Fulek Michal, Frosztega Weronika, Wieckiewicz Mieszko, Szymanska-Chabowska Anna, Gac Pawel, Poreba Rafal, Mazur Grzegorz, Sciskalska Milena, Kepinska Marta, Martuszewski Adrian, Martynowicz Helena
Clinical Department of Diabetology, Hypertension and Internal Diseases, Institute of Internal Diseases, Wroclaw Medical University, 213 Borowska St, Wroclaw, 50-556, Poland.
Department of Experimental Dentistry, Wroclaw Medical University, 26 Krakowska St, Wroclaw, 50-425, Poland.
Sci Rep. 2025 Jan 28;15(1):3567. doi: 10.1038/s41598-025-86833-y.
Oxidative stress is proven to increase cardiovascular risk and to diminish healthy life expectancy. Sleep bruxism (SB) is a prevalent masticatory muscle activity during sleep characterized by heterogeneous etiology and inadequately recognized pathophysiology. Recent theories have proposed a potential association between SB and oxidative stress. The aim of the research was to compare the antioxidant status between individuals with SB in contrast to those without SB. A total of 80 adults participated in a full-night polysomnography, assessed according to the American Academy of Sleep Medicine (AASM) standards. Blood samples were subsequently drawn via venipuncture for analysis. Participants were stratified into two groups based on their bruxism episode index (BEI). Using successive receiver operating characteristic (ROC) curves, optimal cut-off values were identified, enabling the detection of correlations with moderate (BEI > 2) and severe (BEI > 4) sleep bruxism. In the investigated group of patients we observed the relationship between bruxism and the examined parameters: total antioxidant status (TAS), advanced protein products (AOPP) and thiobarbituric acid-reacting substances (TBARS). Low TAS (≤ 0.14 mM and ≤ 0. 16 mM), high AOPP (≥ 82.44 µmol/l) and high TBARS (≥ 723.03 µmol/l and ≥ 1585.45 µmol/l) serum levels result in significantly higher sleep bruxism parameters. Sleep bruxism is related to oxidative stress markers. Elevated markers of lipid and protein peroxidation may be associated with endovascular damage and cardiovascular risk in sleep bruxers, but further research is needed in this topic.
氧化应激已被证明会增加心血管疾病风险并缩短健康预期寿命。睡眠磨牙症(SB)是一种在睡眠期间普遍存在的咀嚼肌活动,其病因多样,病理生理学尚未得到充分认识。最近的理论提出了SB与氧化应激之间的潜在关联。该研究的目的是比较有SB的个体与无SB的个体之间的抗氧化状态。共有80名成年人参加了整夜多导睡眠图监测,并根据美国睡眠医学学会(AASM)标准进行评估。随后通过静脉穿刺采集血样进行分析。参与者根据其磨牙症发作指数(BEI)分为两组。使用连续受试者工作特征(ROC)曲线确定最佳临界值,以检测与中度(BEI>2)和重度(BEI>4)睡眠磨牙症的相关性。在被调查的患者组中,我们观察到磨牙症与所检查参数之间的关系:总抗氧化状态(TAS)、晚期蛋白产物(AOPP)和硫代巴比妥酸反应物质(TBARS)。低TAS(≤0.14 mM和≤0.16 mM)、高AOPP(≥82.44 µmol/l)和高TBARS(≥723.03 µmol/l和≥1585.45 µmol/l)的血清水平导致睡眠磨牙症参数显著升高。睡眠磨牙症与氧化应激标志物有关。脂质和蛋白质过氧化标志物升高可能与睡眠磨牙者的血管内损伤和心血管疾病风险有关,但该主题还需要进一步研究。