Department of Food and Experimental Nutrition, Faculty of Pharmaceutical Sciences, University of São Paulo, Av. Prof. Lineu Prestes 580, Bloco 14, Butantã, São Paulo, SP, Brazil.
Food Funct. 2018 Oct 17;9(10):5313-5322. doi: 10.1039/c8fo01621f.
Considering that oxidative stress is implicated in the pathogenesis and progression of different health conditions, we aimed to evaluate whether the redox balance of a healthy Brazilian population is associated with GPX1 polymorphisms, selenium status, lipid profile, and anthropometric and lifestyle parameters.
343 healthy adults were assessed for redox balance markers [glutathione peroxidase (GPx) and superoxide dismutase (SOD) activity; malondialdehyde (MDA) and oxygen radical absorption capacity (ORAC)]; genotyped for the polymorphisms GPX1 Pro198Leu (rs1050450), -602A/G (rs3811699) and Arg5Pro (rs8179169); evaluated for selenium biomarkers (plasma, erythrocyte, and urine) and intake; and assessed for lipid profile. Anthropometric (BMI) and lifestyle data (physical activity, current smoking habit and alcohol consumption) were collected. Multivariable regression models were applied to investigate the possible associations.
Although there were no differences in GPx activity according to GPX1 Pro198Leu and -602A/G polymorphisms, this redox balance marker was positively associated with erythrocyte selenium and negatively associated with the presence of a minor allele of Pro198Leu. SOD activity was positively associated with the presence of a minor allele for these polymorphisms. ORAC showed the same pattern among Leu and G carriers and was positively associated with Leu allele presence, BMI and alcohol intake. MDA was only associated negatively with the male sex and plasma selenium.
Our findings suggest that the redox balance of a Brazilian healthy population is associated with GPX1 polymorphisms (Pro198Leu and -602A/G), selenium status, BMI, sex, smoking habit and alcohol consumption.
考虑到氧化应激与多种健康状况的发病机制和进展有关,我们旨在评估健康巴西人群的氧化还原平衡是否与 GPX1 多态性、硒状态、脂质谱以及人体测量和生活方式参数相关。
评估 343 名健康成年人的氧化还原平衡标志物[谷胱甘肽过氧化物酶(GPx)和超氧化物歧化酶(SOD)活性;丙二醛(MDA)和氧自由基吸收能力(ORAC)];对 GPX1 Pro198Leu(rs1050450)、-602A/G(rs3811699)和 Arg5Pro(rs8179169)多态性进行基因分型;评估硒生物标志物(血浆、红细胞和尿液)和摄入量;并评估脂质谱。收集人体测量(BMI)和生活方式(体力活动、当前吸烟习惯和饮酒)数据。应用多变量回归模型来探讨可能的关联。
尽管 GPx 活性在 GPX1 Pro198Leu 和 -602A/G 多态性方面没有差异,但这种氧化还原平衡标志物与红细胞硒呈正相关,与 Pro198Leu 等位基因的存在呈负相关。SOD 活性与这些多态性的小等位基因存在呈正相关。ORAC 在 Leu 和 G 携带者中表现出相同的模式,与 Leu 等位基因的存在、BMI 和酒精摄入量呈正相关。MDA 仅与男性和血浆硒呈负相关。
我们的研究结果表明,巴西健康人群的氧化还原平衡与 GPX1 多态性(Pro198Leu 和 -602A/G)、硒状态、BMI、性别、吸烟习惯和饮酒有关。