14:15 |
0111.
|
Response of Quantitative
MRI to Artificial Collagen Cross-linking of Articular
Cartilage
Jari Rautiainen1,2, Mikko J. Nissi1,2,
Elli-Noora Salo3, Harri Kokkonen2,4,
Shalom Michaeli5, Silvi Mangia5,
Olli Gröhn6, Juha Töyräs2,4, and
Miika T. Nieminen1,3
1Medical Research Center Oulu and Department
of Diagnostic Radiology, University of Oulu, Oulu,
Finland, 2Department
of Applied Physics, University of Eastern Finland,
Kuopio, Finland, 3Department
of Diagnostic Radiology, Oulu University Hospital, Oulu,
Finland, 4Diagnostic
Imaging Center, Kuopio University Hospital, Kuopio,
Finland, 5Center
for Magnetic Resonance Research, University of
Minnesota, MN, United States, 6Department
of Neurobiology, A.I.Virtanen Institute for Molecular
Sciences, University of Eastern Finland, Kuopio, Finland
Aging of cartilage results in accumulation of advanced
glycation end products (AGEs), most notably collagen
cross-links in cartilage. Increased cross-linking of the
collagens makes cartilage more stiff and brittle. In
this study, sensitivity of quantitative MRI parameters
to artificial collagen cross-linking induced by L-threose
in bovine articular cartilage was evaluated. Artificial
cross-linking detectably changed the biophysical
properties of cartilage which were also detected with
MRI parameters. While T2 and dGEMRIC responded to the
treatment as expected, T1ρ relaxation time constants
showed unexpected increase, possibly attributed to an
increased cross-linked fraction characterized by the
slow motion or blocking of exchange-mediated relaxation.
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14:27 |
0112. |
Validation of diffusion
tensor imaging of articular cartialge in an animal model of
posttraumatic osteoarthritis
Jose G Raya1, Ignacio Rossi1, Oran
Kennedy1, Natalie Danna1, Bryan
Beutel1, You Jin Lee1, and
Thorsten Kirsch1
1NYU Langone Medical Center, New York, NY,
United States
We validate DTI of articular cartilage in an animal
model of posttraumatic osteoarthritis (PTOA). Eight New
Zeeland white rabbits underwent anterior cruciate
ligament transection (ACLT) on one of the hindlimbs and
sham surgery in the contralateral limb. Rabbits were
scarified at 4 (n=4) and 8 weeks (n=4) after surgery.
Both joints underwent MRI (PD-weighted and DTI),
micro-CT and histology with safranin O. We observe a
trend of increased MD in the ACLT joints compared to the
sham that was significant at 8 weeks. Changes in MD
correlated with areas of PG loss in histology, that only
show changes on PG
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14:39 |
0113.
|
Rapid T1 and T2 mapping of
the hip articular cartilage with radial MR fingerprinting
Martijn A Cloos1, Leeor Alon1,
Christian Geppert2, Daniel K Sodickson1,
and Riccardo Lattanzi1
1Center for Biomedical Imaging, Department of
Radiology, New York University School of Medicine, New
York, NY, United States, 2Siemens
AG Healthcare, Erlangen, Germany
Biochemical assessment is critical for early detection
and staging of hip articular cartilage damage, as well
as to predict risk for progression. We employed the
principles of magnetic resonance fingerprinting to
explore the feasibility of simultaneous T1 and T2
mapping in clinically feasible scan times. In addition
to a PD image, our method quantified T1 and T2 with a
0.8x0.8 mm2 in-plane resolution (scan time of 1:20 min
per slice). By enabling a fast comprehensive
morphological and biochemical assessment, we hope to
improve assessment and staging of cartilage damage,
predict risk for progression and impact patient
management decisions.
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14:51 |
0114. |
Correlation between
Cartilaginous endplate defects and Intervertebral disc
degeneration: An In Vivo MRI Study at 3.0 Tesla
Dong Xing1, Jiao Wang1, Yunfei Zha1,
Lei Hu1, Hui Lin2, and Yuan Lin1
1Department of Radiology, Renmin Hospital of
Wuhan University, Wuhan, Hubei, China, 2GE
Healthcare China, Shanghai, China
Although IVDD is a multifactorial disease, it is well
accepted that limited nutrition is the final common
pathway for IVDD and the changes in the structure or
composition of the cartilaginous endplate (CEP) have
been considered a crucial role in IVDD. The ultrashort
echo time (UTE) sequence has been used in detecting the
CEP defects and the visual classification of IVDD ,
however, a further study utilized the quantitative
parameter of T2*-relaxation time would be benefit to
understand the causes of disc degeneration of early
stage. The purpose of this study was to use 3D-UTE and
T2*- mapping sequence to ascertain the relation between
CEP Integrity and IVDD.
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15:03 |
0115. |
Metal Artifact Reduction
Using a 3D UTE-MSI sequence with Time-Frame Regularized
Compressed Sensing Reconstruction
Yifei Lou1, Qun He2, Xun Jia3,
Eric Chang2, Christine B Chung2,
and Jiang Du2
1Department of Mathematical Sciences,
University of Texas Dallas, Dallas, TX, United States, 2Radiology,
University of California, San Diego, CA, United States, 3Department
of Radiation Oncology, University of Texas Southwestern
Medical Center, Dallas, TX, United States
Metallic implants are routinely used to treat advanced
joint disease. There is a need for non-invasive
diagnosis of wear-induced disease. MRI has obvious
advantages. However, conventional MR sequences are
subject to severe distortion due to strong
susceptibility effects near metal, with little or no
signal from important joint tissues such as tendons and
cortical bone which have very short T2s. 3D ultrashort
echo time (UTE) imaging sequences together with multiple
spectral imaging (MSI) can potentially image short T2
tissues and minimize metal artifact. However, 3D UTE-MSI
is time-consuming. In this study we aimed to develop 3D
UTE-MSI using with vastly undersampling to reduce scan
time and a tight-frame regularized compressive sensing
(TFCS) technique to reduce streak artifacts. T1,
magnetization transfer ratio (MTR) and water content of
tissues near metal can potentially being measured using
a clinical whole-body scanner
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15:15 |
0116. |
Effects of bath solutions
on the quantitative determination of relaxation times in
compressed articular cartilage by microscopic MRI
Nian Wang1 and
Yang Xia1
1Department of Physics and Center for
Biomedical Research, Oakland University, Rochester, MI,
United States
A new type of laminar appearance was found in the deep
region of compressed articular cartilage at the magic
angle by high-resolution MRI, but the origin of this
appearance was unclear. Recently, the molecular origin
of this loading-induced laminar layer in the deep
cartilage was attributed to the GAG loss in cartilage.
To investigate the characteristics of this additional
low-intensity layer, quantitative MRI T1, T2, and T1ρ
experiments were carried out under different
orientations when the tissue was soaked in different
soaking solution.
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15:27 |
0117. |
Determination of
correlation time in articular cartilage by T1rho relaxation
dispersion
Matti Hanni1,2, Mikko J. Nissi3,4,
Jari Rautiainen3,4, Simo Saarakkala2,5,
Jutta Ellermann6, and Miika T. Nieminen2,7
1Department of Radiology, University of Oulu,
Oulu, Finland, 2Medical
Research Center Oulu, Oulu University Hospital and
University of Oulu, Oulu, Finland, 3Department
of Radiology, and Medical Research Center Oulu,
University of Oulu and Oulu University Hospital, Oulu,
Finland, 4Department
of Applied Physics, University of Eastern Finland,
Kuopio, Finland, 5Department
of Diagnostic Radiology, Oulu University Hospital,
Department of Medical Technology, University of Oulu,
Oulu, Finland, 6Center
for Magnetic Resonance Research, Department of
Radiology, University of Minnesota, Minneapolis,
Minnesota, United States, 7Department
of Diagnostic Radiology, University of Oulu and Oulu
University Hospital, Oulu, Finland
Reorientational correlation time is a fundamental
biophysical property that describes the dynamics of
nuclei in any type of tissue. In this abstract,
correlation time is investigated as a potential new MRI
contrast. It is obtained from MRI T1rho relaxation
dispersion measurements of bovine and human articular
cartilage in vitro. The fitted correlation times appear
to be macromolecule-specific, as well as indicative of
early structural changes associated with osteoarthritis.
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15:39 |
0118.
|
Magnetic Resonance Imaging
as Biomarker of Adverse Local Tissue Reactions in Total Hip
Arthroplasty
Matthew F. Koff1, Parina H. Shah1,
Alissa Burge1, Mauro Miranda1,
Christina Esposito2, Elexis Baral2,
Thomas W. Bauer3, Allina Nocon4,
Kara Fields4, Stephen Lyman4, HSS
Adult Reconstruction & Joint Replacement Division5,
Douglas Padgett5, Timothy Wright2,
and Hollis G. Potter1
1Department of Radiology and Imaging - MRI,
Hospital for Special Surgery, New York, New York, United
States, 2Department
of Biomechanics, Hospital for Special Surgery, New York,
New York, United States, 3Department
of Anatomic Pathology, Cleveland Clinic, Cleveland,
Ohio, United States,4Healthcare Research
Institute, Hospital for Special Surgery, New York, New
York, United States, 5Adult
Reconstruction & Joint Replacement Division, Hospital
for Special Surgery, New York, New York, United States
synopsis
|
15:51 |
0119. |
Quantitative Susceptibility
Mapping (QSM) to correlate with histology and quantitative
parametric mapping in surgically induced juvenile
osteochondritis dissecans
Luning Wang1, Mikko J Nissi1,2,
Ferenc Toth3, Michael Garwood1,
Cathy Carlson3, and Jutta Ellermann1
1Center for Magnetic Resonance Research,
University of Minnesota, Twin Cities, Minneapolis, MN,
United States, 2Medical
Research Center Oulu, Oulu University Hospital and
University of Oulu, Finland, 3University
of Minnesota, Twin Cities, Minneapolis, MN, United
States
Juvenile Osteochondritis Dissecans (OCD) is a disease of
epiphyseal cartilage occurring subsequent to failure of
cartilage canal blood vessels. Minimum intensity
projections of MR susceptibility maps together with MR
relaxometry can provide a noninvasive approach for a
direct correlation between the quantitative assessment
of cartilage matrix and the visualization of the canal
degeneration at different time points.
|
16:03 |
0120. |
Cartilage MR T1ρ and T2
quantifications: longitudinal reproducibility and variations
using different coils and scanners at single and multi-sites
Xiaojuan Li1, Valentina Pedoia1,
Deepak Kumar1, Drew Lansdown1,
Cory Wyatt1, Julien Rivorie1,
Narihiro Okazaki1, Dragana Savic1,
Matthew F Koff2, Joel Felmlee3,
Williams Steven3, and Sharmila Majumdar1
1University of California, San Francisco, CA,
United States, 2Hospital
for Special Surgery, New York, NY, United States, 3Mayo
Clinic, Rochester, MN, United States
MR T1ρ and T2 mapping are promising techniques that have
potential as early markers of cartilage degeneration.
Currently, applications of cartilage T1ρ and T2 imaging
in multicenter clinical trials are very limited. One
impeding factor is the lack of documentation of
potential variations of T1ρ and T2 introduced by
different scanners, coils and sites. In this report, we
evaluate the longitudinal reproducibility of T1ρ and T2,
and the variation of T1ρ and T2 by using different
scanners and coils at one site, and the reproducibility
and cross-validation of T1ρ and T2 among three sites.
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