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
Hauptverfasser: Yamamoto, Tetsuya, Isobe, Tomonori, Akutsu, Hiroyoshi, Masumoto, Tomohiko, Ando, Hiroki, Sato, Eisuke, Takada, Kenta, Anno, Izumi, Matsumura, Akira
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container_end_page 648
container_issue 5
container_start_page 644
container_title Magnetic resonance imaging
container_volume 33
creator Yamamoto, Tetsuya
Isobe, Tomonori
Akutsu, Hiroyoshi
Masumoto, Tomohiko
Ando, Hiroki
Sato, Eisuke
Takada, Kenta
Anno, Izumi
Matsumura, Akira
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 &lt; 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 &lt; 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 &amp; 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. 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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 &lt; 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 &lt; 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 &amp; 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 &amp; 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 &lt; 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 &lt; 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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