在50岁以下的人群中,生物年龄加速和结肠多
Chloe M Brown1, Maria V Yow1, Shria Kumar1,2
1Sylvester Comprehensive Cancer Center, Miller School of Medicine at the University of Miami, Miami, Florida.
Cancer prevention research (Philadelphia, Pa.)
|December 10, 2024
概括
通过DNA甲基化测量加速衰老,与50岁以下的个体患前瘤息肉的风险更高有关. 这一发现可能有助于开发针对早期结直肠癌的查.
科学领域:
- 表观遗传学和衰老研究.
- 胃肠道学和瘤学
- 预防医学 预防医学
背景情况:
- 加速衰老,即生物年龄超过时间年龄,与癌症的发展有关.
- 加速衰老在早期结直肠癌 (EOCRC) 和其前体病变中的作用尚不清楚.
- 前新生体多 (PNP) 是结直肠癌风险的关键指标.
研究的目的:
- 调查加速衰老与50岁以下人群中先发性聚体 (PNP) 的存在之间的关联.
- 探索生物年龄指标在EOCRC查风险分层中的潜力.
主要方法:
- 用DNA甲基化分析从外围血液样本中确定生物年龄和年龄加速指标 (GrimAge).
- 进行了后勤回归分析,以评估年龄加速和PNPs之间的关联.
- 该研究包括51名50岁以下的接受结肠镜检查的患者.
主要成果:
- 每一年的加快衰老都与患PNP的几率增加16%有关.
- 在这个队列中,男性性别被确定为PNP的最强风险因素.
- 这项研究是第一个在年轻人中检查加速衰老和PNP的研究之一.
结论:
- 根据GrimAge的量化,加快衰老与50岁以下的个体患前瘤多的风险增加有关.
- 生物年龄计算可以整合到EOCRC查的风险模型中.
- 了解这种关联为开发风险分层查策略提供了一条途径,以打击不断上升的EOCRC率.
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