Show simple item record

dc.creatorMilionis H., Barkas F., Ntaios G., Papavasileiou V., Vemmos K., Michel P., Elisaf M.en
dc.date.accessioned2023-01-31T09:00:05Z
dc.date.available2023-01-31T09:00:05Z
dc.date.issued2016
dc.identifier10.1016/j.ejim.2016.06.023
dc.identifier.issn09536205
dc.identifier.urihttp://hdl.handle.net/11615/76637
dc.description.abstractBackground/purpose A reduction of cardiovascular events has been reported in phase 2 and 3 trials of the proprotein convertase subtilisin kexin 9 (PCSK9) inhibitors alirocumab and evolocumab. We aimed to investigate the effect PCSK9 inhibition on stroke risk in a meta-analysis involving data from randomized studies with alirocumab and evolocumab. Methods Data from pre-specified combined analysis of 4465 patients who completed phase 2 or 3 studies of evolocumab over a period of 1 year and a randomized trial on alirocumab including 2341 patients with hyperlipidemia on maximally tolerated statin who were at high risk for coronary heart disease over a period of 1.5 years were used. Results The number of patients having an ischemic stroke was small in both trials. PCSK9 inhibition showed no significant effect on stroke rate (risk ratio 1.43; 95% CI, 0.45–4.57, p = 0.55). No significant differences in stroke risk were evident when transient ischemic attacks were included in the analysis (risk ratio 0.65; 95% CI, 0.25–1.68, p = 0.37). No hemorrhagic strokes were reported in either study. Conclusion Although a benefit towards reduction of cardiovascular events in the overall has been documented, longer exposure is warranted to be able to evaluate the effect on stroke risk. © 2016 European Federation of Internal Medicine.en
dc.language.isoenen
dc.sourceEuropean Journal of Internal Medicineen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84979680841&doi=10.1016%2fj.ejim.2016.06.023&partnerID=40&md5=2e6bc722c13d8560231aa6c016780427
dc.subjectalirocumaben
dc.subjectevolocumaben
dc.subjecthydroxymethylglutaryl coenzyme A reductase inhibitoren
dc.subjecthypocholesterolemic agenten
dc.subjectplaceboen
dc.subjectproprotein convertase subtilisin kexin 9en
dc.subjectproprotein convertase subtilisin kexin 9 inhibitoren
dc.subjectserine proteinaseen
dc.subjectserine proteinase inhibitoren
dc.subjectunclassified drugen
dc.subjectalirocumaben
dc.subjectevolocumaben
dc.subjecthydroxymethylglutaryl coenzyme A reductase inhibitoren
dc.subjecthypocholesterolemic agenten
dc.subjectlow density lipoprotein cholesterolen
dc.subjectmonoclonal antibodyen
dc.subjectproprotein convertase 9en
dc.subjectbrain hemorrhageen
dc.subjectcerebrovascular accidenten
dc.subjectenzyme inhibitionen
dc.subjecthumanen
dc.subjecthypercholesterolemiaen
dc.subjectischemic heart diseaseen
dc.subjectmeta analysisen
dc.subjectrandomized controlled trial (topic)en
dc.subjectReviewen
dc.subjectantagonists and inhibitorsen
dc.subjectblooden
dc.subjectcombination drug therapyen
dc.subjectcomplicationen
dc.subjecthypercholesterolemiaen
dc.subjectStrokeen
dc.subjectAntibodies, Monoclonalen
dc.subjectAnticholesteremic Agentsen
dc.subjectCholesterol, LDLen
dc.subjectDrug Therapy, Combinationen
dc.subjectHumansen
dc.subjectHydroxymethylglutaryl-CoA Reductase Inhibitorsen
dc.subjectHypercholesterolemiaen
dc.subjectProprotein Convertase 9en
dc.subjectRandomized Controlled Trials as Topicen
dc.subjectStrokeen
dc.subjectElsevier B.V.en
dc.titleProprotein convertase subtilisin kexin 9 (PCSK9) inhibitors to treat hypercholesterolemia: Effect on stroke risken
dc.typeotheren


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record