CMR-based cardiac phenotyping in different forms of heart failure
Heart failure (HF) is a heterogenous disease requiring precise diagnostics and knowledge of pathophysiological processes. Since structural and functional imaging data are scarce we hypothesized that cardiac magnetic resonance (CMR)-based analyses would provide accurate characterization and mechanist...
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Published in | The international journal of cardiovascular imaging Vol. 40; no. 7; pp. 1585 - 1596 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Dordrecht
Springer Netherlands
01.07.2024
Springer Nature B.V |
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Online Access | Get full text |
ISSN | 1875-8312 1569-5794 1875-8312 1573-0743 |
DOI | 10.1007/s10554-024-03145-4 |
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Abstract | Heart failure (HF) is a heterogenous disease requiring precise diagnostics and knowledge of pathophysiological processes. Since structural and functional imaging data are scarce we hypothesized that cardiac magnetic resonance (CMR)-based analyses would provide accurate characterization and mechanistic insights into different HF groups comprising preserved (HFpEF), mid-range (HFmrEF) and reduced ejection fraction (HFrEF). 22 HFpEF, 17 HFmrEF and 15 HFrEF patients as well as 19 healthy volunteers were included. CMR image assessment contained left atrial (LA) and left ventricular (LV) volumetric evaluation as well as left atrioventricular coupling index (LACI). Furthermore, CMR feature-tracking included LV and LA strain in terms of reservoir (Es), conduit (Ee) and active boosterpump (Ea) function. CMR-based tissue characterization comprised T1 mapping as well as late-gadolinium enhancement (LGE) analyses. HFpEF patients showed predominant atrial impairment (Es 20.8%vs.25.4%, p = 0.02 and Ee 8.3%vs.13.5%, p = 0.001) and increased LACI compared to healthy controls (14.5%vs.23.3%, p = 0.004). Patients with HFmrEF showed LV enlargement but mostly preserved LA function with a compensatory increase in LA boosterpump (LA Ea: 15.0%, p = 0.049). In HFrEF LA and LV functional impairment was documented (Es: 14.2%, Ee: 5.4% p < 0.001 respectively; Ea: 8.8%, p = 0.02). This was paralleled by non-invasively assessed progressive fibrosis (T1 mapping and LGE; HFrEF > HFmrEF > HFpEF). CMR-imaging reveals insights into HF phenotypes with mainly atrial affection in HFpEF, ventricular affection with atrial compensation in HFmrEF and global impairment in HFrEF paralleled by progressive LV fibrosis. These data suggest a necessity for a personalized HF management based on imaging findings for future optimized patient management. |
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AbstractList | Heart failure (HF) is a heterogenous disease requiring precise diagnostics and knowledge of pathophysiological processes. Since structural and functional imaging data are scarce we hypothesized that cardiac magnetic resonance (CMR)-based analyses would provide accurate characterization and mechanistic insights into different HF groups comprising preserved (HFpEF), mid-range (HFmrEF) and reduced ejection fraction (HFrEF). 22 HFpEF, 17 HFmrEF and 15 HFrEF patients as well as 19 healthy volunteers were included. CMR image assessment contained left atrial (LA) and left ventricular (LV) volumetric evaluation as well as left atrioventricular coupling index (LACI). Furthermore, CMR feature-tracking included LV and LA strain in terms of reservoir (Es), conduit (Ee) and active boosterpump (Ea) function. CMR-based tissue characterization comprised T1 mapping as well as late-gadolinium enhancement (LGE) analyses. HFpEF patients showed predominant atrial impairment (Es 20.8%vs.25.4%, p = 0.02 and Ee 8.3%vs.13.5%, p = 0.001) and increased LACI compared to healthy controls (14.5%vs.23.3%, p = 0.004). Patients with HFmrEF showed LV enlargement but mostly preserved LA function with a compensatory increase in LA boosterpump (LA Ea: 15.0%, p = 0.049). In HFrEF LA and LV functional impairment was documented (Es: 14.2%, Ee: 5.4% p < 0.001 respectively; Ea: 8.8%, p = 0.02). This was paralleled by non-invasively assessed progressive fibrosis (T1 mapping and LGE; HFrEF > HFmrEF > HFpEF). CMR-imaging reveals insights into HF phenotypes with mainly atrial affection in HFpEF, ventricular affection with atrial compensation in HFmrEF and global impairment in HFrEF paralleled by progressive LV fibrosis. These data suggest a necessity for a personalized HF management based on imaging findings for future optimized patient management. Heart failure (HF) is a heterogenous disease requiring precise diagnostics and knowledge of pathophysiological processes. Since structural and functional imaging data are scarce we hypothesized that cardiac magnetic resonance (CMR)-based analyses would provide accurate characterization and mechanistic insights into different HF groups comprising preserved (HFpEF), mid-range (HFmrEF) and reduced ejection fraction (HFrEF). 22 HFpEF, 17 HFmrEF and 15 HFrEF patients as well as 19 healthy volunteers were included. CMR image assessment contained left atrial (LA) and left ventricular (LV) volumetric evaluation as well as left atrioventricular coupling index (LACI). Furthermore, CMR feature-tracking included LV and LA strain in terms of reservoir (Es), conduit (Ee) and active boosterpump (Ea) function. CMR-based tissue characterization comprised T1 mapping as well as late-gadolinium enhancement (LGE) analyses. HFpEF patients showed predominant atrial impairment (Es 20.8%vs.25.4%, p = 0.02 and Ee 8.3%vs.13.5%, p = 0.001) and increased LACI compared to healthy controls (14.5%vs.23.3%, p = 0.004). Patients with HFmrEF showed LV enlargement but mostly preserved LA function with a compensatory increase in LA boosterpump (LA Ea: 15.0%, p = 0.049). In HFrEF LA and LV functional impairment was documented (Es: 14.2%, Ee: 5.4% p < 0.001 respectively; Ea: 8.8%, p = 0.02). This was paralleled by non-invasively assessed progressive fibrosis (T1 mapping and LGE; HFrEF > HFmrEF > HFpEF). CMR-imaging reveals insights into HF phenotypes with mainly atrial affection in HFpEF, ventricular affection with atrial compensation in HFmrEF and global impairment in HFrEF paralleled by progressive LV fibrosis. These data suggest a necessity for a personalized HF management based on imaging findings for future optimized patient management.Heart failure (HF) is a heterogenous disease requiring precise diagnostics and knowledge of pathophysiological processes. Since structural and functional imaging data are scarce we hypothesized that cardiac magnetic resonance (CMR)-based analyses would provide accurate characterization and mechanistic insights into different HF groups comprising preserved (HFpEF), mid-range (HFmrEF) and reduced ejection fraction (HFrEF). 22 HFpEF, 17 HFmrEF and 15 HFrEF patients as well as 19 healthy volunteers were included. CMR image assessment contained left atrial (LA) and left ventricular (LV) volumetric evaluation as well as left atrioventricular coupling index (LACI). Furthermore, CMR feature-tracking included LV and LA strain in terms of reservoir (Es), conduit (Ee) and active boosterpump (Ea) function. CMR-based tissue characterization comprised T1 mapping as well as late-gadolinium enhancement (LGE) analyses. HFpEF patients showed predominant atrial impairment (Es 20.8%vs.25.4%, p = 0.02 and Ee 8.3%vs.13.5%, p = 0.001) and increased LACI compared to healthy controls (14.5%vs.23.3%, p = 0.004). Patients with HFmrEF showed LV enlargement but mostly preserved LA function with a compensatory increase in LA boosterpump (LA Ea: 15.0%, p = 0.049). In HFrEF LA and LV functional impairment was documented (Es: 14.2%, Ee: 5.4% p < 0.001 respectively; Ea: 8.8%, p = 0.02). This was paralleled by non-invasively assessed progressive fibrosis (T1 mapping and LGE; HFrEF > HFmrEF > HFpEF). CMR-imaging reveals insights into HF phenotypes with mainly atrial affection in HFpEF, ventricular affection with atrial compensation in HFmrEF and global impairment in HFrEF paralleled by progressive LV fibrosis. These data suggest a necessity for a personalized HF management based on imaging findings for future optimized patient management. |
Author | Hasenfuß, Gerd Hashemi, Djawid Schuster, Andreas Kowallick, Johannes T. Lange, Torben Backhaus, Sören J. Kelle, Sebastian Schulz, Alexander Evertz, Ruben |
Author_xml | – sequence: 1 givenname: Torben surname: Lange fullname: Lange, Torben organization: Department of Cardiology and Pneumology, University Medical Center Göttingen, Georg-August University, German Centre of Cardiovascular Research (DZHK), partner site Lower Saxony – sequence: 2 givenname: Sören J. surname: Backhaus fullname: Backhaus, Sören J. organization: Department of Cardiology, Campus Kerckhoff of the Justus-Liebig-Universität Gießen, Kerckhoff-Clinic – sequence: 3 givenname: Alexander surname: Schulz fullname: Schulz, Alexander organization: Department of Cardiology and Pneumology, University Medical Center Göttingen, Georg-August University, German Centre of Cardiovascular Research (DZHK), partner site Lower Saxony – sequence: 4 givenname: Djawid surname: Hashemi fullname: Hashemi, Djawid organization: Department of Internal Medicine/Cardiology, Charité Campus Virchow Clinic, German Centre for Cardiovascular Research (DZHK), partner site Berlin – sequence: 5 givenname: Ruben surname: Evertz fullname: Evertz, Ruben organization: Department of Cardiology and Pneumology, University Medical Center Göttingen, Georg-August University, German Centre of Cardiovascular Research (DZHK), partner site Lower Saxony – sequence: 6 givenname: Johannes T. surname: Kowallick fullname: Kowallick, Johannes T. organization: German Centre of Cardiovascular Research (DZHK), partner site Lower Saxony, Institute for Diagnostic and Interventional Radiology, University Medical Center Göttingen, Georg-August University – sequence: 7 givenname: Gerd surname: Hasenfuß fullname: Hasenfuß, Gerd organization: Department of Cardiology and Pneumology, University Medical Center Göttingen, Georg-August University, German Centre of Cardiovascular Research (DZHK), partner site Lower Saxony – sequence: 8 givenname: Sebastian surname: Kelle fullname: Kelle, Sebastian organization: Department of Internal Medicine/Cardiology, Charité Campus Virchow Clinic, German Centre for Cardiovascular Research (DZHK), partner site Berlin – sequence: 9 givenname: Andreas surname: Schuster fullname: Schuster, Andreas email: andreas_schuster@gmx.net organization: Department of Cardiology and Pneumology, University Medical Center Göttingen, Georg-August University, German Centre of Cardiovascular Research (DZHK), partner site Lower Saxony |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/38878148$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1016_j_ins_2024_121513 crossref_primary_10_3390_jcdd12040110 crossref_primary_10_1002_ehf2_15251 |
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Keywords | Heart failure CMR imaging Left atrioventricular coupling index CMR-based tissue characterization CMR feature-tracking Myocardial strain assessment |
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PublicationSubtitle | X-Ray Imaging, Intravascular Imaging, Echocardiography, Nuclear Cardiology, Computed Tomography and Magnetic Resonance Imaging |
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Snippet | Heart failure (HF) is a heterogenous disease requiring precise diagnostics and knowledge of pathophysiological processes. Since structural and functional... |
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StartPage | 1585 |
SubjectTerms | Cardiac Imaging Cardiology Congestive heart failure Coronary artery disease Fibrosis Gadolinium Heart diseases Heart failure Imaging Impairment Magnetic resonance Magnetic resonance imaging Mapping Medical imaging Medicine Medicine & Public Health Original Paper Phenotypes Phenotyping Radiology Structural analysis Structure-function relationships Ventricle |
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Title | CMR-based cardiac phenotyping in different forms of heart failure |
URI | https://link.springer.com/article/10.1007/s10554-024-03145-4 https://www.ncbi.nlm.nih.gov/pubmed/38878148 https://www.proquest.com/docview/3082426922 https://www.proquest.com/docview/3068751780 |
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