Influence of echo time in quantitative proton MR spectroscopy using LCModel
Abstract Objective The objective of this study was to elucidate the influence on quantitative analysis using LCModel with the condition of echo time (TE) longer than the recommended values in the spectrum acquisition specifications. Methods A 3 T magnetic resonance system was used to perform proton...
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Veröffentlicht in: | Magnetic resonance imaging 2015-06, Vol.33 (5), p.644-648 |
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description | Abstract Objective The objective of this study was to elucidate the influence on quantitative analysis using LCModel with the condition of echo time (TE) longer than the recommended values in the spectrum acquisition specifications. Methods A 3 T magnetic resonance system was used to perform proton magnetic resonance spectroscopy. The participants were 5 healthy volunteers and 11 patients with glioma. Data were collected at TE of 72, 144 and 288 ms. LCModel was used to quantify several metabolites ( N -acetylaspartate, creatine and phosphocreatine, and choline-containing compounds). The results were compared with quantitative values obtained by using the T2-corrected internal reference method. Results In healthy volunteers, when TE was long, the quantitative values obtained using LCModel were up to 6.8-fold larger (p < 0.05) than those obtained using the T2-corrected internal reference method. The ratios of the quantitative values obtained by the two methods differed between metabolites (p < 0.05). In patients with glioma, the ratios of quantitative values obtained by the two methods tended to be larger at longer TE, similarly to the case of healthy volunteers, and large between-individual variation in the ratios was observed. Conclusions In clinical practice, TE is sometimes set longer than the value recommended for LCModel. If TE is long, LCModel overestimates the quantitative value since it cannot compensate for signal attenuation, and this effect is different for each metabolite and condition. Therefore, if TE is longer than recommended, it is necessary to account for the possibly reduced reliability of quantitative values calculated using LCModel. |
doi_str_mv | 10.1016/j.mri.2015.01.015 |
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Methods A 3 T magnetic resonance system was used to perform proton magnetic resonance spectroscopy. The participants were 5 healthy volunteers and 11 patients with glioma. Data were collected at TE of 72, 144 and 288 ms. LCModel was used to quantify several metabolites ( N -acetylaspartate, creatine and phosphocreatine, and choline-containing compounds). The results were compared with quantitative values obtained by using the T2-corrected internal reference method. Results In healthy volunteers, when TE was long, the quantitative values obtained using LCModel were up to 6.8-fold larger (p < 0.05) than those obtained using the T2-corrected internal reference method. The ratios of the quantitative values obtained by the two methods differed between metabolites (p < 0.05). In patients with glioma, the ratios of quantitative values obtained by the two methods tended to be larger at longer TE, similarly to the case of healthy volunteers, and large between-individual variation in the ratios was observed. Conclusions In clinical practice, TE is sometimes set longer than the value recommended for LCModel. If TE is long, LCModel overestimates the quantitative value since it cannot compensate for signal attenuation, and this effect is different for each metabolite and condition. Therefore, if TE is longer than recommended, it is necessary to account for the possibly reduced reliability of quantitative values calculated using LCModel.</description><identifier>ISSN: 0730-725X</identifier><identifier>EISSN: 1873-5894</identifier><identifier>DOI: 10.1016/j.mri.2015.01.015</identifier><identifier>PMID: 25623808</identifier><language>eng</language><publisher>Netherlands: Elsevier Inc</publisher><subject>Aspartic Acid - analogs & derivatives ; Aspartic Acid - metabolism ; Brain - metabolism ; Brain Neoplasms - metabolism ; Choline - metabolism ; Creatine - metabolism ; Echo time ; Glioma - metabolism ; Humans ; Image Processing, Computer-Assisted - methods ; LCModel ; Models, Theoretical ; MRS ; Phosphocreatine - metabolism ; Proton Magnetic Resonance Spectroscopy - methods ; Quantitative analysis ; Radiology ; Reproducibility of Results ; T2 relaxation</subject><ispartof>Magnetic resonance imaging, 2015-06, Vol.33 (5), p.644-648</ispartof><rights>Elsevier Inc.</rights><rights>2015 Elsevier Inc.</rights><rights>Copyright © 2015 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c408t-b36de2a7bb347a3e9da230726311920370b0b571bc5cdae8b77d17b57c0afbc03</citedby><cites>FETCH-LOGICAL-c408t-b36de2a7bb347a3e9da230726311920370b0b571bc5cdae8b77d17b57c0afbc03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.mri.2015.01.015$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25623808$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yamamoto, Tetsuya</creatorcontrib><creatorcontrib>Isobe, Tomonori</creatorcontrib><creatorcontrib>Akutsu, Hiroyoshi</creatorcontrib><creatorcontrib>Masumoto, Tomohiko</creatorcontrib><creatorcontrib>Ando, Hiroki</creatorcontrib><creatorcontrib>Sato, Eisuke</creatorcontrib><creatorcontrib>Takada, Kenta</creatorcontrib><creatorcontrib>Anno, Izumi</creatorcontrib><creatorcontrib>Matsumura, Akira</creatorcontrib><title>Influence of echo time in quantitative proton MR spectroscopy using LCModel</title><title>Magnetic resonance imaging</title><addtitle>Magn Reson Imaging</addtitle><description>Abstract Objective The objective of this study was to elucidate the influence on quantitative analysis using LCModel with the condition of echo time (TE) longer than the recommended values in the spectrum acquisition specifications. Methods A 3 T magnetic resonance system was used to perform proton magnetic resonance spectroscopy. The participants were 5 healthy volunteers and 11 patients with glioma. Data were collected at TE of 72, 144 and 288 ms. LCModel was used to quantify several metabolites ( N -acetylaspartate, creatine and phosphocreatine, and choline-containing compounds). The results were compared with quantitative values obtained by using the T2-corrected internal reference method. Results In healthy volunteers, when TE was long, the quantitative values obtained using LCModel were up to 6.8-fold larger (p < 0.05) than those obtained using the T2-corrected internal reference method. The ratios of the quantitative values obtained by the two methods differed between metabolites (p < 0.05). In patients with glioma, the ratios of quantitative values obtained by the two methods tended to be larger at longer TE, similarly to the case of healthy volunteers, and large between-individual variation in the ratios was observed. Conclusions In clinical practice, TE is sometimes set longer than the value recommended for LCModel. If TE is long, LCModel overestimates the quantitative value since it cannot compensate for signal attenuation, and this effect is different for each metabolite and condition. Therefore, if TE is longer than recommended, it is necessary to account for the possibly reduced reliability of quantitative values calculated using LCModel.</description><subject>Aspartic Acid - analogs & derivatives</subject><subject>Aspartic Acid - metabolism</subject><subject>Brain - metabolism</subject><subject>Brain Neoplasms - metabolism</subject><subject>Choline - metabolism</subject><subject>Creatine - metabolism</subject><subject>Echo time</subject><subject>Glioma - metabolism</subject><subject>Humans</subject><subject>Image Processing, Computer-Assisted - methods</subject><subject>LCModel</subject><subject>Models, Theoretical</subject><subject>MRS</subject><subject>Phosphocreatine - metabolism</subject><subject>Proton Magnetic Resonance Spectroscopy - methods</subject><subject>Quantitative analysis</subject><subject>Radiology</subject><subject>Reproducibility of Results</subject><subject>T2 relaxation</subject><issn>0730-725X</issn><issn>1873-5894</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU9r3DAQxUVoSbZpP0AuQcdevB1JK8tLoVCWpA3dUOgfyE1I8jjR1pY2kh3Yb1-ZTXvooTAgEO89Zn6PkAsGSwasfrdbDskvOTC5BFZGnpAFa5SoZLNevSALUAIqxeXdGXmV8w4AJBfylJxxWXPRQLMgX25C108YHNLYUXQPkY5-QOoDfZxMGP1oRv-EdJ_iGAO9_UbzHt2YYnZxf6BT9uGebje3scX-NXnZmT7jm-f3nPy8vvqx-Vxtv3662XzcVm4FzVhZUbfIjbJWrJQRuG4NF6B4LRhbcxAKLFipmHXStQYbq1TLVPlxYDrrQJyTt8fcstTjhHnUg88O-94EjFPWrG6ANSD4ukjZUerKxjlhp_fJDyYdNAM9M9Q7XRjqmaEGVkYWz-Vz_GQHbP86_kArgvdHAZYjnzwmnZ2fEbY-FTa6jf6_8R_-cbveB-9M_wsPmHdxSqHQ00xnrkF_n0ucO2Sy9MfhTvwG02mWwg</recordid><startdate>20150601</startdate><enddate>20150601</enddate><creator>Yamamoto, Tetsuya</creator><creator>Isobe, Tomonori</creator><creator>Akutsu, Hiroyoshi</creator><creator>Masumoto, Tomohiko</creator><creator>Ando, Hiroki</creator><creator>Sato, Eisuke</creator><creator>Takada, Kenta</creator><creator>Anno, Izumi</creator><creator>Matsumura, Akira</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20150601</creationdate><title>Influence of echo time in quantitative proton MR spectroscopy using LCModel</title><author>Yamamoto, Tetsuya ; Isobe, Tomonori ; Akutsu, Hiroyoshi ; Masumoto, Tomohiko ; Ando, Hiroki ; Sato, Eisuke ; Takada, Kenta ; Anno, Izumi ; Matsumura, Akira</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c408t-b36de2a7bb347a3e9da230726311920370b0b571bc5cdae8b77d17b57c0afbc03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Aspartic Acid - analogs & derivatives</topic><topic>Aspartic Acid - metabolism</topic><topic>Brain - metabolism</topic><topic>Brain Neoplasms - metabolism</topic><topic>Choline - metabolism</topic><topic>Creatine - metabolism</topic><topic>Echo time</topic><topic>Glioma - metabolism</topic><topic>Humans</topic><topic>Image Processing, Computer-Assisted - methods</topic><topic>LCModel</topic><topic>Models, Theoretical</topic><topic>MRS</topic><topic>Phosphocreatine - metabolism</topic><topic>Proton Magnetic Resonance Spectroscopy - methods</topic><topic>Quantitative analysis</topic><topic>Radiology</topic><topic>Reproducibility of Results</topic><topic>T2 relaxation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yamamoto, Tetsuya</creatorcontrib><creatorcontrib>Isobe, Tomonori</creatorcontrib><creatorcontrib>Akutsu, Hiroyoshi</creatorcontrib><creatorcontrib>Masumoto, Tomohiko</creatorcontrib><creatorcontrib>Ando, Hiroki</creatorcontrib><creatorcontrib>Sato, Eisuke</creatorcontrib><creatorcontrib>Takada, Kenta</creatorcontrib><creatorcontrib>Anno, Izumi</creatorcontrib><creatorcontrib>Matsumura, Akira</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Magnetic resonance imaging</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yamamoto, Tetsuya</au><au>Isobe, Tomonori</au><au>Akutsu, Hiroyoshi</au><au>Masumoto, Tomohiko</au><au>Ando, Hiroki</au><au>Sato, Eisuke</au><au>Takada, Kenta</au><au>Anno, Izumi</au><au>Matsumura, Akira</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Influence of echo time in quantitative proton MR spectroscopy using LCModel</atitle><jtitle>Magnetic resonance imaging</jtitle><addtitle>Magn Reson Imaging</addtitle><date>2015-06-01</date><risdate>2015</risdate><volume>33</volume><issue>5</issue><spage>644</spage><epage>648</epage><pages>644-648</pages><issn>0730-725X</issn><eissn>1873-5894</eissn><abstract>Abstract Objective The objective of this study was to elucidate the influence on quantitative analysis using LCModel with the condition of echo time (TE) longer than the recommended values in the spectrum acquisition specifications. Methods A 3 T magnetic resonance system was used to perform proton magnetic resonance spectroscopy. The participants were 5 healthy volunteers and 11 patients with glioma. Data were collected at TE of 72, 144 and 288 ms. LCModel was used to quantify several metabolites ( N -acetylaspartate, creatine and phosphocreatine, and choline-containing compounds). The results were compared with quantitative values obtained by using the T2-corrected internal reference method. Results In healthy volunteers, when TE was long, the quantitative values obtained using LCModel were up to 6.8-fold larger (p < 0.05) than those obtained using the T2-corrected internal reference method. The ratios of the quantitative values obtained by the two methods differed between metabolites (p < 0.05). In patients with glioma, the ratios of quantitative values obtained by the two methods tended to be larger at longer TE, similarly to the case of healthy volunteers, and large between-individual variation in the ratios was observed. Conclusions In clinical practice, TE is sometimes set longer than the value recommended for LCModel. If TE is long, LCModel overestimates the quantitative value since it cannot compensate for signal attenuation, and this effect is different for each metabolite and condition. Therefore, if TE is longer than recommended, it is necessary to account for the possibly reduced reliability of quantitative values calculated using LCModel.</abstract><cop>Netherlands</cop><pub>Elsevier Inc</pub><pmid>25623808</pmid><doi>10.1016/j.mri.2015.01.015</doi><tpages>5</tpages></addata></record> |
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subjects | Aspartic Acid - analogs & derivatives Aspartic Acid - metabolism Brain - metabolism Brain Neoplasms - metabolism Choline - metabolism Creatine - metabolism Echo time Glioma - metabolism Humans Image Processing, Computer-Assisted - methods LCModel Models, Theoretical MRS Phosphocreatine - metabolism Proton Magnetic Resonance Spectroscopy - methods Quantitative analysis Radiology Reproducibility of Results T2 relaxation |
title | Influence of echo time in quantitative proton MR spectroscopy using LCModel |
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