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Effects of adjunctive eslicarbazepine acetate on serum lipids in patients with partial-onset seizures: Impact of concomitant statins and enzyme-inducing antiepileptic drugs.

Artikel i vetenskaplig tidskrift
Författare Scott Mintzer
Robert T Wechsler
Joanne B Rogin
Barry E Gidal
Matthias Schwab
Elinor Ben-Menachem
Mar Carreño
Patrício Soares da Silva
Joana Moreira
Yan Li
David Blum
Todd Grinnell
Publicerad i Epilepsy research
Volym 141
Sidor 83-89
ISSN 1872-6844
Publiceringsår 2018
Publicerad vid Institutionen för neurovetenskap och fysiologi
Sidor 83-89
Språk en
Länkar dx.doi.org/10.1016/j.eplepsyres.201...
www.ncbi.nlm.nih.gov/entrez/query.f...
Ämnesord Eslicarbazepine acetate, Statins, Serum lipids, Partial-onset seizures, Adjunctive, Enzyme-inducing antiepileptic drugs
Ämneskategorier Klinisk medicin

Sammanfattning

To evaluate the effects of eslicarbazepine acetate (ESL) on lipid metabolism and to determine whether reduced statin exposure during ESL therapy has clinical consequences.We conducted a post-hoc analysis of pooled data for serum lipids (laboratory values) from three phase III, multicenter, randomized, double-blind, placebo-controlled trials of adjunctive ESL therapy (400, 800, or 1200 mg once daily) in patients with treatment-refractory partial-onset seizures. Changes from baseline in serum lipid levels were analyzed according to use of statins and/or enzyme-inducing antiepileptic drugs (EIAEDs) during the baseline period.In total, 426 and 1021 placebo- and ESL-treated patients, respectively, were included in the analysis. With regard to the changes from baseline in serum concentrations, there were statistically significant differences between the placebo and ESL 1200 mg QD groups, for both total cholesterol (TC) and high-density lipoprotein cholesterol (HDL-C), but the effect sizes were small (+4.1 mg/dL and +1.8 mg/dL, respectively). A small but significant difference in low-density lipoprotein cholesterol (LDL-C; -5.0 mg/dL) was observed between the ESL 400 mg QD group and the placebo group. In patients not taking a concomitant EIAED, there were no changes with ESL 400 mg QD, but modest and statistically significant increases in cholesterol fractions (TC, LDL-C and HDL-C) with ESL 800 mg QD (<6 mg/dL) and ESL 1200 mg QD (<10 mg/dL). ESL had no consistent effect on lipids in patients taking a concomitant EIAED. In patients taking statins during baseline, there were no clinically relevant changes in serum lipids during use of ESL, although the subgroups were small.These results suggest that ESL does not appear to have clinically significant effects on serum lipids, nor does the pharmacokinetic interaction between ESL and statins have an impact on serum lipid concentrations.

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