Confounder-corrected T 1 mapping in the liver through simultaneous estimation of T 1 , PDFF, R 2 , and B 1 + in a single breath-hold acquisition
Quantitative volumetric T mapping in the liver has the potential to aid in the detection, diagnosis, and quantification of liver fibrosis, inflammation, and spatially resolved liver function. However, accurate measurement of hepatic T is confounded by the presence of fat and inhomogeneous excitation...
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Veröffentlicht in: | Magnetic resonance in medicine 2023-06, Vol.89 (6), p.2186 |
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creator | Roberts, Nathan T Tamada, Daiki Muslu, Yavuz Hernando, Diego Reeder, Scott B |
description | Quantitative volumetric T
mapping in the liver has the potential to aid in the detection, diagnosis, and quantification of liver fibrosis, inflammation, and spatially resolved liver function. However, accurate measurement of hepatic T
is confounded by the presence of fat and inhomogeneous
excitation. Furthermore, scan time constraints related to respiratory motion require tradeoffs of reduced volumetric coverage and/or increased acquisition time. This work presents a novel 3D acquisition and estimation method for confounder-corrected T
measurement over the entire liver within a single breath-hold through simultaneous estimation of T
, fat and
.
The proposed method combines chemical shift encoded MRI and variable flip angle MRI with a
mapping technique to enable confounder-corrected T
mapping. The method was evaluated theoretically and demonstrated in both phantom and in vivo acquisitions at 1.5 and 3.0T. At 1.5T, the method was evaluated both pre- and post- contrast enhancement in healthy volunteers.
The proposed method demonstrated excellent linear agreement with reference inversion-recovery spin-echo based T
in phantom acquisitions at both 1.5 and 3.0T, with minimal bias (5.2 and 45 ms, respectively) over T
ranging from 200-1200 ms. In vivo results were in general agreement with reference saturation-recovery based 2D T
maps (SMART
Map, GE Healthcare).
The proposed 3D T
mapping method accounts for fat and
confounders through simultaneous estimation of T
,
, PDFF and
. It demonstrates strong linear agreement with reference T
measurements, with low bias and high precision, and can achieve full liver coverage in a single breath-hold. |
doi_str_mv | 10.1002/mrm.29590 |
format | Article |
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mapping in the liver has the potential to aid in the detection, diagnosis, and quantification of liver fibrosis, inflammation, and spatially resolved liver function. However, accurate measurement of hepatic T
is confounded by the presence of fat and inhomogeneous
excitation. Furthermore, scan time constraints related to respiratory motion require tradeoffs of reduced volumetric coverage and/or increased acquisition time. This work presents a novel 3D acquisition and estimation method for confounder-corrected T
measurement over the entire liver within a single breath-hold through simultaneous estimation of T
, fat and
.
The proposed method combines chemical shift encoded MRI and variable flip angle MRI with a
mapping technique to enable confounder-corrected T
mapping. The method was evaluated theoretically and demonstrated in both phantom and in vivo acquisitions at 1.5 and 3.0T. At 1.5T, the method was evaluated both pre- and post- contrast enhancement in healthy volunteers.
The proposed method demonstrated excellent linear agreement with reference inversion-recovery spin-echo based T
in phantom acquisitions at both 1.5 and 3.0T, with minimal bias (5.2 and 45 ms, respectively) over T
ranging from 200-1200 ms. In vivo results were in general agreement with reference saturation-recovery based 2D T
maps (SMART
Map, GE Healthcare).
The proposed 3D T
mapping method accounts for fat and
confounders through simultaneous estimation of T
,
, PDFF and
. It demonstrates strong linear agreement with reference T
measurements, with low bias and high precision, and can achieve full liver coverage in a single breath-hold.</description><identifier>EISSN: 1522-2594</identifier><identifier>DOI: 10.1002/mrm.29590</identifier><identifier>PMID: 36656152</identifier><language>eng</language><publisher>United States</publisher><subject>Breath Holding ; Humans ; Liver - diagnostic imaging ; Liver - pathology ; Liver Cirrhosis ; Magnetic Resonance Imaging - methods ; Non-alcoholic Fatty Liver Disease - pathology ; Phantoms, Imaging ; Reproducibility of Results</subject><ispartof>Magnetic resonance in medicine, 2023-06, Vol.89 (6), p.2186</ispartof><rights>2023 The Authors. Magnetic Resonance in Medicine published by Wiley Periodicals LLC on behalf of International Society for Magnetic Resonance in Medicine.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0002-0016-0317 ; 0000-0003-4728-8171 ; 0000-0003-3615-459X ; 0000-0002-2369-3378 ; 0000-0002-5363-8935</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36656152$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Roberts, Nathan T</creatorcontrib><creatorcontrib>Tamada, Daiki</creatorcontrib><creatorcontrib>Muslu, Yavuz</creatorcontrib><creatorcontrib>Hernando, Diego</creatorcontrib><creatorcontrib>Reeder, Scott B</creatorcontrib><title>Confounder-corrected T 1 mapping in the liver through simultaneous estimation of T 1 , PDFF, R 2 , and B 1 + in a single breath-hold acquisition</title><title>Magnetic resonance in medicine</title><addtitle>Magn Reson Med</addtitle><description>Quantitative volumetric T
mapping in the liver has the potential to aid in the detection, diagnosis, and quantification of liver fibrosis, inflammation, and spatially resolved liver function. However, accurate measurement of hepatic T
is confounded by the presence of fat and inhomogeneous
excitation. Furthermore, scan time constraints related to respiratory motion require tradeoffs of reduced volumetric coverage and/or increased acquisition time. This work presents a novel 3D acquisition and estimation method for confounder-corrected T
measurement over the entire liver within a single breath-hold through simultaneous estimation of T
, fat and
.
The proposed method combines chemical shift encoded MRI and variable flip angle MRI with a
mapping technique to enable confounder-corrected T
mapping. The method was evaluated theoretically and demonstrated in both phantom and in vivo acquisitions at 1.5 and 3.0T. At 1.5T, the method was evaluated both pre- and post- contrast enhancement in healthy volunteers.
The proposed method demonstrated excellent linear agreement with reference inversion-recovery spin-echo based T
in phantom acquisitions at both 1.5 and 3.0T, with minimal bias (5.2 and 45 ms, respectively) over T
ranging from 200-1200 ms. In vivo results were in general agreement with reference saturation-recovery based 2D T
maps (SMART
Map, GE Healthcare).
The proposed 3D T
mapping method accounts for fat and
confounders through simultaneous estimation of T
,
, PDFF and
. It demonstrates strong linear agreement with reference T
measurements, with low bias and high precision, and can achieve full liver coverage in a single breath-hold.</description><subject>Breath Holding</subject><subject>Humans</subject><subject>Liver - diagnostic imaging</subject><subject>Liver - pathology</subject><subject>Liver Cirrhosis</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Non-alcoholic Fatty Liver Disease - pathology</subject><subject>Phantoms, Imaging</subject><subject>Reproducibility of Results</subject><issn>1522-2594</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kMtOwzAURC0kREthwQ-gu6cBx3k0XkKhgFQJhMq6un6kMUrsYDtI_AWfTMpjNaO5miPdIeQspZcppeyq890l4wWnB2SaFowlrOD5hByH8EYp5XyRH5FJVpZFOV6n5GvpbO0Gq7RPpPNey6gVbCCFDvve2B0YC7HR0JoP7Ufn3bBrIJhuaCNa7YYAOkTTYTTOgqt_unN4vl2t5vACbPRoFdyM6cWehWPX7loNwmuMTdK4VgHK98EEs0eckMMa26BP_3RGXld3m-VDsn66f1xer5M-pVVM9CLPGFaCSixFKTlWjOaZEsiRa8G5FAx5VVc5ywuqqBKS1wqxFrrEPBMim5HzX24_iE6rbe_HH_zn9n-a7BspkGNV</recordid><startdate>202306</startdate><enddate>202306</enddate><creator>Roberts, Nathan T</creator><creator>Tamada, Daiki</creator><creator>Muslu, Yavuz</creator><creator>Hernando, Diego</creator><creator>Reeder, Scott B</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><orcidid>https://orcid.org/0000-0002-0016-0317</orcidid><orcidid>https://orcid.org/0000-0003-4728-8171</orcidid><orcidid>https://orcid.org/0000-0003-3615-459X</orcidid><orcidid>https://orcid.org/0000-0002-2369-3378</orcidid><orcidid>https://orcid.org/0000-0002-5363-8935</orcidid></search><sort><creationdate>202306</creationdate><title>Confounder-corrected T 1 mapping in the liver through simultaneous estimation of T 1 , PDFF, R 2 , and B 1 + in a single breath-hold acquisition</title><author>Roberts, Nathan T ; Tamada, Daiki ; Muslu, Yavuz ; Hernando, Diego ; Reeder, Scott B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p108t-e7432a8b0ca6b6c9a82043dba9a9eb99cb2a98f842450d0dbc9fdaafbe6a43bb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Breath Holding</topic><topic>Humans</topic><topic>Liver - diagnostic imaging</topic><topic>Liver - pathology</topic><topic>Liver Cirrhosis</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Non-alcoholic Fatty Liver Disease - pathology</topic><topic>Phantoms, Imaging</topic><topic>Reproducibility of Results</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Roberts, Nathan T</creatorcontrib><creatorcontrib>Tamada, Daiki</creatorcontrib><creatorcontrib>Muslu, Yavuz</creatorcontrib><creatorcontrib>Hernando, Diego</creatorcontrib><creatorcontrib>Reeder, Scott B</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Magnetic resonance in medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Roberts, Nathan T</au><au>Tamada, Daiki</au><au>Muslu, Yavuz</au><au>Hernando, Diego</au><au>Reeder, Scott B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Confounder-corrected T 1 mapping in the liver through simultaneous estimation of T 1 , PDFF, R 2 , and B 1 + in a single breath-hold acquisition</atitle><jtitle>Magnetic resonance in medicine</jtitle><addtitle>Magn Reson Med</addtitle><date>2023-06</date><risdate>2023</risdate><volume>89</volume><issue>6</issue><spage>2186</spage><pages>2186-</pages><eissn>1522-2594</eissn><abstract>Quantitative volumetric T
mapping in the liver has the potential to aid in the detection, diagnosis, and quantification of liver fibrosis, inflammation, and spatially resolved liver function. However, accurate measurement of hepatic T
is confounded by the presence of fat and inhomogeneous
excitation. Furthermore, scan time constraints related to respiratory motion require tradeoffs of reduced volumetric coverage and/or increased acquisition time. This work presents a novel 3D acquisition and estimation method for confounder-corrected T
measurement over the entire liver within a single breath-hold through simultaneous estimation of T
, fat and
.
The proposed method combines chemical shift encoded MRI and variable flip angle MRI with a
mapping technique to enable confounder-corrected T
mapping. The method was evaluated theoretically and demonstrated in both phantom and in vivo acquisitions at 1.5 and 3.0T. At 1.5T, the method was evaluated both pre- and post- contrast enhancement in healthy volunteers.
The proposed method demonstrated excellent linear agreement with reference inversion-recovery spin-echo based T
in phantom acquisitions at both 1.5 and 3.0T, with minimal bias (5.2 and 45 ms, respectively) over T
ranging from 200-1200 ms. In vivo results were in general agreement with reference saturation-recovery based 2D T
maps (SMART
Map, GE Healthcare).
The proposed 3D T
mapping method accounts for fat and
confounders through simultaneous estimation of T
,
, PDFF and
. It demonstrates strong linear agreement with reference T
measurements, with low bias and high precision, and can achieve full liver coverage in a single breath-hold.</abstract><cop>United States</cop><pmid>36656152</pmid><doi>10.1002/mrm.29590</doi><orcidid>https://orcid.org/0000-0002-0016-0317</orcidid><orcidid>https://orcid.org/0000-0003-4728-8171</orcidid><orcidid>https://orcid.org/0000-0003-3615-459X</orcidid><orcidid>https://orcid.org/0000-0002-2369-3378</orcidid><orcidid>https://orcid.org/0000-0002-5363-8935</orcidid><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; Access via Wiley Online Library |
subjects | Breath Holding Humans Liver - diagnostic imaging Liver - pathology Liver Cirrhosis Magnetic Resonance Imaging - methods Non-alcoholic Fatty Liver Disease - pathology Phantoms, Imaging Reproducibility of Results |
title | Confounder-corrected T 1 mapping in the liver through simultaneous estimation of T 1 , PDFF, R 2 , and B 1 + in a single breath-hold acquisition |
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