Reduced adrenal stress response in patients on PCSK9 inhibitor therapy.

ACTH stimulation Test Alirocumab Cortisol stress response Evolocumab Low LDL-Levels PCSK9 inhibitor therapy

Journal

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

Informations de publication

Date de publication:
05 2021
Historique:
received: 11 08 2020
revised: 05 02 2021
accepted: 23 03 2021
pubmed: 24 4 2021
medline: 24 6 2021
entrez: 23 4 2021
Statut: ppublish

Résumé

Treatment with proprotein convertase subtilisin-kexin type 9 inhibitors (PCSK9i), in addition to statin therapy, reduces LDL-cholesterol (LDL-c) in some patients to extremely low levels (i.e.< 20 mg/dl or < 0.52 mmol/l). There is concern that at such low levels, the physiologic role of cholesterol may be impaired, e.g. the adrenal cortisol stress response might be compromised. We therefore evaluated the effect of PCSK9i therapy on the cortisol response to ACTH in patients with LDL-c down to extremely low levels. Nineteen patients on PCSK9i therapy and 18 controls matched for age, gender and comorbidities were included. The cortisol response to adrenocorticotropic hormone (ACTH) was tested after application of 250 μg ACTH. LDL-c levels ranged from 0.42 to 3.32 mmol/l (mean 1.38 ± 0.84 mmol/l) in the PCSK9i group and 0.81-4.82 mmol/l (mean 2.10 ± 0.97) in the control group. By analysis of covariance (ANCOVA), the PCSK9i group had significantly lower cortisol response compared to the control group (- 97.26 nmol/l, -178.60 to -15.93, p = 0.02) after 60 min. There was a significant positive correlation between the duration of PCSK9i treatment and cortisol levels (r = 0.59, p = 0.009). Extremely low LDL-c levels down to 0.42 mmol/l were not associated with lower stimulated cortisol levels. Patients on PCSK9i therapy showed a significantly lower cortisol response to ACTH. Stimulated cortisol levels were lower in the first months of PCSK9i treatment, suggesting an adaptive phenomenon. We conclude that the adrenal stress response in patients on PCSK9 inhibitor therapy is reduced.

Sections du résumé

BACKGROUND AND AIMS
Treatment with proprotein convertase subtilisin-kexin type 9 inhibitors (PCSK9i), in addition to statin therapy, reduces LDL-cholesterol (LDL-c) in some patients to extremely low levels (i.e.< 20 mg/dl or < 0.52 mmol/l). There is concern that at such low levels, the physiologic role of cholesterol may be impaired, e.g. the adrenal cortisol stress response might be compromised. We therefore evaluated the effect of PCSK9i therapy on the cortisol response to ACTH in patients with LDL-c down to extremely low levels.
METHODS
Nineteen patients on PCSK9i therapy and 18 controls matched for age, gender and comorbidities were included. The cortisol response to adrenocorticotropic hormone (ACTH) was tested after application of 250 μg ACTH.
RESULTS
LDL-c levels ranged from 0.42 to 3.32 mmol/l (mean 1.38 ± 0.84 mmol/l) in the PCSK9i group and 0.81-4.82 mmol/l (mean 2.10 ± 0.97) in the control group. By analysis of covariance (ANCOVA), the PCSK9i group had significantly lower cortisol response compared to the control group (- 97.26 nmol/l, -178.60 to -15.93, p = 0.02) after 60 min. There was a significant positive correlation between the duration of PCSK9i treatment and cortisol levels (r = 0.59, p = 0.009). Extremely low LDL-c levels down to 0.42 mmol/l were not associated with lower stimulated cortisol levels.
CONCLUSIONS
Patients on PCSK9i therapy showed a significantly lower cortisol response to ACTH. Stimulated cortisol levels were lower in the first months of PCSK9i treatment, suggesting an adaptive phenomenon. We conclude that the adrenal stress response in patients on PCSK9 inhibitor therapy is reduced.

Identifiants

pubmed: 33892329
pii: S0021-9150(21)00149-0
doi: 10.1016/j.atherosclerosis.2021.03.028
pii:
doi:

Substances chimiques

Anticholesteremic Agents 0
Cholesterol, LDL 0
Enzyme Inhibitors 0
Hypolipidemic Agents 0
PCSK9 protein, human EC 3.4.21.-
Proprotein Convertase 9 EC 3.4.21.-

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

63-68

Informations de copyright

Copyright © 2021 Elsevier B.V. All rights reserved.

Auteurs

Simon Meier (S)

Department of Internal Medicine, Cantonal Hospital Baden, Im Ergel 1, 5404, Baden, Switzerland.

Marcel Frick (M)

Department of Internal Medicine, Cantonal Hospital Baden, Im Ergel 1, 5404, Baden, Switzerland.

Michael Liu (M)

Department of Internal Medicine, Cantonal Hospital Baden, Im Ergel 1, 5404, Baden, Switzerland.

Seyed Soheil Saeedi Saravi (SS)

Department of Internal Medicine, Cantonal Hospital Baden, Im Ergel 1, 5404, Baden, Switzerland; Laboratory for Platelet Research and of Endothelial Function, Center for Molecular Cardiology, University of Zurich, Wagistrasse 12, 8952, Schlieren, Switzerland.

Giulia Montrasio (G)

Department of Internal Medicine, Cantonal Hospital Baden, Im Ergel 1, 5404, Baden, Switzerland.

Helga Preiss (H)

Department of Internal Medicine, Cantonal Hospital Baden, Im Ergel 1, 5404, Baden, Switzerland.

Lisa Pasterk (L)

Laboratory for Platelet Research and of Endothelial Function, Center for Molecular Cardiology, University of Zurich, Wagistrasse 12, 8952, Schlieren, Switzerland.

Nicole Bonetti (N)

Laboratory for Platelet Research and of Endothelial Function, Center for Molecular Cardiology, University of Zurich, Wagistrasse 12, 8952, Schlieren, Switzerland.

Michael Egloff (M)

Department of Internal Medicine, Cantonal Hospital Baden, Im Ergel 1, 5404, Baden, Switzerland.

Hans-Rudolf Schmid (HR)

Department of Internal Medicine, Cantonal Hospital Baden, Im Ergel 1, 5404, Baden, Switzerland.

Isabella Sudano (I)

University Heart Center Zürich, University Hospital of Zürich, Rämistrasse 100, 8091, Switzerland.

Giovanni G Camici (GG)

Laboratory for Platelet Research and of Endothelial Function, Center for Molecular Cardiology, University of Zurich, Wagistrasse 12, 8952, Schlieren, Switzerland.

François Mach (F)

Department of Cardiology, University Hospitals of Geneva, Rue Gabrielle-Perret-Gentil 4, 1205, Geneva, Switzerland.

Thomas F Luescher (TF)

Laboratory for Platelet Research and of Endothelial Function, Center for Molecular Cardiology, University of Zurich, Wagistrasse 12, 8952, Schlieren, Switzerland; Heart Division, Royal Brompton & Harefield Hospital and National Heart & Lung Institute, Imperial College, London, United Kingdom.

Georg Ehret (G)

Department of Cardiology, University Hospitals of Geneva, Rue Gabrielle-Perret-Gentil 4, 1205, Geneva, Switzerland.

Jürg H Beer (JH)

Department of Internal Medicine, Cantonal Hospital Baden, Im Ergel 1, 5404, Baden, Switzerland; Laboratory for Platelet Research and of Endothelial Function, Center for Molecular Cardiology, University of Zurich, Wagistrasse 12, 8952, Schlieren, Switzerland. Electronic address: juerg-hans.beer@ksb.ch.

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