Evolocumab, a PCSK9‐Monoclonal Antibody, Rapidly Reverses Coronary Artery Endothelial Dysfunction in People Living With HIV and People With Dyslipidemia

Background PCSK9 (proprotein convertase subtilisin/kexin type 9) is well recognized for its important role in cholesterol metabolism. Elevated levels are associated with increased cardiovascular risk and inhibition with PCSK9 antibodies (PCSK9i) lowers cardiovascular events in patients with coronary...

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Main Authors: Thorsten M. Leucker, Gary Gerstenblith, Michael Schär, Todd T. Brown, Steven R. Jones, Yohannes Afework, Robert G. Weiss, Allison G. Hays
Format: Article
Language:English
Published: Wiley 2020-07-01
Series:Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
Subjects:
Online Access:https://www.ahajournals.org/doi/10.1161/JAHA.120.016263
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author Thorsten M. Leucker
Gary Gerstenblith
Michael Schär
Todd T. Brown
Steven R. Jones
Yohannes Afework
Robert G. Weiss
Allison G. Hays
author_facet Thorsten M. Leucker
Gary Gerstenblith
Michael Schär
Todd T. Brown
Steven R. Jones
Yohannes Afework
Robert G. Weiss
Allison G. Hays
author_sort Thorsten M. Leucker
collection DOAJ
description Background PCSK9 (proprotein convertase subtilisin/kexin type 9) is well recognized for its important role in cholesterol metabolism. Elevated levels are associated with increased cardiovascular risk and inhibition with PCSK9 antibodies (PCSK9i) lowers cardiovascular events in patients with coronary artery disease. PCSK9 levels are also elevated in people living with HIV (PLWH) and those with dyslipidemia. Because increased PCSK9 in PLWH is associated with impaired coronary endothelial function, a barometer of coronary vascular health, we tested the hypothesis that PCSK9i improves impaired coronary endothelial function in dyslipidemia without coronary artery disease and in PLWH with nearly optimal/above goal low‐density lipoprotein cholesterol levels. Methods and Results We performed a single‐center study in 19 PLWH and 11 with dyslipidemia to evaluate the effects of the PCSK9i evolocumab on coronary endothelial function using cine 3T MRI to noninvasively measure coronary endothelial function, assessed as the changes in coronary cross‐sectional area and coronary blood flow from rest to that during isometric handgrip exercise, a known endothelial‐dependent vasodilator. Before evolocumab, there was a decrease or no coronary vasodilation and no increase in coronary blood flow (the normal responses) to isometric handgrip exercise in either group. Following 6 weeks of evolocumab, 480 mg q4 weeks, the % cross‐sectional area changes from rest to isometric handgrip exercise were +5.6±5.5% and +4.5±3.1% in the PLWH and dyslipidemia groups, respectively, both P<0.01 versus baseline. Improved cross‐sectional area was paralleled by a significant coronary blood flow improvement in both groups. Conclusions To our knowledge, these data represent the first evidence that PCSK9 inhibition improves coronary artery health in PLWH and people with dyslipidemia. Registration URL: https://www.clinicaltrials.gov; Unique identifier: NCT03500302.
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spelling doaj.art-950fb299fce848429615e13c278f99712023-11-17T17:03:47ZengWileyJournal of the American Heart Association: Cardiovascular and Cerebrovascular Disease2047-99802020-07-0191410.1161/JAHA.120.016263Evolocumab, a PCSK9‐Monoclonal Antibody, Rapidly Reverses Coronary Artery Endothelial Dysfunction in People Living With HIV and People With DyslipidemiaThorsten M. Leucker0Gary Gerstenblith1Michael Schär2Todd T. Brown3Steven R. Jones4Yohannes Afework5Robert G. Weiss6Allison G. Hays7Division of Cardiology Department of Medicine Johns Hopkins University School of Medicine Baltimore MDDivision of Cardiology Department of Medicine Johns Hopkins University School of Medicine Baltimore MDDivision of Magnetic Resonance Research Department of Radiology Johns Hopkins University School of Medicine Baltimore MDDivision of Endocrinology, Diabetes and Metabolism Department of Medicine Johns Hopkins University School of Medicine Baltimore MDDivision of Cardiology Department of Medicine Johns Hopkins University School of Medicine Baltimore MDDivision of Magnetic Resonance Research Department of Radiology Johns Hopkins University School of Medicine Baltimore MDDivision of Cardiology Department of Medicine Johns Hopkins University School of Medicine Baltimore MDDivision of Cardiology Department of Medicine Johns Hopkins University School of Medicine Baltimore MDBackground PCSK9 (proprotein convertase subtilisin/kexin type 9) is well recognized for its important role in cholesterol metabolism. Elevated levels are associated with increased cardiovascular risk and inhibition with PCSK9 antibodies (PCSK9i) lowers cardiovascular events in patients with coronary artery disease. PCSK9 levels are also elevated in people living with HIV (PLWH) and those with dyslipidemia. Because increased PCSK9 in PLWH is associated with impaired coronary endothelial function, a barometer of coronary vascular health, we tested the hypothesis that PCSK9i improves impaired coronary endothelial function in dyslipidemia without coronary artery disease and in PLWH with nearly optimal/above goal low‐density lipoprotein cholesterol levels. Methods and Results We performed a single‐center study in 19 PLWH and 11 with dyslipidemia to evaluate the effects of the PCSK9i evolocumab on coronary endothelial function using cine 3T MRI to noninvasively measure coronary endothelial function, assessed as the changes in coronary cross‐sectional area and coronary blood flow from rest to that during isometric handgrip exercise, a known endothelial‐dependent vasodilator. Before evolocumab, there was a decrease or no coronary vasodilation and no increase in coronary blood flow (the normal responses) to isometric handgrip exercise in either group. Following 6 weeks of evolocumab, 480 mg q4 weeks, the % cross‐sectional area changes from rest to isometric handgrip exercise were +5.6±5.5% and +4.5±3.1% in the PLWH and dyslipidemia groups, respectively, both P<0.01 versus baseline. Improved cross‐sectional area was paralleled by a significant coronary blood flow improvement in both groups. Conclusions To our knowledge, these data represent the first evidence that PCSK9 inhibition improves coronary artery health in PLWH and people with dyslipidemia. Registration URL: https://www.clinicaltrials.gov; Unique identifier: NCT03500302.https://www.ahajournals.org/doi/10.1161/JAHA.120.016263endothelial functionHIVinflammationmagnetic resonance imagingproprotein convertase subtilisin/kexin type 9
spellingShingle Thorsten M. Leucker
Gary Gerstenblith
Michael Schär
Todd T. Brown
Steven R. Jones
Yohannes Afework
Robert G. Weiss
Allison G. Hays
Evolocumab, a PCSK9‐Monoclonal Antibody, Rapidly Reverses Coronary Artery Endothelial Dysfunction in People Living With HIV and People With Dyslipidemia
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
endothelial function
HIV
inflammation
magnetic resonance imaging
proprotein convertase subtilisin/kexin type 9
title Evolocumab, a PCSK9‐Monoclonal Antibody, Rapidly Reverses Coronary Artery Endothelial Dysfunction in People Living With HIV and People With Dyslipidemia
title_full Evolocumab, a PCSK9‐Monoclonal Antibody, Rapidly Reverses Coronary Artery Endothelial Dysfunction in People Living With HIV and People With Dyslipidemia
title_fullStr Evolocumab, a PCSK9‐Monoclonal Antibody, Rapidly Reverses Coronary Artery Endothelial Dysfunction in People Living With HIV and People With Dyslipidemia
title_full_unstemmed Evolocumab, a PCSK9‐Monoclonal Antibody, Rapidly Reverses Coronary Artery Endothelial Dysfunction in People Living With HIV and People With Dyslipidemia
title_short Evolocumab, a PCSK9‐Monoclonal Antibody, Rapidly Reverses Coronary Artery Endothelial Dysfunction in People Living With HIV and People With Dyslipidemia
title_sort evolocumab a pcsk9 monoclonal antibody rapidly reverses coronary artery endothelial dysfunction in people living with hiv and people with dyslipidemia
topic endothelial function
HIV
inflammation
magnetic resonance imaging
proprotein convertase subtilisin/kexin type 9
url https://www.ahajournals.org/doi/10.1161/JAHA.120.016263
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