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Neurocognitive Disorders Associated with PCSK9 Inhibitors: a Pharmacovigilance Disproportionality Analysis.
Gouverneur, Amandine; Sanchez-Pena, Paola; Veyrac, Gwenaelle; Salem, Joe-Elie; Bégaud, Bernard; Bezin, Julien.
Afiliação
  • Gouverneur A; Team Pharmacoepidemiology, Bordeaux Population Health Research Center, UMR 1219, Inserm, University of Bordeaux, Bordeaux, France.
  • Sanchez-Pena P; Service de Pharmacologie médicale, Pôle de santé Publique, CHU de Bordeaux, Bordeaux, France.
  • Veyrac G; Service de Pharmacologie médicale, Pôle de santé Publique, CHU de Bordeaux, Bordeaux, France.
  • Salem JE; Clinical Pharmacology Department, CHU Nantes, Nantes, France.
  • Bégaud B; Department of Pharmacology and Clinical Investigation Center (CIC-1901), Groupe Hospitalier Pitié-Salpêtrière, Sorbonne Universite, AP-HP, INSERM, Paris, France.
  • Bezin J; Team Pharmacoepidemiology, Bordeaux Population Health Research Center, UMR 1219, Inserm, University of Bordeaux, Bordeaux, France.
Cardiovasc Drugs Ther ; 37(2): 271-276, 2023 04.
Article em En | MEDLINE | ID: mdl-34436707
PURPOSE: PCSK9 might affect central nervous system development, neuronal apoptosis, and differentiation. We investigate the neurocognitive adverse events associated with the use of PCSK9 inhibitors (alirocumab and evolocumab) using pharmacovigilance reports. METHODS: We used the World Health Organization pharmacovigilance database (VigiBase) to perform a disproportionality analysis comparing the proportion of neurocognitive adverse events reported with PCSK9 inhibitors versus the proportion of these effects reported since August 14, 2015 (date of first post-marketing report suspecting a PCSK9 inhibitor), for all drugs in the database. Associations between PCSK9 inhibitor use and neurocognitive adverse events were assessed using both proportional reporting ratio (PRR) and information component (IC). Complementary analyses were performed on other neurologic events, and different sensitivity analyses were conducted to evaluate the robustness of results. RESULTS: Among the 81,108 reports involving at least one PCSK9 inhibitor, 1,941 concerned the occurrence of neurocognitive disorders. Most of patients (52.3%) were aged 45-74 years, and 58.0% were women. Signals of disproportionate reporting were found for PCSK9 inhibitors (PRR 1.22, 95% CI 1.17; 1.28; IC 0.28, IC025 0.21) and for each drug individually. No signal of disproportionality was found for any of the other neurologic events investigated. Signals of disproportionate reporting were found for the positive control (benzodiazepines), but not for the negative control (aspirin). The results of the main analysis were confirmed by sensitivity analyses. CONCLUSIONS: This study identified a signal of neurocognitive disorders associated with PCSK9 inhibitors and encourages paying attention to at-risk populations.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pró-Proteína Convertase 9 / Inibidores de PCSK9 Tipo de estudo: Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: Cardiovasc Drugs Ther Assunto da revista: ANGIOLOGIA / CARDIOLOGIA / TERAPIA POR MEDICAMENTOS Ano de publicação: 2023 Tipo de documento: Article País de afiliação: França País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Pró-Proteína Convertase 9 / Inibidores de PCSK9 Tipo de estudo: Risk_factors_studies Limite: Female / Humans / Male Idioma: En Revista: Cardiovasc Drugs Ther Assunto da revista: ANGIOLOGIA / CARDIOLOGIA / TERAPIA POR MEDICAMENTOS Ano de publicação: 2023 Tipo de documento: Article País de afiliação: França País de publicação: Estados Unidos