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N-glycosylation profiling of plasma provides evidence for accelerated physiological aging in post-traumatic stress disorder

机译:血浆 N 糖基化谱分析为创伤后应激障碍加速生理衰老提供了证据

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The prevalence of age-related diseases is increased in individuals with post-traumatic stress disorder (PTSD). However, the underlying biological mechanisms are still unclear. N -glycosylation is an age-dependent process, identified as a biomarker for physiological aging (GlycoAge Test). To investigate whether traumatic stress accelerates the aging process, we analyzed the N -glycosylation profile in n =13 individuals with PTSD, n =9 trauma-exposed individuals and in n =10 low-stress control subjects. Individuals with PTSD and trauma-exposed individuals presented an upward shift in the GlycoAge Test, equivalent to an advancement of the aging process by 15 additional years. Trauma-exposed individuals presented an intermediate N -glycosylation profile positioned between severely traumatized individuals with PTSD and low-stress control subjects. In conclusion, our data suggest that cumulative exposure to traumatic stressors accelerates the process of physiological aging.
机译:患有创伤后应激障碍(PTSD)的人中与年龄有关的疾病的患病率增加。但是,潜在的生物学机制仍不清楚。 N-糖基化是一个年龄依赖性的过程,被确定为生理性衰老的生物标志物(GlycoAge Test)。为了研究创伤性应激是否会加速衰老过程,我们分析了n = 13例PTSD患者,n = 9暴露于创伤的个体和n = 10例低压力对照组的N-糖基化谱。患有PTSD的人和遭受创伤的人在GlycoAge测试中呈现出上升的趋势,这相当于将衰老过程再延长15年。暴露于创伤的个体表现出中等的N-糖基化分布,位于患有创伤后应激障碍的重度创伤个体与低压力对照组之间。总之,我们的数据表明,累积暴露于外伤性应激会加速生理老化的过程。

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