Heart and Lung Center, Cardiology, Helsinki University Central Hospital, University of Helsinki, Helsinki, Finland.
Department of Food and Environmental Sciences, University of Helsinki, Helsinki, Finland.
J Intern Med. 2018 Jan;283(1):93-101. doi: 10.1111/joim.12682. Epub 2017 Sep 21.
Amiodarone is an effective and widely used antiarrhythmic drug with many possible adverse effects including hypercholesterolaemia and hepatotoxicity.
Our aim was to evaluate how long-term amiodarone treatment affects cholesterol metabolism.
The study population consisted of 56 cardiac patients, of whom 20 were on amiodarone (amiodarone + group) and 36 did not use the drug (amiodarone - group). We also studied a control group of 124 individuals selected randomly from the population. Cholesterol metabolism was evaluated by analysis of serum noncholesterol sterols by gas-liquid chromatography and gas chromatography-mass spectrometry.
Comparisons of serum lipids and noncholesterol sterols across the three groups showed increased serum triglyceride in users of amiodarone but no statistically significant group differences in total, LDL or HDL cholesterol or serum proprotein convertase subtilisin/kexin type 9 concentrations. Nor did the groups differ in the ratios of cholestanol or plant sterols to cholesterol in serum, suggesting that cholesterol absorption was unaltered. However, all users of amiodarone had very markedly elevated serum desmosterol concentrations: the desmosterol-to-cholesterol ratio (10 × μmol mmol ) averaged 1030.7 ± 115.7 (mean ± SE) in the amiodarone + group versus 82.7 ± 3.4 and 75.9 ± 1.4 in the amiodarone - and the population control groups (P < 0.001), respectively.
Use of amiodarone was associated with on average 12-fold serum desmosterol concentrations compared with the control groups. This observation is fully novel and suggests that amiodarone interferes with the conversion of desmosterol to cholesterol in the cholesterol synthesis pathway. Whether accumulation of desmosterol plays a role in amiodarone-induced hepatotoxicity deserves to be studied in the future.
胺碘酮是一种有效的、广泛应用的抗心律失常药物,具有许多可能的不良反应,包括高胆固醇血症和肝毒性。
我们旨在评估长期胺碘酮治疗对胆固醇代谢的影响。
研究人群包括 56 例心脏病患者,其中 20 例服用胺碘酮(胺碘酮+组),36 例未使用该药物(胺碘酮-组)。我们还从人群中随机选择了 124 名对照者组成对照组。通过气相色谱-液相色谱和气相色谱-质谱分析血清非胆固醇甾醇来评估胆固醇代谢。
三组血清脂质和非胆固醇甾醇的比较显示,胺碘酮使用者的血清甘油三酯升高,但总胆固醇、LDL 或 HDL 胆固醇或血清前蛋白转化酶枯草溶菌素/激肽释放酶 9 浓度无统计学显著组间差异。胆固醇吸收也没有改变,因为各组血清胆甾烷醇或植物甾醇与胆固醇的比值没有差异。然而,所有胺碘酮使用者的血清去甲胆固醇浓度均显著升高:胺碘酮+组的去甲胆固醇与胆固醇比值(10×μmolmmol)平均为 1030.7±115.7(均值±SE),而胺碘酮-组和人群对照组分别为 82.7±3.4 和 75.9±1.4(P<0.001)。
与对照组相比,胺碘酮的使用平均使血清去甲胆固醇浓度升高 12 倍。这一观察结果是完全新颖的,提示胺碘酮干扰胆固醇合成途径中去甲胆固醇转化为胆固醇。去甲胆固醇的积累是否在胺碘酮诱导的肝毒性中起作用值得在未来进行研究。