Genetic Predictors of Acute and Chronic Musculoskeletal Pain After Minor MVC

描述（由申请人提供）：每年，超过500万人在“轻微”机动车碰撞（MVC）后在美国急诊室（ED）接受治疗并出院回家。持续性疼痛（最常见的是颈部疼痛）发生在10- 20%的这些人中，仅在美国每年的经济影响就达290亿美元。关于这些常见和昂贵的疾病的发病机制的当代知识总结在MVC后疼痛发病机制的生物心理社会模型。近年来，心理因素对持续性疼痛发展的机制的识别和详细描述大大改善了生物心理社会模型。相比之下，生物心理社会模型中的生物因素仍然相对不明确，并且通常仅限于对碰撞严重程度或初始损伤的估计。有趣的是，越来越多的证据表明，影响肾上腺素能系统功能的遗传特征可能构成重要的生物脆弱性因素的发展创伤后疼痛，因此可能是重要的生物心理社会模型纳入。即时和持续的肾上腺素能反应受重要的肾上腺素能系统组分的功能影响，包括调节突触儿茶酚胺水平的酶和转运蛋白以及协调细胞反应的受体。越来越多的文献记录了这些成分影响疼痛处理的能力，研究人员的试点数据支持这一假设，即这些成分的遗传变异影响轻微MVC后发生立即和持续肌肉骨骼疼痛的脆弱性。拟议研究的目标，轻微MVC后急性和慢性肌肉骨骼疼痛的遗传预测因子，是评估决定与疼痛感知相关的特定肾上腺素能系统过程的基因型，当与碰撞相关，心理和其他因素相结合时，是否会改善轻微MVC后立即和持续颈部疼痛症状的预测。在轻微MVC后接受评价的患者（n = 795）将在艾德中招募，并将接受初始艾德评价，包括用于遗传分析的血液采集。然后，患者将在MVC后1个月、6个月和12个月接受采访，以评估疼痛结局。初步数据证明了研究小组进行拟议研究的能力，并支持选定的肾上腺素能系统相关遗传因素的潜在预测价值。这项研究提供了一个前所未有的机会，可以开发出丰富的MVC后持续性颈部疼痛的生物心理社会预测模型，这些模型整合了多个领域的因素。这些模型将提供重要的新知识，在MVC后疼痛的发展过程中，个体的脆弱性特征和遗传与非遗传因素之间的相互作用。 公共卫生相关性拟议的研究将提供有关持续性创伤后肌肉骨骼疼痛发展过程中个体脆弱性特征以及遗传和非遗传因素之间相互作用的新知识。了解肌肉骨骼疼痛疾病的病因对公众的健康很重要，因为这些疾病很常见，会引起严重的疼痛和痛苦，而且对社会来说代价高昂。

DESCRIPTION (provided by applicant): Each year, more than 5 million people are treated in US Emergency Departments (EDs) after "minor" motor vehicle collision (MVC) and discharged to home. Persistent pain (most commonly neck pain) develops in 10- 20% of these individuals, with an economic impact of $29 billion per year in the United States alone. Contemporary knowledge regarding the pathogenesis of these common and costly disorders is summarized in biopsychosocial models of post-MVC pain pathogenesis. In recent years, the identification and detailed delineation of mechanisms by which psychological factors contribute to persistent pain development has substantially improved the biopsychosocial model. In contrast, biological factors in the biopsychosocial model remain relatively poorly defined, and are generally limited to estimates of crash severity or initial injury only. Interestingly, increasing evidence indicates that genetic characteristics influencing adrenergic system function may constitute important biological vulnerability factors for the development of posttraumatic pain, and thus may be important to incorporate into the biopsychosocial model. The immediate and ongoing adrenergic response is influenced by the function of important adrenergic system components, including enzymes and transporters that modulate synaptic catecholamine levels and receptors that orchestrate the cellular response. A growing literature documents the ability of these components to influence pain processing, and the investigators' pilot data support the hypothesis that genetic variation in these components affects vulnerability to develop immediate and persistent musculoskeletal pain after minor MVC. The goal of the proposed research, Genetic predictors of acute and chronic musculoskeletal pain after minor MVC, is to assess whether genotypes determining specific adrenergic system processes relevant to pain perception will, when combined with crash-related, psychological, and other factors, improve the prediction of immediate and persistent neck pain symptoms after minor MVC. Patients presenting for evaluation after minor MVC (n = 795) will be recruited in the ED and will receive initial ED evaluation including blood collection for genetic analyses. Patients will then be interviewed 1, 6, and 12 months after the MVC to assess pain outcomes. Pilot data demonstrate the ability of the study team to perform the proposed study and support the potential predictive value of the selected adrenergic system-related genetic factors. The proposed study provides an unprecedented opportunity to develop rich biopsychosocial prediction models of persistent post-MVC neck pain which integrate factors across multiple domains. These models will provide important new knowledge regarding both individual vulnerability characteristics and interactions between genetic and non-genetic factors during the development of post-MVC pain. PUBLIC HEALTH RELEVANCE The proposed study will provide new knowledge regarding both individual vulnerability characteristics and interactions between genetic and non-genetic factors during the development of persistent posttraumatic musculoskeletal pain. Understanding the etiology of musculoskeletal pain disorders is important to the public's health because these disorders are common, cause significant pain and suffering, and are very costly to society.