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High-Resolution 3D Cartilage Imaging with IDEAL–SPGR at 3 T

David B. Siepmann1, Jeff McGovern2, Jean H. Brittain3 and Scott B. Reeder1,4

1 Department of Radiology, University of Wisconsin School of Medicine, 600 Highland Ave., CSC E1/374, Madison, WI 53792.
2 GE Healthcare, Waukesha, WI.
3 Global Applied Science Laboratory, GE Healthcare, Madison, WI.
4 Departments of Medical Physics, Biomedical Engineering, and Medicine, University of Wisconsin, Madison, WI.


Figure 1
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Fig. 1A 36-year-old man with healthy knee. Representative lateral parasagittal MR images from IDEAL–SPGR (A–C) and fat-saturated SPGR (D) acquisitions with equal acquired resolution and imaging times. IDEAL–SPGR acquisition provides fat only (C) and combined fat–water images (A) in addition to water images (B). This capability improves signal-to-noise ratio and markedly improves cartilage–fluid contrast compared with that of equivalent fat-saturated SPGR image (D).

 

Figure 2
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Fig. 1B 36-year-old man with healthy knee. Representative lateral parasagittal MR images from IDEAL–SPGR (A–C) and fat-saturated SPGR (D) acquisitions with equal acquired resolution and imaging times. IDEAL–SPGR acquisition provides fat only (C) and combined fat–water images (A) in addition to water images (B). This capability improves signal-to-noise ratio and markedly improves cartilage–fluid contrast compared with that of equivalent fat-saturated SPGR image (D).

 

Figure 3
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Fig. 1C 36-year-old man with healthy knee. Representative lateral parasagittal MR images from IDEAL–SPGR (A–C) and fat-saturated SPGR (D) acquisitions with equal acquired resolution and imaging times. IDEAL–SPGR acquisition provides fat only (C) and combined fat–water images (A) in addition to water images (B). This capability improves signal-to-noise ratio and markedly improves cartilage–fluid contrast compared with that of equivalent fat-saturated SPGR image (D).

 

Figure 4
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Fig. 1D 36-year-old man with healthy knee. Representative lateral parasagittal MR images from IDEAL–SPGR (A–C) and fat-saturated SPGR (D) acquisitions with equal acquired resolution and imaging times. IDEAL–SPGR acquisition provides fat only (C) and combined fat–water images (A) in addition to water images (B). This capability improves signal-to-noise ratio and markedly improves cartilage–fluid contrast compared with that of equivalent fat-saturated SPGR image (D).

 

Figure 5
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Fig. 2A Comparison of calculated signal-to-noise ratio (SNR) and contrast-to-noise ratio (CNR) between patellar cartilage and articular fluid values with IDEAL–SPGR (dark gray) and fat-saturated SPGR (light gray) techniques. Error bars represent standard error above and below mean. Other than SNR of synovial fluid, all results are statistically significant (p < 0.05). Graph shows IDEAL–SPGR provides significant SNR advantage for patellar and femoral cartilage and for muscle. SNR values for synovial fluid are approximately equivalent for the two techniques.

 

Figure 6
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Fig. 2B Comparison of calculated signal-to-noise ratio (SNR) and contrast-to-noise ratio (CNR) between patellar cartilage and articular fluid values with IDEAL–SPGR (dark gray) and fat-saturated SPGR (light gray) techniques. Error bars represent standard error above and below mean. Other than SNR of synovial fluid, all results are statistically significant (p < 0.05). Graph shows IDEAL–SPGR markedly improving CNR between patellar cartilage and articular fluid compared with fat-saturated SPGR for both patellar and femoral cartilage.

 

Figure 7
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Fig. 3A 34-year-old man with healthy knee. Magnified sagittal MR images allow better comparison of contrast-to-noise ratio (CNR) for patellar cartilage and synovial fluid. IDEAL–SPGR image (A) shows lower signal intensity in fluid, and therefore better CNR, than does fat-saturated SPGR image (B).

 

Figure 8
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Fig. 3B 34-year-old man with healthy knee. Magnified sagittal MR images allow better comparison of contrast-to-noise ratio (CNR) for patellar cartilage and synovial fluid. IDEAL–SPGR image (A) shows lower signal intensity in fluid, and therefore better CNR, than does fat-saturated SPGR image (B).

 

Figure 9
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Fig. 4A 35-year-old man with healthy knee. MR images show that in addition to signal-to-noise ratio and contrast-to-noise ratio advantages, IDEAL–SPGR sequence yields not only images with robust fat saturation (A) but also fat-only (B) and in-phase (C) and out-of phase (D) recombined images with no additional imaging time. This capability may lead to methods for evaluating bone marrow abnormalities such as edema, which is common in patients with osteoarthritis.

 

Figure 10
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Fig. 4B 35-year-old man with healthy knee. MR images show that in addition to signal-to-noise ratio and contrast-to-noise ratio advantages, IDEAL–SPGR sequence yields not only images with robust fat saturation (A) but also fat-only (B) and in-phase (C) and out-of phase (D) recombined images with no additional imaging time. This capability may lead to methods for evaluating bone marrow abnormalities such as edema, which is common in patients with osteoarthritis.

 

Figure 11
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Fig. 4C 35-year-old man with healthy knee. MR images show that in addition to signal-to-noise ratio and contrast-to-noise ratio advantages, IDEAL–SPGR sequence yields not only images with robust fat saturation (A) but also fat-only (B) and in-phase (C) and out-of phase (D) recombined images with no additional imaging time. This capability may lead to methods for evaluating bone marrow abnormalities such as edema, which is common in patients with osteoarthritis.

 

Figure 12
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Fig. 4D 35-year-old man with healthy knee. MR images show that in addition to signal-to-noise ratio and contrast-to-noise ratio advantages, IDEAL–SPGR sequence yields not only images with robust fat saturation (A) but also fat-only (B) and in-phase (C) and out-of phase (D) recombined images with no additional imaging time. This capability may lead to methods for evaluating bone marrow abnormalities such as edema, which is common in patients with osteoarthritis.

 

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