Blom Dirk J, Chen Jiyan, Yuan Zuyi, Borges Joao L C, Monsalvo Maria L, Wang Nan, Hamer Andrew W, Ge Junbo
University of Cape Town Cape Town South Africa.
Guangdong Cardiovascular Institute Guangdong General Hospital Guangzhou China.
Endocrinol Diabetes Metab. 2020 Mar 6;3(2):e00123. doi: 10.1002/edm2.123. eCollection 2020 Apr.
We assessed the change from baseline in vitamin E, steroid hormones, adrenocorticotropic hormone (ACTH), and gonadotropins, overall and by lowest achieved low-density lipoprotein-cholesterol (LDL-C) level, in patients with type 2 diabetes and dyslipidaemia after 12 weeks of treatment with evolocumab.
This was a prespecified analysis of vitamin E, cortisol, ACTH, gonadal hormones and gonadotropins in the 12-week, placebo-controlled BERSON trial of evolocumab in patients with type 2 diabetes and dyslipidaemia. In BERSON, 981 (451 in China) patients on daily atorvastatin 20 mg were randomized to placebo or one of two doses of evolocumab. We measured analyte levels at baseline and week 12 (vitamin E in all patients; steroid/gonadal hormones only in Chinese patients).
In both the global and Chinese populations, absolute vitamin E levels decreased from baseline to week 12 by approximately 6 μmol/L ( < .0001) among evolocumab-treated patients; however, when normalized for LDL-C, apoB or non-HDL-C, we observed no decrease in vitamin E levels. In Chinese patients, levels of cortisol and ACTH as well as the cortisol:ACTH ratio did not change significantly from baseline to week 12. No patient had a cortisol:ACTH ratio <3.0 (nmol/pmol), suggestive of adrenocortical deficiency. We did not observe clinically relevant changes for gonadal hormones and gonadotropins (oestradiol and testosterone in female and male patients, respectively, luteinizing and follicle-stimulating hormones for both).
In the BERSON study, evolocumab did not adversely affect vitamin E, steroid hormone or gonadotropin levels in the Chinese or global type 2 diabetic populations.ClinicalTrials.gov NCT02662569.
我们评估了2型糖尿病和血脂血脂血脂异常患者接受阿利西尤单抗治疗12周后,维生素E、类固醇激素、促肾上腺皮质激素(ACTH)和促性腺激素相对于基线水平的变化,以及按达到的最低低密度脂蛋白胆固醇(LDL-C)水平进行分层后的变化情况。
这是一项对阿利西尤单抗治疗2型糖尿病和血脂异常患者的12周安慰剂对照BERSON试验中维生素E、皮质醇、ACTH、性腺激素和促性腺激素的预先设定分析。在BERSON试验中,981名(中国451名)每日服用20mg阿托伐他汀的患者被随机分配至安慰剂组或两种剂量阿利西尤单抗中的一组。我们在基线和第12周测量了分析物水平(所有患者均测量维生素E;仅中国患者测量类固醇/性腺激素)。
在全球和中国人群中,接受阿利西尤单抗治疗的患者,从基线到第12周,维生素E的绝对水平均下降了约6μmol/L(P<0.0001);然而,当以LDL-C、载脂蛋白B或非HDL-C进行标准化后,我们未观察到维生素E水平下降。在中国患者中,从基线到第12周,皮质醇和ACTH水平以及皮质醇:ACTH比值均无显著变化。没有患者的皮质醇:ACTH比值<3.0(nmol/pmol),提示肾上腺皮质功能减退。我们未观察到性腺激素和促性腺激素(分别为女性患者的雌二醇和男性患者的睾酮,以及两者的促黄体生成素和促卵泡生成素)出现具有临床意义的变化。
在BERSON研究中,阿利西尤单抗对中国或全球2型糖尿病患者的维生素E、类固醇激素或促性腺激素水平无不良影响。ClinicalTrials.gov NCT02662569。