Connections Between Clonal Hematopoiesis, Cardiovascular Disease, and Cancer: A Review. (Record no. 4510)

MARC details
000 -LEADER
fixed length control field 03821nam a22005777a 4500
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 190823s20192019 xxu||||| |||| 00| 0 eng d
024 ## - OTHER STANDARD IDENTIFIER
Standard number or code 10.1001/jamacardio.2019.0302 [doi]
024 ## - OTHER STANDARD IDENTIFIER
Standard number or code 2727340 [pii]
040 ## - CATALOGING SOURCE
Original cataloging agency Ovid MEDLINE(R)
099 ## - LOCAL FREE-TEXT CALL NUMBER (OCLC)
PMID 30865214
245 ## - TITLE STATEMENT
Title Connections Between Clonal Hematopoiesis, Cardiovascular Disease, and Cancer: A Review.
251 ## - Source
Source JAMA Cardiology. 4(4):380-387, 2019 Apr 01.
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Abbreviated source JAMA Cardiol. 4(4):380-387, 2019 Apr 01.
253 ## - Journal Name
Journal name JAMA cardiology
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Year 2019
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Manufacturer FY2019
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Publication status ppublish
266 ## - Date added to catalog
Date added to catalog 2019-08-23
520 ## - SUMMARY, ETC.
Abstract Conclusions and Relevance: Clonal hematopoiesis represents a premalignant state, with carriers having an increased risk of hematological malignant conditions. Although most carriers will not develop a malignant condition, CH confers an increased risk of CVD, possibly via inflammation. Clonal hematopoiesis may also contribute to CVD in survivors of cancer, although this hypothesis requires validation. Clinically, as advanced sequencing techniques become available, CH may pave the way for precision medicine in the field of cardio-oncology.
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Abstract Importance: Clonal hematopoiesis (CH) has been recently described as a novel driver for cancer and cardiovascular disease (CVD). Clonal hematopoiesis is a common, age-associated disorder marked by expansion of hematopoietic clones carrying recurrent somatic mutations. Current literature suggests that patients with CH have a higher risk of subsequent hematological malignant conditions and mortality attributable to excess CVD. This review discusses the association of cancer with CVD with CH as a potential unifying factor.
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Abstract Observations: The prevalence of CH varies based on the sequencing depth, diagnostic criteria, and patient age and ranges from less than 1% in those younger than 40 years to more than 15% to 20% in those 90 years and older. Clonal hematopoiesis is associated with a 0.5% to 1.0% absolute annual risk of hematological malignant condition and a 2-fold to 4-fold higher risk of coronary artery disease, stroke, and CVD deaths, independent of traditional cardiovascular risk factors. In fact, CH appears to have a relative risk similar to that of traditional cardiovascular risk factors for CVD. Experimental studies suggest that the link between CVD and CH is causal, with inflammation as 1 potential mechanism. There may be also a link between CH and CVD in survivors of cancer; however, data to support this association are currently limited.
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Language note English
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Topical term or geographic name entry element *Cardiovascular Diseases/ge [Genetics]
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Topical term or geographic name entry element *Clonal Evolution/ph [Physiology]
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Topical term or geographic name entry element *Hematopoiesis/ge [Genetics]
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Topical term or geographic name entry element *Neoplasms/ge [Genetics]
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Topical term or geographic name entry element Adult
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Topical term or geographic name entry element Aged
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Topical term or geographic name entry element Aged, 80 and over
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Topical term or geographic name entry element Cardiovascular Diseases/ep [Epidemiology]
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Topical term or geographic name entry element Cardiovascular Diseases/mo [Mortality]
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Coronary Artery Disease/ge [Genetics]
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Coronary Artery Disease/mo [Mortality]
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Humans
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Topical term or geographic name entry element Inflammation/ge [Genetics]
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Topical term or geographic name entry element Middle Aged
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Topical term or geographic name entry element Mutation/ge [Genetics]
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Topical term or geographic name entry element Neoplasms/ep [Epidemiology]
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Topical term or geographic name entry element Neoplasms/mo [Mortality]
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Topical term or geographic name entry element Prevalence
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Topical term or geographic name entry element Risk Factors
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Topical term or geographic name entry element Stroke/ep [Epidemiology]
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Stroke/ge [Genetics]
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Stroke/mo [Mortality]
651 ## - SUBJECT ADDED ENTRY--GEOGRAPHIC NAME
Institution MedStar Heart & Vascular Institute
657 ## - INDEX TERM--FUNCTION
Medline publication type Journal Article
700 ## - ADDED ENTRY--PERSONAL NAME
Local Authors Barac, Ana
790 ## - Authors
All authors Barac A, Calvillo-Arguelles O, Jaiswal S, Moslehi JJ, Schimmer A, Shlush LI, Thavendiranathan P
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DOI <a href="https://dx.doi.org/10.1001/jamacardio.2019.0302">https://dx.doi.org/10.1001/jamacardio.2019.0302</a>
Public note https://dx.doi.org/10.1001/jamacardio.2019.0302
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Koha item type Journal Article
Item type description Article
Holdings
Withdrawn status Lost status Damaged status Not for loan Collection Home library Current library Date acquired Total Checkouts Full call number Barcode Date last seen Price effective from Koha item type
          MedStar Authors Catalog MedStar Authors Catalog 08/23/2019   30865214 30865214 08/23/2019 08/23/2019 Journal Article

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