Visualization of the saccule and utricle with non-contrast-enhanced FLAIR sequences

Objectives 3D-fluid attenuation inversion recovery (FLAIR) collected 4 h after intravenous gadolinium injection can delineate the perilymphatic space (PLS) from the endolymphatic space (ELS) to capture endolymphatic hydrops, the pathological counterpart of Ménière’s disease. We aimed to optimize vis...

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Veröffentlicht in:European radiology 2022-05, Vol.32 (5), p.3532-3540
Hauptverfasser: Fukutomi, Hikaru, Hamitouche, Lydia, Yamamoto, Takayuki, Denat, Laurent, Zhang, Lijun, Zhang, Bei, Prevost, Valentin, Triaire, Bruno, Dousset, Vincent, Barreau, Xavier, Tourdias, Thomas
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container_end_page 3540
container_issue 5
container_start_page 3532
container_title European radiology
container_volume 32
creator Fukutomi, Hikaru
Hamitouche, Lydia
Yamamoto, Takayuki
Denat, Laurent
Zhang, Lijun
Zhang, Bei
Prevost, Valentin
Triaire, Bruno
Dousset, Vincent
Barreau, Xavier
Tourdias, Thomas
description Objectives 3D-fluid attenuation inversion recovery (FLAIR) collected 4 h after intravenous gadolinium injection can delineate the perilymphatic space (PLS) from the endolymphatic space (ELS) to capture endolymphatic hydrops, the pathological counterpart of Ménière’s disease. We aimed to optimize visualization of such inner ear internal anatomy using 3D-FLAIR without injection. Methods 3D-FLAIR signal from different fluid compartments such as PLS and ELS was first simulated. Then, twenty-two healthy subjects were scanned at 3.0-T MRI with non-injected 3D-FLAIR using variable T2 preparations (T2Preps) (OFF, 200, 400, and 600 ms) and variable inversion times (TIs) (from 224 to 5000 ms) and different resolutions (1.0 × 1.0 × 1.5, 0.6 × 0.6 × 0.8, and 0.6 × 0.6 × 0.6 mm 3 ). The relative contrast between PLS and ELS and the visibility of the saccule and utricle were assessed. Additionally, non-injected 3D-FLAIR with the optimal setting was tested in a Ménière patient and compared with gadolinium-injected 3D-FLAIR. Results The PLS and ELS were differentiated when T2Prep was used but not without. The relative contrast was larger with T2Prep at 400 ms than at 200 or 600 ms (0.72 ± 0.22 vs. 0.44 ± 0.11, p  = 0.019; and 0.72 ± 0.22 vs. 0.46 ± 0.28, p  = 0.034, respectively). The saccule and utricle were best delineated in 87. % cases with T2Prep = 400 and TI = 2100 ms at the highest resolution. Visualization of the saccule and utricle in the optimized non-injected 3D-FLAIR was similar to conventional injected 3D-FLAIR in a patient. Conclusions Combining a specific T2Prep and TI in non-injected 3D-FLAIR could separate PLS and ELS and even the saccule and utricle, paving the way toward future application to diagnose Ménière’s disease. Key Points • MRI can capture the internal anatomy of inner ear without injection of contrast media. • Specific parameters consisting of a T2 preparation of 400 ms and an inversion time of 2100 ms must be used to visualize the saccule and utricle on non-injected 3D-FLAIR.
doi_str_mv 10.1007/s00330-021-08403-w
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We aimed to optimize visualization of such inner ear internal anatomy using 3D-FLAIR without injection. Methods 3D-FLAIR signal from different fluid compartments such as PLS and ELS was first simulated. Then, twenty-two healthy subjects were scanned at 3.0-T MRI with non-injected 3D-FLAIR using variable T2 preparations (T2Preps) (OFF, 200, 400, and 600 ms) and variable inversion times (TIs) (from 224 to 5000 ms) and different resolutions (1.0 × 1.0 × 1.5, 0.6 × 0.6 × 0.8, and 0.6 × 0.6 × 0.6 mm 3 ). The relative contrast between PLS and ELS and the visibility of the saccule and utricle were assessed. Additionally, non-injected 3D-FLAIR with the optimal setting was tested in a Ménière patient and compared with gadolinium-injected 3D-FLAIR. Results The PLS and ELS were differentiated when T2Prep was used but not without. The relative contrast was larger with T2Prep at 400 ms than at 200 or 600 ms (0.72 ± 0.22 vs. 0.44 ± 0.11, p  = 0.019; and 0.72 ± 0.22 vs. 0.46 ± 0.28, p  = 0.034, respectively). The saccule and utricle were best delineated in 87. % cases with T2Prep = 400 and TI = 2100 ms at the highest resolution. Visualization of the saccule and utricle in the optimized non-injected 3D-FLAIR was similar to conventional injected 3D-FLAIR in a patient. Conclusions Combining a specific T2Prep and TI in non-injected 3D-FLAIR could separate PLS and ELS and even the saccule and utricle, paving the way toward future application to diagnose Ménière’s disease. Key Points • MRI can capture the internal anatomy of inner ear without injection of contrast media. • Specific parameters consisting of a T2 preparation of 400 ms and an inversion time of 2100 ms must be used to visualize the saccule and utricle on non-injected 3D-FLAIR.</description><identifier>ISSN: 1432-1084</identifier><identifier>ISSN: 0938-7994</identifier><identifier>EISSN: 1432-1084</identifier><identifier>DOI: 10.1007/s00330-021-08403-w</identifier><identifier>PMID: 34928414</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Anatomy ; Contrast Media ; Diagnostic Radiology ; Ear ; Edema ; Endolymphatic Hydrops - diagnosis ; Gadolinium ; Gadolinium DTPA ; Head and Neck ; Humans ; Imaging ; Imaging, Three-Dimensional ; Injection ; Injections, Intravenous ; Inner ear ; Internal Medicine ; Interventional Radiology ; Intravenous administration ; Inversion ; Life Sciences ; Magnetic Resonance Imaging ; Male ; Medicine ; Medicine &amp; Public Health ; Meniere Disease - diagnostic imaging ; Meniere's disease ; Neurons and Cognition ; Neuroradiology ; Optimization ; Radiology ; Saccule ; Saccule and Utricle ; Ultrasound ; Utricle ; Visualization</subject><ispartof>European radiology, 2022-05, Vol.32 (5), p.3532-3540</ispartof><rights>The Author(s), under exclusive licence to European Society of Radiology 2021</rights><rights>2021. 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We aimed to optimize visualization of such inner ear internal anatomy using 3D-FLAIR without injection. Methods 3D-FLAIR signal from different fluid compartments such as PLS and ELS was first simulated. Then, twenty-two healthy subjects were scanned at 3.0-T MRI with non-injected 3D-FLAIR using variable T2 preparations (T2Preps) (OFF, 200, 400, and 600 ms) and variable inversion times (TIs) (from 224 to 5000 ms) and different resolutions (1.0 × 1.0 × 1.5, 0.6 × 0.6 × 0.8, and 0.6 × 0.6 × 0.6 mm 3 ). The relative contrast between PLS and ELS and the visibility of the saccule and utricle were assessed. Additionally, non-injected 3D-FLAIR with the optimal setting was tested in a Ménière patient and compared with gadolinium-injected 3D-FLAIR. Results The PLS and ELS were differentiated when T2Prep was used but not without. The relative contrast was larger with T2Prep at 400 ms than at 200 or 600 ms (0.72 ± 0.22 vs. 0.44 ± 0.11, p  = 0.019; and 0.72 ± 0.22 vs. 0.46 ± 0.28, p  = 0.034, respectively). The saccule and utricle were best delineated in 87. % cases with T2Prep = 400 and TI = 2100 ms at the highest resolution. Visualization of the saccule and utricle in the optimized non-injected 3D-FLAIR was similar to conventional injected 3D-FLAIR in a patient. Conclusions Combining a specific T2Prep and TI in non-injected 3D-FLAIR could separate PLS and ELS and even the saccule and utricle, paving the way toward future application to diagnose Ménière’s disease. Key Points • MRI can capture the internal anatomy of inner ear without injection of contrast media. • Specific parameters consisting of a T2 preparation of 400 ms and an inversion time of 2100 ms must be used to visualize the saccule and utricle on non-injected 3D-FLAIR.</description><subject>Anatomy</subject><subject>Contrast Media</subject><subject>Diagnostic Radiology</subject><subject>Ear</subject><subject>Edema</subject><subject>Endolymphatic Hydrops - diagnosis</subject><subject>Gadolinium</subject><subject>Gadolinium DTPA</subject><subject>Head and Neck</subject><subject>Humans</subject><subject>Imaging</subject><subject>Imaging, Three-Dimensional</subject><subject>Injection</subject><subject>Injections, Intravenous</subject><subject>Inner ear</subject><subject>Internal Medicine</subject><subject>Interventional Radiology</subject><subject>Intravenous administration</subject><subject>Inversion</subject><subject>Life Sciences</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Meniere Disease - diagnostic imaging</subject><subject>Meniere's disease</subject><subject>Neurons and Cognition</subject><subject>Neuroradiology</subject><subject>Optimization</subject><subject>Radiology</subject><subject>Saccule</subject><subject>Saccule and Utricle</subject><subject>Ultrasound</subject><subject>Utricle</subject><subject>Visualization</subject><issn>1432-1084</issn><issn>0938-7994</issn><issn>1432-1084</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kU1vFDEMhiNERUvhD3BAI3Eph4Cdj53JcVVRWmklpPJxjdKMw041m5RkhlX59aRMKYgDJ9vx49eOXsZeILxBgPZtAZASOAjk0CmQfP-IHaGSgmOtH_-VH7KnpVwDgEHVPmGHUhnRKVRH7OOXocxuHH64aUixSaGZttQU5_08UuNi38xTHnzN98O0bWKK3Kc4ZVcmTnHroqe-OdusLy6bQt9mqnV5xg6CGws9v4_H7PPZu0-n53zz4f3F6XrDvQIzcR-oNXqlFAjyQncIGg0FHZSSTgcXsPMgWiJD2vQeV1Lqlq686rvQIoE8Zq8X3a0b7U0edi7f2uQGe77e2Ls3qNItSv0dK3uysDc51TPLZHdD8TSOLlKaixUrFKDQdF1FX_2DXqc5x_qTSmnVCWXAVEoslM-plEzh4QIEe2ePXeyx1R77yx67r0Mv76Xnqx31DyO__aiAXIBSW_Er5T-7_yP7E5j_mVc</recordid><startdate>20220501</startdate><enddate>20220501</enddate><creator>Fukutomi, Hikaru</creator><creator>Hamitouche, Lydia</creator><creator>Yamamoto, Takayuki</creator><creator>Denat, Laurent</creator><creator>Zhang, Lijun</creator><creator>Zhang, Bei</creator><creator>Prevost, Valentin</creator><creator>Triaire, Bruno</creator><creator>Dousset, Vincent</creator><creator>Barreau, Xavier</creator><creator>Tourdias, Thomas</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><general>Springer Verlag</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>3V.</scope><scope>7QO</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>1XC</scope><orcidid>https://orcid.org/0000-0002-7151-6325</orcidid></search><sort><creationdate>20220501</creationdate><title>Visualization of the saccule and utricle with non-contrast-enhanced FLAIR sequences</title><author>Fukutomi, Hikaru ; 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Public Health</topic><topic>Meniere Disease - diagnostic imaging</topic><topic>Meniere's disease</topic><topic>Neurons and Cognition</topic><topic>Neuroradiology</topic><topic>Optimization</topic><topic>Radiology</topic><topic>Saccule</topic><topic>Saccule and Utricle</topic><topic>Ultrasound</topic><topic>Utricle</topic><topic>Visualization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fukutomi, Hikaru</creatorcontrib><creatorcontrib>Hamitouche, Lydia</creatorcontrib><creatorcontrib>Yamamoto, Takayuki</creatorcontrib><creatorcontrib>Denat, Laurent</creatorcontrib><creatorcontrib>Zhang, Lijun</creatorcontrib><creatorcontrib>Zhang, Bei</creatorcontrib><creatorcontrib>Prevost, Valentin</creatorcontrib><creatorcontrib>Triaire, Bruno</creatorcontrib><creatorcontrib>Dousset, Vincent</creatorcontrib><creatorcontrib>Barreau, Xavier</creatorcontrib><creatorcontrib>Tourdias, Thomas</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Proquest Nursing &amp; 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We aimed to optimize visualization of such inner ear internal anatomy using 3D-FLAIR without injection. Methods 3D-FLAIR signal from different fluid compartments such as PLS and ELS was first simulated. Then, twenty-two healthy subjects were scanned at 3.0-T MRI with non-injected 3D-FLAIR using variable T2 preparations (T2Preps) (OFF, 200, 400, and 600 ms) and variable inversion times (TIs) (from 224 to 5000 ms) and different resolutions (1.0 × 1.0 × 1.5, 0.6 × 0.6 × 0.8, and 0.6 × 0.6 × 0.6 mm 3 ). The relative contrast between PLS and ELS and the visibility of the saccule and utricle were assessed. Additionally, non-injected 3D-FLAIR with the optimal setting was tested in a Ménière patient and compared with gadolinium-injected 3D-FLAIR. Results The PLS and ELS were differentiated when T2Prep was used but not without. The relative contrast was larger with T2Prep at 400 ms than at 200 or 600 ms (0.72 ± 0.22 vs. 0.44 ± 0.11, p  = 0.019; and 0.72 ± 0.22 vs. 0.46 ± 0.28, p  = 0.034, respectively). The saccule and utricle were best delineated in 87. % cases with T2Prep = 400 and TI = 2100 ms at the highest resolution. Visualization of the saccule and utricle in the optimized non-injected 3D-FLAIR was similar to conventional injected 3D-FLAIR in a patient. Conclusions Combining a specific T2Prep and TI in non-injected 3D-FLAIR could separate PLS and ELS and even the saccule and utricle, paving the way toward future application to diagnose Ménière’s disease. Key Points • MRI can capture the internal anatomy of inner ear without injection of contrast media. • Specific parameters consisting of a T2 preparation of 400 ms and an inversion time of 2100 ms must be used to visualize the saccule and utricle on non-injected 3D-FLAIR.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>34928414</pmid><doi>10.1007/s00330-021-08403-w</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0002-7151-6325</orcidid></addata></record>
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source MEDLINE; Springer Nature - Complete Springer Journals
subjects Anatomy
Contrast Media
Diagnostic Radiology
Ear
Edema
Endolymphatic Hydrops - diagnosis
Gadolinium
Gadolinium DTPA
Head and Neck
Humans
Imaging
Imaging, Three-Dimensional
Injection
Injections, Intravenous
Inner ear
Internal Medicine
Interventional Radiology
Intravenous administration
Inversion
Life Sciences
Magnetic Resonance Imaging
Male
Medicine
Medicine & Public Health
Meniere Disease - diagnostic imaging
Meniere's disease
Neurons and Cognition
Neuroradiology
Optimization
Radiology
Saccule
Saccule and Utricle
Ultrasound
Utricle
Visualization
title Visualization of the saccule and utricle with non-contrast-enhanced FLAIR sequences
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