Quantification of Spinal Cord Atrophy From Magnetic
Resonance Images Via a B-Spline Active Surface Model
O. Coulon,
1,4
* S.J. Hickman,
2
G.J. Parker,
3
G.J. Barker,
2
D.H. Miller,
2
and S.R. Arridge
1
A method is presented that aims at segmenting and measuring
the surface of the spinal cord from MR images in order to detect
and quantify atrophy. A semiautomatic segmentation with very
little intervention from an operator is proposed. It is based on
the optimization of a B-spline active surface. The method al-
lows for the computation of orthogonal cross-sections at any
level along the cord, from which measurements are derived,
such as cross-sectional area or curvature. An evaluation of the
accuracy and reproducibility of the method is presented. Magn
Reson Med 47:1176 –1185, 2002. © 2002 Wiley-Liss, Inc.
Key words: active surface; atrophy; spinal cord; multiple scle-
rosis
Quantitative assessment of disease progression in multiple
sclerosis (MS) using MRI is an important issue for thera-
peutic monitoring and understanding the development of
disability. In particular, the relationship between spinal
cord atrophy and development of disability has been the
subject of recent interest (5,7,13,16,17) and a correlation
between atrophy and disability has been demonstrated.
Although imaging techniques have improved signifi-
cantly and provide convenient images to study the spinal
cord, reliable and reproducible postprocessing and image
analysis techniques to measure spinal cord atrophy are
still limited. Atrophy is mostly assessed by measuring
cross-sectional area at specific levels, typically C2 and C5
(5,17), along the cervical cord. This creates several prob-
lems, including the choice of the level at which the mea-
surements are performed, the cord orientation, and the
cord segmentation process. To provide nonbiased area
measurements, the image, or part of the image, needs to be
reformatted (17), or acquired (5), with slices perpendicular
to the cord. The concept of “perpendicular to the cord” is
somewhat imprecise and operator-dependent for a struc-
ture which is not a strict cylinder or a surface of revolu-
tion. It has not been formally defined in the above-men-
tioned publications. Moreover, spinal cord cross-sectional
area has often been measured either manually or using
intensity-based 2D processing techniques. The limitations
of such methods are various: because the orientation of the
cord changes along its axis, measurements are restricted to
a predefined level at which cord and slices are orthogonal;
intensity-based segmentation is hindered by the signifi-
cant intensity variations caused by surface coils typically
used during acquisition; 2D measurements are more prone
to being biased by partial volume effect than 3D measure-
ments; manual analysis are more time-consuming and
more sensitive to intra- and interoperator variability.
We present here a method that aims to solve those prob-
lems. The method is based on a 3D extraction of the cer-
vical cord surface and the computation of a medial axis,
used to define orthogonal cross-sections anywhere along
the cord. The segmentation method is semiautomated with
very few interventions by the operator, based on the opti-
mization of a parameterized active surface. Cross-sectional
area measurements can be provided globally as well as
locally at any point along the cord. We show that the
method provides accurate and reproducible measure-
ments.
MATERIALS AND METHODS
MR Images were acquired on a Signa 1.5T system (GE
Medical Systems, Milwaukee, WI), with a phased array
spinal coil for data reception. Volume-acquired inversion-
prepared fast spoiled gradient echo (IR-FSPGR) acquisi-
tion was performed (60 1 mm slices, TI 450 ms, TE
4.2 ms, TR 17.8 ms, flip angle 20°, matrix 256 256, field
of view 25 25 cm, 7-min acquisition time). A group of
nine control subjects were scanned with scan-rescan (two
sessions on the same day).
Segmentation
In IR-FSPGR images, the cervical cord appears as a bright
structure against a dark background (the cerebrospinal
fluid space), with cylindrical topology (Fig. 3a). Segmen-
tation difficulties can arise due to artifacts (e.g., move-
ment-induced, see Ref. 11), noise, and proximity of other
structures such as vertebrae (particularly at the C5/C6
level). Because of its cylindrical topology and the ultimate
goal of making measurements, we chose to represent the
cord surface with a B-spline parametric surface. B-spline
functions have been used successfully to represent general
(15) or anatomical shapes (1,2,14) and have several advan-
tages. They provide a compact representation, because the
whole surface is defined by a mesh of control points (Fig.
1a), and the resulting surface is smooth and differentiable
(in our case the surface is defined with bicubic splines and
therefore C
2
). Curvatures and other differential character-
istics can be computed analytically from the representa-
tion. An interesting property of B-spline surfaces is local-
1
Department of Computer Science, University College London, London, UK.
2
NMR Research Unit, Institute of Neurology, University College London,
London, UK.
3
Imaging Science and Biomedical Engineering, University of Manchester,
Manchester, UK.
4
Laboratoire des Sciences de l’Information et des Syste ` mes, Centre National
de la Recherche Scientifique, Marseille, France.
Grant sponsors: Wellcome Trust (to O.C. and S.J.H.); AstraZeneca Pharma-
ceuticals PLC (to G.J.P.); Multiple Sclerosis Society of Great Britain and
Northern Ireland (to G.J.P.).
*Correspondence to: Olivier Coulon, Laboratoire des Sciences de
l’Information et des Syste ` mes, e ´ quipe LXAO, Ecole Supe ´ rieure d’Inge ´ nieurs
de Luminy, Campus de Luminy, case 925, 13288 Marseille cedex 9, France.
E-mail: Olivier.Coulon@esil.univ-mrs.fr
Received 12 July 2001; revised 13 January 2002; accepted 13 January 2002.
DOI 10.1002/mrm.10162
Published online in Wiley InterScience (www.interscience.wiley.com).
Magnetic Resonance in Medicine 47:1176 –1185 (2002)
© 2002 Wiley-Liss, Inc. 1176