Literature DB >> 19552745

Amiodarone concentrations in plasma and fat tissue during chronic treatment and related toxicity.

Carmelo Lafuente-Lafuente1, Jean-Claude Alvarez, Antoine Leenhardt, Stéphane Mouly, Fabrice Extramiana, Charles Caulin, Christian Funck-Brentano, Jean-François Bergmann.   

Abstract

AIMS: To determine if amiodarone, highly lipophilic, accumulates in excess with respect to dose in fat tissue during long-term administration, and study if plasma and fat tissue concentrations are correlated with adverse effects.
METHODS: Trough concentrations of amiodarone and N-desethyl-amiodarone were measured simultaneously in plasma and fat tissue, in 30 consecutive patients treated with amiodarone for 3 months to 12 years. Subcutaneous adipose tissue was obtained by needle aspiration from lumbar and abdominal areas. Concentrations were measured by liquid chromatography-tandem mass spectrometry.
RESULTS: Plasma levels of amiodarone and N-desethyl-amiodarone were significantly correlated with daily maintenance doses (R= 0.52, P= 0.003). Amiodarone concentrations in fat tissue were four to 226 times (mean 55) higher than in plasma, and well correlated with plasma levels (R= 0.68, P < 0.001). Concentrations of amiodarone and N-desethyl-amiodarone in adipose tissue did not significantly increase with higher total cumulated doses or longer treatment duration. Nine of 12 patients who had received amiodarone for > or =2 years developed clinically important adverse effects, predominantly hypothyroidism (n= 6), compared with two of 18 patients treated for less time (relative risk 6.75; 95% confidence interval 1.8, 26). The incidence of those adverse effects was not significantly associated with amiodarone concentrations, whether in plasma or in adipose tissue.
CONCLUSIONS: We found no evidence of excessive or unexpected accumulation of amiodarone in fat tissue on long-term administration. Late amiodarone adverse effects, particularly hypothyroidism, are associated with longer exposure times, but do not seem to be explained by higher concentrations in plasma or in fat tissue.

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Year:  2009        PMID: 19552745      PMCID: PMC2686067          DOI: 10.1111/j.1365-2125.2009.03381.x

Source DB:  PubMed          Journal:  Br J Clin Pharmacol        ISSN: 0306-5251            Impact factor:   4.335


  24 in total

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Review 6.  Antiarrhythmics for maintaining sinus rhythm after cardioversion of atrial fibrillation.

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2.  Association between N-desethylamiodarone/amiodarone ratio and amiodarone-induced thyroid dysfunction.

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4.  WAT-on-a-chip: a physiologically relevant microfluidic system incorporating white adipose tissue.

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5.  The role of CYP 3A4 and 1A1 in amiodarone-induced hepatocellular toxicity.

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6.  Antiarrhythmics for maintaining sinus rhythm after cardioversion of atrial fibrillation.

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Journal:  Cochrane Database Syst Rev       Date:  2019-09-04

7.  Lifespan-increasing drug nordihydroguaiaretic acid inhibits p300 and activates autophagy.

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8.  Influence of concomitant medication on plasma concentration of amiodarone in patients with atrial fibrillation - a pilot study.

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9.  Prediction of the dose range for adverse neurological effects of amiodarone in patients from an in vitro toxicity test by in vitro-in vivo extrapolation.

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10.  Therapeutic monitoring of amiodarone and desethylamiodarone after surgical ablation of atrial fibrillation-evaluation of the relationship between clinical effect and the serum concentration.

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