Sutter Charlotte, Helbling Daniel, Haas Cordula, Neubauer Jacqueline
Zurich Institute of Forensic Medicine, University of Zurich, Zurich 8006, Switzerland.
Onkozentrum Zurich, Zurich 8038, Switzerland.
Aging (Albany NY). 2025 Jul 17;17(7):1679-1701. doi: 10.18632/aging.206281.
The use of epigenetic clocks for measuring age acceleration in the field of cancer research has been a common practice for many years. In forensic genetics, DNA methylation can be used to estimate the age of a stain donor. As lifestyle and disease can alter a person's methylation profile, the accuracy of forensic age estimation tools might decrease compared to the chronological age when estimating a person affected by cancer. In our study, we applied the VISAGE enhanced age estimation tool on blood samples from cancer patients suffering from a variety of cancer entities, including solid and hematologic tumours. A comparison of the age estimation errors between the cancer patients (n = 100) and a healthy control cohort (n = 102) revealed small statistically significant differences and a tendency towards age acceleration in the blood of these patients. Although this study showed that in patients with aggressive cancers (like CLL or AML) estimation accuracy is clearly decreased, for most entities the observed differences were subtle and an analysis of individual CpG sites did not reveal strikingly different methylation patterns. Conclusively, age estimation on blood stains from cancer patients might not result in significantly higher estimation errors, except for very aggressive forms of cancer.
在癌症研究领域,使用表观遗传时钟来测量年龄加速已经是多年来的常见做法。在法医遗传学中,DNA甲基化可用于估计污渍捐赠者的年龄。由于生活方式和疾病会改变一个人的甲基化谱,与估计癌症患者的实际年龄相比,法医年龄估计工具的准确性可能会降低。在我们的研究中,我们将VISAGE增强年龄估计工具应用于患有各种癌症实体(包括实体瘤和血液肿瘤)的癌症患者的血液样本。对癌症患者(n = 100)和健康对照队列(n = 102)之间的年龄估计误差进行比较,发现这些患者血液中的差异在统计学上有小的显著差异以及年龄加速的趋势。虽然这项研究表明,在患有侵袭性癌症(如慢性淋巴细胞白血病或急性髓细胞白血病)的患者中,估计准确性明显降低,但对于大多数实体瘤来说,观察到的差异很细微,对单个CpG位点的分析并未揭示出明显不同的甲基化模式。总之,除了非常侵袭性的癌症形式外,对癌症患者血迹的年龄估计可能不会导致显著更高的估计误差。