Pathological Ventricular Remodeling: Mechanisms: Part 1 of 2

Despite declines in heart failure morbidity and mortality with current therapies, rehospitalization rates remain distressingly high, substantially affecting individuals, society, and the economy. As a result, the need for new therapeutic advances and novel medical devices is urgent. Disease-related...

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Published inCirculation (New York, N.Y.) Vol. 128; no. 4; pp. 388 - 400
Main Authors Burchfield, Jana S., Xie, Min, Hill, Joseph A.
Format Journal Article
LanguageEnglish
Published Hagerstown, MD by the American College of Cardiology Foundation and the American Heart Association, Inc 23.07.2013
Lippincott Williams & Wilkins
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Abstract Despite declines in heart failure morbidity and mortality with current therapies, rehospitalization rates remain distressingly high, substantially affecting individuals, society, and the economy. As a result, the need for new therapeutic advances and novel medical devices is urgent. Disease-related left ventricular remodeling is a complex process involving cardiac myocyte growth and death, vascular rarefaction, fibrosis, inflammation, and electrophysiological remodeling. Because these events are highly interrelated, targeting a single molecule or process may not be sufficient. Here, we review molecular and cellular mechanisms governing pathological ventricular remodeling.
AbstractList Despite declines in heart failure morbidity and mortality with current therapies, rehospitalization rates remain distressingly high, substantially affecting individuals, society, and the economy. As a result, the need for new therapeutic advances and novel medical devices is urgent. Disease-related left ventricular remodeling is a complex process involving cardiac myocyte growth and death, vascular rarefaction, fibrosis, inflammation, and electrophysiological remodeling. Because these events are highly interrelated, targeting a single molecule or process may not be sufficient. Here, we review molecular and cellular mechanisms governing pathological ventricular remodeling.
Despite declines in heart failure morbidity and mortality with current therapies, re-hospitalization rates remain distressingly high, impacting substantially on individuals, society, and the economy. As a result, the need for new therapeutic advances and novel medical devices is urgent. Disease-related left ventricular remodeling is a complex process involving cardiac myocyte growth and death, vascular rarefaction, fibrosis, inflammation, and electrophysiological remodeling. As these events are highly inter-related, targeting one single molecule or process may not be sufficient. Here, we review molecular and cellular mechanisms governing pathological ventricular remodeling.
Despite declines in heart failure morbidity and mortality with current therapies, rehospitalization rates remain distressingly high, substantially affecting individuals, society, and the economy. As a result, the need for new therapeutic advances and novel medical devices is urgent. Disease-related left ventricular remodeling is a complex process involving cardiac myocyte growth and death, vascular rarefaction, fibrosis, inflammation, and electrophysiological remodeling. Because these events are highly interrelated, targeting a single molecule or process may not be sufficient. Here, we review molecular and cellular mechanisms governing pathological ventricular remodeling.Despite declines in heart failure morbidity and mortality with current therapies, rehospitalization rates remain distressingly high, substantially affecting individuals, society, and the economy. As a result, the need for new therapeutic advances and novel medical devices is urgent. Disease-related left ventricular remodeling is a complex process involving cardiac myocyte growth and death, vascular rarefaction, fibrosis, inflammation, and electrophysiological remodeling. Because these events are highly interrelated, targeting a single molecule or process may not be sufficient. Here, we review molecular and cellular mechanisms governing pathological ventricular remodeling.
Author Xie, Min
Hill, Joseph A.
Burchfield, Jana S.
AuthorAffiliation From the Texas Heart Institute, Houston, TX (J.B.); and Departments of Internal Medicine (Cardiology) (M.X., J.A.H.) and Molecular Biology (J.A.H.), University of Texas Southwestern Medical Center, Dallas
AuthorAffiliation_xml – name: From the Texas Heart Institute, Houston, TX (J.B.); and Departments of Internal Medicine (Cardiology) (M.X., J.A.H.) and Molecular Biology (J.A.H.), University of Texas Southwestern Medical Center, Dallas
– name: 2 Dept of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX
– name: 1 Depts of Internal Medicine (Cardiology)
Author_xml – sequence: 1
  givenname: Jana
  surname: Burchfield
  middlename: S.
  fullname: Burchfield, Jana S.
  organization: From the Texas Heart Institute, Houston, TX (J.B.); and Departments of Internal Medicine (Cardiology) (M.X., J.A.H.) and Molecular Biology (J.A.H.), University of Texas Southwestern Medical Center, Dallas
– sequence: 2
  givenname: Min
  surname: Xie
  fullname: Xie, Min
– sequence: 3
  givenname: Joseph
  surname: Hill
  middlename: A.
  fullname: Hill, Joseph A.
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ID FETCH-LOGICAL-c4473-df759e8547c841f19d8bc784f92a50aceb7dc767e24aeb45589b9afd850cc0f53
ISSN 0009-7322
1524-4539
IngestDate Thu Aug 21 13:55:06 EDT 2025
Thu Jul 10 16:28:45 EDT 2025
Wed Feb 19 02:05:40 EST 2025
Mon Jul 21 09:17:30 EDT 2025
Tue Jul 01 03:20:31 EDT 2025
Thu Apr 24 22:59:44 EDT 2025
Fri May 16 03:43:48 EDT 2025
IsPeerReviewed true
IsScholarly true
Issue 4
Keywords Heart
cardiac electrophysiology
stem cells
Stem cell
Electrophysiology
ventricular remodeling
Cardiovascular disease
Inflammation
Mechanism
Vascular remodeling
Fibrosis
Circulatory system
Cardiology
fibrosis
inflammation
Language English
License CC BY 4.0
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c4473-df759e8547c841f19d8bc784f92a50aceb7dc767e24aeb45589b9afd850cc0f53
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content type line 23
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crossref_citationtrail_10_1161_CIRCULATIONAHA_113_001878
crossref_primary_10_1161_CIRCULATIONAHA_113_001878
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PublicationDate 2013-July-23
PublicationDateYYYYMMDD 2013-07-23
PublicationDate_xml – month: 07
  year: 2013
  text: 2013-July-23
  day: 23
PublicationDecade 2010
PublicationPlace Hagerstown, MD
PublicationPlace_xml – name: Hagerstown, MD
– name: United States
PublicationTitle Circulation (New York, N.Y.)
PublicationTitleAlternate Circulation
PublicationYear 2013
Publisher by the American College of Cardiology Foundation and the American Heart Association, Inc
Lippincott Williams & Wilkins
Publisher_xml – name: by the American College of Cardiology Foundation and the American Heart Association, Inc
– name: Lippincott Williams & Wilkins
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Snippet Despite declines in heart failure morbidity and mortality with current therapies, rehospitalization rates remain distressingly high, substantially affecting...
Despite declines in heart failure morbidity and mortality with current therapies, re-hospitalization rates remain distressingly high, impacting substantially...
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SubjectTerms Animals
Biological and medical sciences
Blood and lymphatic vessels
Cardiology. Vascular system
Cardiomegaly - pathology
Cardiomegaly - physiopathology
Cardiomegaly - therapy
Disease Progression
Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous
Heart Failure - pathology
Heart Failure - physiopathology
Heart Failure - therapy
Humans
Medical sciences
Myocardium - pathology
Ventricular Remodeling - physiology
Title Pathological Ventricular Remodeling: Mechanisms: Part 1 of 2
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https://www.ncbi.nlm.nih.gov/pubmed/23877061
https://www.proquest.com/docview/1412163104
https://pubmed.ncbi.nlm.nih.gov/PMC3801217
Volume 128
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