Publication: Eligibility for PCSK9 Inhibitors According to American College of Cardiology (ACC) and European Society of Cardiology/European Atherosclerosis Society (ESC/EAS) Guidelines After Acute Coronary Syndromes.
cris.virtual.author-orcid | 0000-0002-8766-7945 | |
cris.virtualsource.author-orcid | a5541bd1-b9f4-4ca5-9876-de5d6a047370 | |
cris.virtualsource.author-orcid | 3fda0c3a-0cd0-438e-8e23-e3486ee2ffe0 | |
cris.virtualsource.author-orcid | e48f797a-09e5-4a05-8aea-6ff39d24e57e | |
cris.virtualsource.author-orcid | 9c78047b-8526-4ad2-8f55-167f7aa55063 | |
cris.virtualsource.author-orcid | f066d906-a45d-4400-9e07-830bd9478529 | |
cris.virtualsource.author-orcid | dcf039b3-51b9-457e-aa4f-439d935925b3 | |
cris.virtualsource.author-orcid | 101f1394-72d5-4dda-b28f-666a3dee6c70 | |
datacite.rights | open.access | |
dc.contributor.author | Gencer, Baris | |
dc.contributor.author | Koskinas, Konstantinos | |
dc.contributor.author | Räber, Lorenz | |
dc.contributor.author | Karagiannis Voules, Alexios | |
dc.contributor.author | Nanchen, David | |
dc.contributor.author | Auer, Reto | |
dc.contributor.author | Carballo, David | |
dc.contributor.author | Carballo, Sebastian | |
dc.contributor.author | Klingenberg, Roland | |
dc.contributor.author | Heg, Dierik Hans | |
dc.contributor.author | Matter, Christian M | |
dc.contributor.author | Lüscher, Thomas F | |
dc.contributor.author | Rodondi, Nicolas | |
dc.contributor.author | Mach, François | |
dc.contributor.author | Windecker, Stephan | |
dc.date.accessioned | 2024-10-25T13:12:47Z | |
dc.date.available | 2024-10-25T13:12:47Z | |
dc.date.issued | 2017-11-09 | |
dc.description.abstract | BACKGROUND The American College of Cardiology (ACC) and European Society of Cardiology/European Atherosclerosis Society (ESC/EAS) have recently published recommendations for the use of proprotein convertase subtilisin/kexin-9 (PCSK9) inhibitors in situations of very high risk. We aim to assess in the real world the suitability of PCSK9 inhibitors for acute coronary syndromes. METHODS AND RESULTS We analyzed a prospective Swiss cohort of 2023 patients hospitalized for acute coronary syndromes between 2009 and 2014 with available data for low-density lipoprotein cholesterol and lipid-lowering therapy at 1 year. Clinical familial hypercholesterolemia was defined using the Dutch Lipid Clinic Network algorithm as unlikely, possible, probable, or definite. We simulated a fixed relative reduction of 24% in low-density lipoprotein cholesterol levels at 1 year in all patients not treated with ezetimibe, irrespective of the low-density lipoprotein cholesterol levels and statin regimen. At 1 year, 94.3% of patients were treated with statin, 5.8% with ezetimibe, and 35.8% of patients had on-target low-density lipoprotein cholesterol levels (<1.8 mmol/L); 25.6% met criteria for possible or probable/definite familial hypercholesterolemia. After a simulation of the lipid-lowering effect of ezetimibe, the proportion of patients who would be eligible for PCSK9 inhibitors at 1 year was 13.4% using American College of Cardiology criteria and 2.7% using European Society of Cardiology/European Atherosclerosis Society criteria. Patients with possible or probable/definite familial hypercholesterolemia were more eligible for PCSK9 inhibitors compared with their non-familial hypercholesterolemia counterparts: 27.6% versus 8.8% according to American College of Cardiology criteria and 6.6% versus 1.8% according to European Society of Cardiology/European Atherosclerosis Society criteria (P<0.001). CONCLUSIONS Recommendations made by the American College of Cardiology guidelines would lead to 5-fold higher eligibility rates for PCSK9 inhibitors compared to the European Society of Cardiology/European Atherosclerosis Society consensus statement in acute coronary syndrome patients. | |
dc.description.note | Gencer and Koskinas contributed equally to this work (as co-first authors). Mach and Windecker contributed equally to this work (as co-last authors). | |
dc.description.numberOfPages | 10 | |
dc.description.sponsorship | Universitätsklinik für Kardiologie | |
dc.description.sponsorship | Berner Institut für Hausarztmedizin (BIHAM) | |
dc.description.sponsorship | Clinical Trials Unit Bern (CTU) | |
dc.identifier.doi | 10.7892/boris.107400 | |
dc.identifier.pmid | 29122809 | |
dc.identifier.publisherDOI | 10.1161/JAHA.117.006537 | |
dc.identifier.uri | https://boris-portal.unibe.ch/handle/20.500.12422/155801 | |
dc.language.iso | en | |
dc.publisher | American Heart Association | |
dc.relation.ispartof | Journal of the American Heart Association | |
dc.relation.issn | 2047-9980 | |
dc.relation.organization | Clinic of General Internal Medicine | |
dc.relation.organization | DCD5A442BDB9E17DE0405C82790C4DE2 | |
dc.relation.organization | DCD5A442BECFE17DE0405C82790C4DE2 | |
dc.relation.organization | DCD5A442BE42E17DE0405C82790C4DE2 | |
dc.relation.organization | DCD5A442BB15E17DE0405C82790C4DE2 | |
dc.subject | PCSK9 lipids secondary prevention | |
dc.subject.ddc | 600 - Technology::610 - Medicine & health | |
dc.subject.ddc | 300 - Social sciences, sociology & anthropology::360 - Social problems & social services | |
dc.title | Eligibility for PCSK9 Inhibitors According to American College of Cardiology (ACC) and European Society of Cardiology/European Atherosclerosis Society (ESC/EAS) Guidelines After Acute Coronary Syndromes. | |
dc.type | article | |
dspace.entity.type | Publication | |
dspace.file.type | text | |
oaire.citation.issue | 11 | |
oaire.citation.startPage | e006537 | |
oaire.citation.volume | 6 | |
oairecerif.author.affiliation | Universitätsklinik für Kardiologie | |
oairecerif.author.affiliation | Universitätsklinik für Kardiologie | |
oairecerif.author.affiliation | Clinical Trials Unit Bern (CTU) | |
oairecerif.author.affiliation | Berner Institut für Hausarztmedizin (BIHAM) | |
oairecerif.author.affiliation | Clinical Trials Unit Bern (CTU) | |
oairecerif.author.affiliation | Berner Institut für Hausarztmedizin (BIHAM) | |
oairecerif.author.affiliation | Universitätsklinik für Kardiologie | |
oairecerif.author.affiliation2 | Institut für Sozial- und Präventivmedizin (ISPM) | |
oairecerif.author.affiliation2 | Institut für Sozial- und Präventivmedizin (ISPM) | |
oairecerif.author.affiliation2 | Clinic of General Internal Medicine | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.date.licenseChanged | 2019-10-23 17:58:46 | |
unibe.description.ispublished | pub | |
unibe.eprints.legacyId | 107400 | |
unibe.journal.abbrevTitle | J Am Heart Assoc | |
unibe.refereed | true | |
unibe.subtype.article | journal |
Files
Original bundle
1 - 1 of 1
- Name:
- Gencer JAmHeartAssoc 2017.pdf
- Size:
- 1.18 MB
- Format:
- Adobe Portable Document Format
- File Type:
- text
- License:
- https://creativecommons.org/licenses/by-nc/4.0
- Content:
- published