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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Proprotein convertase subtilisin kexin 9 (PCSK9) inhibitors to treat hypercholesterolemia: Effect on stroke risk

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Συγγραφέας
Milionis H., Barkas F., Ntaios G., Papavasileiou V., Vemmos K., Michel P., Elisaf M.
Ημερομηνία
2016
Γλώσσα
en
DOI
10.1016/j.ejim.2016.06.023
Λέξη-κλειδί
alirocumab
evolocumab
hydroxymethylglutaryl coenzyme A reductase inhibitor
hypocholesterolemic agent
placebo
proprotein convertase subtilisin kexin 9
proprotein convertase subtilisin kexin 9 inhibitor
serine proteinase
serine proteinase inhibitor
unclassified drug
alirocumab
evolocumab
hydroxymethylglutaryl coenzyme A reductase inhibitor
hypocholesterolemic agent
low density lipoprotein cholesterol
monoclonal antibody
proprotein convertase 9
brain hemorrhage
cerebrovascular accident
enzyme inhibition
human
hypercholesterolemia
ischemic heart disease
meta analysis
randomized controlled trial (topic)
Review
antagonists and inhibitors
blood
combination drug therapy
complication
hypercholesterolemia
Stroke
Antibodies, Monoclonal
Anticholesteremic Agents
Cholesterol, LDL
Drug Therapy, Combination
Humans
Hydroxymethylglutaryl-CoA Reductase Inhibitors
Hypercholesterolemia
Proprotein Convertase 9
Randomized Controlled Trials as Topic
Stroke
Elsevier B.V.
Εμφάνιση Μεταδεδομένων
Επιτομή
Background/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.
URI
http://hdl.handle.net/11615/76637
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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