Zrnić-Ćirić Milica, Kotur-Stevuljević Jelena, Stanković Ivan, Đordjević Brižita, Baralić Ivana, Ostojić Miodrag
University of Belgrade, Faculty of Pharmacy, Department of Bromatology, Belgrade.
University of Belgrade, Faculty of Pharmacy, Department of Medical Biochemistry, Belgrade.
J Med Biochem. 2023 Jan 20;42(1):47-57. doi: 10.5937/jomb0-38224.
The uneven lipid-lowering statin effects and statin intolerance raise interest regarding the involvement of coadministration of statins and dietary supplements. This study aimed to evaluate the effects of octacosanol supplementation on markers of redox status in cardiovascular patients on chronic atorvastatin therapy.
A double-blind, randomized, placebo-controlled, single-centre study was conducted. Redox status homeostasis parameters [i.e., advanced oxidation protein products (AOPP), pro-oxidant-antioxidant balance (PAB), total oxidant status (TOS), total antioxidant status (TAS), superoxide dismutase activity (SOD), total protein sulfhydryl (SHgroups), and paraoxonase 1 (PO N 1) activity] were assessed in 81 patients. According to favorable changes in lipid profile, patients were classified into two groups: responders (n = 35) and non-responders (n = 46), and followed for 13 weeks. A principal component analysis (PCA) was applied to explore the effect of octacosanol supplementation and the relationship between investigated parameters as predictors of responders' and non-responders' status.
Significant decrease in Oxy-score value was found at the endpoint compared to baseline in responders' group (21.0 (13.4-25.5) versus 15.1 (12.4-18.0); < 0.01). PCA analysis extracted 4 significant factors in the both groups, whereas extracted factors containing "octacosanol status" variable explained 14.7% and 11.5% of the variance in responders' and non-responders' subgroups, respectively.
Octacosanol supplementation leads to an improvement of lipid profile and markers of redox status in responders' group. New studies are needed to validate our results in order to find the best approach for personalized supplementation as a useful adjunct to standard statin therapy.
他汀类药物降脂效果不均一以及他汀不耐受引发了人们对他汀类药物与膳食补充剂联合使用的关注。本研究旨在评估补充二十八烷醇对接受慢性阿托伐他汀治疗的心血管疾病患者氧化还原状态标志物的影响。
进行了一项双盲、随机、安慰剂对照、单中心研究。在81例患者中评估了氧化还原状态稳态参数[即晚期氧化蛋白产物(AOPP)、促氧化剂-抗氧化剂平衡(PAB)、总氧化状态(TOS)、总抗氧化状态(TAS)、超氧化物歧化酶活性(SOD)、总蛋白巯基(SH基团)和对氧磷酶1(PON1)活性]。根据血脂谱的有利变化,将患者分为两组:反应者(n = 35)和无反应者(n = 46),并随访13周。应用主成分分析(PCA)来探讨补充二十八烷醇的效果以及所研究参数之间的关系,这些参数可作为反应者和无反应者状态的预测指标。
与基线相比,反应者组在终点时Oxy评分值显著降低(21.0(13.4 - 25.5)对15.1(12.4 - 18.0);P < 0.01)。PCA分析在两组中均提取了4个显著因素,而包含“二十八烷醇状态”变量的提取因素分别解释了反应者和无反应者亚组中14.7%和11.5%的方差。
补充二十八烷醇可改善反应者组的血脂谱和氧化还原状态标志物。需要新的研究来验证我们的结果,以便找到个性化补充的最佳方法,作为标准他汀治疗的有益辅助手段。