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-orcid0000-0002-8766-7945
cris.virtualsource.author-orcida5541bd1-b9f4-4ca5-9876-de5d6a047370
cris.virtualsource.author-orcid3fda0c3a-0cd0-438e-8e23-e3486ee2ffe0
cris.virtualsource.author-orcide48f797a-09e5-4a05-8aea-6ff39d24e57e
cris.virtualsource.author-orcid9c78047b-8526-4ad2-8f55-167f7aa55063
cris.virtualsource.author-orcidf066d906-a45d-4400-9e07-830bd9478529
cris.virtualsource.author-orciddcf039b3-51b9-457e-aa4f-439d935925b3
cris.virtualsource.author-orcid101f1394-72d5-4dda-b28f-666a3dee6c70
datacite.rightsopen.access
dc.contributor.authorGencer, Baris
dc.contributor.authorKoskinas, Konstantinos
dc.contributor.authorRäber, Lorenz
dc.contributor.authorKaragiannis Voules, Alexios
dc.contributor.authorNanchen, David
dc.contributor.authorAuer, Reto
dc.contributor.authorCarballo, David
dc.contributor.authorCarballo, Sebastian
dc.contributor.authorKlingenberg, Roland
dc.contributor.authorHeg, Dierik Hans
dc.contributor.authorMatter, Christian M
dc.contributor.authorLüscher, Thomas F
dc.contributor.authorRodondi, Nicolas
dc.contributor.authorMach, François
dc.contributor.authorWindecker, Stephan
dc.date.accessioned2024-10-25T13:12:47Z
dc.date.available2024-10-25T13:12:47Z
dc.date.issued2017-11-09
dc.description.abstractBACKGROUND 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.noteGencer 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.numberOfPages10
dc.description.sponsorshipUniversitätsklinik für Kardiologie
dc.description.sponsorshipBerner Institut für Hausarztmedizin (BIHAM)
dc.description.sponsorshipClinical Trials Unit Bern (CTU)
dc.identifier.doi10.7892/boris.107400
dc.identifier.pmid29122809
dc.identifier.publisherDOI10.1161/JAHA.117.006537
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/155801
dc.language.isoen
dc.publisherAmerican Heart Association
dc.relation.ispartofJournal of the American Heart Association
dc.relation.issn2047-9980
dc.relation.organizationClinic of General Internal Medicine
dc.relation.organizationDCD5A442BDB9E17DE0405C82790C4DE2
dc.relation.organizationDCD5A442BECFE17DE0405C82790C4DE2
dc.relation.organizationDCD5A442BE42E17DE0405C82790C4DE2
dc.relation.organizationDCD5A442BB15E17DE0405C82790C4DE2
dc.subjectPCSK9 lipids secondary prevention
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.subject.ddc300 - Social sciences, sociology & anthropology::360 - Social problems & social services
dc.titleEligibility 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.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue11
oaire.citation.startPagee006537
oaire.citation.volume6
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
oairecerif.author.affiliationClinical Trials Unit Bern (CTU)
oairecerif.author.affiliationBerner Institut für Hausarztmedizin (BIHAM)
oairecerif.author.affiliationClinical Trials Unit Bern (CTU)
oairecerif.author.affiliationBerner Institut für Hausarztmedizin (BIHAM)
oairecerif.author.affiliationUniversitätsklinik für Kardiologie
oairecerif.author.affiliation2Institut für Sozial- und Präventivmedizin (ISPM)
oairecerif.author.affiliation2Institut für Sozial- und Präventivmedizin (ISPM)
oairecerif.author.affiliation2Clinic of General Internal Medicine
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.date.licenseChanged2019-10-23 17:58:46
unibe.description.ispublishedpub
unibe.eprints.legacyId107400
unibe.journal.abbrevTitleJ Am Heart Assoc
unibe.refereedtrue
unibe.subtype.articlejournal

Files

Original bundle
Now showing 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

Collections