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
Hauptverfasser: Troncone, Luca, Luciani, Marco, Coggins, Matthew, Wilker, Elissa H, Ho, Cheng-Ying, Codispoti, Kari Elise, Frosch, Matthew P, Kayed, Rakez, Del Monte, Federica
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container_end_page 2407
container_issue 22
container_start_page 2395
container_title Journal of the American College of Cardiology
container_volume 68
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.
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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. 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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. 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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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