Wild-type transthyretin cardiac amyloidosis is not rare in elderly subjects: the CATCH screening study

Abstract Aims Wild-type transthyretin cardiac amyloidosis (ATTRwt-CA) affects older adults and is currently considered as a rare disorder. We investigated for the first time the prevalence of ATTRwt-CA in elderly individuals from the general population. Methods and results General practitioners from...

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Veröffentlicht in:European journal of preventive cardiology 2024-08, Vol.31 (11), p.1410-1417
Hauptverfasser: Aimo, Alberto, Vergaro, Giuseppe, Castiglione, Vincenzo, Fabiani, Iacopo, Barison, Andrea, Gentile, Francesco, Ferrari Chen, Yu Fu, Giorgetti, Assuero, Genovesi, Dario, Buda, Gabriele, Franzini, Maria, Piepoli, Massimo, Moscardini, Stefano, Rapezzi, Claudio, Fontana, Marianna, Passino, Claudio, Emdin, Michele
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container_issue 11
container_start_page 1410
container_title European journal of preventive cardiology
container_volume 31
creator Aimo, Alberto
Vergaro, Giuseppe
Castiglione, Vincenzo
Fabiani, Iacopo
Barison, Andrea
Gentile, Francesco
Ferrari Chen, Yu Fu
Giorgetti, Assuero
Genovesi, Dario
Buda, Gabriele
Franzini, Maria
Piepoli, Massimo
Moscardini, Stefano
Rapezzi, Claudio
Fontana, Marianna
Passino, Claudio
Emdin, Michele
description Abstract Aims Wild-type transthyretin cardiac amyloidosis (ATTRwt-CA) affects older adults and is currently considered as a rare disorder. We investigated for the first time the prevalence of ATTRwt-CA in elderly individuals from the general population. Methods and results General practitioners from Pisa, Italy, proposed a screening for ATTRwt-CA to all their patients aged 65–90 years, until 1000 accepted. The following red flags were searched: interventricular septal thickness ≥ 12 mm, any echocardiographic, electrocardiographic or clinical hallmark of CA, or high-sensitivity troponin T ≥ 14 ng/L. Individuals with at least one red flag (n = 346) were asked to undergo the search for a monoclonal protein and bone scintigraphy, and 216 accepted. Four patients received a non-invasive diagnosis of ATTRwt-CA. All complained of dyspnoea on moderate effort. A woman and a man aged 79 and 85 years, respectively, showed an intense cardiac tracer uptake (Grade 3), left ventricular (LV) wall thickening, Grade 2 and 3 diastolic dysfunction, and N-terminal pro-B-type natriuretic peptide (NT-proBNP) > 1000 ng/L. Two other patients (a man aged 74 years and a woman aged 83 years) showed a Grade 2 uptake, an increased LV septal thickness, but preserved diastolic function, and NT-proBNP < 300 ng/L. The prevalence of ATTR-CA in subjects ≥ 65 years was calculated as 0.46% (i.e. 4 out of the 870 subjects completing the screening, namely 654 not meeting the criteria for Step 2 and 216 progressing to Step 2). Conclusion Wild-type transthyretin cardiac amyloidosis is uncommon in elderly subjects from the general population, but more frequent than expected for a rare disease. Lay Summary Wild-type transthyretin cardiac amyloidosis (ATTRwt-CA) is a heart condition mostly found in older adults. Wild-type transthyretin cardiac amyloidosis is considered a rare disease, although no systematic screening has been performed yet. The study aimed to understand how common this disease is among the general population aged 65–90 years in Pisa, Italy. To do this, general practitioners offered screening for ATTRwt-CA to their patients within this age group. The initial step of the screening involved checking for certain warning signs (red flags), like abnormal thickness in a part of the heart called the interventricular septum, unusual heart function observed through various tests, or elevated levels of a specific heart protein. Out of 1000 individuals who began the screening process, 346 showed
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We investigated for the first time the prevalence of ATTRwt-CA in elderly individuals from the general population. Methods and results General practitioners from Pisa, Italy, proposed a screening for ATTRwt-CA to all their patients aged 65–90 years, until 1000 accepted. The following red flags were searched: interventricular septal thickness ≥ 12 mm, any echocardiographic, electrocardiographic or clinical hallmark of CA, or high-sensitivity troponin T ≥ 14 ng/L. Individuals with at least one red flag (n = 346) were asked to undergo the search for a monoclonal protein and bone scintigraphy, and 216 accepted. Four patients received a non-invasive diagnosis of ATTRwt-CA. All complained of dyspnoea on moderate effort. A woman and a man aged 79 and 85 years, respectively, showed an intense cardiac tracer uptake (Grade 3), left ventricular (LV) wall thickening, Grade 2 and 3 diastolic dysfunction, and N-terminal pro-B-type natriuretic peptide (NT-proBNP) &gt; 1000 ng/L. Two other patients (a man aged 74 years and a woman aged 83 years) showed a Grade 2 uptake, an increased LV septal thickness, but preserved diastolic function, and NT-proBNP &lt; 300 ng/L. The prevalence of ATTR-CA in subjects ≥ 65 years was calculated as 0.46% (i.e. 4 out of the 870 subjects completing the screening, namely 654 not meeting the criteria for Step 2 and 216 progressing to Step 2). Conclusion Wild-type transthyretin cardiac amyloidosis is uncommon in elderly subjects from the general population, but more frequent than expected for a rare disease. Lay Summary Wild-type transthyretin cardiac amyloidosis (ATTRwt-CA) is a heart condition mostly found in older adults. Wild-type transthyretin cardiac amyloidosis is considered a rare disease, although no systematic screening has been performed yet. The study aimed to understand how common this disease is among the general population aged 65–90 years in Pisa, Italy. To do this, general practitioners offered screening for ATTRwt-CA to their patients within this age group. The initial step of the screening involved checking for certain warning signs (red flags), like abnormal thickness in a part of the heart called the interventricular septum, unusual heart function observed through various tests, or elevated levels of a specific heart protein. Out of 1000 individuals who began the screening process, 346 showed at least one of these red flags and were further examined using bone scintigraphy (a type of imaging test) and tests for a specific protein related to this condition. Of these, 216 agreed to proceed with these additional tests. The results showed that four of these patients actually had ATTRwt-CA. Their conditions varied in severity, with some showing more intense signs of the disease on the heart scans, thicker heart walls, and higher levels of heart stress proteins. All four patients experienced mild difficulty in breathing during physical activity. Based on these findings, the study concluded that about 0.46% of elderly individuals in the general population might have ATTRwt-CA, indicating that the disease is somewhat more common in this age group than previously thought. Graphical Abstract Graphical Abstract Main findings of the CATCH study. ATTR-CA, transthyretin cardiac amyloidosis; ECG, electrocardiogram; GP, general practitioner; hs-TnT, high-sensitivity troponin T; IVS, interventricular septum; NT-proBNP, N-terminal pro-B-type natriuretic peptide.</description><identifier>ISSN: 2047-4873</identifier><identifier>ISSN: 2047-4881</identifier><identifier>EISSN: 2047-4881</identifier><identifier>DOI: 10.1093/eurjpc/zwae093</identifier><identifier>PMID: 38456769</identifier><language>eng</language><publisher>UK: Oxford University Press</publisher><ispartof>European journal of preventive cardiology, 2024-08, Vol.31 (11), p.1410-1417</ispartof><rights>The Author(s) 2024. Published by Oxford University Press on behalf of the European Society of Cardiology. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com. 2024</rights><rights>The Author(s) 2024. Published by Oxford University Press on behalf of the European Society of Cardiology. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.</rights><rights>The Author(s) 2024. Published by Oxford University Press on behalf of the European Society of Cardiology. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c214t-7a892edf0386ed1f17c7c7e14599956eeac398c61d2493f733570f1646ded3233</cites><orcidid>0000-0002-9233-9831 ; 0000-0002-0723-4753 ; 0000-0002-8541-1962 ; 0000-0001-7453-3748 ; 0000-0002-9198-2657</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1578,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38456769$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Aimo, Alberto</creatorcontrib><creatorcontrib>Vergaro, Giuseppe</creatorcontrib><creatorcontrib>Castiglione, Vincenzo</creatorcontrib><creatorcontrib>Fabiani, Iacopo</creatorcontrib><creatorcontrib>Barison, Andrea</creatorcontrib><creatorcontrib>Gentile, Francesco</creatorcontrib><creatorcontrib>Ferrari Chen, Yu Fu</creatorcontrib><creatorcontrib>Giorgetti, Assuero</creatorcontrib><creatorcontrib>Genovesi, Dario</creatorcontrib><creatorcontrib>Buda, Gabriele</creatorcontrib><creatorcontrib>Franzini, Maria</creatorcontrib><creatorcontrib>Piepoli, Massimo</creatorcontrib><creatorcontrib>Moscardini, Stefano</creatorcontrib><creatorcontrib>Rapezzi, Claudio</creatorcontrib><creatorcontrib>Fontana, Marianna</creatorcontrib><creatorcontrib>Passino, Claudio</creatorcontrib><creatorcontrib>Emdin, Michele</creatorcontrib><title>Wild-type transthyretin cardiac amyloidosis is not rare in elderly subjects: the CATCH screening study</title><title>European journal of preventive cardiology</title><addtitle>Eur J Prev Cardiol</addtitle><description>Abstract Aims Wild-type transthyretin cardiac amyloidosis (ATTRwt-CA) affects older adults and is currently considered as a rare disorder. We investigated for the first time the prevalence of ATTRwt-CA in elderly individuals from the general population. Methods and results General practitioners from Pisa, Italy, proposed a screening for ATTRwt-CA to all their patients aged 65–90 years, until 1000 accepted. The following red flags were searched: interventricular septal thickness ≥ 12 mm, any echocardiographic, electrocardiographic or clinical hallmark of CA, or high-sensitivity troponin T ≥ 14 ng/L. Individuals with at least one red flag (n = 346) were asked to undergo the search for a monoclonal protein and bone scintigraphy, and 216 accepted. Four patients received a non-invasive diagnosis of ATTRwt-CA. All complained of dyspnoea on moderate effort. A woman and a man aged 79 and 85 years, respectively, showed an intense cardiac tracer uptake (Grade 3), left ventricular (LV) wall thickening, Grade 2 and 3 diastolic dysfunction, and N-terminal pro-B-type natriuretic peptide (NT-proBNP) &gt; 1000 ng/L. Two other patients (a man aged 74 years and a woman aged 83 years) showed a Grade 2 uptake, an increased LV septal thickness, but preserved diastolic function, and NT-proBNP &lt; 300 ng/L. The prevalence of ATTR-CA in subjects ≥ 65 years was calculated as 0.46% (i.e. 4 out of the 870 subjects completing the screening, namely 654 not meeting the criteria for Step 2 and 216 progressing to Step 2). Conclusion Wild-type transthyretin cardiac amyloidosis is uncommon in elderly subjects from the general population, but more frequent than expected for a rare disease. Lay Summary Wild-type transthyretin cardiac amyloidosis (ATTRwt-CA) is a heart condition mostly found in older adults. Wild-type transthyretin cardiac amyloidosis is considered a rare disease, although no systematic screening has been performed yet. The study aimed to understand how common this disease is among the general population aged 65–90 years in Pisa, Italy. To do this, general practitioners offered screening for ATTRwt-CA to their patients within this age group. The initial step of the screening involved checking for certain warning signs (red flags), like abnormal thickness in a part of the heart called the interventricular septum, unusual heart function observed through various tests, or elevated levels of a specific heart protein. Out of 1000 individuals who began the screening process, 346 showed at least one of these red flags and were further examined using bone scintigraphy (a type of imaging test) and tests for a specific protein related to this condition. Of these, 216 agreed to proceed with these additional tests. The results showed that four of these patients actually had ATTRwt-CA. Their conditions varied in severity, with some showing more intense signs of the disease on the heart scans, thicker heart walls, and higher levels of heart stress proteins. All four patients experienced mild difficulty in breathing during physical activity. Based on these findings, the study concluded that about 0.46% of elderly individuals in the general population might have ATTRwt-CA, indicating that the disease is somewhat more common in this age group than previously thought. Graphical Abstract Graphical Abstract Main findings of the CATCH study. ATTR-CA, transthyretin cardiac amyloidosis; ECG, electrocardiogram; GP, general practitioner; hs-TnT, high-sensitivity troponin T; IVS, interventricular septum; NT-proBNP, N-terminal pro-B-type natriuretic peptide.</description><issn>2047-4873</issn><issn>2047-4881</issn><issn>2047-4881</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkD1PwzAQhi0Eoqh0ZUQeYUjrj8SO2aqKL6kSC4gxcu0LTZUmwXaEwq_HKKUrPkt3Jz33Dg9CV5TMKVF8Ab3bdWbx_aUhrifogpFUJmme09PjLPkEzbzfkfgEYSzPz9GE52kmpFAXqHyvapuEoQMcnG582A4OQtVgo52ttMF6P9RtZVtfeRx_0wbstAMcEagtuHrAvt_swAR_h8MW8Gr5unrC3jiApmo-sA-9HS7RWalrD7NDn6K3h_vIJeuXx-fVcp0YRtOQSJ0rBrYkPBdgaUmliQU0zZRSmQDQhqvcCGpZqngpOc8kKalIhQXLGedTdDPmdq797MGHYl95A3WtG2h7XzCVpVJmVImIzkfUuNZ7B2XRuWqv3VBQUvzqLUa9xUFvPLg-ZPebPdgj_iczArcj0Pbdf2E_3CyHcg</recordid><startdate>20240822</startdate><enddate>20240822</enddate><creator>Aimo, Alberto</creator><creator>Vergaro, Giuseppe</creator><creator>Castiglione, Vincenzo</creator><creator>Fabiani, Iacopo</creator><creator>Barison, Andrea</creator><creator>Gentile, Francesco</creator><creator>Ferrari Chen, Yu Fu</creator><creator>Giorgetti, Assuero</creator><creator>Genovesi, Dario</creator><creator>Buda, Gabriele</creator><creator>Franzini, Maria</creator><creator>Piepoli, Massimo</creator><creator>Moscardini, Stefano</creator><creator>Rapezzi, Claudio</creator><creator>Fontana, Marianna</creator><creator>Passino, Claudio</creator><creator>Emdin, Michele</creator><general>Oxford University Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9233-9831</orcidid><orcidid>https://orcid.org/0000-0002-0723-4753</orcidid><orcidid>https://orcid.org/0000-0002-8541-1962</orcidid><orcidid>https://orcid.org/0000-0001-7453-3748</orcidid><orcidid>https://orcid.org/0000-0002-9198-2657</orcidid></search><sort><creationdate>20240822</creationdate><title>Wild-type transthyretin cardiac amyloidosis is not rare in elderly subjects: the CATCH screening study</title><author>Aimo, Alberto ; Vergaro, Giuseppe ; Castiglione, Vincenzo ; Fabiani, Iacopo ; Barison, Andrea ; Gentile, Francesco ; Ferrari Chen, Yu Fu ; Giorgetti, Assuero ; Genovesi, Dario ; Buda, Gabriele ; Franzini, Maria ; Piepoli, Massimo ; Moscardini, Stefano ; Rapezzi, Claudio ; Fontana, Marianna ; Passino, Claudio ; Emdin, Michele</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c214t-7a892edf0386ed1f17c7c7e14599956eeac398c61d2493f733570f1646ded3233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aimo, Alberto</creatorcontrib><creatorcontrib>Vergaro, Giuseppe</creatorcontrib><creatorcontrib>Castiglione, Vincenzo</creatorcontrib><creatorcontrib>Fabiani, Iacopo</creatorcontrib><creatorcontrib>Barison, Andrea</creatorcontrib><creatorcontrib>Gentile, Francesco</creatorcontrib><creatorcontrib>Ferrari Chen, Yu Fu</creatorcontrib><creatorcontrib>Giorgetti, Assuero</creatorcontrib><creatorcontrib>Genovesi, Dario</creatorcontrib><creatorcontrib>Buda, Gabriele</creatorcontrib><creatorcontrib>Franzini, Maria</creatorcontrib><creatorcontrib>Piepoli, Massimo</creatorcontrib><creatorcontrib>Moscardini, Stefano</creatorcontrib><creatorcontrib>Rapezzi, Claudio</creatorcontrib><creatorcontrib>Fontana, Marianna</creatorcontrib><creatorcontrib>Passino, Claudio</creatorcontrib><creatorcontrib>Emdin, Michele</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of preventive cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aimo, Alberto</au><au>Vergaro, Giuseppe</au><au>Castiglione, Vincenzo</au><au>Fabiani, Iacopo</au><au>Barison, Andrea</au><au>Gentile, Francesco</au><au>Ferrari Chen, Yu Fu</au><au>Giorgetti, Assuero</au><au>Genovesi, Dario</au><au>Buda, Gabriele</au><au>Franzini, Maria</au><au>Piepoli, Massimo</au><au>Moscardini, Stefano</au><au>Rapezzi, Claudio</au><au>Fontana, Marianna</au><au>Passino, Claudio</au><au>Emdin, Michele</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Wild-type transthyretin cardiac amyloidosis is not rare in elderly subjects: the CATCH screening study</atitle><jtitle>European journal of preventive cardiology</jtitle><addtitle>Eur J Prev Cardiol</addtitle><date>2024-08-22</date><risdate>2024</risdate><volume>31</volume><issue>11</issue><spage>1410</spage><epage>1417</epage><pages>1410-1417</pages><issn>2047-4873</issn><issn>2047-4881</issn><eissn>2047-4881</eissn><abstract>Abstract Aims Wild-type transthyretin cardiac amyloidosis (ATTRwt-CA) affects older adults and is currently considered as a rare disorder. We investigated for the first time the prevalence of ATTRwt-CA in elderly individuals from the general population. Methods and results General practitioners from Pisa, Italy, proposed a screening for ATTRwt-CA to all their patients aged 65–90 years, until 1000 accepted. The following red flags were searched: interventricular septal thickness ≥ 12 mm, any echocardiographic, electrocardiographic or clinical hallmark of CA, or high-sensitivity troponin T ≥ 14 ng/L. Individuals with at least one red flag (n = 346) were asked to undergo the search for a monoclonal protein and bone scintigraphy, and 216 accepted. Four patients received a non-invasive diagnosis of ATTRwt-CA. All complained of dyspnoea on moderate effort. A woman and a man aged 79 and 85 years, respectively, showed an intense cardiac tracer uptake (Grade 3), left ventricular (LV) wall thickening, Grade 2 and 3 diastolic dysfunction, and N-terminal pro-B-type natriuretic peptide (NT-proBNP) &gt; 1000 ng/L. Two other patients (a man aged 74 years and a woman aged 83 years) showed a Grade 2 uptake, an increased LV septal thickness, but preserved diastolic function, and NT-proBNP &lt; 300 ng/L. The prevalence of ATTR-CA in subjects ≥ 65 years was calculated as 0.46% (i.e. 4 out of the 870 subjects completing the screening, namely 654 not meeting the criteria for Step 2 and 216 progressing to Step 2). Conclusion Wild-type transthyretin cardiac amyloidosis is uncommon in elderly subjects from the general population, but more frequent than expected for a rare disease. Lay Summary Wild-type transthyretin cardiac amyloidosis (ATTRwt-CA) is a heart condition mostly found in older adults. Wild-type transthyretin cardiac amyloidosis is considered a rare disease, although no systematic screening has been performed yet. The study aimed to understand how common this disease is among the general population aged 65–90 years in Pisa, Italy. To do this, general practitioners offered screening for ATTRwt-CA to their patients within this age group. The initial step of the screening involved checking for certain warning signs (red flags), like abnormal thickness in a part of the heart called the interventricular septum, unusual heart function observed through various tests, or elevated levels of a specific heart protein. Out of 1000 individuals who began the screening process, 346 showed at least one of these red flags and were further examined using bone scintigraphy (a type of imaging test) and tests for a specific protein related to this condition. Of these, 216 agreed to proceed with these additional tests. The results showed that four of these patients actually had ATTRwt-CA. Their conditions varied in severity, with some showing more intense signs of the disease on the heart scans, thicker heart walls, and higher levels of heart stress proteins. All four patients experienced mild difficulty in breathing during physical activity. Based on these findings, the study concluded that about 0.46% of elderly individuals in the general population might have ATTRwt-CA, indicating that the disease is somewhat more common in this age group than previously thought. Graphical Abstract Graphical Abstract Main findings of the CATCH study. ATTR-CA, transthyretin cardiac amyloidosis; ECG, electrocardiogram; GP, general practitioner; hs-TnT, high-sensitivity troponin T; IVS, interventricular septum; NT-proBNP, N-terminal pro-B-type natriuretic peptide.</abstract><cop>UK</cop><pub>Oxford University Press</pub><pmid>38456769</pmid><doi>10.1093/eurjpc/zwae093</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-9233-9831</orcidid><orcidid>https://orcid.org/0000-0002-0723-4753</orcidid><orcidid>https://orcid.org/0000-0002-8541-1962</orcidid><orcidid>https://orcid.org/0000-0001-7453-3748</orcidid><orcidid>https://orcid.org/0000-0002-9198-2657</orcidid></addata></record>
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title Wild-type transthyretin cardiac amyloidosis is not rare in elderly subjects: the CATCH screening study
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