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UCEPR: Ultrafast localized CEST-spectroscopy with PRESS in phantoms and in vivo
Purpose Chemical exchange saturation transfer (CEST) is a contrast mechanism enhancing low‐concentration molecules through saturation transfer from their exchangeable protons to bulk water. Often many scans are acquired to form a Z‐spectrum, making the CEST method time‐consuming. Here, an ultrafast...
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Published in: | Magnetic resonance in medicine 2016-05, Vol.75 (5), p.1875-1885 |
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container_title | Magnetic resonance in medicine |
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creator | Liu, Zheng Dimitrov, Ivan E. Lenkinski, Robert E. Hajibeigi, Asghar Vinogradov, Elena |
description | Purpose
Chemical exchange saturation transfer (CEST) is a contrast mechanism enhancing low‐concentration molecules through saturation transfer from their exchangeable protons to bulk water. Often many scans are acquired to form a Z‐spectrum, making the CEST method time‐consuming. Here, an ultrafast localized CEST‐spectroscopy with PRESS (UCEPR) is proposed to obtain the entire Z‐spectrum of a voxel using only two scans, significantly accelerating CEST.
Theory and Methods
The approach combines ultrafast nonlocalized CEST spectroscopy with localization using PRESS. A field gradient is applied concurrently with the saturation pulse producing simultaneous saturation of all Z‐spectrum frequencies that are also spatially encoded. A readout gradient during data acquisition resolves the spatial dependence of the CEST responses into frequency. UCEPR was tested on a 3T scanner both in phantoms and in vivo.
Results
In phantoms, a fast Z‐spectroscopy acquisition of multiple pH‐variant iopamidol samples was achieved with four‐ to seven‐fold acceleration as compared to the conventional CEST methods. In vivo, amide proton transfer (APT) in white matter of healthy human brain was measured rapidly in 48 s and with high frequency resolution (≤ 0.2 ppm).
Conclusion
Compared with conventional CEST methods, UCEPR has the advantage of rapidly acquiring high‐resolution Z‐spectra. Potential in vivo applications include ultrafast localized Z‐spectroscopy, quantitative, or dynamic CEST studies. Magn Reson Med 75:1875–1885, 2016. © 2015 Wiley Periodicals, Inc. |
doi_str_mv | 10.1002/mrm.25780 |
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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4663188</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>4022848901</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4800-5307af69d6ff701a0ca8ce3c62755d5a0848821c14634f61720d71842f78c67b3</originalsourceid><addsrcrecordid>eNqNkU9v0zAYxi0EYmXswBdAkbjsku31f4cDEqq6DandqnYVEhfLcxzqkcQhTju6T0_ajgo47WDZ1vt7Hj_yg9A7DGcYgJxXbXVGuFTwAg0wJyQlPGMv0QAkg5TijB2hNzHeA0CWSfYaHREBlFIuB-hmMRxNZx-TRdm1pjCxS8pgTekfXZ4MR_PbNDbOdm2INjSb5MF3y2Q6G83nia-TZmnqLlQxMXW-va_9OrxFrwpTRnfytB-jxcXodniVjm8uvww_j1PLFEDKKUhTiCwXRSEBG7BGWUetIJLznBtQTCmCLWaCskJgSSCXWDFSSGWFvKPH6NPet1ndVS63ru7zl7ppfWXajQ7G638ntV_q72GtmRAUK9UbnD4ZtOHnysVOVz5aV5amdmEVNZZKZqJf5Dko5pRJLnv0w3_ofVi1df8TOwoykrHt2-__Dn9I_aeWHjjfAw--dJvDHIPe9q37vvWubz2ZTXaHXpHuFT527tdBYdofWkgquf56fanlNZt-G0-4zuhvfQWprg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1781092948</pqid></control><display><type>article</type><title>UCEPR: Ultrafast localized CEST-spectroscopy with PRESS in phantoms and in vivo</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Liu, Zheng ; Dimitrov, Ivan E. ; Lenkinski, Robert E. ; Hajibeigi, Asghar ; Vinogradov, Elena</creator><creatorcontrib>Liu, Zheng ; Dimitrov, Ivan E. ; Lenkinski, Robert E. ; Hajibeigi, Asghar ; Vinogradov, Elena</creatorcontrib><description>Purpose
Chemical exchange saturation transfer (CEST) is a contrast mechanism enhancing low‐concentration molecules through saturation transfer from their exchangeable protons to bulk water. Often many scans are acquired to form a Z‐spectrum, making the CEST method time‐consuming. Here, an ultrafast localized CEST‐spectroscopy with PRESS (UCEPR) is proposed to obtain the entire Z‐spectrum of a voxel using only two scans, significantly accelerating CEST.
Theory and Methods
The approach combines ultrafast nonlocalized CEST spectroscopy with localization using PRESS. A field gradient is applied concurrently with the saturation pulse producing simultaneous saturation of all Z‐spectrum frequencies that are also spatially encoded. A readout gradient during data acquisition resolves the spatial dependence of the CEST responses into frequency. UCEPR was tested on a 3T scanner both in phantoms and in vivo.
Results
In phantoms, a fast Z‐spectroscopy acquisition of multiple pH‐variant iopamidol samples was achieved with four‐ to seven‐fold acceleration as compared to the conventional CEST methods. In vivo, amide proton transfer (APT) in white matter of healthy human brain was measured rapidly in 48 s and with high frequency resolution (≤ 0.2 ppm).
Conclusion
Compared with conventional CEST methods, UCEPR has the advantage of rapidly acquiring high‐resolution Z‐spectra. Potential in vivo applications include ultrafast localized Z‐spectroscopy, quantitative, or dynamic CEST studies. Magn Reson Med 75:1875–1885, 2016. © 2015 Wiley Periodicals, Inc.</description><identifier>ISSN: 0740-3194</identifier><identifier>EISSN: 1522-2594</identifier><identifier>DOI: 10.1002/mrm.25780</identifier><identifier>PMID: 26033357</identifier><identifier>CODEN: MRMEEN</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>APT ; Brain - diagnostic imaging ; Brain - physiology ; broadband saturation ; Contrast Media - chemistry ; Healthy Volunteers ; Humans ; Hydrogen-Ion Concentration ; Image Processing, Computer-Assisted - methods ; iopamidol ; Iopamidol - chemistry ; Magnetic Resonance Imaging ; Methods ; Phantoms, Imaging ; PRESS ; Protons ; Radio Waves ; Spectrophotometry - methods ; Spectrum analysis ; ultrafast localized CEST ; Water - chemistry</subject><ispartof>Magnetic resonance in medicine, 2016-05, Vol.75 (5), p.1875-1885</ispartof><rights>2015 Wiley Periodicals, Inc.</rights><rights>2016 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4800-5307af69d6ff701a0ca8ce3c62755d5a0848821c14634f61720d71842f78c67b3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26033357$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Zheng</creatorcontrib><creatorcontrib>Dimitrov, Ivan E.</creatorcontrib><creatorcontrib>Lenkinski, Robert E.</creatorcontrib><creatorcontrib>Hajibeigi, Asghar</creatorcontrib><creatorcontrib>Vinogradov, Elena</creatorcontrib><title>UCEPR: Ultrafast localized CEST-spectroscopy with PRESS in phantoms and in vivo</title><title>Magnetic resonance in medicine</title><addtitle>Magn. Reson. Med</addtitle><description>Purpose
Chemical exchange saturation transfer (CEST) is a contrast mechanism enhancing low‐concentration molecules through saturation transfer from their exchangeable protons to bulk water. Often many scans are acquired to form a Z‐spectrum, making the CEST method time‐consuming. Here, an ultrafast localized CEST‐spectroscopy with PRESS (UCEPR) is proposed to obtain the entire Z‐spectrum of a voxel using only two scans, significantly accelerating CEST.
Theory and Methods
The approach combines ultrafast nonlocalized CEST spectroscopy with localization using PRESS. A field gradient is applied concurrently with the saturation pulse producing simultaneous saturation of all Z‐spectrum frequencies that are also spatially encoded. A readout gradient during data acquisition resolves the spatial dependence of the CEST responses into frequency. UCEPR was tested on a 3T scanner both in phantoms and in vivo.
Results
In phantoms, a fast Z‐spectroscopy acquisition of multiple pH‐variant iopamidol samples was achieved with four‐ to seven‐fold acceleration as compared to the conventional CEST methods. In vivo, amide proton transfer (APT) in white matter of healthy human brain was measured rapidly in 48 s and with high frequency resolution (≤ 0.2 ppm).
Conclusion
Compared with conventional CEST methods, UCEPR has the advantage of rapidly acquiring high‐resolution Z‐spectra. Potential in vivo applications include ultrafast localized Z‐spectroscopy, quantitative, or dynamic CEST studies. Magn Reson Med 75:1875–1885, 2016. © 2015 Wiley Periodicals, Inc.</description><subject>APT</subject><subject>Brain - diagnostic imaging</subject><subject>Brain - physiology</subject><subject>broadband saturation</subject><subject>Contrast Media - chemistry</subject><subject>Healthy Volunteers</subject><subject>Humans</subject><subject>Hydrogen-Ion Concentration</subject><subject>Image Processing, Computer-Assisted - methods</subject><subject>iopamidol</subject><subject>Iopamidol - chemistry</subject><subject>Magnetic Resonance Imaging</subject><subject>Methods</subject><subject>Phantoms, Imaging</subject><subject>PRESS</subject><subject>Protons</subject><subject>Radio Waves</subject><subject>Spectrophotometry - methods</subject><subject>Spectrum analysis</subject><subject>ultrafast localized CEST</subject><subject>Water - chemistry</subject><issn>0740-3194</issn><issn>1522-2594</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqNkU9v0zAYxi0EYmXswBdAkbjsku31f4cDEqq6DandqnYVEhfLcxzqkcQhTju6T0_ajgo47WDZ1vt7Hj_yg9A7DGcYgJxXbXVGuFTwAg0wJyQlPGMv0QAkg5TijB2hNzHeA0CWSfYaHREBlFIuB-hmMRxNZx-TRdm1pjCxS8pgTekfXZ4MR_PbNDbOdm2INjSb5MF3y2Q6G83nia-TZmnqLlQxMXW-va_9OrxFrwpTRnfytB-jxcXodniVjm8uvww_j1PLFEDKKUhTiCwXRSEBG7BGWUetIJLznBtQTCmCLWaCskJgSSCXWDFSSGWFvKPH6NPet1ndVS63ru7zl7ppfWXajQ7G638ntV_q72GtmRAUK9UbnD4ZtOHnysVOVz5aV5amdmEVNZZKZqJf5Dko5pRJLnv0w3_ofVi1df8TOwoykrHt2-__Dn9I_aeWHjjfAw--dJvDHIPe9q37vvWubz2ZTXaHXpHuFT527tdBYdofWkgquf56fanlNZt-G0-4zuhvfQWprg</recordid><startdate>201605</startdate><enddate>201605</enddate><creator>Liu, Zheng</creator><creator>Dimitrov, Ivan E.</creator><creator>Lenkinski, Robert E.</creator><creator>Hajibeigi, Asghar</creator><creator>Vinogradov, Elena</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>8FD</scope><scope>FR3</scope><scope>K9.</scope><scope>M7Z</scope><scope>P64</scope><scope>7X8</scope><scope>7QO</scope><scope>5PM</scope></search><sort><creationdate>201605</creationdate><title>UCEPR: Ultrafast localized CEST-spectroscopy with PRESS in phantoms and in vivo</title><author>Liu, Zheng ; Dimitrov, Ivan E. ; Lenkinski, Robert E. ; Hajibeigi, Asghar ; Vinogradov, Elena</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4800-5307af69d6ff701a0ca8ce3c62755d5a0848821c14634f61720d71842f78c67b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>APT</topic><topic>Brain - diagnostic imaging</topic><topic>Brain - physiology</topic><topic>broadband saturation</topic><topic>Contrast Media - chemistry</topic><topic>Healthy Volunteers</topic><topic>Humans</topic><topic>Hydrogen-Ion Concentration</topic><topic>Image Processing, Computer-Assisted - methods</topic><topic>iopamidol</topic><topic>Iopamidol - chemistry</topic><topic>Magnetic Resonance Imaging</topic><topic>Methods</topic><topic>Phantoms, Imaging</topic><topic>PRESS</topic><topic>Protons</topic><topic>Radio Waves</topic><topic>Spectrophotometry - methods</topic><topic>Spectrum analysis</topic><topic>ultrafast localized CEST</topic><topic>Water - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Zheng</creatorcontrib><creatorcontrib>Dimitrov, Ivan E.</creatorcontrib><creatorcontrib>Lenkinski, Robert E.</creatorcontrib><creatorcontrib>Hajibeigi, Asghar</creatorcontrib><creatorcontrib>Vinogradov, Elena</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biochemistry Abstracts 1</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Biotechnology Research Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Magnetic resonance in medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Zheng</au><au>Dimitrov, Ivan E.</au><au>Lenkinski, Robert E.</au><au>Hajibeigi, Asghar</au><au>Vinogradov, Elena</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>UCEPR: Ultrafast localized CEST-spectroscopy with PRESS in phantoms and in vivo</atitle><jtitle>Magnetic resonance in medicine</jtitle><addtitle>Magn. Reson. Med</addtitle><date>2016-05</date><risdate>2016</risdate><volume>75</volume><issue>5</issue><spage>1875</spage><epage>1885</epage><pages>1875-1885</pages><issn>0740-3194</issn><eissn>1522-2594</eissn><coden>MRMEEN</coden><abstract>Purpose
Chemical exchange saturation transfer (CEST) is a contrast mechanism enhancing low‐concentration molecules through saturation transfer from their exchangeable protons to bulk water. Often many scans are acquired to form a Z‐spectrum, making the CEST method time‐consuming. Here, an ultrafast localized CEST‐spectroscopy with PRESS (UCEPR) is proposed to obtain the entire Z‐spectrum of a voxel using only two scans, significantly accelerating CEST.
Theory and Methods
The approach combines ultrafast nonlocalized CEST spectroscopy with localization using PRESS. A field gradient is applied concurrently with the saturation pulse producing simultaneous saturation of all Z‐spectrum frequencies that are also spatially encoded. A readout gradient during data acquisition resolves the spatial dependence of the CEST responses into frequency. UCEPR was tested on a 3T scanner both in phantoms and in vivo.
Results
In phantoms, a fast Z‐spectroscopy acquisition of multiple pH‐variant iopamidol samples was achieved with four‐ to seven‐fold acceleration as compared to the conventional CEST methods. In vivo, amide proton transfer (APT) in white matter of healthy human brain was measured rapidly in 48 s and with high frequency resolution (≤ 0.2 ppm).
Conclusion
Compared with conventional CEST methods, UCEPR has the advantage of rapidly acquiring high‐resolution Z‐spectra. Potential in vivo applications include ultrafast localized Z‐spectroscopy, quantitative, or dynamic CEST studies. Magn Reson Med 75:1875–1885, 2016. © 2015 Wiley Periodicals, Inc.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>26033357</pmid><doi>10.1002/mrm.25780</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record> |
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subjects | APT Brain - diagnostic imaging Brain - physiology broadband saturation Contrast Media - chemistry Healthy Volunteers Humans Hydrogen-Ion Concentration Image Processing, Computer-Assisted - methods iopamidol Iopamidol - chemistry Magnetic Resonance Imaging Methods Phantoms, Imaging PRESS Protons Radio Waves Spectrophotometry - methods Spectrum analysis ultrafast localized CEST Water - chemistry |
title | UCEPR: Ultrafast localized CEST-spectroscopy with PRESS in phantoms and in vivo |
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