Aortic valve calcification is subject to aortic stenosis severity and the underlying flow pattern
Sex- and flow-related aortic valve calcification (AVC) studies are still limited in number, and data on the exact calcium quantity and distribution are scarce. Therefore, we aimed to (1) re-define the best threshold of AVC load to distinguish severe from moderate aortic stenosis (AS) in common AS en...
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Published in | Heart and vessels Vol. 36; no. 2; pp. 242 - 251 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
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01.02.2021
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Abstract | Sex- and flow-related aortic valve calcification (AVC) studies are still limited in number, and data on the exact calcium quantity and distribution are scarce. Therefore, we aimed to (1) re-define the best threshold of AVC load to distinguish severe from moderate aortic stenosis (AS) in common AS entities and to (2) evaluate differences in the aortic annulus and left ventricular outflow tract (LVOT) calcium load. Nine hundred and thirty-eight patients with contrast-enhanced cardiac MSCT and moderate-to-severe aortic stenosis (AS) were retrospectively enrolled. Patients with severe AS ≤ 1.0 cm
2
(
n
= 841) were further separated into three AS entities: high gradient (HGAS,
n
= 370, 44.0%), paradoxical low gradient (pLGAS,
n
= 333, 39.6%), and classical low gradient (LGAS,
n
= 138, 16.4%). AVC, leaflet, and LVOT calcification were quantified. Aortic valve calcification scores were highest in severe HGAS, and lower in severe pLGAS and classical LGAS. In all severity and AS entities, the non-coronary cusp (NCC) was the most calcified one. LVOT calcification was consistently comparable between gender and AS entities. Accuracy of logistic regression was the highest in HGAS (male vs. female: AVC > 2156 Agatston units (AU), c-index 0.76; vs. AVC > 1292 AU, c-index 0.85; or AVC density > 406 AU/cm
2
, c-index 0.82; vs. > 259 AU/cm
2
, c-index 0.86; each
p
< 0.0001*) to diagnose severe AS. AVC could only be used in men to differentiate between severe LGAS and moderate AS. Data from this retrospective analysis indicate that the NCC is subject to pre-dominant degeneration throughout gender, AS severity, and several AS entities. AVC was consistently comparable in severe pLGAS and classical LGAS, but only AVC in severe LGAS could sufficiently distinguish from moderate AS in men. LVOT calcification failed to be a reliable indicator of accelerating AS. |
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AbstractList | Sex- and flow-related aortic valve calcification (AVC) studies are still limited in number, and data on the exact calcium quantity and distribution are scarce. Therefore, we aimed to (1) re-define the best threshold of AVC load to distinguish severe from moderate aortic stenosis (AS) in common AS entities and to (2) evaluate differences in the aortic annulus and left ventricular outflow tract (LVOT) calcium load. Nine hundred and thirty-eight patients with contrast-enhanced cardiac MSCT and moderate-to-severe aortic stenosis (AS) were retrospectively enrolled. Patients with severe AS ≤ 1.0 cm
2
(
n
= 841) were further separated into three AS entities: high gradient (HGAS,
n
= 370, 44.0%), paradoxical low gradient (pLGAS,
n
= 333, 39.6%), and classical low gradient (LGAS,
n
= 138, 16.4%). AVC, leaflet, and LVOT calcification were quantified. Aortic valve calcification scores were highest in severe HGAS, and lower in severe pLGAS and classical LGAS. In all severity and AS entities, the non-coronary cusp (NCC) was the most calcified one. LVOT calcification was consistently comparable between gender and AS entities. Accuracy of logistic regression was the highest in HGAS (male vs. female: AVC > 2156 Agatston units (AU), c-index 0.76; vs. AVC > 1292 AU, c-index 0.85; or AVC density > 406 AU/cm
2
, c-index 0.82; vs. > 259 AU/cm
2
, c-index 0.86; each
p
< 0.0001*) to diagnose severe AS. AVC could only be used in men to differentiate between severe LGAS and moderate AS. Data from this retrospective analysis indicate that the NCC is subject to pre-dominant degeneration throughout gender, AS severity, and several AS entities. AVC was consistently comparable in severe pLGAS and classical LGAS, but only AVC in severe LGAS could sufficiently distinguish from moderate AS in men. LVOT calcification failed to be a reliable indicator of accelerating AS. Sex- and flow-related aortic valve calcification (AVC) studies are still limited in number, and data on the exact calcium quantity and distribution are scarce. Therefore, we aimed to (1) re-define the best threshold of AVC load to distinguish severe from moderate aortic stenosis (AS) in common AS entities and to (2) evaluate differences in the aortic annulus and left ventricular outflow tract (LVOT) calcium load. Nine hundred and thirty-eight patients with contrast-enhanced cardiac MSCT and moderate-to-severe aortic stenosis (AS) were retrospectively enrolled. Patients with severe AS ≤ 1.0 cm2 (n = 841) were further separated into three AS entities: high gradient (HGAS, n = 370, 44.0%), paradoxical low gradient (pLGAS, n = 333, 39.6%), and classical low gradient (LGAS, n = 138, 16.4%). AVC, leaflet, and LVOT calcification were quantified. Aortic valve calcification scores were highest in severe HGAS, and lower in severe pLGAS and classical LGAS. In all severity and AS entities, the non-coronary cusp (NCC) was the most calcified one. LVOT calcification was consistently comparable between gender and AS entities. Accuracy of logistic regression was the highest in HGAS (male vs. female: AVC > 2156 Agatston units (AU), c-index 0.76; vs. AVC > 1292 AU, c-index 0.85; or AVC density > 406 AU/cm2, c-index 0.82; vs. > 259 AU/cm2, c-index 0.86; each p < 0.0001*) to diagnose severe AS. AVC could only be used in men to differentiate between severe LGAS and moderate AS. Data from this retrospective analysis indicate that the NCC is subject to pre-dominant degeneration throughout gender, AS severity, and several AS entities. AVC was consistently comparable in severe pLGAS and classical LGAS, but only AVC in severe LGAS could sufficiently distinguish from moderate AS in men. LVOT calcification failed to be a reliable indicator of accelerating AS. Sex- and flow-related aortic valve calcification (AVC) studies are still limited in number, and data on the exact calcium quantity and distribution are scarce. Therefore, we aimed to (1) re-define the best threshold of AVC load to distinguish severe from moderate aortic stenosis (AS) in common AS entities and to (2) evaluate differences in the aortic annulus and left ventricular outflow tract (LVOT) calcium load. Nine hundred and thirty-eight patients with contrast-enhanced cardiac MSCT and moderate-to-severe aortic stenosis (AS) were retrospectively enrolled. Patients with severe AS ≤ 1.0 cm (n = 841) were further separated into three AS entities: high gradient (HGAS, n = 370, 44.0%), paradoxical low gradient (pLGAS, n = 333, 39.6%), and classical low gradient (LGAS, n = 138, 16.4%). AVC, leaflet, and LVOT calcification were quantified. Aortic valve calcification scores were highest in severe HGAS, and lower in severe pLGAS and classical LGAS. In all severity and AS entities, the non-coronary cusp (NCC) was the most calcified one. LVOT calcification was consistently comparable between gender and AS entities. Accuracy of logistic regression was the highest in HGAS (male vs. female: AVC > 2156 Agatston units (AU), c-index 0.76; vs. AVC > 1292 AU, c-index 0.85; or AVC density > 406 AU/cm , c-index 0.82; vs. > 259 AU/cm , c-index 0.86; each p < 0.0001*) to diagnose severe AS. AVC could only be used in men to differentiate between severe LGAS and moderate AS. Data from this retrospective analysis indicate that the NCC is subject to pre-dominant degeneration throughout gender, AS severity, and several AS entities. AVC was consistently comparable in severe pLGAS and classical LGAS, but only AVC in severe LGAS could sufficiently distinguish from moderate AS in men. LVOT calcification failed to be a reliable indicator of accelerating AS. Sex- and flow-related aortic valve calcification (AVC) studies are still limited in number, and data on the exact calcium quantity and distribution are scarce. Therefore, we aimed to (1) re-define the best threshold of AVC load to distinguish severe from moderate aortic stenosis (AS) in common AS entities and to (2) evaluate differences in the aortic annulus and left ventricular outflow tract (LVOT) calcium load. Nine hundred and thirty-eight patients with contrast-enhanced cardiac MSCT and moderate-to-severe aortic stenosis (AS) were retrospectively enrolled. Patients with severe AS ≤ 1.0 cm2 (n = 841) were further separated into three AS entities: high gradient (HGAS, n = 370, 44.0%), paradoxical low gradient (pLGAS, n = 333, 39.6%), and classical low gradient (LGAS, n = 138, 16.4%). AVC, leaflet, and LVOT calcification were quantified. Aortic valve calcification scores were highest in severe HGAS, and lower in severe pLGAS and classical LGAS. In all severity and AS entities, the non-coronary cusp (NCC) was the most calcified one. LVOT calcification was consistently comparable between gender and AS entities. Accuracy of logistic regression was the highest in HGAS (male vs. female: AVC > 2156 Agatston units (AU), c-index 0.76; vs. AVC > 1292 AU, c-index 0.85; or AVC density > 406 AU/cm2, c-index 0.82; vs. > 259 AU/cm2, c-index 0.86; each p < 0.0001*) to diagnose severe AS. AVC could only be used in men to differentiate between severe LGAS and moderate AS. Data from this retrospective analysis indicate that the NCC is subject to pre-dominant degeneration throughout gender, AS severity, and several AS entities. AVC was consistently comparable in severe pLGAS and classical LGAS, but only AVC in severe LGAS could sufficiently distinguish from moderate AS in men. LVOT calcification failed to be a reliable indicator of accelerating AS.Sex- and flow-related aortic valve calcification (AVC) studies are still limited in number, and data on the exact calcium quantity and distribution are scarce. Therefore, we aimed to (1) re-define the best threshold of AVC load to distinguish severe from moderate aortic stenosis (AS) in common AS entities and to (2) evaluate differences in the aortic annulus and left ventricular outflow tract (LVOT) calcium load. Nine hundred and thirty-eight patients with contrast-enhanced cardiac MSCT and moderate-to-severe aortic stenosis (AS) were retrospectively enrolled. Patients with severe AS ≤ 1.0 cm2 (n = 841) were further separated into three AS entities: high gradient (HGAS, n = 370, 44.0%), paradoxical low gradient (pLGAS, n = 333, 39.6%), and classical low gradient (LGAS, n = 138, 16.4%). AVC, leaflet, and LVOT calcification were quantified. Aortic valve calcification scores were highest in severe HGAS, and lower in severe pLGAS and classical LGAS. In all severity and AS entities, the non-coronary cusp (NCC) was the most calcified one. LVOT calcification was consistently comparable between gender and AS entities. Accuracy of logistic regression was the highest in HGAS (male vs. female: AVC > 2156 Agatston units (AU), c-index 0.76; vs. AVC > 1292 AU, c-index 0.85; or AVC density > 406 AU/cm2, c-index 0.82; vs. > 259 AU/cm2, c-index 0.86; each p < 0.0001*) to diagnose severe AS. AVC could only be used in men to differentiate between severe LGAS and moderate AS. Data from this retrospective analysis indicate that the NCC is subject to pre-dominant degeneration throughout gender, AS severity, and several AS entities. AVC was consistently comparable in severe pLGAS and classical LGAS, but only AVC in severe LGAS could sufficiently distinguish from moderate AS in men. LVOT calcification failed to be a reliable indicator of accelerating AS. |
Author | Westenfeld, Ralf Hellhammer, Katharina Zeus, Tobias Bosbach, Georg Dannenberg, Lisa Kelm, Malte Maier, Oliver Jung, Christian Polzin, Amin Klein, Kathrin Zako, Saif Afzal, Shazia Piayda, Kerstin Veulemans, Verena |
Author_xml | – sequence: 1 givenname: Verena orcidid: 0000-0002-2744-2154 surname: Veulemans fullname: Veulemans, Verena email: verena.veulemanns@med.uni-duesseldorf.de organization: Division of Cardiology, Pulmonology and Vascular Medicine, Heinrich Heine University – sequence: 2 givenname: Kerstin surname: Piayda fullname: Piayda, Kerstin organization: Division of Cardiology, Pulmonology and Vascular Medicine, Heinrich Heine University – sequence: 3 givenname: Oliver surname: Maier fullname: Maier, Oliver organization: Division of Cardiology, Pulmonology and Vascular Medicine, Heinrich Heine University – sequence: 4 givenname: Georg surname: Bosbach fullname: Bosbach, Georg organization: Division of Cardiology, Pulmonology and Vascular Medicine, Heinrich Heine University – sequence: 5 givenname: Amin surname: Polzin fullname: Polzin, Amin organization: Division of Cardiology, Pulmonology and Vascular Medicine, Heinrich Heine University – sequence: 6 givenname: Katharina surname: Hellhammer fullname: Hellhammer, Katharina organization: Division of Cardiology, Pulmonology and Vascular Medicine, Heinrich Heine University – sequence: 7 givenname: Shazia surname: Afzal fullname: Afzal, Shazia organization: Division of Cardiology, Pulmonology and Vascular Medicine, Heinrich Heine University – sequence: 8 givenname: Kathrin surname: Klein fullname: Klein, Kathrin organization: Division of Cardiology, Pulmonology and Vascular Medicine, Heinrich Heine University – sequence: 9 givenname: Lisa surname: Dannenberg fullname: Dannenberg, Lisa organization: Division of Cardiology, Pulmonology and Vascular Medicine, Heinrich Heine University – sequence: 10 givenname: Saif surname: Zako fullname: Zako, Saif organization: Division of Cardiology, Pulmonology and Vascular Medicine, Heinrich Heine University – sequence: 11 givenname: Christian surname: Jung fullname: Jung, Christian organization: Division of Cardiology, Pulmonology and Vascular Medicine, Heinrich Heine University – sequence: 12 givenname: Ralf surname: Westenfeld fullname: Westenfeld, Ralf organization: Division of Cardiology, Pulmonology and Vascular Medicine, Heinrich Heine University – sequence: 13 givenname: Malte surname: Kelm fullname: Kelm, Malte organization: Division of Cardiology, Pulmonology and Vascular Medicine, Heinrich Heine University, CARID (Cardiovascular Research Institute Düsseldorf), Heinrich Heine University – sequence: 14 givenname: Tobias surname: Zeus fullname: Zeus, Tobias organization: Division of Cardiology, Pulmonology and Vascular Medicine, Heinrich Heine University |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32894344$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1007_s00380_022_02187_9 crossref_primary_10_1016_j_amjcard_2023_03_024 crossref_primary_10_3390_jcm11133902 crossref_primary_10_1161_CIRCIMAGING_121_012884 crossref_primary_10_1093_eurheartj_ehab757 crossref_primary_10_1016_j_compmedimag_2023_102289 crossref_primary_10_1007_s00380_021_01818_x crossref_primary_10_1186_s43044_022_00311_8 crossref_primary_10_1016_j_jcmg_2024_03_014 crossref_primary_10_3390_jcm13144064 crossref_primary_10_3390_ijms232416139 crossref_primary_10_1016_j_cmpb_2023_107882 |
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Keywords | Aortic valve calcification AS entities TAVR TAVI |
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References_xml | – volume: 12 start-page: 1835 year: 2019 end-page: 1848 ident: CR11 article-title: Why and how to measure aortic valve calcification in patients with aortic stenosis publication-title: JACC Cardiovasc Imaging doi: 10.1016/j.jcmg.2019.01.045 – volume: 368 start-page: 1005 year: 2006 end-page: 1011 ident: CR1 article-title: Burden of valvular heart diseases: a population-based study publication-title: Lancet doi: 10.1016/S0140-6736(06)69208-8 – volume: 76 start-page: 431 year: 2010 end-page: 439 ident: CR12 article-title: “Device landing zone” calcification, assessed by MSCT, as a predictive factor for pacemaker implantation after TAVI publication-title: Catheter Cardiovasc Interv doi: 10.1002/ccd.22563 – volume: 110 start-page: 356 year: 2004 end-page: 362 ident: CR2 article-title: Evaluation and clinical implications of aortic valve calcification measured by electron-beam computed tomography publication-title: Circulation doi: 10.1161/01.CIR.0000135469.82545.D0 – 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Snippet | Sex- and flow-related aortic valve calcification (AVC) studies are still limited in number, and data on the exact calcium quantity and distribution are scarce.... |
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SubjectTerms | Aorta Aortic stenosis Aortic valve Biomedical Engineering and Bioengineering Calcification Calcification (ectopic) Calcium Cardiac Surgery Cardiology Degeneration Gender Heart Heart valves Medicine Medicine & Public Health Men Original Original Article Regression analysis Stenosis Vascular Surgery Ventricle |
Title | Aortic valve calcification is subject to aortic stenosis severity and the underlying flow pattern |
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