Hippocampal Surface Analysis using Spherical Harmonic Function - Paper | MATH 0209A, Papers of Cryptography and System Security

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HIPPOCAMPAL SURFACE ANALYSIS USING SPHERICAL HARMONIC FUNCTION
APPLIED TO SURFACE CONFORMAL MAPPING
Boris Gutman
1
, Yalin Wang
1
;
2
, Lok Ming Lui
1
, Tony F. Chan
1
, Paul M. Thompson
2
1
Department of Mathematics, University of California, Los Angeles, CA USA
2
Department of Neurology, UCLA Medical School, Los Angeles, CA USA
ABSTRACT
Using spherical harmonics of an inverse conformal map, we com-
pared hippocampal surfaces of sixteen Alzheimer (AD) and fourteen
control subjects. Hippocampal surfaces were conformally mapped
to a sphere. Maps were regularly sampled and exact, high-degree
spherical harmonic transforms of the inverse maps were computed.
Using the transforms shape descriptors corresponding to the degree
of the harmonics and invariant to translation, rotation, and scale were
obtained and normalized against sample mean. Two-dimensional vi-
sualizations of the shape descriptors were indicative of global as well
as local shape features of hippocampal surfaces. These descriptors
are potentially useful for visual detection of global patterns and cre-
ation of population-based, probabilistic, disease-specific digital at-
lases, especially for comparison of global shape features.
1. INTRODUCTION
Recent studies have confirmed a long-observed correlation be-
tween changes in hippocampal shape and volume, and Alzheimer
disease. Csernansky et al. [1] have found shape analysis methods
that could potentially predict the onset of symptoms using high di-
mensional diffeomorphic transformations of a neuroanatomical tem-
plate. Goldman et al. [2] have found that some patients with con-
firmed Alzheimer sometimes show few or no symptoms through-
out much of their lives. Thus, changes in hippocampal shape char-
acteristic of Alzheimer may take place years before patients show
symptoms. Others [3] have even suggested the possibility of drug
treatments capable of preventing or significantly slowing the pro-
gression of the disease. All these studies suggest a future need for
accurate methods of analyzing local as well as global features of
hippocampal shape. In our study, we compared the shapes of 14 left
and 14 right hippocampi of control subjects with 16 left and 16 right
hippocampi of Alzheimer subjects using spherical harmonic trans-
form applied to surface conformal mapping. The procedure went as
follows: (1) Triangulation meshes were reconstructed from 3-D T1
weighted SPGR (spoiled gradient) MRI images, by using an active
surface algorithm that deforms a mesh onto the hippocampal surface
[4]. (2) The meshes were then conformally mapped to a 2-sphere ac-
cording to [5] and regularly sampled using linear interpolation, thus
creating a spherical parameterization of the mesh. (3) A fast spheri-
cal harmonic transform algorithm (FST) was then performed on the
regularly sampled meshes according to [6]. (4)Lastly, rotationally
invariant shape descriptors were calculated, normalized for easy vi-
sual analysis and plotted in
R
2
. We hope these two-dimensional
visualizations of global shape descriptors will serve as a guide for
future statistical analysis similar to that in [1] and the creation of
disease-specific brain atlases as in [7].
2. PREVIOUS WORK
Various methods have been employed in the field of brain sub-
manifold shape analysis. Gerig et al. [8] used spherical harmon-
ics to compute mean squared distance between lateral ventricles of
twins as a measure of pairwise shape difference by normalizing co-
efficients with respect to volume and applying Parseval’s equation.
Although mathematically elegant, this method involves much com-
putational error due to irregularity of sample points. This is be-
cause spherical harmonic coefficients are approximated using a least
squares solution. Another method is a high dimensional diffeomor-
phic map directly from a subject manifold onto an exemplar target
manifold following Miller [9]. With this method, manifolds are di-
vided into subregions and an overall mean transformation between
all subjects and the target manifold is found for each of (usually)
many thousands of points. Then, using the mean transformation, the
mean manifold is constructed. Thus, the perpendicular displacement
between each subject’s surface and the overall mean for each subre-
gion is calculated as a measure of shape variation. Csernanksi et al.
[1] have employed this method in their study of Alzheimer’s.
Fig. 1. Low-Pass Filtering: (a) through (d) are hippocampal sur-
faces reconstructed from harmonics up to degree 10, 20, 63 and 127,
respectively. (e) is the original hippocampus
Use of spherical harmonic shape descriptors as initial representa-
tion of shape is advantageous to methods involving neuroanatomical
templates in that the transform is independent of any population-
based averages and that it describes global shape features in addition
to locally detailed features. Figure 1 illustrates this property: lower-
order spherical harmonics correspond to the major shape features of
a hippocampus, while those of higher order correspond to noise and
local features. Further, the analogue of a template in this method is a
fixed target space, the sphere, which eliminates error due to variabil-
ity of subject-based templates. As shown in [5], the conformal map
onto the sphere is invariant to the specifics of triangulation and rota-
tion. That spherical harmonics-based shape descriptors are also rota-
tionally invariant in effect guarantees rotational invariance through-
out the entire procedure of our method. In addition, the regularity
of sampled grid points allows for a fast calculation of spherical har-
monic coefficients which are exact up to numerical error associated
pf3
pf4

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HIPPOCAMPAL SURFACE ANALYSIS USING SPHERICAL HARMONIC FUNCTION

APPLIED TO SURFACE CONFORMAL MAPPING

Boris Gutman

, Yalin Wang

, Lok Ming Lui

, Tony F. Chan

, Paul M. Thompson

Department of Mathematics, University of California, Los Angeles, CA USA 2 Department of Neurology, UCLA Medical School, Los Angeles, CA USA

[email protected]

ABSTRACT

Using spherical harmonics of an inverse conformal map, we com-

pared hippocampal surfaces of sixteen Alzheimer (AD) and fourteen

control subjects. Hippocampal surfaces were conformally mapped

to a sphere. Maps were regularly sampled and exact, high-degree

spherical harmonic transforms of the inverse maps were computed.

Using the transforms shape descriptors corresponding to the degree

of the harmonics and invariant to translation, rotation, and scale were

obtained and normalized against sample mean. Two-dimensional vi-

sualizations of the shape descriptors were indicative of global as well

as local shape features of hippocampal surfaces. These descriptors

are potentially useful for visual detection of global patterns and cre-

ation of population-based, probabilistic, disease-specific digital at-

lases, especially for comparison of global shape features.

1. INTRODUCTION

Recent studies have confirmed a long-observed correlation be-

tween changes in hippocampal shape and volume, and Alzheimer

disease. Csernansky et al. [1] have found shape analysis methods

that could potentially predict the onset of symptoms using high di-

mensional diffeomorphic transformations of a neuroanatomical tem-

plate. Goldman et al. [2] have found that some patients with con-

firmed Alzheimer sometimes show few or no symptoms through-

out much of their lives. Thus, changes in hippocampal shape char-

acteristic of Alzheimer may take place years before patients show

symptoms. Others [3] have even suggested the possibility of drug

treatments capable of preventing or significantly slowing the pro-

gression of the disease. All these studies suggest a future need for

accurate methods of analyzing local as well as global features of

hippocampal shape. In our study, we compared the shapes of 14 left

and 14 right hippocampi of control subjects with 16 left and 16 right

hippocampi of Alzheimer subjects using spherical harmonic trans-

form applied to surface conformal mapping. The procedure went as

follows: (1) Triangulation meshes were reconstructed from 3-D T

weighted SPGR (spoiled gradient) MRI images, by using an active

surface algorithm that deforms a mesh onto the hippocampal surface

[4]. (2) The meshes were then conformally mapped to a 2-sphere ac-

cording to [5] and regularly sampled using linear interpolation, thus

creating a spherical parameterization of the mesh. (3) A fast spheri-

cal harmonic transform algorithm (FST) was then performed on the

regularly sampled meshes according to [6]. (4)Lastly, rotationally

invariant shape descriptors were calculated, normalized for easy vi-

sual analysis and plotted in R

. We hope these two-dimensional

visualizations of global shape descriptors will serve as a guide for

future statistical analysis similar to that in [1] and the creation of

disease-specific brain atlases as in [7].

2. PREVIOUS WORK

Various methods have been employed in the field of brain sub-

manifold shape analysis. Gerig et al. [8] used spherical harmon-

ics to compute mean squared distance between lateral ventricles of

twins as a measure of pairwise shape difference by normalizing co-

efficients with respect to volume and applying Parseval’s equation.

Although mathematically elegant, this method involves much com-

putational error due to irregularity of sample points. This is be-

cause spherical harmonic coefficients are approximated using a least

squares solution. Another method is a high dimensional diffeomor-

phic map directly from a subject manifold onto an exemplar target

manifold following Miller [9]. With this method, manifolds are di-

vided into subregions and an overall mean transformation between

all subjects and the target manifold is found for each of (usually)

many thousands of points. Then, using the mean transformation, the

mean manifold is constructed. Thus, the perpendicular displacement

between each subject’s surface and the overall mean for each subre-

gion is calculated as a measure of shape variation. Csernanksi et al.

[1] have employed this method in their study of Alzheimer’s.

Fig. 1. Low-Pass Filtering: (a) through (d) are hippocampal sur-

faces reconstructed from harmonics up to degree 10, 20, 63 and 127,

respectively. (e) is the original hippocampus

Use of spherical harmonic shape descriptors as initial representa-

tion of shape is advantageous to methods involving neuroanatomical

templates in that the transform is independent of any population-

based averages and that it describes global shape features in addition

to locally detailed features. Figure 1 illustrates this property: lower-

order spherical harmonics correspond to the major shape features of

a hippocampus, while those of higher order correspond to noise and

local features. Further, the analogue of a template in this method is a

fixed target space, the sphere, which eliminates error due to variabil-

ity of subject-based templates. As shown in [5], the conformal map

onto the sphere is invariant to the specifics of triangulation and rota-

tion. That spherical harmonics-based shape descriptors are also rota-

tionally invariant in effect guarantees rotational invariance through-

out the entire procedure of our method. In addition, the regularity

of sampled grid points allows for a fast calculation of spherical har-

monic coefficients which are exact up to numerical error associated

with floating-point implementation.

3. CONFORMAL MAPPING ONTO THE 2-SPHERE

In this section we give the idea behind the conformal mapping

algorithm following X. Gu, Y. Wang, et al. [5]. The idea is to first

find a homeomorphism

f : M! S

(monomorphism between two

topological spaces that is continuous in both directions) and then op-

timize it by minimizing harmonic energy. Here M is the manifold

represented by a triangulation mesh of the object surface embedded

in R

, defined by , (K ; g ) where K is a simplicial complex and

g : jK j! R

is a function mapping the vertices of K to R

. For

simplicity, consider a scalar piecewise-linear continuous function

f : M! R. Let u; v 2 K be vertices, fu; v g 2 K the edge formed

by u; v. (Here, we approximate all functions on M by continuous

piecewise linear (PL) functions. Thus, the range-space of the confor-

mal map is also a triangulation mesh.) Define the inner product on

the space of PL functions by < f ; g >=

P

fu;v g2K ku;v (f (u)

f (v ))(g (u) g (v )), where ku;v is string energy. By choosing

the correct string energy constants, harmonic energy is defined by

E (f ) =< f ; f >=

P

fu;v g2K ku;v jjf (u) f (v )jj

. Vector func-

tions on M to are defined by

f = (f 1 ; f 2 ; f 3 ). Vector harmonic

energy is E (

f ) =

P

i= E (fi ). Minimizing the harmonic en-

ergy ensures that the map is harmonic i.e. that the laplacian is

equal to zero. That the map is harmonic guarantees its conformality.

Here, the initial homeomorphism used is the Gauss map defined by ! f (v ) =

n (v ); v 2 M. For details on the algorithm minimizing

harmonic energy and additional constraints placed on the function

to ensure convergence as well as an explanation in a more general

setting, see [5].

4. SPHERICAL HARMONICS

A function f : S

! C is a spherical harmonic if it is the eigen-

function of the Laplacian operator f = f where  is a scalar

multiplier. A countable set of spherical harmonics provides an or-

thonormal basis for the space of square-integrable functions on the

sphere L

(S

). If we parameterize the sphere with a latitudinal co-

ordinate c and a colatitudinal coordinate p, spherical harmonics are

expressed explicitly:

Y

m l (^ ;^ )^ =^

s

(2l + 1)(l m)!

4(l + m)!

P

m l (^ os^ )e

im

for the degree l and order m, where l and m are integers with

jmj < l. Here, P

m l (^ os^ )^ is the associated Legendre polynomial

P

m l (^ os^ )^ =^

(1)m 2 l^ l! (1 x

m 2 d

m+

dxm+^ (x

l , which is a solution

to the associated Legendre differential equation. Let f be in L

(S

. For a given order l and degree m, a spherical harmonic coefficient

is defined by fb (l ; m) =< f ; Y

m l >^ , where^ <^ f^ ;^ g^ >^ is the usual

L

inner product in spherical coordinates. The spherical harmonic

expansion is the series f ( ; ) =

P 1

l=

Pl m=l fb (l ; m)Y m l (^ ;^ ).

The set of all coefficients b f (l ; m) is called the spherical harmonic

transform of f. In practice, the transform is computed with a fast

algorithm described in [6], which relies on regular mesh sampling.

The transform is only computed up to a certain degree l < B , where

the limit B is called the bandwidth.

A consequence of Parseval’s equation is that any function in

L

(S

) is uniquely determined by its spherical harmonic coeffi-

cients, implying that linear transformations (scaling, rotation, trans-

lation) in the object space alter an object’s spectrum. Thus, further

registration is needed to make each individual coefficient completely

invariant to linear transformations. While translational invariance is

achieved easily, rotational invariance will be the subject of the con-

cluding section. For now, we have achieved a limited rotational in-

variance by simplifying the spectrum as described below.

Fig. 2. Rotational invariance: A hippocampal surface was rotated

45 degrees around each axis, mapped conformally and decomposed

into new spherical harmonics. The plot shows the relative difference

between the new and the original descriptors: [s(l ) s(l

)℄=s(l )

versus degree l. Error is within 1%.

5. SPHERICAL HARMONIC ANALYSIS AND THE

SURFACE CONFORMAL MAP

Let

f : M  R

! S

be a conformal homeomorphism defined

discretely by

f = (f 1 ; f 2 ; f 3 ), as described in section (3), where

M is a mesh representing the object. Let

f

: S

! R

be the

inverse map from the sphere onto the hippocampal surface, defined

by the isomorphic property of the homeomorphism. We regularly

sample

f

= (f

1 ;^ f^

2 ;^ f^

3 )^ using a matching area algorithm and linear interpolation, and apply the FST to each scalar component

of the inverse map. This amounts to projecting the inverse of the dis-

crete conformal map onto a finite-dimensional subspace of L

(S

The result is a set of vector spherical harmonic coefficients in C

f

![

f

(l ; m) = f b f

1 (l^ ;^ m);^

b f

2 (l^ ;^ m);^

b f

3 (l^ ;^ m)jjmj^ ^ l^ ^ B^ gg

, where B is the bandwidth. The spectrum simplification neces-

sary for rotational invariance comes from two key observations.

One is that the norm of a function in L

(S

) does not change

with rotation. The other is that for a spherical function pl 2

S panfY

l l

; Y

l+ l

; :::; Y

l l g, given an element of the rotation group g 2 S O (3) and its associated operator (g ), the transformed

function remains in the same subspace of L

(S

) : (g )(pl ) 2

S panfY

l l ;^ Y^

l+ l ;^ :::;^ Y^

l l g^. Thus,

X^ l

m=l

j pbl (l ; m)j

= jjpl jj

2 =^ jj(g^ )(pl^ )jj

2 =^

Xl

m=l

j(g )(pl )(l ; m)j

Further, the linearity of (g ) implies f ( ; ) =

P

B 1

l= pl )

(g )[f ( ; )℄ =

PB 1

l= (g )(pl ). This motivates the following

definition. Returning to our original notation, we define spherical

harmonic shape descriptors s(l ) =

P

i=

P

l m=l jj fbi

(l ; m)jj

to be the squared Euclidean norms of squared L

-norms of the vector

than 122 new hippocampal models. To make the first step in this di-

rection, we are currently transforming the models into mesh format.

8. REFERENCES

[1] J. G. Csernansky, L. Wang, J. Swank, J. P. Miller, M. Gado, D.

McKeel, M. I. Miller, and J. C. Morris, ”Preclinical detection

of Alzheimer’s disease: hippocampal shape and volume predict

dementia onset in the elderly,” Neuroimage. Vol 25 Issue 3, pp

783-792, 15 April 2005

[2] W. P. Goldman, J. L. Price, M. Storandt, E. A. Grant, D. W.

McKeel Jr., E. H. Rubin and J. C. Morris, ”Absence of cogni-

tive impairment or decline in preclinical Alzheimer’s disease,”

Neurology 56, pp. 361-367, 2001.

[3] N. Bodick, F. Forette, D. Hadler, R. J. Harvey, P. Leber, I. G.

McKeith, P. J. Riekkinen, M. N. Rossor, P. Scheltens, S. Shi-

mohama, R. Spiegel, S. Tanaka, L. J. Thal, Y. Urata, P. White-

house and G. Wilcock, ”Protocols to demonstrate slowing of

Alzheimer disease progression.” The Disease Progression Sub-

Group, Alzheimer Dis. Assoc. Disord. (Suppl 3), pp. 50-53.

November 1997

[4] P. M. Thompson and A. Toga, ”A framework for computational

anatomy,” in Comput. Visual. Sci., vol. 5, 2002, pp. 1-

[5] X. Gu, Y. Wang, T. F. Chan, P. M. Thompson, and S. Yau ”Genus

Zero Surface Conformal Mapping and Its Application to Brain

Surface Mapping” IEEE Transactions on Medical Imaging, Vol.

23, No. 8, p. 949, August 2004

[6] D. Healy, D. Rockmore, P. Kostelec, and S. Moore, ”Ffts for the

2-sphere-Improvements and variations,” J. Fourier Anal. Appli-

cat., vol. 9, no. 4, pp. 341-385, 2003.

[7] P. Thompson, M. Mega, C. Vidal, J. Rapoport, and A. Toga,

”Detecting disease-specific patterns of brain structure using cor-

tical pattern matching and a population-based probabilistic brain

atlas,” in Proc.17th Int. Conf. Information Processing in Medi-

cal Imaging (IPMI2001), Davis, CA, June 18-22, 2001, pp. 488-

[8] G. Gerig, M. Styner, D. Jones, D. Weinberger, and J. Lieberman,

”Shape analysis of brain ventricles using spharm,” presented at

the IEEE Workshop on Mathematical Methods in Biomedical

Image Analysis (MMBIA’01), Kauai, HI, December 2001.

[9] M. I. Miller, ”Computational anatomy: shape, growth, and at-

rophy comparison via diffeomorphisms” Neuroimage Vol. 23,

Supp 1, pp. S19-S33, 2004.

[10] C. Brechbuhler, G. Gerig, and O. Kubler, ”Surface

parametrization and shape description,” Proc. SPIE (Visualiza-

tion Biomed. Comp. 1992), vol. 1808, pp. 80-89, 1992.

[11] A. Cuyt, J. Sijbers, B. Verdonk, D. Van Dyck, ”Region and

Contour Identification of Physical Objects” Appl. Num. Anal.

Comp. Math. 1, No. 2, 343 - 352, 2004

[12] J. G. Csernansky, S. Joshi, L. Wang, J. W. Haller, M. Gado,

J. P. Miller, U. Grenander, and M. I. Miller ”Hippocampal mor-

phometry in schizophrenia by high dimensional brain mapping,”

Proc. Natl. Acad. Sci. USA Vol. 95, pp. 11406-11411, Septem-

ber 1998.

[13] P. M. Thompson, M.S. Mega, R.P. Woods, C.I. Zoumalan,

C.J. Lindshield, R.E. Blanton, J. Moussai, C.J. Holmes, J.L.

Cummings, A.W. Toga ”Cortical change in Alzheimer’s disease

detected with a disease-specific population-based brain atlas.”

Cereb Cortex. January 2001; 11(1):1-16.

[14] M. Kazhdan, T. Funkhouser, S. Rusinkiewicz ”Rotation Invari-

ant Spherical Harmonic Representation of 3D Shape Descrip-

tors” Proc. of Symposium on Geometry Processing pp. 167-175,

June 2003