Prognosis of Transthyretin Cardiac Amyloidosis Without Heart Failure Symptoms

BackgroundTransthyretin amyloid cardiomyopathy (ATTR-CM) is increasingly recognized as a treatable cause of heart failure (HF). Advances in diagnosis and therapy have increased the number of patients diagnosed at early stages, but prognostic data on patients without HF symptoms are lacking. Moreover...

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Veröffentlicht in:JACC CardioOncology 2022-11, Vol.4 (4), p.442-454
Hauptverfasser: Gonzalez-Lopez, Esther, Escobar-Lopez, Luis, Obici, Laura, Saturi, Giulia, Bezard, Mélanie, Saith, Sunil E., AbouEzzeddine, Omar F., Mussinelli, Roberta, Gagliardi, Christian, Kharoubi, Mounira, Griffin, Jan M., Dispenzieri, Angela, Vilches, Silvia, Perlini, Stefano, Longhi, Simone, Oghina, Silvia, Rivas, Adrian, Grogan, Martha, Maurer, Mathew S., Damy, Thibaud, Palladini, Giovanni, Rapezzi, Claudio, Garcia-Pavia, Pablo
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container_end_page 454
container_issue 4
container_start_page 442
container_title JACC CardioOncology
container_volume 4
creator Gonzalez-Lopez, Esther
Escobar-Lopez, Luis
Obici, Laura
Saturi, Giulia
Bezard, Mélanie
Saith, Sunil E.
AbouEzzeddine, Omar F.
Mussinelli, Roberta
Gagliardi, Christian
Kharoubi, Mounira
Griffin, Jan M.
Dispenzieri, Angela
Vilches, Silvia
Perlini, Stefano
Longhi, Simone
Oghina, Silvia
Rivas, Adrian
Grogan, Martha
Maurer, Mathew S.
Damy, Thibaud
Palladini, Giovanni
Rapezzi, Claudio
Garcia-Pavia, Pablo
description BackgroundTransthyretin amyloid cardiomyopathy (ATTR-CM) is increasingly recognized as a treatable cause of heart failure (HF). Advances in diagnosis and therapy have increased the number of patients diagnosed at early stages, but prognostic data on patients without HF symptoms are lacking. Moreover, it is unknown whether asymptomatic patients benefit from early initiation of transthyretin (TTR) stabilizers. ObjectivesThe aim of this study was to describe the natural history and prognosis of ATTR-CM in patients without HF symptoms. MethodsClinical characteristics and outcomes of patients with ATTR-CM without HF symptoms were retrospectively collected at 6 international amyloidosis centers. ResultsA total of 118 patients (78.8% men, median age 66 years [IQR: 53.8-75 years], 68 [57.6%] with variant transthyretin amyloidosis, mean left ventricular ejection fraction 60.5% ± 9.9%, mean left ventricular wall thickness 15.4 ± 3.1 mm, and 53 [45%] treated with TTR stabilizers at baseline or during follow-up) were included. During a median follow-up period of 3.7 years (IQR: 1-6 years), 38 patients developed HF symptoms (23 New York Heart Association functional class II and 14 functional class III or IV), 32 died, and 2 required cardiac transplantation. Additionally, 20 patients received pacemakers, 13 developed AF, and 1 had a stroke. Overall survival was 96.5% (95% CI: 91%-99%), 90.4% (95% CI: 82%-95%), and 82% (95% CI: 71%-89%) at 1, 3, and 5 years, respectively. Treatment with TTR stabilizers was associated with improved survival (HR: 0.31; 95% CI: 0.12-0.82; P = 0.019) and remained significant after adjusting for sex, age, ATTR-CM type, and estimated glomerular filtration rate (HR: 0.18; 95% CI: 0.06-0.55; P = 0.002). ConclusionsAfter a median follow-up period of 3.7 years, 1 in 3 patients with asymptomatic ATTR-CM developed HF symptoms, and nearly as many died or required cardiac transplantation. Treatment with TTR stabilizers was associated with improved prognosis.
doi_str_mv 10.1016/j.jaccao.2022.07.007
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Advances in diagnosis and therapy have increased the number of patients diagnosed at early stages, but prognostic data on patients without HF symptoms are lacking. Moreover, it is unknown whether asymptomatic patients benefit from early initiation of transthyretin (TTR) stabilizers. ObjectivesThe aim of this study was to describe the natural history and prognosis of ATTR-CM in patients without HF symptoms. MethodsClinical characteristics and outcomes of patients with ATTR-CM without HF symptoms were retrospectively collected at 6 international amyloidosis centers. ResultsA total of 118 patients (78.8% men, median age 66 years [IQR: 53.8-75 years], 68 [57.6%] with variant transthyretin amyloidosis, mean left ventricular ejection fraction 60.5% ± 9.9%, mean left ventricular wall thickness 15.4 ± 3.1 mm, and 53 [45%] treated with TTR stabilizers at baseline or during follow-up) were included. During a median follow-up period of 3.7 years (IQR: 1-6 years), 38 patients developed HF symptoms (23 New York Heart Association functional class II and 14 functional class III or IV), 32 died, and 2 required cardiac transplantation. Additionally, 20 patients received pacemakers, 13 developed AF, and 1 had a stroke. Overall survival was 96.5% (95% CI: 91%-99%), 90.4% (95% CI: 82%-95%), and 82% (95% CI: 71%-89%) at 1, 3, and 5 years, respectively. Treatment with TTR stabilizers was associated with improved survival (HR: 0.31; 95% CI: 0.12-0.82; P = 0.019) and remained significant after adjusting for sex, age, ATTR-CM type, and estimated glomerular filtration rate (HR: 0.18; 95% CI: 0.06-0.55; P = 0.002). ConclusionsAfter a median follow-up period of 3.7 years, 1 in 3 patients with asymptomatic ATTR-CM developed HF symptoms, and nearly as many died or required cardiac transplantation. Treatment with TTR stabilizers was associated with improved prognosis.</description><identifier>ISSN: 2666-0873</identifier><identifier>EISSN: 2666-0873</identifier><identifier>DOI: 10.1016/j.jaccao.2022.07.007</identifier><language>eng</language><publisher>Elsevier</publisher><subject>Life Sciences ; Mini-Focus Issue: Amyloidosis</subject><ispartof>JACC CardioOncology, 2022-11, Vol.4 (4), p.442-454</ispartof><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><rights>2022 The Authors 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c419t-87f26abffa577890d153e16dbe0007c9b122ea1a5d62a38d46181b33ca58c9ab3</citedby><cites>FETCH-LOGICAL-c419t-87f26abffa577890d153e16dbe0007c9b122ea1a5d62a38d46181b33ca58c9ab3</cites><orcidid>0000-0002-5470-2257 ; 0000-0002-8154-3538</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9700255/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9700255/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://hal.science/hal-04392150$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Gonzalez-Lopez, Esther</creatorcontrib><creatorcontrib>Escobar-Lopez, Luis</creatorcontrib><creatorcontrib>Obici, Laura</creatorcontrib><creatorcontrib>Saturi, Giulia</creatorcontrib><creatorcontrib>Bezard, Mélanie</creatorcontrib><creatorcontrib>Saith, Sunil E.</creatorcontrib><creatorcontrib>AbouEzzeddine, Omar F.</creatorcontrib><creatorcontrib>Mussinelli, Roberta</creatorcontrib><creatorcontrib>Gagliardi, Christian</creatorcontrib><creatorcontrib>Kharoubi, Mounira</creatorcontrib><creatorcontrib>Griffin, Jan M.</creatorcontrib><creatorcontrib>Dispenzieri, Angela</creatorcontrib><creatorcontrib>Vilches, Silvia</creatorcontrib><creatorcontrib>Perlini, Stefano</creatorcontrib><creatorcontrib>Longhi, Simone</creatorcontrib><creatorcontrib>Oghina, Silvia</creatorcontrib><creatorcontrib>Rivas, Adrian</creatorcontrib><creatorcontrib>Grogan, Martha</creatorcontrib><creatorcontrib>Maurer, Mathew S.</creatorcontrib><creatorcontrib>Damy, Thibaud</creatorcontrib><creatorcontrib>Palladini, Giovanni</creatorcontrib><creatorcontrib>Rapezzi, Claudio</creatorcontrib><creatorcontrib>Garcia-Pavia, Pablo</creatorcontrib><title>Prognosis of Transthyretin Cardiac Amyloidosis Without Heart Failure Symptoms</title><title>JACC CardioOncology</title><description>BackgroundTransthyretin amyloid cardiomyopathy (ATTR-CM) is increasingly recognized as a treatable cause of heart failure (HF). Advances in diagnosis and therapy have increased the number of patients diagnosed at early stages, but prognostic data on patients without HF symptoms are lacking. Moreover, it is unknown whether asymptomatic patients benefit from early initiation of transthyretin (TTR) stabilizers. ObjectivesThe aim of this study was to describe the natural history and prognosis of ATTR-CM in patients without HF symptoms. MethodsClinical characteristics and outcomes of patients with ATTR-CM without HF symptoms were retrospectively collected at 6 international amyloidosis centers. ResultsA total of 118 patients (78.8% men, median age 66 years [IQR: 53.8-75 years], 68 [57.6%] with variant transthyretin amyloidosis, mean left ventricular ejection fraction 60.5% ± 9.9%, mean left ventricular wall thickness 15.4 ± 3.1 mm, and 53 [45%] treated with TTR stabilizers at baseline or during follow-up) were included. During a median follow-up period of 3.7 years (IQR: 1-6 years), 38 patients developed HF symptoms (23 New York Heart Association functional class II and 14 functional class III or IV), 32 died, and 2 required cardiac transplantation. Additionally, 20 patients received pacemakers, 13 developed AF, and 1 had a stroke. Overall survival was 96.5% (95% CI: 91%-99%), 90.4% (95% CI: 82%-95%), and 82% (95% CI: 71%-89%) at 1, 3, and 5 years, respectively. Treatment with TTR stabilizers was associated with improved survival (HR: 0.31; 95% CI: 0.12-0.82; P = 0.019) and remained significant after adjusting for sex, age, ATTR-CM type, and estimated glomerular filtration rate (HR: 0.18; 95% CI: 0.06-0.55; P = 0.002). ConclusionsAfter a median follow-up period of 3.7 years, 1 in 3 patients with asymptomatic ATTR-CM developed HF symptoms, and nearly as many died or required cardiac transplantation. Treatment with TTR stabilizers was associated with improved prognosis.</description><subject>Life Sciences</subject><subject>Mini-Focus Issue: Amyloidosis</subject><issn>2666-0873</issn><issn>2666-0873</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNpdkcFKw0AQhoMoWGrfwEOOemjc3SS7yUUoxVqhYMGKx2Wy2bRbkmzd3RT6Nn2WPpmJKaKeZpj555sZfs-7xSjACNOHbbAFIUAHBBESIBYgxC68AaGUjlHCwstf-bU3snaLECIxxjRKBt5yafS61lZZXxf-ykBt3eZgpFO1PwWTKxCn46Q6lFrl36oP5Ta6cf5cgnGn4wxU2Rh5Or4dqp3Tlb3xrgoorRyd49B7nz2tpvPx4vX5ZTpZjEWEUzdOWEEoZEUBMWNJinIchxLTPJPtdUykGSZEAoY4pwTCJI8oTnAWhgLiRKSQhUPvsefumqySuZC1M1DynVEVmAPXoPjfTq02fK33PGXd-3ELuO8Bm39j88mCdzUUhSnBMdrjVnt3Xmb0ZyOt45WyQpYl1FI3lhMWERpTwpJWGvVSYbS1RhY_bIx4Zxjf8t4w3hnGEePtw-EX_-CPKA</recordid><startdate>20221101</startdate><enddate>20221101</enddate><creator>Gonzalez-Lopez, Esther</creator><creator>Escobar-Lopez, Luis</creator><creator>Obici, Laura</creator><creator>Saturi, Giulia</creator><creator>Bezard, Mélanie</creator><creator>Saith, Sunil E.</creator><creator>AbouEzzeddine, Omar F.</creator><creator>Mussinelli, Roberta</creator><creator>Gagliardi, Christian</creator><creator>Kharoubi, Mounira</creator><creator>Griffin, Jan M.</creator><creator>Dispenzieri, Angela</creator><creator>Vilches, Silvia</creator><creator>Perlini, Stefano</creator><creator>Longhi, Simone</creator><creator>Oghina, Silvia</creator><creator>Rivas, Adrian</creator><creator>Grogan, Martha</creator><creator>Maurer, Mathew S.</creator><creator>Damy, Thibaud</creator><creator>Palladini, Giovanni</creator><creator>Rapezzi, Claudio</creator><creator>Garcia-Pavia, Pablo</creator><general>Elsevier</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>1XC</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-5470-2257</orcidid><orcidid>https://orcid.org/0000-0002-8154-3538</orcidid></search><sort><creationdate>20221101</creationdate><title>Prognosis of Transthyretin Cardiac Amyloidosis Without Heart Failure Symptoms</title><author>Gonzalez-Lopez, Esther ; Escobar-Lopez, Luis ; Obici, Laura ; Saturi, Giulia ; Bezard, Mélanie ; Saith, Sunil E. ; AbouEzzeddine, Omar F. ; Mussinelli, Roberta ; Gagliardi, Christian ; Kharoubi, Mounira ; Griffin, Jan M. ; Dispenzieri, Angela ; Vilches, Silvia ; Perlini, Stefano ; Longhi, Simone ; Oghina, Silvia ; Rivas, Adrian ; Grogan, Martha ; Maurer, Mathew S. ; Damy, Thibaud ; Palladini, Giovanni ; Rapezzi, Claudio ; Garcia-Pavia, Pablo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c419t-87f26abffa577890d153e16dbe0007c9b122ea1a5d62a38d46181b33ca58c9ab3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Life Sciences</topic><topic>Mini-Focus Issue: Amyloidosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gonzalez-Lopez, Esther</creatorcontrib><creatorcontrib>Escobar-Lopez, Luis</creatorcontrib><creatorcontrib>Obici, Laura</creatorcontrib><creatorcontrib>Saturi, Giulia</creatorcontrib><creatorcontrib>Bezard, Mélanie</creatorcontrib><creatorcontrib>Saith, Sunil E.</creatorcontrib><creatorcontrib>AbouEzzeddine, Omar F.</creatorcontrib><creatorcontrib>Mussinelli, Roberta</creatorcontrib><creatorcontrib>Gagliardi, Christian</creatorcontrib><creatorcontrib>Kharoubi, Mounira</creatorcontrib><creatorcontrib>Griffin, Jan M.</creatorcontrib><creatorcontrib>Dispenzieri, Angela</creatorcontrib><creatorcontrib>Vilches, Silvia</creatorcontrib><creatorcontrib>Perlini, Stefano</creatorcontrib><creatorcontrib>Longhi, Simone</creatorcontrib><creatorcontrib>Oghina, Silvia</creatorcontrib><creatorcontrib>Rivas, Adrian</creatorcontrib><creatorcontrib>Grogan, Martha</creatorcontrib><creatorcontrib>Maurer, Mathew S.</creatorcontrib><creatorcontrib>Damy, Thibaud</creatorcontrib><creatorcontrib>Palladini, Giovanni</creatorcontrib><creatorcontrib>Rapezzi, Claudio</creatorcontrib><creatorcontrib>Garcia-Pavia, Pablo</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>JACC CardioOncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gonzalez-Lopez, Esther</au><au>Escobar-Lopez, Luis</au><au>Obici, Laura</au><au>Saturi, Giulia</au><au>Bezard, Mélanie</au><au>Saith, Sunil E.</au><au>AbouEzzeddine, Omar F.</au><au>Mussinelli, Roberta</au><au>Gagliardi, Christian</au><au>Kharoubi, Mounira</au><au>Griffin, Jan M.</au><au>Dispenzieri, Angela</au><au>Vilches, Silvia</au><au>Perlini, Stefano</au><au>Longhi, Simone</au><au>Oghina, Silvia</au><au>Rivas, Adrian</au><au>Grogan, Martha</au><au>Maurer, Mathew S.</au><au>Damy, Thibaud</au><au>Palladini, Giovanni</au><au>Rapezzi, Claudio</au><au>Garcia-Pavia, Pablo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prognosis of Transthyretin Cardiac Amyloidosis Without Heart Failure Symptoms</atitle><jtitle>JACC CardioOncology</jtitle><date>2022-11-01</date><risdate>2022</risdate><volume>4</volume><issue>4</issue><spage>442</spage><epage>454</epage><pages>442-454</pages><issn>2666-0873</issn><eissn>2666-0873</eissn><abstract>BackgroundTransthyretin amyloid cardiomyopathy (ATTR-CM) is increasingly recognized as a treatable cause of heart failure (HF). Advances in diagnosis and therapy have increased the number of patients diagnosed at early stages, but prognostic data on patients without HF symptoms are lacking. Moreover, it is unknown whether asymptomatic patients benefit from early initiation of transthyretin (TTR) stabilizers. ObjectivesThe aim of this study was to describe the natural history and prognosis of ATTR-CM in patients without HF symptoms. MethodsClinical characteristics and outcomes of patients with ATTR-CM without HF symptoms were retrospectively collected at 6 international amyloidosis centers. ResultsA total of 118 patients (78.8% men, median age 66 years [IQR: 53.8-75 years], 68 [57.6%] with variant transthyretin amyloidosis, mean left ventricular ejection fraction 60.5% ± 9.9%, mean left ventricular wall thickness 15.4 ± 3.1 mm, and 53 [45%] treated with TTR stabilizers at baseline or during follow-up) were included. During a median follow-up period of 3.7 years (IQR: 1-6 years), 38 patients developed HF symptoms (23 New York Heart Association functional class II and 14 functional class III or IV), 32 died, and 2 required cardiac transplantation. Additionally, 20 patients received pacemakers, 13 developed AF, and 1 had a stroke. Overall survival was 96.5% (95% CI: 91%-99%), 90.4% (95% CI: 82%-95%), and 82% (95% CI: 71%-89%) at 1, 3, and 5 years, respectively. Treatment with TTR stabilizers was associated with improved survival (HR: 0.31; 95% CI: 0.12-0.82; P = 0.019) and remained significant after adjusting for sex, age, ATTR-CM type, and estimated glomerular filtration rate (HR: 0.18; 95% CI: 0.06-0.55; P = 0.002). ConclusionsAfter a median follow-up period of 3.7 years, 1 in 3 patients with asymptomatic ATTR-CM developed HF symptoms, and nearly as many died or required cardiac transplantation. Treatment with TTR stabilizers was associated with improved prognosis.</abstract><pub>Elsevier</pub><doi>10.1016/j.jaccao.2022.07.007</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-5470-2257</orcidid><orcidid>https://orcid.org/0000-0002-8154-3538</orcidid><oa>free_for_read</oa></addata></record>
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Mini-Focus Issue: Amyloidosis
title Prognosis of Transthyretin Cardiac Amyloidosis Without Heart Failure Symptoms
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