Literature DB >> 28813214

Cognitive Function in a Randomized Trial of Evolocumab.

Robert P Giugliano1, François Mach1, Kenton Zavitz1, Christopher Kurtz1, Kyungah Im1, Estella Kanevsky1, Jingjing Schneider1, Huei Wang1, Anthony Keech1, Terje R Pedersen1, Marc S Sabatine1, Peter S Sever1, Jennifer G Robinson1, Narimon Honarpour1, Scott M Wasserman1, Brian R Ott1.   

Abstract

Background Findings from clinical trials of proprotein convertase subtilisin-kexin type 9 (PCSK9) inhibitors have led to concern that these drugs or the low levels of low-density lipoprotein (LDL) cholesterol that result from their use are associated with cognitive deficits. Methods In a subgroup of patients from a randomized, placebo-controlled trial of evolocumab added to statin therapy, we prospectively assessed cognitive function using the Cambridge Neuropsychological Test Automated Battery. The primary end point was the score on the spatial working memory strategy index of executive function (scores range from 4 to 28, with lower scores indicating a more efficient use of strategy and planning). Secondary end points were the scores for working memory (scores range from 0 to 279, with lower scores indicating fewer errors), episodic memory (scores range from 0 to 70, with lower scores indicating fewer errors), and psychomotor speed (scores range from 100 to 5100 msec, with faster times representing better performance). Assessments of cognitive function were performed at baseline, week 24, yearly, and at the end of the trial. The primary analysis was a noninferiority comparison of the mean change from baseline in the score on the spatial working memory strategy index of executive function between the patients who received evolocumab and those who received placebo; the noninferiority margin was set at 20% of the standard deviation of the score in the placebo group. Results A total of 1204 patients were followed for a median of 19 months; the mean (±SD) change from baseline over time in the raw score for the spatial working memory strategy index of executive function (primary end point) was -0.21±2.62 in the evolocumab group and -0.29±2.81 in the placebo group (P<0.001 for noninferiority; P=0.85 for superiority). There were no significant between-group differences in the secondary end points of scores for working memory (change in raw score, -0.52 in the evolocumab group and -0.93 in the placebo group), episodic memory (change in raw score, -1.53 and -1.53, respectively), or psychomotor speed (change in raw score, 5.2 msec and 0.9 msec, respectively). In an exploratory analysis, there were no associations between LDL cholesterol levels and cognitive changes. Conclusions In a randomized trial involving patients who received either evolocumab or placebo in addition to statin therapy, no significant between-group difference in cognitive function was observed over a median of 19 months. (Funded by Amgen; EBBINGHAUS ClinicalTrials.gov number, NCT02207634 .).

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Year:  2017        PMID: 28813214     DOI: 10.1056/NEJMoa1701131

Source DB:  PubMed          Journal:  N Engl J Med        ISSN: 0028-4793            Impact factor:   91.245


  93 in total

1.  PCSK9 is Increased in Cerebrospinal Fluid of Individuals With Alcohol Use Disorder.

Authors:  Ji Soo Lee; Daniel Rosoff; Audrey Luo; Martha Longley; Monte Phillips; Katrin Charlet; Christine Muench; Jeesun Jung; Falk W Lohoff
Journal:  Alcohol Clin Exp Res       Date:  2019-05-03       Impact factor: 3.455

Review 2.  Low Density Lipoprotein (LDL) Cholesterol as a Causal Role for Atherosclerotic Disease: Potential Role of PCSK9 Inhibitors.

Authors:  Rita Del Pinto; Davide Grassi; Giuliana Properzi; Giovambattista Desideri; Claudio Ferri
Journal:  High Blood Press Cardiovasc Prev       Date:  2019-06-24

Review 3.  New Insights in the Control of Low-Density Lipoprotein Cholesterol to Prevent Cardiovascular Disease.

Authors:  Julius L Katzmann; Ulrich Laufs
Journal:  Curr Cardiol Rep       Date:  2019-06-21       Impact factor: 2.931

Review 4.  Novel strategies to target proprotein convertase subtilisin kexin 9: beyond monoclonal antibodies.

Authors:  Nabil G Seidah; Annik Prat; Angela Pirillo; Alberico Luigi Catapano; Giuseppe Danilo Norata
Journal:  Cardiovasc Res       Date:  2019-03-01       Impact factor: 10.787

Review 5.  Alirocumab as add-on therapy to statins: current evidence and clinical potential.

Authors:  Johann Auer; Robert Berent
Journal:  Ther Adv Cardiovasc Dis       Date:  2018-05-24

Review 6.  PCSK9 Inhibition: New Treatment Options and Perspectives to Lower Atherogenic Lipoprotein Particles and Cardiovascular Risk.

Authors:  Julia Brandts; Dirk Müller-Wieland
Journal:  Curr Atheroscler Rep       Date:  2019-07-27       Impact factor: 5.113

7.  Proprotein convertase subtilisin/kexin type 9 and lipid metabolism.

Authors:  Stefano Spolitu; Wen Dai; John A Zadroga; Lale Ozcan
Journal:  Curr Opin Lipidol       Date:  2019-06       Impact factor: 4.776

8.  PCSK9 Variants, Low-Density Lipoprotein Cholesterol, and Neurocognitive Impairment: Reasons for Geographic and Racial Differences in Stroke Study (REGARDS).

Authors:  Matthew T Mefford; Robert S Rosenson; Mary Cushman; Michael E Farkouh; Leslie A McClure; Virginia G Wadley; Marguerite R Irvin; Vera Bittner; Monika M Safford; Ransi Somaratne; Keri L Monda; Paul Muntner; Emily B Levitan
Journal:  Circulation       Date:  2017-11-16       Impact factor: 29.690

Review 9.  Lipid-lowering Drugs and Neurocognitive Function: A Systematic Review.

Authors:  Georgios Kyriakos; Lourdes Victoria Quiles-SÁnchez; Evangelos Diamantis; Paraskevi Farmaki; Nikolaos Garmpis; Christos Damaskos; Spyridon Savvanis; Alexandros Patsouras; Athanasia Stelianidi; Errika Voutyritsa; Vasiliki E Georgakopoulou; Anna Garmpi
Journal:  In Vivo       Date:  2020 Nov-Dec       Impact factor: 2.155

Review 10.  A Clinical Guide to Combination Lipid-Lowering Therapy.

Authors:  Cori Russell; Samip Sheth; Douglas Jacoby
Journal:  Curr Atheroscler Rep       Date:  2018-03-07       Impact factor: 5.113

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