Department of Internal Medicine, Medical University of Silesia, 44-902 Bytom, Poland.
Department of Laboratory Diagnostics, Poznan University of Medical Science, 60-569 Poznan, Poland.
Clin Interv Aging. 2019 May 9;14:789-796. doi: 10.2147/CIA.S196016. eCollection 2019.
Ageing is one of the major risks for atherosclerosis. The age-related changes of interactions between plasma lipids, oxidative stress, antioxidant defense, and glycation processes are still not established while we age. Thus, the aim of the study was to analyze such relationships in individuals at risk for atherosclerosis due to their age. Elderly and middle-aged persons with no acute disease or severe chronic disorder were assessed. Fasting plasma lipids (total cholesterol (T-C), high-density lipoprotein-cholesterol (HDL-C), low-density lipoprotein-cholesterol, and triacylglycerols), thiobarbituric acid reacting substances (TBARS), plasma total antioxidant status (TAS), and glucose and glycated proteins (fructosamine (FA) and glycated hemoglobin (HbA)) were determined. An oral glucose tolerance test allowed exclusion of persons with type 2 diabetes. Lipid profiles were significantly profitable, increased HDL-C especially (p<0.0001), in the elderly versus middle-aged group. Decreased TBARS and TAS were found in the elderly versus middle-aged group (=0.0001 and p=0.00002, respectively). Increased fructosamine was found in the elderly (255±30 μmol/L) versus middle-aged (236±33 μmol/L) group (p=0.006). Multiple regression analysis showed that in the middle-aged group TBARS correlated with T-C and HDL-C, and in the elderly group with HbA and FA independently of other factors. The factors which have an impact on oxidant-antioxidant status are crucial to understanding the pathomechanisms of senescence as well as the development of chronic diseases. Healthy aging may be maintained throughout proper lipid control. Moreover, data support the premise that the balance between lipid metabolism and oxidative stress may play a role in the initial phases of glycation plasma proteins particularly among elderly persons.
衰老是动脉粥样硬化的主要危险因素之一。随着年龄的增长,血浆脂质、氧化应激、抗氧化防御和糖基化过程之间相互作用的变化尚不清楚。因此,本研究旨在分析由于年龄而处于动脉粥样硬化风险中的个体的这些关系。评估了无急性疾病或严重慢性疾病的老年和中年个体。测定空腹血浆脂质(总胆固醇(T-C)、高密度脂蛋白胆固醇(HDL-C)、低密度脂蛋白胆固醇和三酰甘油)、硫代巴比妥酸反应物质(TBARS)、血浆总抗氧化状态(TAS)以及葡萄糖和糖基化蛋白(果糖胺(FA)和糖化血红蛋白(HbA))。口服葡萄糖耐量试验排除了 2 型糖尿病患者。脂质谱在老年组中明显有益,尤其是 HDL-C 增加(p<0.0001)。与中年组相比,老年组的 TBARS 和 TAS 降低(=0.0001 和 p=0.00002)。老年组的果糖胺增加(255±30 μmol/L)与中年组(236±33 μmol/L)相比(p=0.006)。多元回归分析显示,在中年组中,TBARS 与 T-C 和 HDL-C 相关,而在老年组中与 HbA 和 FA 独立于其他因素相关。影响氧化还原状态的因素对于理解衰老的发病机制以及慢性疾病的发展至关重要。通过适当的脂质控制,可以保持健康的衰老。此外,数据支持这样的前提,即脂质代谢和氧化应激之间的平衡可能在糖基化血浆蛋白的初始阶段,特别是在老年人中发挥作用。