Optimization and validation of a rapid high-resolution T1-w 3D FLASH waterexcitation MRI sequence for the quantitative assessment of articular cartilage volume and thickness
C. Glaser et al., Optimization and validation of a rapid high-resolution T1-w 3D FLASH waterexcitation MRI sequence for the quantitative assessment of articular cartilage volume and thickness, MAGN RES IM, 19(2), 2001, pp. 177-185
In view of follow up. survey and development of therapeutic strategies for
osteoarthritis where cartilage deterioration plays an important role, a non
invasive, reliable and quantitative assessment of the articular cartilage
is desirable. The currently available high resolution T-1-weighted (T1-w) 3
D FLASH pulse sequences with frequency selective fat suppression are very t
ime consuming. We have I)optimized a high resolution T1-w 3D FLASH water ex
citation (WE) sequence for short acquisition time and cartilage visualizati
on, and 2) validated this sequence for cartilage volume and thickness quant
ification. The spectral fat presaturation was replaced by selective water e
xcitation. The flip angle of the WE sequence was optimized for the contrast
to noise (C/N-cart) ratio of cartilage. Sagittal datasets (voxel size: 0.3
1 x 0.31 x 2 mm(3)) of the knees of nine healthy volunteers were acquired b
oth, with the 3D FLASH WE (17.2/6.6/30 degrees) sequence (WE) and a previou
sly validated 3D FLASH fat saturated (42/11/30 degrees) sequence (FS). For
validation of the WE sequence, cartilage volume, mean and maximal cartilage
thickness of the two sequences were compared. Reproducibility was assessed
by calculating the coefficient of variation (COV %) of 4 consecutive WE da
ta sets in the volunteers. The acquisition rime was reduced from 16 ' 30 "
(FS) down to 7 ' 14 " for the WE sequence. Image contrast and visualization
of the cartilage was very similar, but delineation of the basal layer of t
he cartilage was slightly improved with the WE sequence. A flip angle of 30
degrees provided the best C/N-cart ratios (WE). Reproducibility (COV) was
between 1.9 and 5.9%. Cartilage volume and thickness agreed within 4% betwe
en FS and WE sequence. The WE sequence allows for rapid, valid and reproduc
ible quantification of articular cartilage volume and thickness, prerequisi
tes for follow-up examinations. The reduced acquisition time (50% of FS) en
ables routine clinical application and thus may contribute to a broader ass
essment of osteoarthritis. (C) 2001 Elsevier Science Inc. All rights reserv
ed.