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MicroRNA circulating in the early aftermath of motor vehicle collision predict persistent pain development and suggest a role for microRNA in sex-specific pain differences

机译:机动车碰撞后早期循环的MicroRNA预测持续的疼痛发展并提示microRNA在性别特异性疼痛差异中的作用

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摘要

BackgroundMolecular mediators influencing the transition from acute to persistent musculoskeletal pain following common stress exposures such as motor vehicle collision (MVC) remain poorly understood. In this exploratory, proof of concept study, we compared circulating microRNA (miRNA) expression profiles in the early aftermath of MVC among individuals who did and did not subsequently develop persistent pain. Blood RNA samples were obtained from African American individuals (n = 53) who presented to the emergency department after MVC and were discharged to home after evaluation. The presence or absence of severe pain in the axial region, the most common and morbid region in which post-MVC pain occurs, was assessed 6 weeks following MVC via standardized questionnaire. miRNA expression was determined using miRNA-sequencing; nonparametric analyses were used to compare miRNA expression levels among individuals with and without persistent pain.
机译:背景技术在常见的压力暴露(例如机动车碰撞(MVC))之后,影响从急性肌肉骨骼疼痛向持久性肌肉骨骼疼痛过渡的分子介质仍然知之甚少。在这项探索性的概念验证研究中,我们比较了在MVC发生早期和以后没有出现持续性疼痛的个体中循环microRNA(miRNA)表达谱。血液RNA样本是从非裔美国人(n = 53)获得的,他们在MVC之后出现在急诊室,经过评估后被送回家中。在MVC术后6周,通过标准化问卷调查评估了MVC后疼痛发生的最常见和病态的轴向区域是否存在严重疼痛。使用miRNA测序确定miRNA表达;非参数分析用于比较有持续疼痛和无持续疼痛的个体之间的miRNA表达水平。

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