Department of Anesthesiology, University of North Carolina, Chapel Hill, North Carolina, USA.
BMC Emerg Med. 2011 Sep 26;11:14. doi: 10.1186/1471-227X-11-14.
Persistent musculoskeletal pain and psychological sequelae following minor motor vehicle collision (MVC) are common problems with a large economic cost. Prospective studies of pain following MVC have demonstrated that demographic characteristics, including female gender and low education level, and psychological characteristics, including high pre-collision anxiety, are independent predictors of persistent pain. These results have contributed to the psychological and social components of a biopsychosocial model of post-MVC pain pathogenesis, but the biological contributors to the model remain poorly defined. Recent experimental studies indicate that genetic variations in adrenergic system function influence the vulnerability to post-traumatic pain, but no studies have examined the contribution of genetic factors to existing predictive models of vulnerability to persistent pain.
METHODS/DESIGN: The Project CRASH study is a federally supported, multicenter, prospective study designed to determine whether variations in genes affecting synaptic catecholamine levels and alpha and beta adrenergic receptor function augment social and psychological factors in a predictive model of persistent musculoskeletal pain and posttraumatic stress disorder (PTSD) following minor MVC. The Project CRASH study will assess pain, pain interference and PTSD symptoms at 6 weeks, 6 months, and 1 year in approximately 1,000 patients enrolled from 8 Emergency Departments in four states with no-fault accident laws.
The results from this study will provide insights into the pathophysiology of persistent pain and PTSD following MVC and may serve to improve the ability of clinicians and researchers to identify individuals at high risk for adverse outcomes following minor MVC.
轻微机动车碰撞(MVC)后持续的肌肉骨骼疼痛和心理后遗症是一个常见的问题,具有巨大的经济成本。对 MVC 后疼痛的前瞻性研究表明,人口统计学特征,包括女性性别和低教育水平,以及心理特征,包括高碰撞前焦虑,是持续疼痛的独立预测因素。这些结果为 MVC 后疼痛发病机制的心理和社会因素生物心理社会模型做出了贡献,但该模型的生物学贡献仍未得到明确界定。最近的实验研究表明,肾上腺素能系统功能的遗传变异影响创伤后疼痛的易感性,但尚无研究探讨遗传因素对现有易发性预测模型的贡献。
方法/设计:CRASH 项目是一项联邦资助的、多中心的前瞻性研究,旨在确定影响突触儿茶酚胺水平和α和β肾上腺素能受体功能的基因变异是否在预测 MVC 后持续肌肉骨骼疼痛和创伤后应激障碍(PTSD)的社会和心理因素模型中增强。CRASH 项目将在四个州的 8 个急诊部门招募的大约 1000 名患者中,在 6 周、6 个月和 1 年评估疼痛、疼痛干扰和 PTSD 症状。
这项研究的结果将为 MVC 后持续疼痛和 PTSD 的发病机制提供深入的了解,并可能有助于提高临床医生和研究人员识别轻度 MVC 后不良后果高风险个体的能力。