Geuter Joschua, Seizer Lennart, Cornelissen Guillaume Germaine, Engin Ayse Basak, Fuchs Dietmar, Schubert Christian
Sainsbury Wellcome Centre, London, United Kingdom.
Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, University Hospital of Tübingen, Tübingen, Germany.
J Circadian Rhythms. 2025 May 19;23:6. doi: 10.5334/jcr.252. eCollection 2025.
8-hydroxy-2'deoxyguanosine (8-OHdG) is an oxidative product removed from DNA following radical oxygen species-induced damage. As a water-soluble molecule, it can be measured non-invasively in urine and is commonly used as a marker for 'whole-body' oxidative stress. However, its validity and reliability in assessing oxidative stress across various chronic diseases and in early carcinogenesis screening in clinical diagnosis and research remain subjects of debate. To determine optimal measurement timing and duration, it is essential to establish the circadian profile of 8-OHdG under everyday life conditions. Here, applying the integrative single-case design, we show the presence of day-night differences for 8-OHdG in continuous time series of two breast cancer survivors while considering different correction approaches. The participants sampled their urine in 12-h-pooled collections over one month. In both subjects, 8-OHdG levels were significantly higher during the day than at night regardless of whether they were corrected by creatinine or urine volume (creatinine corrected: t = -6.43, < 0.01 [subject 1], t = -2.69, = 0.01 [subject 2]; volume corrected: t = -7.30, < 0.01 [subject 1], t = -3.69, < 0.01 [subject 2]). Notably, urinary 8-OHdG levels show higher variability in night samples compared to day samples. These findings underscore the importance of considering daily fluctuations in 8-OHdG levels in both clinical and research studies, as well as the need to account for the dynamic characteristics of stress markers to minimize the risk of inconsistent or misleading results in clinical diagnostics.
8-羟基-2'-脱氧鸟苷(8-OHdG)是一种在活性氧诱导的DNA损伤后从DNA中去除的氧化产物。作为一种水溶性分子,它可以在尿液中进行非侵入性测量,并且通常用作“全身”氧化应激的标志物。然而,其在评估各种慢性疾病中的氧化应激以及临床诊断和研究中的早期癌症筛查中的有效性和可靠性仍然存在争议。为了确定最佳测量时间和持续时间,在日常生活条件下建立8-OHdG的昼夜分布至关重要。在这里,应用综合单病例设计,我们在考虑不同校正方法的同时,展示了两名乳腺癌幸存者连续时间序列中8-OHdG的昼夜差异。参与者在一个月内以12小时汇总收集的方式采集尿液样本。在两名受试者中,无论是否通过肌酐或尿量进行校正,白天的8-OHdG水平均显著高于夜间(肌酐校正:t = -6.43,P < 0.01 [受试者1],t = -2.69,P = 0.01 [受试者2];尿量校正:t = -7.30,P < 0.01 [受试者1],t = -3.69,P < 0.01 [受试者2])。值得注意的是,与白天样本相比,夜间样本中尿8-OHdG水平的变异性更高。这些发现强调了在临床和研究中考虑8-OHdG水平每日波动的重要性,以及考虑应激标志物动态特征以尽量减少临床诊断中结果不一致或误导性风险的必要性。