Enhanced MR for morphological characterization of ligaments, tendons and bone
Project Number5U01EB023829-06
Former Number1U01EB023829-01A1
Contact PI/Project LeaderZHANG, XIAOLIANG Other PIs
Awardee OrganizationSTATE UNIVERSITY OF NEW YORK AT BUFFALO
Description
Abstract Text
PROJECT SUMMARY/ABSTRACT
According to Council for Disability Awareness, diseases of the musculoskeletal system and connective tissue,
such as the ligaments, tendons and bone are the #1 cause of disability in the United States. MR imaging has
been increasingly becoming the diagnostic tool of choice for evaluation and management of these diseases
and injuries due to its potential of providing information on not only anatomic structure but also function
noninvasively. However, the capability of MRI in studying human ligaments, tendons and bone is limited by
inadequate sensitivity and slow acquisitions of conventional MR technology. Semi-solid/solid tissues, including
collagen-rich tissues such as calcified ligaments and tendons, as well as periosteum, cortical bone and
trabecular bone, provide very little MR signal with traditional MRI due to their very short transverse (T2)
relaxation time of a few milliseconds or less. In addition, during the long acquisition times, involuntary
movements of human subjects introduce motion artifacts, posing a critical challenge in obtaining high-
resolution images with diagnostic value. Several recently developed technologies have the potential to address
these limitations. Ultrahigh field 7T MRI, parallel imaging, and compressed sensing have demonstrated unique
advantages of high sensitivity and fast acquisitions in vivo. Studies on musculoskeletal imaging using ultra-
short echo time (UTE) and zero echo time (ZTE) methods have shown unparalleled capability to image short
T2 species normally invisible in MRI. However, the implementation of these technologies at ultrahigh fields is
challenging due to design difficulties of the required high frequency multichannel coil arrays, as well as the
problems associated with ultrahigh fields, e.g. increased susceptibility, B1 inhomogeneity, and increased SAR.
In this study, through a synergistic bioengineering research partnership, we propose a comprehensive project
for developing advanced hardware and imaging methods at 7T to enable morphological and functional
characterization of human ligaments, tendons and bone. These developments aim to produce highly sensitive,
isotropic ~100-150um resolution images of semi-solid connective tissues with clinically relevant contrast in 1
minute scan time. Hardware developments will include multichannel coil arrays for knee and extremities using
quadrature and flexible array technology with metamaterial decoupling, as well as application of pyrolytic
graphite materials for reducing susceptibility artifacts. Imaging acquisition developments will be based on
improved UTE/ZTE sequences, and we propose new integrated techniques for improved semi-solid tissue
contrast, motion correction, and acceleration using parallel imaging and compressed sensing. We will also
validate the methods developed and assess the performance and safety/SAR. This research would provide
sensitive imaging tools for morphological and functional characterization of ligaments, tendons and bone,
which are highly demanded and essential for studying semi-solid connective tissues. We expect this research
will have a long-term clinical impact in the management of musculoskeletal system diseases and injuries.
Public Health Relevance Statement
Relevance to Public Health:
The successful outcome of the proposed project will provide a whole new imaging technique with highly
efficient acquisition technique and RF hardware dedicated to human ligament, tendon and bone MR imaging.
With this package of novel hardware and software, people can visualize the invisible structures in regular MR
technology. This would advance and benefit the biomedical research and clinical diagnosis on musculoskeletal
diseases, joint/cartilage disorders, connective tissue diseases and injuries, rheumatism, osteoporosis, and
complications associated with diabetes in lower and upper extremities.
National Institute of Biomedical Imaging and Bioengineering
CFDA Code
286
DUNS Number
038633251
UEI
LMCJKRFW5R81
Project Start Date
05-August-2020
Project End Date
31-July-2025
Budget Start Date
01-August-2024
Budget End Date
31-July-2025
Project Funding Information for 2024
Total Funding
$5,583
Direct Costs
$3,500
Indirect Costs
$2,083
Year
Funding IC
FY Total Cost by IC
2024
National Institute of Biomedical Imaging and Bioengineering
$5,583
Year
Funding IC
FY Total Cost by IC
Sub Projects
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