Orientational dependence of T2 relaxation in articular cartilage: A microscopic MRI (μMRI) study

The experiments reported herein are the first MRI investigations of the orientational dependence of T2 relaxation in articular cartilage at microscopic resolution over the 360° angular space. For each of six canine cartilage specimens, 48 independent T2‐weighted proton images were acquired for 12 di...

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Published inMagnetic resonance in medicine Vol. 48; no. 3; pp. 460 - 469
Main Authors Xia, Yang, Moody, Jonathan B., Alhadlaq, Hisham
Format Journal Article
LanguageEnglish
Published New York Wiley Subscription Services, Inc., A Wiley Company 01.09.2002
Williams & Wilkins
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Summary:The experiments reported herein are the first MRI investigations of the orientational dependence of T2 relaxation in articular cartilage at microscopic resolution over the 360° angular space. For each of six canine cartilage specimens, 48 independent T2‐weighted proton images were acquired for 12 different specimen orientations. Pixel‐wise monoexponential fits of these proton images produced 12 T2 relaxation images, each with an in‐plane pixel resolution of 13.7 μm. Cartilage T2 as a function of specimen orientation was shown to follow approximately the angular dependence of the nuclear dipole–dipole interaction, with local maxima at approximately 55°, 125°, 235°, and 305°. However, the relative amplitudes of the T2 maxima deviated somewhat from those expected from the dipolar interaction. The amplitudes of these maxima also varied with tissue depth: the largest amplitudes were found in the radial zone, intermediate amplitudes were found in the superficial zone, and there was a continuous decrease in amplitude approaching the transitional zone from the superficial zone above and the radial zone below. We explain the discrepancy between the observed T2 anisotropy and the angular dependence of the dipolar interaction by means of a simple model which considers the average of one isotropic and two anisotropic spin populations—the first being associated with “free” water, and the latter two arising from collagen‐associated waters. We show that even for the “long” T2 components, which arise in multiple‐compartment studies of collagen‐water systems, there appears to be two subpopulations. Each has the same peak value of T2, but the angular dependence of one is shifted in phase by 90° relative to the other by virtue of the fact that each is associated with groups of mutually perpendicular fibrils. Magn Reson Med 48:460–469, 2002. © 2002 Wiley‐Liss, Inc.
Bibliography:R.B. and J.N. Bennett
ArticleID:MRM10216
Research Excellence Fund in Biotechnology, Oakland University
NIH - No. R01 AR 45172
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istex:BC13B583F817E05555FBD273F5F74EA895816E41
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0740-3194
1522-2594
DOI:10.1002/mrm.10216