Evidence of an anti-inflammatory effect of PCSK9 inhibitors within the human atherosclerotic plaque.


Journal

Atherosclerosis
ISSN: 1879-1484
Titre abrégé: Atherosclerosis
Pays: Ireland
ID NLM: 0242543

Informations de publication

Date de publication:
08 2023
Historique:
received: 16 05 2023
revised: 28 06 2023
accepted: 28 06 2023
medline: 14 8 2023
pubmed: 9 7 2023
entrez: 8 7 2023
Statut: ppublish

Résumé

Preclinical evidence suggests that proprotein convertase subtilisin-kexin type 9 (PCSK9) inhibitors hold anti-inflammatory properties independently of their ability to lower LDL-cholesterol (C). However, whether PCSK9 inhibitors exert anti-inflammatory effects within the atherosclerotic plaque in humans is unknown. We explored the impact of PCSK9 inhibitors, used as monotherapy, compared with other lipid-lowering drugs (oLLD) on the expression of inflammatory markers within the plaque, assessing also the subsequent incidence of cardiovascular events. In an observational study, we recruited 645 patients on stable therapy for at least six months and undergoing carotid endarterectomy, categorizing patients according to the use of PCSK9 inhibitors only (n = 159) or oLLD (n = 486). We evaluated the expression of NLRP3, caspase-1, IL-1β, TNFα, NF-kB, PCSK9, SIRT3, CD68, MMP-9, and collagen within the plaques in the two groups through immunohistochemistry, ELISA, or immunoblot. A composite outcome including non-fatal myocardial infarction, non-fatal stroke, and all-cause mortality was assessed during a 678 ± 120 days follow-up after the procedure. Patients treated with PCSK9 inhibitors had a lower expression of pro-inflammatory proteins and a higher abundance of SIRT3 and collagen within the plaque, a result obtained despite comparable levels of circulating hs-CRP and observed also in LDL-C-matched subgroups with LDL-C levels <100 mg/dL. Patients treated with PCSK9 inhibitors showed a decreased risk of developing the outcome compared with patients on oLLD, also after adjustment for multiple variables including LDL-C (adjusted hazard ratio 0.262; 95% CI 0.131-0.524; p < 0.001). The expression of PCSK9 correlated positively with that of pro-inflammatory proteins, which burden was associated with a higher risk of developing the outcome, independently of the therapeutic regimen. The use of PCSK9 inhibitors is accompanied by a beneficial remodelling of the inflammatory burden within the human atheroma, an effect possibly or partly independent of their LDL-C lowering ability. This phenomenon might provide an additional cardiovascular benefit.

Sections du résumé

BACKGROUND AND AIMS
Preclinical evidence suggests that proprotein convertase subtilisin-kexin type 9 (PCSK9) inhibitors hold anti-inflammatory properties independently of their ability to lower LDL-cholesterol (C). However, whether PCSK9 inhibitors exert anti-inflammatory effects within the atherosclerotic plaque in humans is unknown. We explored the impact of PCSK9 inhibitors, used as monotherapy, compared with other lipid-lowering drugs (oLLD) on the expression of inflammatory markers within the plaque, assessing also the subsequent incidence of cardiovascular events.
METHODS
In an observational study, we recruited 645 patients on stable therapy for at least six months and undergoing carotid endarterectomy, categorizing patients according to the use of PCSK9 inhibitors only (n = 159) or oLLD (n = 486). We evaluated the expression of NLRP3, caspase-1, IL-1β, TNFα, NF-kB, PCSK9, SIRT3, CD68, MMP-9, and collagen within the plaques in the two groups through immunohistochemistry, ELISA, or immunoblot. A composite outcome including non-fatal myocardial infarction, non-fatal stroke, and all-cause mortality was assessed during a 678 ± 120 days follow-up after the procedure.
RESULTS
Patients treated with PCSK9 inhibitors had a lower expression of pro-inflammatory proteins and a higher abundance of SIRT3 and collagen within the plaque, a result obtained despite comparable levels of circulating hs-CRP and observed also in LDL-C-matched subgroups with LDL-C levels <100 mg/dL. Patients treated with PCSK9 inhibitors showed a decreased risk of developing the outcome compared with patients on oLLD, also after adjustment for multiple variables including LDL-C (adjusted hazard ratio 0.262; 95% CI 0.131-0.524; p < 0.001). The expression of PCSK9 correlated positively with that of pro-inflammatory proteins, which burden was associated with a higher risk of developing the outcome, independently of the therapeutic regimen.
CONCLUSIONS
The use of PCSK9 inhibitors is accompanied by a beneficial remodelling of the inflammatory burden within the human atheroma, an effect possibly or partly independent of their LDL-C lowering ability. This phenomenon might provide an additional cardiovascular benefit.

Identifiants

pubmed: 37422356
pii: S0021-9150(23)05074-8
doi: 10.1016/j.atherosclerosis.2023.06.971
pii:
doi:

Substances chimiques

PCSK9 protein, human EC 3.4.21.-
Proprotein Convertase 9 EC 3.4.21.-
PCSK9 Inhibitors 0
Cholesterol, LDL 0
Sirtuin 3 EC 3.5.1.-
Anti-Inflammatory Agents 0
Anticholesteremic Agents 0

Types de publication

Observational Study Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

117180

Subventions

Organisme : NHLBI NIH HHS
ID : T32 HL144456
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK033823
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK123259
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL146691
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL159062
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL164772
Pays : United States

Informations de copyright

Copyright © 2023 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Raffaele Marfella (R)

Università degli Studi della Campania "Luigi Vanvitelli", Piazza Luigi Miraglia 2, 80138, Naples, Italy; Mediterranea Cardiocentro, 80122, Naples, Italy. Electronic address: antonio.ceriello@hotmail.it.

Francesco Prattichizzo (F)

IRCCS MultiMedica, Via Fantoli 16/15, 20138, Milan, Italy.

Celestino Sardu (C)

Università degli Studi della Campania "Luigi Vanvitelli", Piazza Luigi Miraglia 2, 80138, Naples, Italy.

Pasquale Paolisso (P)

Cardiovascular Center Aalst, OLV-Clinic, Aalst, Belgium; Department of Advanced Biomedical Sciences, University of Naples Federico II, Naples, Italy.

Nunzia D'Onofrio (N)

Department of Precision Medicine, The University of Campania "Luigi Vanvitelli", Italy.

Lucia Scisciola (L)

Università degli Studi della Campania "Luigi Vanvitelli", Piazza Luigi Miraglia 2, 80138, Naples, Italy.

Rosalba La Grotta (R)

IRCCS MultiMedica, Via Fantoli 16/15, 20138, Milan, Italy.

Chiara Frigé (C)

IRCCS MultiMedica, Via Fantoli 16/15, 20138, Milan, Italy.

Franca Ferraraccio (F)

Department of Mental Health and Public Medicine, Section of Statistic, The University of Campania "Luigi Vanvitelli", Naples, Italy.

Iacopo Panarese (I)

Department of Mental Health and Public Medicine, Section of Statistic, The University of Campania "Luigi Vanvitelli", Naples, Italy.

Mara Fanelli (M)

Laboratory of Molecular Oncology, Gemelli Molise SpA, Campobasso, Italy.

Piero Modugno (P)

Department of Cardiovascular Medicine, Gemelli Molise SpA, Campobasso, Italy.

Antonio Maria Calafiore (AM)

Department of Cardiovascular Medicine, Gemelli Molise SpA, Campobasso, Italy.

Mario Melchionna (M)

Department of Cardiovascular Medicine, Gemelli Molise SpA, Campobasso, Italy.

Ferdinando Carlo Sasso (FC)

Università degli Studi della Campania "Luigi Vanvitelli", Piazza Luigi Miraglia 2, 80138, Naples, Italy.

Fulvio Furbatto (F)

Department of Cardiology, Hospital Cardarelli, Naples, Italy.

Davide D'Andrea (D)

Department of Cardiology, Hospital Cardarelli, Naples, Italy.

Mario Siniscalchi (M)

Department of Cardiology, Hospital Cardarelli, Naples, Italy.

Ciro Mauro (C)

Department of Cardiology, Hospital Cardarelli, Naples, Italy.

Arturo Cesaro (A)

Department of Translational Medical Sciences, University of Campania 'Luigi Vanvitelli', Naples, Italy.

Paolo Calabrò (P)

Department of Translational Medical Sciences, University of Campania 'Luigi Vanvitelli', Naples, Italy.

Gaetano Santulli (G)

Albert Einstein College of Medicine, USA.

Maria Luisa Balestrieri (ML)

Department of Precision Medicine, The University of Campania "Luigi Vanvitelli", Italy.

Emanuele Barbato (E)

Cardiovascular Center Aalst, OLV-Clinic, Aalst, Belgium; Department of Advanced Biomedical Sciences, University of Naples Federico II, Naples, Italy.

Antonio Ceriello (A)

IRCCS MultiMedica, Via Fantoli 16/15, 20138, Milan, Italy. Electronic address: raffaele.marfella@unicampania.it.

Giuseppe Paolisso (G)

Università degli Studi della Campania "Luigi Vanvitelli", Piazza Luigi Miraglia 2, 80138, Naples, Italy; Mediterranea Cardiocentro, 80122, Naples, Italy.

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Classifications MeSH