Aβ Amyloid Pathology Affects the Hearts of Patients With Alzheimer's Disease: Mind the Heart
Individually, heart failure (HF) and Alzheimer's disease (AD) are severe threats to population health, and their potential coexistence is an alarming prospect. In addition to sharing analogous epidemiological and genetic profiles, biochemical characteristics, and common triggers, the authors re...
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Veröffentlicht in: | Journal of the American College of Cardiology 2016-12, Vol.68 (22), p.2395-2407 |
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creator | Troncone, Luca Luciani, Marco Coggins, Matthew Wilker, Elissa H Ho, Cheng-Ying Codispoti, Kari Elise Frosch, Matthew P Kayed, Rakez Del Monte, Federica |
description | Individually, heart failure (HF) and Alzheimer's disease (AD) are severe threats to population health, and their potential coexistence is an alarming prospect. In addition to sharing analogous epidemiological and genetic profiles, biochemical characteristics, and common triggers, the authors recently recognized common molecular and pathological features between the 2 conditions. Whereas cognitive impairment has been linked to HF through perfusion defects, angiopathy, and inflammation, whether patients with AD present with myocardial dysfunction, and if the 2 conditions bear a common pathogenesis as neglected siblings are unknown.
Here, the authors investigated whether amyloid beta (Aβ) protein aggregates are present in the hearts of patients with a primary diagnosis of AD, affecting myocardial function.
The authors examined myocardial function in a retrospective cross-sectional study from a cohort of AD patients and age-matched controls. Imaging and proteomics approaches were used to identify and quantify Aβ deposits in AD heart and brain specimens compared with controls. Cell shortening and calcium transients were measured on isolated adult cardiomyocytes.
Echocardiographic measurements of myocardial function suggest that patients with AD present with an anticipated diastolic dysfunction. As in the brain, Aβ
and Aβ
are present in the heart, and their expression is increased in AD.
Here, the authors provide the first report of the presence of compromised myocardial function and intramyocardial deposits of Aβ in AD patients. The findings depict a novel biological framework in which AD may be viewed either as a systemic disease or as a metastatic disorder leading to heart, and possibly multiorgan failure. AD and HF are both debilitating and life-threatening conditions, affecting enormous patient populations. Our findings underline a previously dismissed problem of a magnitude that will require new diagnostic approaches and treatments for brain and heart disease, and their combination. |
doi_str_mv | 10.1016/j.jacc.2016.08.073 |
format | Article |
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Here, the authors investigated whether amyloid beta (Aβ) protein aggregates are present in the hearts of patients with a primary diagnosis of AD, affecting myocardial function.
The authors examined myocardial function in a retrospective cross-sectional study from a cohort of AD patients and age-matched controls. Imaging and proteomics approaches were used to identify and quantify Aβ deposits in AD heart and brain specimens compared with controls. Cell shortening and calcium transients were measured on isolated adult cardiomyocytes.
Echocardiographic measurements of myocardial function suggest that patients with AD present with an anticipated diastolic dysfunction. As in the brain, Aβ
and Aβ
are present in the heart, and their expression is increased in AD.
Here, the authors provide the first report of the presence of compromised myocardial function and intramyocardial deposits of Aβ in AD patients. The findings depict a novel biological framework in which AD may be viewed either as a systemic disease or as a metastatic disorder leading to heart, and possibly multiorgan failure. AD and HF are both debilitating and life-threatening conditions, affecting enormous patient populations. Our findings underline a previously dismissed problem of a magnitude that will require new diagnostic approaches and treatments for brain and heart disease, and their combination.</description><identifier>ISSN: 0735-1097</identifier><identifier>EISSN: 1558-3597</identifier><identifier>DOI: 10.1016/j.jacc.2016.08.073</identifier><identifier>PMID: 27908343</identifier><language>eng</language><publisher>United States</publisher><subject>Aged ; Aged, 80 and over ; Aging - metabolism ; Alzheimer Disease - complications ; Alzheimer Disease - diagnosis ; Alzheimer Disease - metabolism ; Amyloid beta-Peptides - metabolism ; Brain - metabolism ; Brain - ultrastructure ; Cardiomyopathies - diagnosis ; Cardiomyopathies - etiology ; Cardiomyopathies - metabolism ; Cross-Sectional Studies ; Enzyme-Linked Immunosorbent Assay ; Female ; Humans ; Immunoblotting ; Immunohistochemistry ; Male ; Microscopy, Electron, Transmission ; Myocardium - metabolism ; Myocardium - ultrastructure ; Retrospective Studies</subject><ispartof>Journal of the American College of Cardiology, 2016-12, Vol.68 (22), p.2395-2407</ispartof><rights>Copyright © 2016 American College of Cardiology Foundation. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27908343$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Troncone, Luca</creatorcontrib><creatorcontrib>Luciani, Marco</creatorcontrib><creatorcontrib>Coggins, Matthew</creatorcontrib><creatorcontrib>Wilker, Elissa H</creatorcontrib><creatorcontrib>Ho, Cheng-Ying</creatorcontrib><creatorcontrib>Codispoti, Kari Elise</creatorcontrib><creatorcontrib>Frosch, Matthew P</creatorcontrib><creatorcontrib>Kayed, Rakez</creatorcontrib><creatorcontrib>Del Monte, Federica</creatorcontrib><title>Aβ Amyloid Pathology Affects the Hearts of Patients With Alzheimer's Disease: Mind the Heart</title><title>Journal of the American College of Cardiology</title><addtitle>J Am Coll Cardiol</addtitle><description>Individually, heart failure (HF) and Alzheimer's disease (AD) are severe threats to population health, and their potential coexistence is an alarming prospect. In addition to sharing analogous epidemiological and genetic profiles, biochemical characteristics, and common triggers, the authors recently recognized common molecular and pathological features between the 2 conditions. Whereas cognitive impairment has been linked to HF through perfusion defects, angiopathy, and inflammation, whether patients with AD present with myocardial dysfunction, and if the 2 conditions bear a common pathogenesis as neglected siblings are unknown.
Here, the authors investigated whether amyloid beta (Aβ) protein aggregates are present in the hearts of patients with a primary diagnosis of AD, affecting myocardial function.
The authors examined myocardial function in a retrospective cross-sectional study from a cohort of AD patients and age-matched controls. Imaging and proteomics approaches were used to identify and quantify Aβ deposits in AD heart and brain specimens compared with controls. Cell shortening and calcium transients were measured on isolated adult cardiomyocytes.
Echocardiographic measurements of myocardial function suggest that patients with AD present with an anticipated diastolic dysfunction. As in the brain, Aβ
and Aβ
are present in the heart, and their expression is increased in AD.
Here, the authors provide the first report of the presence of compromised myocardial function and intramyocardial deposits of Aβ in AD patients. The findings depict a novel biological framework in which AD may be viewed either as a systemic disease or as a metastatic disorder leading to heart, and possibly multiorgan failure. AD and HF are both debilitating and life-threatening conditions, affecting enormous patient populations. Our findings underline a previously dismissed problem of a magnitude that will require new diagnostic approaches and treatments for brain and heart disease, and their combination.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Aging - metabolism</subject><subject>Alzheimer Disease - complications</subject><subject>Alzheimer Disease - diagnosis</subject><subject>Alzheimer Disease - metabolism</subject><subject>Amyloid beta-Peptides - metabolism</subject><subject>Brain - metabolism</subject><subject>Brain - ultrastructure</subject><subject>Cardiomyopathies - diagnosis</subject><subject>Cardiomyopathies - etiology</subject><subject>Cardiomyopathies - metabolism</subject><subject>Cross-Sectional Studies</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Female</subject><subject>Humans</subject><subject>Immunoblotting</subject><subject>Immunohistochemistry</subject><subject>Male</subject><subject>Microscopy, Electron, Transmission</subject><subject>Myocardium - metabolism</subject><subject>Myocardium - ultrastructure</subject><subject>Retrospective Studies</subject><issn>0735-1097</issn><issn>1558-3597</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkEtOwzAQhi0EoqVwARYoO9gkjOM4ttlF5VGkIliAWAbHD-IqaUqcLsppegaO0ANwJoIorFnNp_m_mcWP0DGGCANOz2fRTCoVxT1HwCNgZAcNMaU8JFSwXTTsNzTEINgAHXg_A4CUY7GPBjETwElChugl-_wIsnpVNU4HD7Irm6p5XQWZtUZ1PuhKE0yMbHts7HfuzLzzm_Wz68rNOqveS-Nq05764NJ5I725CO7cXG_Wf4eHaM_Kypuj7Ryhp-urx_EknN7f3I6zabjAVHShwEprmRCllUxlASkQAkJwnYBhPLWWaOBW6bgQhOIChMEJxTbmKZFMUUNG6Ozn76Jt3pbGd3ntvDJVJeemWfoccxZzwoiAf6gJ5bGgNO7Vk626LGqj80Xratmu8t8CyRdOv3XC</recordid><startdate>20161206</startdate><enddate>20161206</enddate><creator>Troncone, Luca</creator><creator>Luciani, Marco</creator><creator>Coggins, Matthew</creator><creator>Wilker, Elissa H</creator><creator>Ho, Cheng-Ying</creator><creator>Codispoti, Kari Elise</creator><creator>Frosch, Matthew P</creator><creator>Kayed, Rakez</creator><creator>Del Monte, Federica</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope><scope>7T5</scope><scope>7TK</scope><scope>H94</scope></search><sort><creationdate>20161206</creationdate><title>Aβ Amyloid Pathology Affects the Hearts of Patients With Alzheimer's Disease: Mind the Heart</title><author>Troncone, Luca ; Luciani, Marco ; Coggins, Matthew ; Wilker, Elissa H ; Ho, Cheng-Ying ; Codispoti, Kari Elise ; Frosch, Matthew P ; Kayed, Rakez ; Del Monte, Federica</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p159t-91cdda43cdca6ab060330998d40e786ff3d08fcd2b9351b09e1451f2863a7c5e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Aging - metabolism</topic><topic>Alzheimer Disease - complications</topic><topic>Alzheimer Disease - diagnosis</topic><topic>Alzheimer Disease - metabolism</topic><topic>Amyloid beta-Peptides - metabolism</topic><topic>Brain - metabolism</topic><topic>Brain - ultrastructure</topic><topic>Cardiomyopathies - diagnosis</topic><topic>Cardiomyopathies - etiology</topic><topic>Cardiomyopathies - metabolism</topic><topic>Cross-Sectional Studies</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Female</topic><topic>Humans</topic><topic>Immunoblotting</topic><topic>Immunohistochemistry</topic><topic>Male</topic><topic>Microscopy, Electron, Transmission</topic><topic>Myocardium - metabolism</topic><topic>Myocardium - ultrastructure</topic><topic>Retrospective Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Troncone, Luca</creatorcontrib><creatorcontrib>Luciani, Marco</creatorcontrib><creatorcontrib>Coggins, Matthew</creatorcontrib><creatorcontrib>Wilker, Elissa H</creatorcontrib><creatorcontrib>Ho, Cheng-Ying</creatorcontrib><creatorcontrib>Codispoti, Kari Elise</creatorcontrib><creatorcontrib>Frosch, Matthew P</creatorcontrib><creatorcontrib>Kayed, Rakez</creatorcontrib><creatorcontrib>Del Monte, Federica</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Journal of the American College of Cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Troncone, Luca</au><au>Luciani, Marco</au><au>Coggins, Matthew</au><au>Wilker, Elissa H</au><au>Ho, Cheng-Ying</au><au>Codispoti, Kari Elise</au><au>Frosch, Matthew P</au><au>Kayed, Rakez</au><au>Del Monte, Federica</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Aβ Amyloid Pathology Affects the Hearts of Patients With Alzheimer's Disease: Mind the Heart</atitle><jtitle>Journal of the American College of Cardiology</jtitle><addtitle>J Am Coll Cardiol</addtitle><date>2016-12-06</date><risdate>2016</risdate><volume>68</volume><issue>22</issue><spage>2395</spage><epage>2407</epage><pages>2395-2407</pages><issn>0735-1097</issn><eissn>1558-3597</eissn><abstract>Individually, heart failure (HF) and Alzheimer's disease (AD) are severe threats to population health, and their potential coexistence is an alarming prospect. In addition to sharing analogous epidemiological and genetic profiles, biochemical characteristics, and common triggers, the authors recently recognized common molecular and pathological features between the 2 conditions. Whereas cognitive impairment has been linked to HF through perfusion defects, angiopathy, and inflammation, whether patients with AD present with myocardial dysfunction, and if the 2 conditions bear a common pathogenesis as neglected siblings are unknown.
Here, the authors investigated whether amyloid beta (Aβ) protein aggregates are present in the hearts of patients with a primary diagnosis of AD, affecting myocardial function.
The authors examined myocardial function in a retrospective cross-sectional study from a cohort of AD patients and age-matched controls. Imaging and proteomics approaches were used to identify and quantify Aβ deposits in AD heart and brain specimens compared with controls. Cell shortening and calcium transients were measured on isolated adult cardiomyocytes.
Echocardiographic measurements of myocardial function suggest that patients with AD present with an anticipated diastolic dysfunction. As in the brain, Aβ
and Aβ
are present in the heart, and their expression is increased in AD.
Here, the authors provide the first report of the presence of compromised myocardial function and intramyocardial deposits of Aβ in AD patients. The findings depict a novel biological framework in which AD may be viewed either as a systemic disease or as a metastatic disorder leading to heart, and possibly multiorgan failure. AD and HF are both debilitating and life-threatening conditions, affecting enormous patient populations. Our findings underline a previously dismissed problem of a magnitude that will require new diagnostic approaches and treatments for brain and heart disease, and their combination.</abstract><cop>United States</cop><pmid>27908343</pmid><doi>10.1016/j.jacc.2016.08.073</doi><tpages>13</tpages></addata></record> |
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subjects | Aged Aged, 80 and over Aging - metabolism Alzheimer Disease - complications Alzheimer Disease - diagnosis Alzheimer Disease - metabolism Amyloid beta-Peptides - metabolism Brain - metabolism Brain - ultrastructure Cardiomyopathies - diagnosis Cardiomyopathies - etiology Cardiomyopathies - metabolism Cross-Sectional Studies Enzyme-Linked Immunosorbent Assay Female Humans Immunoblotting Immunohistochemistry Male Microscopy, Electron, Transmission Myocardium - metabolism Myocardium - ultrastructure Retrospective Studies |
title | Aβ Amyloid Pathology Affects the Hearts of Patients With Alzheimer's Disease: Mind the Heart |
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