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Article: Assessment of glycosaminoglycan distribution in human lumbar intervertebral discs using chemical exchange saturation transfer at 3 T: Feasibility and initial experience
Title | Assessment of glycosaminoglycan distribution in human lumbar intervertebral discs using chemical exchange saturation transfer at 3 T: Feasibility and initial experience | ||||||
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Authors | |||||||
Keywords | CEST Glycosaminoglycan Intervertebral disc MRI | ||||||
Issue Date | 2011 | ||||||
Publisher | John Wiley & Sons Ltd. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/13087 | ||||||
Citation | Nmr In Biomedicine, 2011, v. 24 n. 9, p. 1137-1144 How to Cite? | ||||||
Abstract | Recent studies have proposed that glycosaminoglycan chemical exchange saturation transfer (gagCEST) is associated with a loss of glycosaminoglycans (GAGs), which may be an initiating factor in intervertebral disc (IVD) degeneration. Despite its promising potential, this application has not been reported in human in vivo IVD studies because of the challenges of B 0 magnetic field inhomogeneity in gagCEST. This study aimed to evaluate the feasibility of quantifying CEST values in IVDs of healthy volunteers using a clinical 3 T scanner. A single-slice turbo spin echo sequence was used to quantify the CEST effect in various GAG phantoms and in IVDs of 12 volunteers. The phantom results indicated high correlation between gagCEST and GAG concentrations (R 2=0.95). With optimal B 0 inhomogeneity correction, in vivo CEST maps of IVDs showed robust contrast between the nucleus pulposus (NP) and the annulus fibrosus (AF) (p<0.01), as well as higher signal in the central relative to the peripheral NP. In addition, a trend of decreasing CEST values from upper to lower disc levels was evident in NP. Our results demonstrate that in vivo gagCEST quantification in human lumbar IVDs is feasible at 3T in combination with successful B 0 inhomogeneity correction, but without significant hardware modifications. Our initial findings suggest that it would be worthwhile to perform direct correlation studies between CEST and GAGs using cadaver samples, and to extend this novel technique to studies on patients with degenerative discs to better understand its distinct imaging features relative to conventional techniques. Copyright © 2011 John Wiley & Sons, Ltd. The feasibility of in vivo glycosaminoglycan chemical exchange saturation transfer (gagCEST) quantification was investigated for the first time in human lumbar intervertebral discs (IVDs) using a clinical MRI scanner. Our data showed robust contrast between the nucleus pulposus (NP) and the annulus fibrosus, a higher signal in the central relative to peripheral NP and a trend of decreasing CEST values from upper to lower disc levels with successful B 0 inhomogeneity correction. Our initial findings suggest that it would be worthwhile to perform direct correlation studies between CEST and glycosaminoglycans using cadaver samples, and to extend this novel technique to studies on patients with degenerative discs to better understand its distinct imaging features relative to conventional techniques. © 2011 John Wiley & Sons, Ltd. | ||||||
Persistent Identifier | http://hdl.handle.net/10722/139132 | ||||||
ISSN | 2023 Impact Factor: 2.7 2023 SCImago Journal Rankings: 0.949 | ||||||
ISI Accession Number ID |
Funding Information: The authors wish to thank Professor Peter van Zijl and Mr Joseph Gillen (Johns Hopkins School of Medicine, Baltimore, MD, USA) for sharing a CEST pulse sequence and Dr Barbara Chan (University of Hong Kong) for producing GAG phantoms. This work was supported by a grant from the General Research Fund sponsored by the Research Grants Council of Hong Kong. | ||||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kim, M | en_HK |
dc.contributor.author | Chan, Q | en_HK |
dc.contributor.author | Anthony, MP | en_HK |
dc.contributor.author | Cheung, KM | en_HK |
dc.contributor.author | Samartzis, D | en_HK |
dc.contributor.author | Khong, PL | en_HK |
dc.date.accessioned | 2011-09-23T05:45:39Z | - |
dc.date.available | 2011-09-23T05:45:39Z | - |
dc.date.issued | 2011 | en_HK |
dc.identifier.citation | Nmr In Biomedicine, 2011, v. 24 n. 9, p. 1137-1144 | en_HK |
dc.identifier.issn | 0952-3480 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/139132 | - |
dc.description.abstract | Recent studies have proposed that glycosaminoglycan chemical exchange saturation transfer (gagCEST) is associated with a loss of glycosaminoglycans (GAGs), which may be an initiating factor in intervertebral disc (IVD) degeneration. Despite its promising potential, this application has not been reported in human in vivo IVD studies because of the challenges of B 0 magnetic field inhomogeneity in gagCEST. This study aimed to evaluate the feasibility of quantifying CEST values in IVDs of healthy volunteers using a clinical 3 T scanner. A single-slice turbo spin echo sequence was used to quantify the CEST effect in various GAG phantoms and in IVDs of 12 volunteers. The phantom results indicated high correlation between gagCEST and GAG concentrations (R 2=0.95). With optimal B 0 inhomogeneity correction, in vivo CEST maps of IVDs showed robust contrast between the nucleus pulposus (NP) and the annulus fibrosus (AF) (p<0.01), as well as higher signal in the central relative to the peripheral NP. In addition, a trend of decreasing CEST values from upper to lower disc levels was evident in NP. Our results demonstrate that in vivo gagCEST quantification in human lumbar IVDs is feasible at 3T in combination with successful B 0 inhomogeneity correction, but without significant hardware modifications. Our initial findings suggest that it would be worthwhile to perform direct correlation studies between CEST and GAGs using cadaver samples, and to extend this novel technique to studies on patients with degenerative discs to better understand its distinct imaging features relative to conventional techniques. Copyright © 2011 John Wiley & Sons, Ltd. The feasibility of in vivo glycosaminoglycan chemical exchange saturation transfer (gagCEST) quantification was investigated for the first time in human lumbar intervertebral discs (IVDs) using a clinical MRI scanner. Our data showed robust contrast between the nucleus pulposus (NP) and the annulus fibrosus, a higher signal in the central relative to peripheral NP and a trend of decreasing CEST values from upper to lower disc levels with successful B 0 inhomogeneity correction. Our initial findings suggest that it would be worthwhile to perform direct correlation studies between CEST and glycosaminoglycans using cadaver samples, and to extend this novel technique to studies on patients with degenerative discs to better understand its distinct imaging features relative to conventional techniques. © 2011 John Wiley & Sons, Ltd. | en_HK |
dc.language | eng | en_US |
dc.publisher | John Wiley & Sons Ltd. The Journal's web site is located at http://www3.interscience.wiley.com/cgi-bin/jhome/13087 | en_HK |
dc.relation.ispartof | NMR in Biomedicine | en_HK |
dc.rights | NMR in Biomedicine. Copyright © John Wiley & Sons Ltd. | - |
dc.subject | CEST | en_HK |
dc.subject | Glycosaminoglycan | en_HK |
dc.subject | Intervertebral disc | en_HK |
dc.subject | MRI | en_HK |
dc.subject.mesh | Glycosaminoglycans - metabolism | - |
dc.subject.mesh | Intervertebral Disc - metabolism | - |
dc.subject.mesh | Lumbar Vertebrae - metabolism | - |
dc.subject.mesh | Magnetic Resonance Imaging - methods | - |
dc.subject.mesh | Phantoms, Imaging | - |
dc.title | Assessment of glycosaminoglycan distribution in human lumbar intervertebral discs using chemical exchange saturation transfer at 3 T: Feasibility and initial experience | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Kim, M: minakim@hku.hk | en_HK |
dc.identifier.email | Anthony, MP: anthonym@hku.hk | en_HK |
dc.identifier.email | Cheung, KM: cheungmc@hku.hk | en_HK |
dc.identifier.email | Samartzis, D: dspine@hku.hk | en_HK |
dc.identifier.email | Khong, PL: plkhong@hkucc.hku.hk | en_HK |
dc.identifier.authority | Kim, M=rp00292 | en_HK |
dc.identifier.authority | Anthony, MP=rp01302 | en_HK |
dc.identifier.authority | Cheung, KM=rp00387 | en_HK |
dc.identifier.authority | Samartzis, D=rp01430 | en_HK |
dc.identifier.authority | Khong, PL=rp00467 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1002/nbm.1671 | en_HK |
dc.identifier.pmid | 21387446 | - |
dc.identifier.scopus | eid_2-s2.0-80053197189 | en_HK |
dc.identifier.hkuros | 192105 | en_US |
dc.identifier.hkuros | 189132 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-80053197189&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 24 | en_HK |
dc.identifier.issue | 9 | en_HK |
dc.identifier.spage | 1137 | en_HK |
dc.identifier.epage | 1144 | en_HK |
dc.identifier.isi | WOS:000296419200014 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.f1000 | 13154958 | - |
dc.identifier.scopusauthorid | Kim, M=8146283400 | en_HK |
dc.identifier.scopusauthorid | Chan, Q=6602497305 | en_HK |
dc.identifier.scopusauthorid | Anthony, MP=35270974300 | en_HK |
dc.identifier.scopusauthorid | Cheung, KM=7402406754 | en_HK |
dc.identifier.scopusauthorid | Samartzis, D=34572771100 | en_HK |
dc.identifier.scopusauthorid | Khong, PL=7006693233 | en_HK |
dc.identifier.issnl | 0952-3480 | - |