多重蛋白质组学识别了与炎症相关的血生物标志物,用于衰老和心脏代谢障碍
Siting Wu1, Yulin Li1, Xue Zhao1
1Department of Neurology, Tianjin Neurological Institute, Tianjin Medical University General Hospital, Tianjin, 300070, China.
Clinical proteomics
|April 22, 2024
概括
像EGF和MMP1这样的炎症蛋白质是衰老和心脏代谢障碍 (CMD) 的关键. 十个重叠的蛋白质显示CMD在衰老中的诊断价值,有助于了解疾病的进展.
科学领域:
- 蛋白质组学是指蛋白质组学.
- 分子生物学分子生物学
- 老年学是指老年学的学科.
背景情况:
- 心脏代谢障碍 (CMD) 在老年人群中很普遍,是心血管疾病 (CVD) 的重要危险因素.
- 炎症在心血管疾病和衰老的发展中起着作用,但具体的炎症分子表型尚不清楚.
研究的目的:
- 确定与正常衰老和CMD相关的炎症分子表型.
- 在老龄化人口中探索CMD的潜在蛋白质生物标志物.
主要方法:
- 利用近距离延伸试验 (PEA) 来分析来自年轻人,老年人和患有CMD的老年人血中的368种炎症蛋白.
- 构建了蛋白质-蛋白质相互作用 (PPI) 网络,以在差异表达蛋白 (DEP) 中识别枢纽蛋白.
- 评估了已识别的蛋白质和临床特征之间的相关性,并使用ROC曲线分析评估了诊断价值.
主要成果:
- 在正常衰老中确定了161个DEP (枢纽蛋白:EGF) 和28个在患有CMD的老年人中发现的DEP (枢纽蛋白:MMP1).
- 发现10种重叠的蛋白质 (例如,SHMT1,EGLN1,NCF2) 与脂质和葡萄糖水平有显著的相关性.
- 这10种蛋白质在老龄化中显示出CMD的良好诊断价值 (AUC>0.7),EGLN1,NCF2,REG4和SLC39A2在两个老龄化群体中都增加.
结论:
- 该研究确定了正常衰老和CMD的潜在分子标志物.
- 需要进一步研究更大的样本大小来验证这些发现,并预测它们对心血管疾病的意义.
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