes
F
x,
∇L
u(x)
k∇L
u(x)k
!= 1.
(3.5)
ForM
=I, this simplifies the H-J PDE to the Eikonal PDE:
The solution provides a geodesic distance
L
ufor all locations of Ω. The geodesic distance
r
in
Equation 3.4 is chosen under the assumption that the sulcal regions are separated from each
other by at least
r. In this chapter, this quantity was empirically set
r= 4.0
mmbased on
the average width of the sulcal regions in the MNI-305 template [70]. This geodesic distance
can be adjusted depending on the target population.
The candidate points are determined as endpoints if every point holding
R(u,·) = 1 is
located within an octant centered at
u
as shown in Figure 3.6. This is easily achieved by
testing the sign of the inner products of all neighboring points holdingR(u,·) = 1, i.e., no
line between the neighboring points and the center point
u
has a separating angle above
90 degrees. Let
E
⊆
U
be the set of the endpoints determined by this way. To find the
neighboring sulcal point at
u∈E, the weighted shortest distance is employed from
u
to
s,
such that
s
holds
R(u,s) = 1. The distance weighting is based on the assumption that the
tangent direction of the sulcal curve changes smoothly along the curve. Thus, the weighted
distance is given by the following form:
C(s,u) =k(s−u)×T(u)k,
(3.7)
where
T(u) is the tangent vector at
u. Therefore, the neighboring sulcal point ˆs
at
u
is
obtained by
ˆ
s= argmin
s
C(s,u).
(3.8)
However,
T(u) is unknown due to no prior knowledge of the sulcal curve available. Instead
T(u) is estimated using the local principal direction,T
k2(u). This is an incremental procedure;
ݑݑ
ݏ
ݏ
ଵFigure 3.6: A schematic overview of the proposed endpoint detection. An example of the
octant of the sphere is determined by three orthogonal axes.
u
is determined as an endpoint
if its neighboring points in a geodesic kernel
S(u) belong to one of the octants.
us
0and
us
1form the maximum angle across every possible line starting from
u, such that
R(u,s
0) = 1
and
R(u,s
1) = 1.
R(ˆs,·) = 1 and it stops if ˆs∈E
or ˆs
is a part of the other already delineated curve (junction
point). Starting at an arbitrary endpoint, the curve estimation is finished if every element in
E
has been connected. Figure 3.7 shows the estimated curves from sulcal points. The sulcal
endpoints are located in the end of each sulcal curve.
3.6
Materials
I chose the Kirby reproducibility dataset [53] to evaluate my sulcal extraction method
for reproducibility. Briefly, the Kirby reproducibility dataset was aquired on 21 healthy
volunteers with no history of neurological disease and is publicly available on NITRC
2. Scan-
2
Figure 3.7: The estimated curves with endpoints in the lateral (left) and medial (right) views.
The sulcal curves are reconstructed from the detected sulcal points. Each curve is labeled
with a distinct color. End points are highlighted via larger dots. Sulcal regions with branches
are represented as several curves with junction points.
rescan imaging sessions withT
1-weighted scans were acquired at the F.M. Kirby Research
Center (Baltimore, MD, USA), using the MP-RAGE sequence on 3T Philips Achieva scanners
at 1.0mm
×1.0mm
×1.2mm
resolution (204 slices with TR = 6.7ms, TE = 3.1ms, flip
angle = 8
◦, matrix = 240×256) scans. The central cortical surfaces were created using the
standard Freesurfer v5.3 pipeline. For validation, the left hemispheres were resampled with
163,842 points via spherical icosahedron subdivision.
3.7
Results
All experiments were performed on a PC equipped with an Intel Core (TM) i5-3570K 3.4
GHz CPU with 12.00 GB memory, and only a single core was used. It took 1-2 minutes to
obtain a full set of complete curves on a cortical surface on average. Quantitative verification
on clinical data is extremely difficult as there is no ground truth for such sulcal curve data.
Qualitatively I compared the results to standards in the field such as BrainVisa. The following
sections mainly focus on the reliability and reproducibility of the proposed method versus
other methods.
3.7.1
Noise Sensitivity
To evaluate noise sensitivity, synthetic surfaces were generated by vertex-wise perturbation
of an existing brain surface model. Perturbations were simulated via uniformly distributed
independent displacements of the vertices. The left hemisphere of the MNI-305 average
healthy control template surface was used for this evaluation purpose, also employed in [70],
as the original brain surface model. Figure 3.8 shows the detected sulcal curves with different
levels of perturbation. Visually, there is no significant difference from the original surface.
For quantitative evaluation of the robustness to noise, for each sulcal point on the original
surface, the Euclidean distance was measured to the closest point on the perturbed surface
as no ground truth is available. Quantitatively, the experimental result showed that for each
level of noise, the average distance was 0.505±0.616, 0.776±0.629, and 0.982±0.702
mm,
respectively. This indicates that the average distances are reasonable given the original MR
image resolution (1.0
mm).
3.7.2
Reproducibility
From the KIRBY dataset, the BrainVISA pipeline
3[107] was used to generate surfaces from
the dataset with sulcal ribbon extraction, and the extracted sulcal ribbons then were projected
onto the sulcal fundi to have sulcal curves for comparison. Figure 3.9 shows an example of
Original Surface
Δ
max=2.27 mm
Δ
max=4.54 mm
Δ
max=6.81 mm
Figure 3.8: Robustness to noise. Sulcal points are detected on the surface perturbed by a
random noise. ∆
maxindicates the maximum displacement of the vertex. The detected sulcal
points (blue) and the estimated curves (red) are stable across levels of noise. The quantitative
evaluation also shows that the average distance to the corresponding points is less than 1.0
mm.
the sulcal curves extracted by using the proposed method. Again, the closest distances were
measured at sulcal points between two corresponding surfaces and then averaged along each
sulcus. Since the closest distance computation is asymmetric (one-way), it took the maximum
of the two possible distances from both corresponding surfaces. Figure 3.10 illustrates a
statistics on the maximum average distances of the corresponding surfaces. Importantly,
the sulcal extraction in the BrainVISA pipeline generates only the set of the labeled major
(a)
(b)
(c)
Figure 3.9: Sulcal curve extraction from the different scans for the same subject. (a)-(b) Two
sets of curves are labeled with respective colors (red
and
blue). (c) The two sets are well
aligned in the same space.
curves as its output (unlabeled curves provided in this pipeline). On the other hand, the
proposed method extracted both major and minor curves (major curve labeling is out of
scope in this chapter). Thus, it could be a unfair evaluation for the proposed method without
a major curve labeling procedure as one would expect higher reproducibility errors in those
smaller curves. Despite that disadvantage, the experimental results show that the proposed
method has less average distance than BrainVISA. The proposed method achieved 2.01
±
0.33
mm
(average±
standard deviation across all 21 cases), whereas BrainVISA showed an
average distance of 2.89
±
0.73
mm. To obtain statistical significance, I applied a paired
t-test between the maximum average distances obtained from BrainVISA and the proposed
method (total 21 maximum average distances for each method as shown in Figure 3.10). This
reveals that the proposed method achieves a statistically significant smaller average distance
(p
0.0001).
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 Subject # A v er age Distance (mm) 0 1 2 3 4 5
Proposed Method BrainVISA
Figure 3.10: The maximum average distances of the extracted sulcal curves on the 21 subjects
in the Kirby reproducibility dataset. The proposed method achieves consistent results over
those obtained in the BrainVISA pipeline.
3.8
Summary
This chapter presented a fast and accurate automatic sulcal curve extraction method to
provide cortical geometric landmarks based on the observation that sulcal fundic regions
are well defined as local extrema. A set of candidate sulcal points is chosen by the line
simplification method. The extracted sulcal points are further connected to form a set of sulcal
curves on the cortex. The resulting landmarks showed a high reliability in the multi-scan
dataset as well as robustness to a high level of noise.
The experimental results showed that the proposed method captures sulcal curves robustly
in the presence of noise and shows high computational efficiency. In comparison to Brain-
VISA, a standard neuroimaging tool, the proposed method showed significantly improved
reproducibility. The proposed method has several advantages: First, the parameter tuning is
quite simple as there is a small set of parameters and the results are robust to reasonable
CHAPTER 4: ROBUST ESTIMATION OF SURFACE
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