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<article xmlns:xlink="http://www.w3.org/1999/xlink">
  <front>
    <journal-meta />
    <article-meta>
      <title-group>
        <article-title>Anisotropy analysis of 2D and 3D textures using anisotropic fractional Brownian field</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <string-name>Ferdaous OUERTANI</string-name>
          <xref ref-type="aff" rid="aff0">0</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Dep. Of Maths</string-name>
          <xref ref-type="aff" rid="aff0">0</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Informatics</string-name>
          <xref ref-type="aff" rid="aff0">0</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>Paris Descartes Paris</string-name>
          <xref ref-type="aff" rid="aff0">0</xref>
        </contrib>
        <contrib contrib-type="author">
          <string-name>France ferdaous.ouertani@gmail.com</string-name>
          <xref ref-type="aff" rid="aff0">0</xref>
        </contrib>
        <aff id="aff0">
          <label>0</label>
          <institution>a) Introduction</institution>
        </aff>
      </contrib-group>
      <pub-date>
        <year>2003</year>
      </pub-date>
      <abstract>
        <p>This paper aims first at implementing two algorithms to extract Region Of Interest (ROI) from 2D (mammography) and 3D images (tomosynthesis) so that to gather ROI databases and second, at analyzing anisotropy of these images textures using an anisotropic fractional Brownian field to check whether the model being studied helps apprehend the breast anisotropy. This analysis includes the estimation and the comparison of indices (already presented in [17]). We detail two algorithms: the automatic and the manual extraction of ROI implemented to gather 2D and 3D Region Of Interest (ROI) databases. Tests performed are described and results are reported.</p>
      </abstract>
      <kwd-group>
        <kwd>-medical imaging</kwd>
        <kwd>fractional Brownian fields</kwd>
        <kwd>tomosynthesis</kwd>
        <kwd>mammography</kwd>
        <kwd>anisotropy</kwd>
        <kwd>texture</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <body>
    <sec id="sec-1">
      <title>-</title>
      <p>INTRODUCTION</p>
      <p>Medical imaging techniques have revolutionized health
care delivery around the world. Melding medical imaging
advances with the power of digital and information technology
that is offering highly personalized and targeted means of
powerful diagnosis generation is fostering greater quality and
efficiency in health care.</p>
      <p>Depending on the imaging modality, the resulting images
are whether 2D or 3D. In the present work, we will be
restricted to the analysis of mammographic images as 2D ones
and tomosynthesis images as 3D ones. To take advantage from
information provided by these images, these ones are analyzed
based on different aspects. Texture consists one of these
aspects.</p>
      <p>Considered as a periodic aspect of images, texture has been
modeled using various mathematical approaches.</p>
      <p>In the current work based on the model definition of [17],
texture analysis is performed from a probabilistic point of view
considering the image as a realization of a random field whose
properties reflect those of the texture.</p>
      <p>Model definitions have varied depending on texture
properties among which texture anisotropy is one of the most
important. It can be apprehended using some directional
processes that are either defined as a restriction of the image on
an oriented line or as a projection of the image along a given
direction [17]. Anisotropy can then be analyzed by looking at
regularity variations of these processes when the extraction
direction changes.</p>
      <p>In this work we propose two algorithms to extract ROI
from either mammography or tomosynthesis. We describe a
tool for image segmentation and region of interest (ROI)
extraction (under some specific conditions) to end-up with
gathering the 2D and 3D extracted ROI into two databases.
We also analyze anisotropy of the images textures using an
anisotropic fractional Brownian field whose definition is
presented in the next section of this paper. We perform
statistical tests on the ROI databases to check whether the
model being studied is adequate and if it helps apprehend the
anisotropy of the breast. In this context, it makes sense to note
that images segmentation, which is a key step for the ROI
extraction, is a difficult and very important part of the current
work. A wrong segmentation can invalidate all the processing
steps that come after and thus lead to a wrong analysis.</p>
      <p>This paper is organized as follows: In the first part, we
summarize materials and methods: We make an overall
presentation of the anisotropic fractional Brownian field model
used as well as a brief description of mammography and
tomosynthesis . We also describe the algorithms used and the
different steps followed so that to exploit and analyze the
images database. In the second part, we expose the different
statistical tests performed and discuss results.</p>
      <p>II.</p>
    </sec>
    <sec id="sec-2">
      <title>MATERIALS AND METHODS</title>
      <sec id="sec-2-1">
        <title>A. Anisotropic Fractional Brownian Field (AFBF) a) Introduction</title>
        <p>Textures are normally ranging from micro (statistical
textures) to macro (structural textures), and depending on the
texture type, several models (namely structural models,
probabilistic models,...) can be used to represent it [4]. In the
current work, tissues we analyze via mammograms and
tomosynthesis will restrict us to statistical textures and the
approach is to consider it as a realization of a random field.</p>
      </sec>
      <sec id="sec-2-2">
        <title>b) Model presentation</title>
        <p>It has been put forward that anisotropy can be captured from
processes extracted from the image [3] [17], either
lineprocess defined by restricting the image on oriented lines of
the image domain, or projection-process obtained by
projecting the image parallel to a given direction. From these
processes, anisotropy can be analyzed by looking at their
regularity variations when the extraction direction changes.
In the sequel, we present the AFBF model used in this work
referring to the model presented by Frederic Richard and
Hermine Bierme in [16] and [17].</p>
        <p>
          Description:
The anisotropic fractional Brownian field is mathematically
defined as the unique centered Gaussian field, null at origin,
with stationary increments and self similar of order H ϵ (0, 1).
Parameter H, called the Hurst index, is a fundamental
parameter which is an indicator of texture roughness. [3], [16],
[
          <xref ref-type="bibr" rid="ref12 ref9">10</xref>
          ] and [17].
        </p>
        <p>Its variogram, which is of the form (1.1) is characterized by a
positive function f called spectral density. This function is
of the form (1.2).
where arg ( ) is the direction of the frequency  and h is a
measurable periodic function ranging in [H;M](0;1) with:
H =essinf h() and M=esssup h().</p>
        <p>Since its spectral density f depends on the spectral direction
arg( ), this model is anisotropic.</p>
        <p>Its anisotropy is characterized by parameters whose estimation
characterizes the anisotropy of the field.</p>
        <p>In [3], Bonami and Estrade proposed to use windowed Radon
transforms of a field to get information about its anisotropy.
These transforms are defined for any direction  of R3 by
projecting a field X along lines of R3 directed by  With:
 .</p>
        <p>Given a window function  of the Schwartz class such that
 = 1, the projection of X along lines oriented in the
direction  through the window  is defined as follows:
As mentioned, the Hurst index h(q) of an anisotropic
fractional Brownian field in a given direction can be
deduced from the Hurst index of the projected field
perpendicular to this direction. Consequently the problem of
estimating the directional Hurst index of an AFBF
reduces to the problem of estimating the Hurst indices of
projected fields [16]. Let f be a projection angle and let
 = ( x,  y,  z) then, if we refer to fig.1
In [17], some estimators of the parameters h(x), h(y ) and
h(z ) are proposed based on projections and quadratic
variations.</p>
        <p>
          These estimators differ in two categories defined as follows:
 Estimators obtained by projecting the field X along
lines oriented in the direction  through the
window  (previously described) which are:
hˆ1: estimator of h(x)
hˆ2: estimator of h(y )
 Estimators obtained by restriction of the field X on a
line, which are: hˆ 01 and hˆ 02, estimators of
min h() (The reader is referred to [
          <xref ref-type="bibr" rid="ref14">14</xref>
          ] and [17] for
detailed explanation).
        </p>
        <p>It was proved in [3] that the Hölder regularity of the projected
field Px, is equal to h()+1/2(d-1) for all directions  of Rd.
In the case of d = 3, Px, regularity is equal to h()+1.
whose regularity is h(x)+1.
whose regularity is h(y )+1.</p>
      </sec>
      <sec id="sec-2-3">
        <title>B. Imaging Modalities a)</title>
      </sec>
      <sec id="sec-2-4">
        <title>Mammography</title>
        <p>Mammography is a type of imaging that, by the use of a dose
of x-ray system, helps examine breasts and detect changes in
tissues before they are noticeable or visible.</p>
        <p>This technique provides two-dimensional information that
allows the radiologist to make a diagnosis.</p>
      </sec>
      <sec id="sec-2-5">
        <title>b) Tomosynthesis</title>
        <p>A technique, which, from a set of projection images acquired
as the X-ray tube moves along a prescribed path, enables the
reconstruction of multiple section images. In fact, by
combining projections, it is possible to reconstruct the
threedimensional projected volume and thus to obtain 3D
information on the organ examined. [7] fig.2 illustrates one
among Tomosynthesis acquisition techniques.
The current work is done in collaboration with the department
of Radiology, University of Pennsylvania, that have provided
the database of breast tomosynthesis and mammography on
which we have performed our tests.</p>
        <p>This database includes information about 40 patients: For each
patient, nine projections for the breast tomosynthesis and
three mammographies are provided.</p>
        <p>For the tomosynthesis cases, each projection was done under
6.25 degrees to each other. The distance from the detector to
the pivot point (i.e., the center of tube rotation) was 20 cm.
The distance from the pivot point to the x-ray tube (i.e., focal
spot) was 46 cm. (Thus the distance from the detector to the
focal spot for the orthogonal projection was 66cm.)
This information is usefull to implement the second algorithm
described in the next section.</p>
      </sec>
      <sec id="sec-2-6">
        <title>D. Methods</title>
        <p>Two Region of Interest (ROI) extraction methods were
developed:</p>
      </sec>
      <sec id="sec-2-7">
        <title>a) An automatic method: where the extraction of the ROI is automatically computed according to specific conditions.</title>
        <p>To automatically extract the region of interest, it comes to
distinguish the three big parts that form a given image in the
database previously described. These three parts are visible
to the unaided eye, namely, the collimator, the breast and the
backgroud.</p>
        <p> Background segmentation</p>
        <p>It makes sense here to note that the threshold value is
computed based on Otsu’s method.
 Collimator segmentation</p>
        <p>A collimator is a device that allows only the rays
going parallel to a particular direction to pass, and
this is by filtering these rays. For this reason,
depending on the source angle, some of the resulting
images lose some or most of their information.</p>
        <p>After being exposed to the x-rays, in the resulting
image, the collimator area appears to be less opaque
than the whole image.</p>
        <p>A possible solution to segment the collimator is to
use the standard deviation.</p>
        <p>In fact, for each line in the image, its standard
deviation is calculated (as shown in fig.3 (a) and
(2.1)) with line= image(i,:)
s(i) = std(line),</p>
        <p>(2.1)
The derivative is applied, computing thus the rate at
which the standard deviation changes with respect to
the change in the image lines (2.2 ).</p>
        <p>S’= diff (s), (2.2)
This standard deviation derivative with respect to the
image lines allows locating and thus segmenting the
collimator (as illustrated in fig.2.2 (b). Its location
corresponds to the position of the pick,
Once the collimator location is known and having the
binary labeled image, objects and boundaries are
localizable. We can separate the three parts of the
image by assigning a label to every pixel as shown in
the fig.4
the breast. That is why, for one patient, it is not
always necessary to find that all the projections are
exploitable (fig.7).
At this level, our purpose is to locate the optimal
position from which a region of interest will be
extracted. To do this, we have to understand the
breast structure and which area of the breast is more
likely to be most interesting for our analysis.</p>
        <p>Breast structure :
The breast is an organ composed mainly of fatty
tissue which also has milk glands contained within it.
A series of ducts connect the milk glands to the
nipple [20].</p>
        <p>The breast is rich in blood vessels and lymphatic
channels. (fig.5)
Breast cancer develops from breast tissue, almost
from the internal lining of milk ducts or the lobule
that supply the ducts with milk.
Ductal carcinomas is the appellation of cancers
originating from ducts whereas lobular carcinomasis
the appellation of those originating from lobules.</p>
      </sec>
    </sec>
    <sec id="sec-3">
      <title>Region of interest axis:</title>
      <p>Based on the breast structure, the region of interest
extracted should be as close as possible to the nipple.
In practice, we browse the image and, in the region
labeled as the breast part (label (1) in fig.4-(b)), we
select the furthest point that constitutes the nipple as
shown in fig.5.</p>
      <p>Given its size, the ROI must fulfill conditions
including the fact that it must not exceed the limits of</p>
      <sec id="sec-3-1">
        <title>b) A manual method: where the ROI is defined manually by the user.</title>
        <p>In this part, we will refer to the tomosynthesis reconstruction
strategy defined in [7] based on the fact that tomosynthesis
means, commonly, generating a set of slice images from the
summation of a set of shifted projection images acquired at
different orientations of the tube.</p>
        <p>Assuming that the x-ray tube and the detector each move in a
linear path along the x-direction, the function for
linearmotion tomosynthesis may be derived by considering the
imaging geometry depicted in fig.8.
The idea here is to manually choose and extract a ROI from
the fifth projection (which is the projection of reference)
among the nine others and automatically compute the
coordinates of this extracted ROI in the other projections. In
this figure, for the first projection image, the x-ray tube is at
location x = x0 and the detector is centred at location x = a0.
The fulcrum plane about which the tube and detector move in
synchrony is at height p. The x-ray tube is at height z = b0
above the plane of the detector.
Let zr be the half height of the breast, Si(ai , 0 , bi): the x-ray
tube source and R(xr , yr , zr) the reference point.</p>
        <p>Given these coordinates (x0, y0,z), our purpose is to find out
T(xi, yi , z).</p>
        <p>In this geometry, it may be demonstrated that:
If SR is a line through the points S and R, then:
SR =  M(x, y, z); SM = SR
(2.3)</p>
      </sec>
    </sec>
    <sec id="sec-4">
      <title>According to (2.3):</title>
      <p>(x - ai) = (xr - ai)
(y - 0) = yr
(z - bi) = (zr - bi)
T(xi, yi , z) = SR ᴖ z = 0 This leads to
 =(bi) / (bi zr)
xi = (xr ai)+ai
yi = yr
with ai and bi are the x-ray tube coordinates.</p>
      <p>Referring to the fig.8, the location of the x-ray tube may be
shown to be:</p>
      <p>bi = cos(i) (b0 - p) + p (2.10)
Having cos(i) = (bi – p) / (b0 – p)
and ai = ( (b0 - p)2 - (bi - p)2)
(2.11)
III.</p>
      <p>TESTS AND RESULTS</p>
      <p>Our tests aim at computing and comparing on each
projection the four indices mentioned in the first part, which
are: H01: on horizontal line;</p>
    </sec>
    <sec id="sec-5">
      <title>H02: on vertical line;</title>
    </sec>
    <sec id="sec-6">
      <title>H1: on horizontal projection;</title>
    </sec>
    <sec id="sec-7">
      <title>H2: on vertical projection; Our tests treat NaN values as missing data, and ignore them.</title>
      <p>Tests are realized on ROI extracted according to the first
algorithm presented in the last part of the paper, which is based
on the automatic extraction.</p>
      <p>The parameter , one of the important parameters present in
our tests, presents the subsampling factor; In fact, when
discretizing each projection, there is an estimation bias. To
compensate this bias, each projection is subsampled with a
subsampling factor of 2The bigger this parameter is, the smaller
the biais is and the bigger the variance is.</p>
      <p>In the sequel, we expose results obtained from varying this
parameter n twice.</p>
      <p>a)
</p>
      <p>ROI size= 512,  = 3</p>
    </sec>
    <sec id="sec-8">
      <title>H01, H02 equality test</title>
      <p>The global regularity is being mesured at first. For
this, we use the ANOVA test so that to check the
correlation between H01 and H02, and we fix a
hypothesis test to the following:
Assuming that N is the global number of projections,
the linear model is of the form:
H01,i = 1+i with i = 1,…, N
H02,i = 2+i
The null-hypothesis being tested is H0: 1= 2
against the alternative one H1: 1 ≠ 2
The estimates of the minimal Hurst index we
obtained using line-based estimators on the extracted
regions of interest are with an average of ≈ 0.11 and
a standard deviation of 0.12.</p>
      <p>In fig.9, it’s shown that the line-based estimates of
the minimal Hurst in both directions are almost equal
on each image and have equivalent empirical
distributions.
This observation is reinforced by the ANOVA test,
illustrated in fig.10, in which the p-value is equal to
0.5767.</p>
      <p>Assuming that the significant risk level is about 0.05,
this value (p-value) suggests that data are not
inconsistent (at this level of risk) with the null
hypothesis which is the means equality. Thereby, we
conclude that:
H01= H02= H0 ≈ 0.11 ± 0.12.
The second test measures the regularity in the
horizontal direction.</p>
      <p>The estimate of the horizontal Hurst index we
obtained using projection based estimator on the
extracted regions of interest is with an average of
H1 ≈ 0.15 and a standard deviation of 0.19.
Let H j1,i be H1 estimated on the jth projection of the
ith acquisition, j0 = 5 the projection reference and
 j 1,i = H j1,i - H j01,i
 j 1,i = +i
By perfoming the t-test on our data, we aim at
demonstrating one of these assumptions:
The null-hypothesis H0:  = 0 against the alternative
one H1:  ≠ 0.</p>
      <p>Results are reported in tables 1, 2 and 3.</p>
    </sec>
    <sec id="sec-9">
      <title>H2 equality test</title>
      <p>We focus now at measuring the regularity in the
vertical direction. The estimate of the vertical Hurst
index we obtained using projection-based estimator
on the extracted regions of interest is with an average
of H2 ≈ 0.12 and a standard deviation of 0.18.
As for the horizontal estimation, let H j2,i be H2
estimated on the jth projection of the ith acquisition,
j0 = 5 the projection reference and:
 j 2,i = H j2,i - H j02,i
 j 2,i = +i
As we proceeded in the H1 test, we perform a t-test
on our data under the null-hypothesis H0:  = 0
against the alternative one H1:  ≠ 0.</p>
      <p>Results showed that, at the 5% significance level, the
t-test indicates a failure to reject the null hypothesis.
In other words, anisotropy, at the level of 5%, could
not be detected.
</p>
    </sec>
    <sec id="sec-10">
      <title>H1, H2 equality test</title>
      <p>b)</p>
      <p>ROI size= 512, n= 4
In this part, our interest is to measure the regularity
by testing the difference between indices in the
horizontal and vertical direction.</p>
      <p>For this, we apply a t-test on our data under the
nullhypothesis
H0: j = 0 against the alternative one H1:  j ≠ 0.
with  j is defined as follows:
Let H j1,i and H j2,i be respectively H1 and H2
estimated on the jth projection of the ith acquisition,

 j,i = H j1,i - H j2,i
 ji =  j+ji
Results indicate that, at the 5% significance level, the
t-test failed to reject the null hypothesis and
therefore, to detect anisotropy.</p>
      <p>These results could be explained by the choice of
some of our parameters( for example).</p>
      <p>In fact, the smaller this parameter is, the more biased
the estimator is.</p>
      <p>In what follows, the  parameter value is increased
so that to decrease the biais.</p>
      <p>The same procedure is repeated to study the
regularity, by increasing our sub sampling
parameter . Results are described as follows: The
estimates of the minimal Hurst index we obtained
using line-based estimators on the extracted regions
of interest are with an average of ≈ 0. 25 and a
standard deviation of 0.03.</p>
      <p>The estimate of the horizontal Hurst index obtained
using projection-based estimator on the extracted
regions of interest is with an average of H1 ≈ 0.39
and a standard deviation of 0.16.</p>
      <p>When it comes to regularity in the vertical direction,
the estimate of the vertical Hurst index obtained
using projection-based estimator on the extracted
regions of interest is with an average of H2 ≈ 0.39
and a standard deviation of 0.15.</p>
      <p>The difference between H1 and H0 as well as the
difference between H2 and H0 casts doubt on
isotropy.</p>
      <p>The same t-test previously performed is applied to
our data with the new parameter and results
showed that, at the 5% significance level, there is an
isotropy in H1.</p>
      <p>As previously mentioned, this result seems logical
since we are dealing with the same angle in the
horizontal axis.</p>
      <p>When it comes to the vertical direction, at the 5%
significance level, anisotropy is detected on some
projections according to table4.
In this section, our objective is to study the x-ray dose effect
through the comparison between mammograms and
tomosynthesis projection for each index (we will
take the fifth projection as the reference one).</p>
      <p>Mammograms used in this test are those whose view is
MedioLateral Oblique: MLO.</p>
      <p>In the sequel, tests will be performed as follows: for both
mammograms and the fifth projection of each patient, the four
indices will be computed, and then we will compare each
index computed on the two types of image, in other words, to
compare H 01,i computed on both mammograms and the fifth
projection, we use the following test:
H0,5 1,i be H01 estimated on the 5th projection of the ith
acquisition, and H0,M1,i be H0 1 estimated on the
mammogram of the ith acquisition, and
 0 1,i = H0,5 1,i - H0,M1,i
 0 1,i = +i
By perfoming the t-test on our data, we aim at demonstrating
one of these two assumptions:
The null-hypothesis H0:  = 0 against the alternative one H1:
 ≠ 0.</p>
      <p>Results cast doubt on the null-hypothesis and allow us to
conclude that, at 5% significance level, there is no equality
between the fifth projection and the mammogram on H 01,i on
the on horizontal line.</p>
      <p>This result is illustrated in fig.12 where the x axis represents
the estimates of H01 on the 5th projections and the y axis is the
estimates of H01 on the mammograms.
In this paper , we present two algorithms for the extraction of
region of interest. We also describe statistical tests on the ROI
databases gathered to see whether the model of Fractional
Brownian Field helps apprehend the anisotropy of the breast.
We end up with the following results:
When it comes to 3D images, tests done on tomosynthesis
reveal that, at a significance level of 5%, and with a
subsampling factor  of 3, our estimator is more likely to be
biased and therefore unable to detect anisotrpy.</p>
      <p>When we increase this subsampling factor to 4, we note that
the estimator improves and therefore is able to detect
anisotropy.</p>
      <p>When comparing indices computed on both mammograms and
the reference tomosynthesis projection which differ on the
amount of the x-ray the patient receives, we note that indices
computed on mammograms are not equals to those computed
on thomosynthesis projections, this suggests that the reduction
of xray dose has an effect on the estimation of H and therefore
on the analysis of anisotropy.
2002.</p>
      <p>.</p>
      <p>Aline Bonami and Anne Estrade. Anisotropic analysis of some gaussian
tumeurs cerebrales. Technical report, Laboratoire de Modelisation et
Calcul de l’IMAG.</p>
      <p>FDA: Food and Drug Administration.
digital
Vision,
[17] Frederic Richard and Hermine Bierme. Analysis of texture anisotropy
based on some gaussian fields with spectral density. analysis of texture
anisotropy through extended fractional brownian fields. February 2011.
[18] Andrew Smith.
[20] virtual medical centre.</p>
    </sec>
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