在患有亚形性皮肤炎的儿童中,表观遗传和生物衰老加速
Richie Jeremian1,2, Alexandra Malinowski3, Edward S Oh3
1Faculty of Medicine & Health Sciences, McGill University, Montreal, Quebec, Canada.
概括
在患有亚托皮性皮炎 (AD) 的儿童中,表观遗传和生物衰老加速,由DNA甲基化变化和改变的炎症生物标志物表明,这表明早期疾病的病理生理学.
科学领域:
- 遗传学和表观遗传学
- 皮肤病学 皮肤病学
- 免疫学 免疫学 免疫学
背景情况:
- 亚托皮炎 (AD) 是一种由遗传和环境因素影响的慢性炎症性皮肤病.
- 表观遗传年龄加速与喘等炎症状况有关.
研究的目的:
- 调查表观遗传衰老,生物衰老,端粒长度和儿科亚托皮炎炎炎症生物标志物的作用.
主要方法:
- 对儿科阿尔茨海默症患者 (n=24) 和年龄相匹配的健康对照组 (n=24) 的血液样本进行了DNA甲基化分析.
- 五个经过验证的算法评估了表观遗传年龄,生物年龄,端粒长度和推断的炎症生物标志物水平.
主要成果:
- 在AD患者中,表观遗传和生物年龄通过四种算法 (Horvath,Skin&Blood,PhenoAge,GrimAge) 加速.
- 端粒长度在两组之间没有显著差异.
- 在AD患者中观察到特定炎症生物标志物 (β2微球蛋白,等离子体激活抑制剂1,cystatin C) 的水平升高以及组织抑制剂金属蛋白酶1的水平降低.
结论:
- 与衰老和炎症相关的DNA甲基化变化在儿科阿尔茨海默病的早期存在.
- 这些发现表明AD病理生理学的潜在临床生物标志物.
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