肾上腺皮质癌中米托坦继发高脂血症的特征。

Nadia Gagnon, Sophie Bernard, Martine Paquette, Catherine Alguire, André Lacroix, Pierre-Olivier Hétu, Harold J Olney, Isabelle Bourdeau
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引用次数: 0

摘要

背景:本研究考察了引入米托坦后LDL-c、HDL-c、甘油三酯(Tg)和非HDL-c的变化幅度和观察最大变化所需的时间。方法:回顾性分析在蒙特里萨大学中心医院接受治疗的45例肾上腺皮质癌患者。收集临床和生化数据,包括米托坦治疗前和第一年的脂质谱。结果:在研究的45例患者中,26例(58%)在引入米托坦之前具有完整的脂质谱,并且在治疗的第一年至少具有1种脂质谱,19例(42%)患者在开始治疗后具有脂质谱。在26例引入米托坦前后血脂的患者中,LDL-c升高2.19 mmol/L (76%) (P< 0.0001), HDL-c升高0.54 mmol/L (35%) (P= 0.0002), Tg升高1.80 mmol/L (129%) (P< 0.0001),非HDL-c升高2.73 mmol/L (79%) (P< 0.0001)。在米托坦治疗的第1 - 6个月期间,LDL-c和非HDL-c分别在42例(93%)和37例(82%)患者中达到峰值(n = 45),而HDL-c在米托坦治疗6个月后达到峰值的患者有29例(66%)。第一年Tg的峰值基本相等。HDL-c、Tg和非HDL-c的平均峰值与其各自的米托坦浓度呈显著相关(β = 0.352, P= 0.03;β = 0.406, P= 0.02; β = 0.339, P= 0.05)。结论:在治疗的第一年,米托坦的引入会导致血脂参数(LDL-c、HDL-c、Tg和非HDL-c)的临床显著升高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Characterization of hyperlipidemia secondary to mitotane in adrenocortical carcinoma.

Characterization of hyperlipidemia secondary to mitotane in adrenocortical carcinoma.

Characterization of hyperlipidemia secondary to mitotane in adrenocortical carcinoma.

Characterization of hyperlipidemia secondary to mitotane in adrenocortical carcinoma.

Background: This study examined the magnitude of changes and the time required to observe maximal changes in LDL-c, HDL-c, triglycerides (Tg) and non-HDL-c after the introduction of mitotane.

Methods: Retrospective study of 45 patients with adrenocortical carcinoma who were treated at the Centre hospitalier de l'Université de Montréal. Clinical and biochemical data were collected, including lipid profiles before and during the first year of treatment with mitotane.

Results: Among the 45 studied patients, 26 (58%) had a complete lipid profile before the introduction of mitotane and at least 1 lipid profile during the first year of treatment, and 19 patients (42%) had a lipid profile following initiation of the treatment. Among the 26 patients who had lipid profiles before and after the introduction of mitotane, the increase of LDL-c was 2.19 mmol/L (76%) (P< 0.0001), HDL-c was 0.54 mmol/L (35%) (P= 0.0002), Tg was 1.80 mmol/L (129%) (P< 0.0001) and non-HDL-c was 2.73 mmol/L (79%) (P< 0.0001). Between the first and the sixth month of mitotane treatment, peak values (n  = 45) of LDL-c and non-HDL-c were reached in 42 patients (93%) and 37 patients (82%), respectively, whereas peak values of HDL-c were reached after 6 months of mitotane treatment in 29 patients (66%). The peak value of Tg was almost equal throughout the first year. The mean peak values of HDL-c, Tg and non-HDL-c showed significant associations with their respective mitotane concentrations (β = 0.352, P= 0.03; β = 0.406, P= 0.02 and β = 0.339, P= 0.05).

Conclusion: The introduction of mitotane produces a clinically significant elevation of lipid parameters (LDL-c, HDL-c, Tg and non-HDL-c) during the first year of treatment.

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