TY - JOUR
T1 - Myofiber ellipticity as an explanation for transverse asymmetry of skeletal muscle diffusion MRI in vivo signal
AU - Karampinos, Dimitrios C.
AU - King, Kevin F.
AU - Sutton, Bradley P.
AU - Georgiadis, John G.
N1 - Funding Information:
The present work was supported by the National Institutes of Health (grant R21HL090455), the Beckman Institute at the University of Illinois at Urbana-Champaign, IL, and the Applied Science Laboratory of GE Healthcare, Waukesha, WI, USA. DCK and JGG also thank Dr. Bruce Damon for a stimulating discussion regarding the possible role of the sarcoplasmic reticulum in diffusion, and Ms. Elise Corbin for her artwork.
PY - 2009/12
Y1 - 2009/12
N2 - Due to its unique non-invasive microstructure probing capabilities, diffusion tensor imaging (DTI) constitutes a valuable tool in the study of fiber orientation in skeletal muscles. By implementing a DTI sequence with judiciously chosen directional encoding to quantify in vivo the microarchitectural properties in the calf muscles of three healthy volunteers at rest, we report that the secondary eigenvalue is significantly higher than the tertiary eigenvalue, a phenomenon corroborated by prior DTI findings. Toward a physics-based explanation of this phenomenon, we propose a composite medium model that accounts for water diffusion in the space within the muscle fiber and the extracellular space. The muscle fibers are abstracted as cylinders of infinite length with an elliptical cross section, the latter closely approximating microstructural features well documented in prior histological studies of excised muscle. The range of values of fiber ellipticity predicted by our model agrees with these studies, and the spatial orientation of the cross-sectional ellipses is consistent with local muscle strain fields and the putative direction of lateral transmission of stress between fibers in certain regions in three antigravity muscles (Tibialis Anterior, Soleus, and Gastrocnemius), as well as independent measurements of deformation in active calf muscles. As a metric, fiber cross-sectional ellipticity may be useful for quantifying morphological changes in skeletal muscle fibers with aging, hypertrophy, or sarcopenia.
AB - Due to its unique non-invasive microstructure probing capabilities, diffusion tensor imaging (DTI) constitutes a valuable tool in the study of fiber orientation in skeletal muscles. By implementing a DTI sequence with judiciously chosen directional encoding to quantify in vivo the microarchitectural properties in the calf muscles of three healthy volunteers at rest, we report that the secondary eigenvalue is significantly higher than the tertiary eigenvalue, a phenomenon corroborated by prior DTI findings. Toward a physics-based explanation of this phenomenon, we propose a composite medium model that accounts for water diffusion in the space within the muscle fiber and the extracellular space. The muscle fibers are abstracted as cylinders of infinite length with an elliptical cross section, the latter closely approximating microstructural features well documented in prior histological studies of excised muscle. The range of values of fiber ellipticity predicted by our model agrees with these studies, and the spatial orientation of the cross-sectional ellipses is consistent with local muscle strain fields and the putative direction of lateral transmission of stress between fibers in certain regions in three antigravity muscles (Tibialis Anterior, Soleus, and Gastrocnemius), as well as independent measurements of deformation in active calf muscles. As a metric, fiber cross-sectional ellipticity may be useful for quantifying morphological changes in skeletal muscle fibers with aging, hypertrophy, or sarcopenia.
KW - Diffusion tensor imaging
KW - Gastrocnemius
KW - Myocytes
KW - Myofiber ellipticity
KW - Skeletal muscle
KW - Soleus
UR - http://www.scopus.com/inward/record.url?scp=70450253112&partnerID=8YFLogxK
U2 - 10.1007/s10439-009-9783-1
DO - 10.1007/s10439-009-9783-1
M3 - Article
C2 - 19763830
AN - SCOPUS:70450253112
SN - 0090-6964
VL - 37
SP - 2532
EP - 2546
JO - Annals of Biomedical Engineering
JF - Annals of Biomedical Engineering
IS - 12
ER -