AJR:189, October 2007 923
AJR 2007; 189:923–927
0361–803X/07/1894–923
© American Roentgen Ray Society
Kabakci et al.
Tractography of Median
Nerve
Musculoskeletal Imaging • Original Research
Diffusion Tensor Imaging and
Tractography of Median Nerve:
Normative Diffusion Values
Neslihan Kabakci
1
Bengi Gürses
1
Zeynep Firat
1
Ali Bayram
1
Aziz Müfit Uluğ
2,3
Arzu Kovanlıkaya
1
İlhami Kovanlıkaya
1
Kabakci N, Gürses B, Firat Z, et al.
Keywords: diffusion tensor imaging, median nerve, MRI
DOI:10.2214/AJR.07.2423
Received January 29, 2007; accepted after revision
May 13, 2007.
Preliminary data presented at the 2006 Annual Scientific
Meeting of the European Society for Magnetic Resonance
in Medicine and Biology, Warsaw, Poland.
1
Department of Radiology, Yeditepe University Hospital,
Devlet Yolu Ankara Cad. 102-104, 34752 Kozyataği,
Istanbul, Turkey. Address correspondence to N. Kabakci
(nkabakci@yeditepe.edu.tr).
2
Department of Biomedical Engineering, Yeditepe
University School of Engineering, Istanbul, Turkey.
3
Department of Radiology, Weill Medical College of Cornell
University, New York, NY.
OBJECTIVE. The purposes of this study were to visualize the human median nerve on dif-
fusion tensor imaging and to determine the normal fractional anisotropy (FA) value and appar-
ent diffusion coefficient (ADC) of the normal median nerve.
SUBJECTS AND METHODS. The wrists of 20 healthy volunteers and of two patients
with carpel tunnel syndrome were examined with a 3-T MRI system with a standard eight-chan-
nel sensitivity-encoding head coil. Diffusion tensor imaging was performed with a spin-echo
echo-planar sequence. A T1-weighted sequence was performed for anatomic reference. After
tractography, the FA value and ADC of the whole nerve were calculated automatically. Manual
focal measurements also were obtained at the levels of the flexor retinaculum, wrist, and forearm.
RESULTS. We visualized the median nerve with MR diffusion tensor tractography and fol-
lowed the nerve for approximately 77.5 mm. We found the normative diffusion values of the me-
dian nerve were an FA of 0.709 ± 0.046 (SD) and an ADC of 1.016 ± 0.129 × 10
−3
mm
2
/s. There
was a statistically significant difference between the FA values obtained at the level of the flexor
retinaculum and the values obtained from the other parts of the median nerve (p < 0.0001). We
found a decrease in FA value (p < 0.01) and an increase in ADC (p < 0.05) with advancing age.
CONCLUSION. The normative diffusion values of the human median nerve can be used
as a reference in evaluation, diagnosis, and follow-up of entrapment, trauma, and regeneration
of the median nerve.
he median nerve is one of three
main nerves of the forearm. It
arises from the lateral and medial
cords of the brachial plexus
(C6–T1). At the wrist level, it passes under the
flexor retinaculum deep in relation to the flexor
digitorum superficialis tendons through the car-
pal tunnel and divides into digital and muscular
branches distal in relation to the flexor retinac-
ulum. Several entrapment and compression
syndromes affect these nerves of the forearm.
Carpal tunnel syndrome (CTS) is the most
common peripheral neuropathy of the upper
extremity resulting from dysfunction of the me-
dian nerve. CTS is characterized by numbness
in the first three digits and the radial aspect of
the fourth digit and by thenar atrophy. There are
several diagnostic methods for CTS, such as the
Phalen maneuver, Flick test, and electromy-
ography [1, 2]. Although the sensitivity and
specificity of MRI in the diagnosis of CTS are
low (sensitivity, 23–96%; specificity, 39–87%),
a few signs, such as nerve enlargement, nerve
flattening, and increased nerve signal intensity,
do occur [1].
With application of the appropriate magnetic
field gradients, MRI can be sensitized to the ther-
mally driven random motion (diffusion) of water
molecules in the direction of the field gradient.
This technique is called diffusion-weighted im-
aging (DWI) [3]. Many materials have intrinsic
structural properties that hinder diffusion so that
diffusivity is greater in some directions than in
others. This property is known as anisotropy. If
there is no directional variation in diffusion rate,
diffusion is said to be isotropic. Biologic tissues
often are anisotropic because structures such as
cell membranes and large protein molecules re-
strict the motion of water molecules. This prop-
erty is called restricted diffusion. DWI usually
shows diffusion information in one direction. In
an anisotropic sample, diffusion tensor imaging
(DTI) is required to fully characterize diffusion.
In theory, to determine all elements of the diffu-
sion tensor, at least six independent measure-
ments with diffusion gradients applied sequen-
tially along six noncollinear directions are
required [4–7]. The direction of maximum diffu-
sivity has been shown to coincide with the fiber
tract orientation [6, 7]. In white matter fiber bun-
T
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