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Value of Longitudinal Strain to Identify Wild-Type Transthyretin Amyloidosis in Patients With Aortic Stenosis
Background:Wild-type transthyretin-related amyloidosis (ATTRwt) and degenerative aortic stenosis (AS) are both age-related. Diagnosis of cardiac amyloidosis (CA) among patients with AS may be difficult due to overlapping morphological and functional criteria. The aim of this study was to describe an...
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Published in: | Circulation Journal 2021/08/25, Vol.85(9), pp.1494-1504 |
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creator | Robin, Guillaume Cognet, Thomas Bouisset, Frédéric Cariou, Eve Méjean, Simon Pradel, Sarah Colombat, Magali Galinier, Michel Carrié, Didier Lairez, Olivier on behalf of the Toulouse Amyloidosis Research Network Collaborators |
description | Background:Wild-type transthyretin-related amyloidosis (ATTRwt) and degenerative aortic stenosis (AS) are both age-related. Diagnosis of cardiac amyloidosis (CA) among patients with AS may be difficult due to overlapping morphological and functional criteria. The aim of this study was to describe an echocardiographic longitudinal strain (LS) pattern among patients with AS with and without ATTRwt.Methods and Results:Patients who have AS with ATTRwt (n=30), AS without ATTRwt (n=50) and ATTRwt without AS (n=31) underwent two-dimensional speckle-tracking echocardiography. Transthyretin CA was based on positive bone scintigraphy without monoclonal gammopathy. All patients showed a gradual decrease in LS from the base to the apex resulting in a decrease of the global LS. A cut-off value of 1.0 for relative apical LS (average apical LS/[average basal LS+mid-LS]) was sensitive (88%) but less specific (68%) in differentiating ATTRwt among patients with severe AS. The best cut-off value for relative apical LS for identifying patients with ATTRwt among the whole population was 0.9 (sensitivity 74%, specificity 66%); however, 35%, 25% and 11% of patients who have ATTRwt without AS, with moderate AS and with severe AS, respectively, did not reach this threshold.Conclusions:A decrease of global and relative apical LS is common in patients with AS, even in the absence of ATTRwt. ATTRwt CA can be present even in the absence of relative apical sparing of LS. |
doi_str_mv | 10.1253/circj.CJ-20-1064 |
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Diagnosis of cardiac amyloidosis (CA) among patients with AS may be difficult due to overlapping morphological and functional criteria. The aim of this study was to describe an echocardiographic longitudinal strain (LS) pattern among patients with AS with and without ATTRwt.Methods and Results:Patients who have AS with ATTRwt (n=30), AS without ATTRwt (n=50) and ATTRwt without AS (n=31) underwent two-dimensional speckle-tracking echocardiography. Transthyretin CA was based on positive bone scintigraphy without monoclonal gammopathy. All patients showed a gradual decrease in LS from the base to the apex resulting in a decrease of the global LS. A cut-off value of 1.0 for relative apical LS (average apical LS/[average basal LS+mid-LS]) was sensitive (88%) but less specific (68%) in differentiating ATTRwt among patients with severe AS. The best cut-off value for relative apical LS for identifying patients with ATTRwt among the whole population was 0.9 (sensitivity 74%, specificity 66%); however, 35%, 25% and 11% of patients who have ATTRwt without AS, with moderate AS and with severe AS, respectively, did not reach this threshold.Conclusions:A decrease of global and relative apical LS is common in patients with AS, even in the absence of ATTRwt. ATTRwt CA can be present even in the absence of relative apical sparing of LS.</description><identifier>ISSN: 1346-9843</identifier><identifier>ISSN: 1347-4820</identifier><identifier>EISSN: 1347-4820</identifier><identifier>DOI: 10.1253/circj.CJ-20-1064</identifier><identifier>PMID: 33980765</identifier><language>eng</language><publisher>Japan: The Japanese Circulation Society</publisher><subject>Amyloid Neuropathies, Familial - complications ; Amyloid Neuropathies, Familial - diagnostic imaging ; Aortic stenosis ; Aortic Valve Stenosis - diagnostic imaging ; Cardiac amyloidosis ; Cardiology and cardiovascular system ; Echocardiography ; Echocardiography - methods ; Human health and pathology ; Humans ; Life Sciences ; Longitudinal strain ; Tomography, X-Ray Computed</subject><ispartof>Circulation Journal, 2021/08/25, Vol.85(9), pp.1494-1504</ispartof><rights>2021, THE JAPANESE CIRCULATION SOCIETY</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c528t-aeea73ae6e1038cc915306fa791508ff993e63b7d8301034c5bb5d0e91236d723</citedby><cites>FETCH-LOGICAL-c528t-aeea73ae6e1038cc915306fa791508ff993e63b7d8301034c5bb5d0e91236d723</cites><orcidid>0000-0001-8642-0273</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33980765$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://ut3-toulouseinp.hal.science/hal-04511264$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Robin, Guillaume</creatorcontrib><creatorcontrib>Cognet, Thomas</creatorcontrib><creatorcontrib>Bouisset, Frédéric</creatorcontrib><creatorcontrib>Cariou, Eve</creatorcontrib><creatorcontrib>Méjean, Simon</creatorcontrib><creatorcontrib>Pradel, Sarah</creatorcontrib><creatorcontrib>Colombat, Magali</creatorcontrib><creatorcontrib>Galinier, Michel</creatorcontrib><creatorcontrib>Carrié, Didier</creatorcontrib><creatorcontrib>Lairez, Olivier</creatorcontrib><creatorcontrib>on behalf of the Toulouse Amyloidosis Research Network Collaborators</creatorcontrib><creatorcontrib>Toulouse Amyloidosis Research Network Collaborators</creatorcontrib><creatorcontrib>on behalf of the Toulouse Amyloidosis Research Network Collaborators</creatorcontrib><title>Value of Longitudinal Strain to Identify Wild-Type Transthyretin Amyloidosis in Patients With Aortic Stenosis</title><title>Circulation Journal</title><addtitle>Circ J</addtitle><description>Background:Wild-type transthyretin-related amyloidosis (ATTRwt) and degenerative aortic stenosis (AS) are both age-related. Diagnosis of cardiac amyloidosis (CA) among patients with AS may be difficult due to overlapping morphological and functional criteria. The aim of this study was to describe an echocardiographic longitudinal strain (LS) pattern among patients with AS with and without ATTRwt.Methods and Results:Patients who have AS with ATTRwt (n=30), AS without ATTRwt (n=50) and ATTRwt without AS (n=31) underwent two-dimensional speckle-tracking echocardiography. Transthyretin CA was based on positive bone scintigraphy without monoclonal gammopathy. All patients showed a gradual decrease in LS from the base to the apex resulting in a decrease of the global LS. A cut-off value of 1.0 for relative apical LS (average apical LS/[average basal LS+mid-LS]) was sensitive (88%) but less specific (68%) in differentiating ATTRwt among patients with severe AS. The best cut-off value for relative apical LS for identifying patients with ATTRwt among the whole population was 0.9 (sensitivity 74%, specificity 66%); however, 35%, 25% and 11% of patients who have ATTRwt without AS, with moderate AS and with severe AS, respectively, did not reach this threshold.Conclusions:A decrease of global and relative apical LS is common in patients with AS, even in the absence of ATTRwt. ATTRwt CA can be present even in the absence of relative apical sparing of LS.</description><subject>Amyloid Neuropathies, Familial - complications</subject><subject>Amyloid Neuropathies, Familial - diagnostic imaging</subject><subject>Aortic stenosis</subject><subject>Aortic Valve Stenosis - diagnostic imaging</subject><subject>Cardiac amyloidosis</subject><subject>Cardiology and cardiovascular system</subject><subject>Echocardiography</subject><subject>Echocardiography - methods</subject><subject>Human health and pathology</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Longitudinal strain</subject><subject>Tomography, X-Ray Computed</subject><issn>1346-9843</issn><issn>1347-4820</issn><issn>1347-4820</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNpFkUuP2yAURq2q1bw6-64qL9uFpxcwtllGUeelSK3UdGaJCL6eEGGTAq7kf188STMbuFyd7yz4suwTgRtCOfumjde7m-VjQaEgUJXvsgvCyrooGwrvX-eqEE3JzrPLEHYAVAAXZ9k5Y6KBuuIXWf-k7Ii56_KVG15MHFszKJv_il6ZIY8uf2hxiKab8mdj22I97TFfezWEuJ08xsQs-sk607pgQp6eP1U0KRESH7f5wvlodNLhMAMfsw-dsgGvj_dV9vv2-3p5X6x-3D0sF6tCc9rEQiGqmimskABrtBaEM6g6VacBmq4TgmHFNnXbMEhEqflmw1tAQSir2pqyq-zrwbtVVu696ZWfpFNG3i9Wct5ByQmhVfmXJPbLgd1792fEEGVvgkZr1YBuDJJyWjFgACKhcEC1dyF47E5uAnIuRL4WIpePkqZFKiRFPh_t46bH9hT430ACbg_ALkT1gidAzR9n8WhsuBTz8WZ-A7bKSxzYP-V2oPI</recordid><startdate>20210825</startdate><enddate>20210825</enddate><creator>Robin, Guillaume</creator><creator>Cognet, Thomas</creator><creator>Bouisset, Frédéric</creator><creator>Cariou, Eve</creator><creator>Méjean, Simon</creator><creator>Pradel, Sarah</creator><creator>Colombat, Magali</creator><creator>Galinier, Michel</creator><creator>Carrié, Didier</creator><creator>Lairez, Olivier</creator><creator>on behalf of the Toulouse Amyloidosis Research Network Collaborators</creator><general>The Japanese Circulation Society</general><general>Japanese Circulation Society</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><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0001-8642-0273</orcidid></search><sort><creationdate>20210825</creationdate><title>Value of Longitudinal Strain to Identify Wild-Type Transthyretin Amyloidosis in Patients With Aortic Stenosis</title><author>Robin, Guillaume ; Cognet, Thomas ; Bouisset, Frédéric ; Cariou, Eve ; Méjean, Simon ; Pradel, Sarah ; Colombat, Magali ; Galinier, Michel ; Carrié, Didier ; Lairez, Olivier ; on behalf of the Toulouse Amyloidosis Research Network Collaborators</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c528t-aeea73ae6e1038cc915306fa791508ff993e63b7d8301034c5bb5d0e91236d723</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Amyloid Neuropathies, Familial - complications</topic><topic>Amyloid Neuropathies, Familial - diagnostic imaging</topic><topic>Aortic stenosis</topic><topic>Aortic Valve Stenosis - diagnostic imaging</topic><topic>Cardiac amyloidosis</topic><topic>Cardiology and cardiovascular system</topic><topic>Echocardiography</topic><topic>Echocardiography - methods</topic><topic>Human health and pathology</topic><topic>Humans</topic><topic>Life Sciences</topic><topic>Longitudinal strain</topic><topic>Tomography, X-Ray Computed</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Robin, Guillaume</creatorcontrib><creatorcontrib>Cognet, Thomas</creatorcontrib><creatorcontrib>Bouisset, Frédéric</creatorcontrib><creatorcontrib>Cariou, Eve</creatorcontrib><creatorcontrib>Méjean, Simon</creatorcontrib><creatorcontrib>Pradel, Sarah</creatorcontrib><creatorcontrib>Colombat, Magali</creatorcontrib><creatorcontrib>Galinier, Michel</creatorcontrib><creatorcontrib>Carrié, Didier</creatorcontrib><creatorcontrib>Lairez, Olivier</creatorcontrib><creatorcontrib>on behalf of the Toulouse Amyloidosis Research Network Collaborators</creatorcontrib><creatorcontrib>Toulouse Amyloidosis Research Network Collaborators</creatorcontrib><creatorcontrib>on behalf of the Toulouse Amyloidosis Research Network Collaborators</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><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Circulation Journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Robin, Guillaume</au><au>Cognet, Thomas</au><au>Bouisset, Frédéric</au><au>Cariou, Eve</au><au>Méjean, Simon</au><au>Pradel, Sarah</au><au>Colombat, Magali</au><au>Galinier, Michel</au><au>Carrié, Didier</au><au>Lairez, Olivier</au><au>on behalf of the Toulouse Amyloidosis Research Network Collaborators</au><aucorp>Toulouse Amyloidosis Research Network Collaborators</aucorp><aucorp>on behalf of the Toulouse Amyloidosis Research Network Collaborators</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Value of Longitudinal Strain to Identify Wild-Type Transthyretin Amyloidosis in Patients With Aortic Stenosis</atitle><jtitle>Circulation Journal</jtitle><addtitle>Circ J</addtitle><date>2021-08-25</date><risdate>2021</risdate><volume>85</volume><issue>9</issue><spage>1494</spage><epage>1504</epage><pages>1494-1504</pages><artnum>CJ-20-1064</artnum><issn>1346-9843</issn><issn>1347-4820</issn><eissn>1347-4820</eissn><abstract>Background:Wild-type transthyretin-related amyloidosis (ATTRwt) and degenerative aortic stenosis (AS) are both age-related. Diagnosis of cardiac amyloidosis (CA) among patients with AS may be difficult due to overlapping morphological and functional criteria. The aim of this study was to describe an echocardiographic longitudinal strain (LS) pattern among patients with AS with and without ATTRwt.Methods and Results:Patients who have AS with ATTRwt (n=30), AS without ATTRwt (n=50) and ATTRwt without AS (n=31) underwent two-dimensional speckle-tracking echocardiography. Transthyretin CA was based on positive bone scintigraphy without monoclonal gammopathy. All patients showed a gradual decrease in LS from the base to the apex resulting in a decrease of the global LS. A cut-off value of 1.0 for relative apical LS (average apical LS/[average basal LS+mid-LS]) was sensitive (88%) but less specific (68%) in differentiating ATTRwt among patients with severe AS. The best cut-off value for relative apical LS for identifying patients with ATTRwt among the whole population was 0.9 (sensitivity 74%, specificity 66%); however, 35%, 25% and 11% of patients who have ATTRwt without AS, with moderate AS and with severe AS, respectively, did not reach this threshold.Conclusions:A decrease of global and relative apical LS is common in patients with AS, even in the absence of ATTRwt. ATTRwt CA can be present even in the absence of relative apical sparing of LS.</abstract><cop>Japan</cop><pub>The Japanese Circulation Society</pub><pmid>33980765</pmid><doi>10.1253/circj.CJ-20-1064</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-8642-0273</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Amyloid Neuropathies, Familial - complications Amyloid Neuropathies, Familial - diagnostic imaging Aortic stenosis Aortic Valve Stenosis - diagnostic imaging Cardiac amyloidosis Cardiology and cardiovascular system Echocardiography Echocardiography - methods Human health and pathology Humans Life Sciences Longitudinal strain Tomography, X-Ray Computed |
title | Value of Longitudinal Strain to Identify Wild-Type Transthyretin Amyloidosis in Patients With Aortic Stenosis |
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