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Lomitapide affects HDL composition and function.
Yahya, R; Favari, E; Calabresi, L; Verhoeven, A J M; Zimetti, F; Adorni, M P; Gomaraschi, M; Averna, M; Cefalù, A B; Bernini, F; Sijbrands, E J G; Mulder, M T; Roeters van Lennep, J E.
Afiliação
  • Yahya R; Department of Internal Medicine, Division Pharmacology, Vascular and Metabolic Diseases, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Favari E; Department of Pharmacy, University of Parma, Parma, Italy.
  • Calabresi L; Centro Grosi Paoletti, Dipartimento di Scienze Farmacologiche e Biomolecolari, Università degli Studi di Milano, Milan, Italy.
  • Verhoeven AJM; Department of Internal Medicine, Division Pharmacology, Vascular and Metabolic Diseases, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Zimetti F; Department of Pharmacy, University of Parma, Parma, Italy.
  • Adorni MP; Department of Pharmacy, University of Parma, Parma, Italy.
  • Gomaraschi M; Centro Grosi Paoletti, Dipartimento di Scienze Farmacologiche e Biomolecolari, Università degli Studi di Milano, Milan, Italy.
  • Averna M; Department of Internal Medicine and Medical Specialties - DIBIMIS, School of Medicine, University of Palermo, Palermo, Italy.
  • Cefalù AB; Department of Internal Medicine and Medical Specialties - DIBIMIS, School of Medicine, University of Palermo, Palermo, Italy.
  • Bernini F; Department of Pharmacy, University of Parma, Parma, Italy.
  • Sijbrands EJG; Department of Internal Medicine, Division Pharmacology, Vascular and Metabolic Diseases, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Mulder MT; Department of Internal Medicine, Division Pharmacology, Vascular and Metabolic Diseases, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Roeters van Lennep JE; Department of Internal Medicine, Division Pharmacology, Vascular and Metabolic Diseases, Erasmus University Medical Center, Rotterdam, The Netherlands. Electronic address: j.roetersvanlennep@erasmusmc.nl.
Atherosclerosis ; 251: 15-18, 2016 08.
Article em En | MEDLINE | ID: mdl-27232459
ABSTRACT

BACKGROUND:

Lomitapide reduces low-density lipoprotein-cholesterol (LDL-C) but also high-density lipoprotein-cholesterol (HDL-C) levels. The latter may reduce the clinical efficacy of lomitapide. We investigated the effect of lomitapide on HDL-C levels and on cholesterol efflux capacity (CEC) of HDL in patients with homozygous familial hypercholesterolemia (HoFH). METHODS AND

RESULTS:

Four HoFH patients were treated with increasing dosages of lomitapide. Lomitapide decreased LDL-C (range -34 to -89%). Total HDL-C levels decreased (range -16 to -34%) with a shift to buoyant HDL. ABCA1-mediated CEC decreased in all patients (range -39 to -99%). The changes of total, ABCG1- and SR-BI-mediated CEC were less consistent.

CONCLUSION:

Lomitapide decreased LDL-C and HDL-C levels. Our report raises the hypothesis that the anti-atherogenic potential of HDL seems to be unaffected as total CEC did not seem to change consistently. Combined with the reduction of atherogenic lipoproteins, the net effect of lomitapide appears to be beneficial in HoFH patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Benzimidazóis / Transportador 1 de Cassete de Ligação de ATP / Lipoproteínas HDL Limite: Adult / Female / Humans / Male Idioma: En Revista: Atherosclerosis Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Benzimidazóis / Transportador 1 de Cassete de Ligação de ATP / Lipoproteínas HDL Limite: Adult / Female / Humans / Male Idioma: En Revista: Atherosclerosis Ano de publicação: 2016 Tipo de documento: Article País de afiliação: Holanda