In Vivo Cardiovascular Molecular Imaging: Contributions to Precision Medicine and Drug Development
Conventional forms of noninvasive cardiovascular imaging that evaluate morphology, function, flow, and metabolism play a vital role in individual treatment decisions, often based on guidelines. Innovations in molecular imaging have enhanced our ability to spatially quantify the expression of a wider...
Gespeichert in:
Veröffentlicht in: | Circulation (New York, N.Y.) N.Y.), 2024-12, Vol.150 (23), p.1885-1897 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1897 |
---|---|
container_issue | 23 |
container_start_page | 1885 |
container_title | Circulation (New York, N.Y.) |
container_volume | 150 |
creator | Lindner, Jonathan R Morello, Matteo |
description | Conventional forms of noninvasive cardiovascular imaging that evaluate morphology, function, flow, and metabolism play a vital role in individual treatment decisions, often based on guidelines. Innovations in molecular imaging have enhanced our ability to spatially quantify the expression of a wider array of disease-related proteins, genes, or cell types, or the activity of specific pathogenic pathways. These techniques, which usually rely on design of targeted imaging probes, have already been used extensively in cancer medicine and have now become part of cardiovascular care in conditions such as amyloidosis and sarcoidosis. The recognition that common cardiovascular conditions are caused by a substantial diversity of pathobiologic pathways and the diversity of therapies available for use have rekindled interest in expanding the role of molecular imaging of tissue phenotype to improve precision in diagnosis and therapeutic decision-making. The intent of this article is to raise awareness and understanding of approaches to molecular or cellular imaging of phenotype with targeted probes, and their potential to promote the principles of precision medicine. Also addressed are the diverse roles of molecular imaging to improve precision and efficiency of new drug development at the stages of candidate identification, preclinical testing, and clinical trials. |
doi_str_mv | 10.1161/CIRCULATIONAHA.124.066522 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_3140922652</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3140922652</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1062-93477ac2947a3f0f67823960e56cfac60012be69df59aad1c830a31395e2a20c3</originalsourceid><addsrcrecordid>eNpVkF9LwzAUxYMobk6_gsQ3Xzrzp00X30qnrrA5kc3XkKXpiLTJTNqB395KVfDp3gPn3Hv4AXCD0RRjhu_y4jXfLrNNsX7OFtkUk3iKGEsIOQFjnJA4ihPKT8EYIcSjlBIyAhchvPeS0TQ5ByPKGcEpI2OwKyx8M0cHc-lL444yqK6WHq5crYetaOTe2P09zJ1tvdl1rXE2wNbBF6-VCb2CK10aZayG0pZw7rs9nOujrt2h0ba9BGeVrIO--pkTsH182OSLaLl-KvJsGSmMGIk4jdNUKsLjVNIKVSydkb4n0glTlVQMIUx2mvGySriUJVYziiTFlCeaSIIUnYDb4e7Bu49Oh1Y0Jihd19Jq1wVBcYw4IT2n3soHq_IuBK8rcfCmkf5TYCS-EYv_iEWPWAyI--z1z5tu1-jyL_nLlH4B1Ax5Eg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3140922652</pqid></control><display><type>article</type><title>In Vivo Cardiovascular Molecular Imaging: Contributions to Precision Medicine and Drug Development</title><source>MEDLINE</source><source>American Heart Association</source><source>Journals@Ovid Complete</source><creator>Lindner, Jonathan R ; Morello, Matteo</creator><creatorcontrib>Lindner, Jonathan R ; Morello, Matteo</creatorcontrib><description>Conventional forms of noninvasive cardiovascular imaging that evaluate morphology, function, flow, and metabolism play a vital role in individual treatment decisions, often based on guidelines. Innovations in molecular imaging have enhanced our ability to spatially quantify the expression of a wider array of disease-related proteins, genes, or cell types, or the activity of specific pathogenic pathways. These techniques, which usually rely on design of targeted imaging probes, have already been used extensively in cancer medicine and have now become part of cardiovascular care in conditions such as amyloidosis and sarcoidosis. The recognition that common cardiovascular conditions are caused by a substantial diversity of pathobiologic pathways and the diversity of therapies available for use have rekindled interest in expanding the role of molecular imaging of tissue phenotype to improve precision in diagnosis and therapeutic decision-making. The intent of this article is to raise awareness and understanding of approaches to molecular or cellular imaging of phenotype with targeted probes, and their potential to promote the principles of precision medicine. Also addressed are the diverse roles of molecular imaging to improve precision and efficiency of new drug development at the stages of candidate identification, preclinical testing, and clinical trials.</description><identifier>ISSN: 0009-7322</identifier><identifier>ISSN: 1524-4539</identifier><identifier>EISSN: 1524-4539</identifier><identifier>DOI: 10.1161/CIRCULATIONAHA.124.066522</identifier><identifier>PMID: 39621762</identifier><language>eng</language><publisher>United States</publisher><subject>Animals ; Cardiovascular Diseases - diagnostic imaging ; Cardiovascular Diseases - metabolism ; Drug Development ; Humans ; Molecular Imaging - methods ; Precision Medicine - methods</subject><ispartof>Circulation (New York, N.Y.), 2024-12, Vol.150 (23), p.1885-1897</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1062-93477ac2947a3f0f67823960e56cfac60012be69df59aad1c830a31395e2a20c3</cites><orcidid>0009-0006-4848-523X ; 0000-0003-2604-5277</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,3674,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39621762$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lindner, Jonathan R</creatorcontrib><creatorcontrib>Morello, Matteo</creatorcontrib><title>In Vivo Cardiovascular Molecular Imaging: Contributions to Precision Medicine and Drug Development</title><title>Circulation (New York, N.Y.)</title><addtitle>Circulation</addtitle><description>Conventional forms of noninvasive cardiovascular imaging that evaluate morphology, function, flow, and metabolism play a vital role in individual treatment decisions, often based on guidelines. Innovations in molecular imaging have enhanced our ability to spatially quantify the expression of a wider array of disease-related proteins, genes, or cell types, or the activity of specific pathogenic pathways. These techniques, which usually rely on design of targeted imaging probes, have already been used extensively in cancer medicine and have now become part of cardiovascular care in conditions such as amyloidosis and sarcoidosis. The recognition that common cardiovascular conditions are caused by a substantial diversity of pathobiologic pathways and the diversity of therapies available for use have rekindled interest in expanding the role of molecular imaging of tissue phenotype to improve precision in diagnosis and therapeutic decision-making. The intent of this article is to raise awareness and understanding of approaches to molecular or cellular imaging of phenotype with targeted probes, and their potential to promote the principles of precision medicine. Also addressed are the diverse roles of molecular imaging to improve precision and efficiency of new drug development at the stages of candidate identification, preclinical testing, and clinical trials.</description><subject>Animals</subject><subject>Cardiovascular Diseases - diagnostic imaging</subject><subject>Cardiovascular Diseases - metabolism</subject><subject>Drug Development</subject><subject>Humans</subject><subject>Molecular Imaging - methods</subject><subject>Precision Medicine - methods</subject><issn>0009-7322</issn><issn>1524-4539</issn><issn>1524-4539</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkF9LwzAUxYMobk6_gsQ3Xzrzp00X30qnrrA5kc3XkKXpiLTJTNqB395KVfDp3gPn3Hv4AXCD0RRjhu_y4jXfLrNNsX7OFtkUk3iKGEsIOQFjnJA4ihPKT8EYIcSjlBIyAhchvPeS0TQ5ByPKGcEpI2OwKyx8M0cHc-lL444yqK6WHq5crYetaOTe2P09zJ1tvdl1rXE2wNbBF6-VCb2CK10aZayG0pZw7rs9nOujrt2h0ba9BGeVrIO--pkTsH182OSLaLl-KvJsGSmMGIk4jdNUKsLjVNIKVSydkb4n0glTlVQMIUx2mvGySriUJVYziiTFlCeaSIIUnYDb4e7Bu49Oh1Y0Jihd19Jq1wVBcYw4IT2n3soHq_IuBK8rcfCmkf5TYCS-EYv_iEWPWAyI--z1z5tu1-jyL_nLlH4B1Ax5Eg</recordid><startdate>20241203</startdate><enddate>20241203</enddate><creator>Lindner, Jonathan R</creator><creator>Morello, Matteo</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0009-0006-4848-523X</orcidid><orcidid>https://orcid.org/0000-0003-2604-5277</orcidid></search><sort><creationdate>20241203</creationdate><title>In Vivo Cardiovascular Molecular Imaging: Contributions to Precision Medicine and Drug Development</title><author>Lindner, Jonathan R ; Morello, Matteo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1062-93477ac2947a3f0f67823960e56cfac60012be69df59aad1c830a31395e2a20c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Animals</topic><topic>Cardiovascular Diseases - diagnostic imaging</topic><topic>Cardiovascular Diseases - metabolism</topic><topic>Drug Development</topic><topic>Humans</topic><topic>Molecular Imaging - methods</topic><topic>Precision Medicine - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lindner, Jonathan R</creatorcontrib><creatorcontrib>Morello, Matteo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Circulation (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lindner, Jonathan R</au><au>Morello, Matteo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>In Vivo Cardiovascular Molecular Imaging: Contributions to Precision Medicine and Drug Development</atitle><jtitle>Circulation (New York, N.Y.)</jtitle><addtitle>Circulation</addtitle><date>2024-12-03</date><risdate>2024</risdate><volume>150</volume><issue>23</issue><spage>1885</spage><epage>1897</epage><pages>1885-1897</pages><issn>0009-7322</issn><issn>1524-4539</issn><eissn>1524-4539</eissn><abstract>Conventional forms of noninvasive cardiovascular imaging that evaluate morphology, function, flow, and metabolism play a vital role in individual treatment decisions, often based on guidelines. Innovations in molecular imaging have enhanced our ability to spatially quantify the expression of a wider array of disease-related proteins, genes, or cell types, or the activity of specific pathogenic pathways. These techniques, which usually rely on design of targeted imaging probes, have already been used extensively in cancer medicine and have now become part of cardiovascular care in conditions such as amyloidosis and sarcoidosis. The recognition that common cardiovascular conditions are caused by a substantial diversity of pathobiologic pathways and the diversity of therapies available for use have rekindled interest in expanding the role of molecular imaging of tissue phenotype to improve precision in diagnosis and therapeutic decision-making. The intent of this article is to raise awareness and understanding of approaches to molecular or cellular imaging of phenotype with targeted probes, and their potential to promote the principles of precision medicine. Also addressed are the diverse roles of molecular imaging to improve precision and efficiency of new drug development at the stages of candidate identification, preclinical testing, and clinical trials.</abstract><cop>United States</cop><pmid>39621762</pmid><doi>10.1161/CIRCULATIONAHA.124.066522</doi><tpages>13</tpages><orcidid>https://orcid.org/0009-0006-4848-523X</orcidid><orcidid>https://orcid.org/0000-0003-2604-5277</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0009-7322 |
ispartof | Circulation (New York, N.Y.), 2024-12, Vol.150 (23), p.1885-1897 |
issn | 0009-7322 1524-4539 1524-4539 |
language | eng |
recordid | cdi_proquest_miscellaneous_3140922652 |
source | MEDLINE; American Heart Association; Journals@Ovid Complete |
subjects | Animals Cardiovascular Diseases - diagnostic imaging Cardiovascular Diseases - metabolism Drug Development Humans Molecular Imaging - methods Precision Medicine - methods |
title | In Vivo Cardiovascular Molecular Imaging: Contributions to Precision Medicine and Drug Development |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-17T16%3A13%3A27IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=In%20Vivo%20Cardiovascular%20Molecular%20Imaging:%20Contributions%20to%20Precision%20Medicine%20and%20Drug%20Development&rft.jtitle=Circulation%20(New%20York,%20N.Y.)&rft.au=Lindner,%20Jonathan%20R&rft.date=2024-12-03&rft.volume=150&rft.issue=23&rft.spage=1885&rft.epage=1897&rft.pages=1885-1897&rft.issn=0009-7322&rft.eissn=1524-4539&rft_id=info:doi/10.1161/CIRCULATIONAHA.124.066522&rft_dat=%3Cproquest_cross%3E3140922652%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3140922652&rft_id=info:pmid/39621762&rfr_iscdi=true |