Literature DB >> 12353281

Spatial assessment of articular cartilage proteoglycans with Gd-DTPA-enhanced T1 imaging.

Miika T Nieminen1, Jarno Rieppo, Johanna Silvennoinen, Juha Töyräs, Juhana M Hakumäki, Mika M Hyttinen, Heikki J Helminen, Jukka S Jurvelin.   

Abstract

In Gd-DTPA-enhanced T(1) imaging of articular cartilage, the MRI contrast agent with two negative charges is understood to accumulate in tissue inversely to the negative charge of cartilage glycosaminoglycans (GAGs) of proteoglycans (PGs), and this leads to a decrease in the T(1) relaxation time of tissue relative to the charge in tissue. By assuming a constant relaxivity for Gd-DTPA in cartilage, it has further been hypothesized that the contrast agent concentration in tissue could be estimated from consecutive T(1) measurements in the absence or presence of the contrast agent. The spatial sensitivity of the technique was examined at 9.4 T in normal and PG-depleted bovine patellar cartilage samples. As a reference, spatial PG concentration was assessed with digital densitometry from safranin O-stained cartilage sections. An excellent linear correlation between spatial optical density (OD) of stained GAGs and T(1) with Gd-DTPA was observed in the control and chondroitinase ABC-treated cartilage specimens, and the MR parameter accounted for approximately 80% of the variations in GAG concentration within samples. Further, the MR-resolved Gd-DTPA concentration proved to be an even better estimate for PGs, with an improved correlation. However, the linear relation between MR parameters and PG concentration did not apply in the deep tissue, where MR measurements overestimated the PG content. While the absolute [Gd-DTPA] determination may be prone to error due to uncertainty of relaxivity in cartilage, or to other contributing factors such as variations in tissue permeability, the experimental evidence highlights the sensitivity of this technique to reflect spatial changes in cartilage PG concentration in normal and degenerated tissue. Copyright 2002 Wiley-Liss, Inc.

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Year:  2002        PMID: 12353281     DOI: 10.1002/mrm.10273

Source DB:  PubMed          Journal:  Magn Reson Med        ISSN: 0740-3194            Impact factor:   4.668


  32 in total

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Authors:  Zhao Wei; Ya-Jun Ma; Hyungseok Jang; Wenhui Yang; Jiang Du
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3.  In vivo T(1rho) mapping in cartilage using 3D magnetization-prepared angle-modulated partitioned k-space spoiled gradient echo snapshots (3D MAPSS).

Authors:  Xiaojuan Li; Eric T Han; Reed F Busse; Sharmila Majumdar
Journal:  Magn Reson Med       Date:  2008-02       Impact factor: 4.668

Review 4.  Emerging MRI methods in rheumatoid arthritis.

Authors:  Camilo G Borrero; James M Mountz; John D Mountz
Journal:  Nat Rev Rheumatol       Date:  2010-11-02       Impact factor: 20.543

Review 5.  MR imaging of articular cartilage physiology.

Authors:  Jung-Ah Choi; Garry E Gold
Journal:  Magn Reson Imaging Clin N Am       Date:  2011-05       Impact factor: 2.266

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Review 7.  [Delayed gadolinium enhanced MRI of cartilage (dGEMRIC): molecular MRI of hip joint cartilage].

Authors:  C Zilkens; M Jäger; B Bittersohl; M Dudda; M B Millis; Y-J Kim; G Muhr; R Krauspe; T C Mamisch
Journal:  Orthopade       Date:  2009-07       Impact factor: 1.087

8.  Toward imaging biomarkers for glycosaminoglycans.

Authors:  Martha L Gray
Journal:  J Bone Joint Surg Am       Date:  2009-02       Impact factor: 5.284

9.  Depth-dependent profiles of glycosaminoglycans in articular cartilage by microMRI and histochemistry.

Authors:  Yang Xia; Shaokuan Zheng; Aruna Bidthanapally
Journal:  J Magn Reson Imaging       Date:  2008-07       Impact factor: 4.813

10.  Molecular imaging of fibrin in a breast cancer xenograft mouse model.

Authors:  Ritika Uppal; Zdravka Medarova; Christian T Farrar; Guangping Dai; Anna Moore; Peter Caravan
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