Sleep Bruxism and Central Sensitization in Myofascial Face Pain

描述（由申请人提供）：肌筋膜面痛（MFP）是颞下颌关节紊乱病（TMD）最常见的类型，其发病机制仍存在争议。其中一个关键的争议涉及睡眠磨牙症（SB）的作用。虽然相对较弱的SB测量支持了SB在至少一些MFP患者中的作用，但尚未进行基于实验室的睡眠研究来明确解决这个问题。该申请提出了作为其主要目的的SB在MFP维护中的确定性研究的进行，其中研磨和紧握的单独作用将被检查。我们还将探讨SB和压力引起的磨牙症之间的关系，以及遗传异常在调节SB患者疼痛风险中的作用。第二个目的是评估中枢致敏（CS）在MFP维持中的作用。支持CS在MFP中的作用的证据受到患者和解剖部位采样偏倚的限制。因此，我们将在更具代表性的MFP患者和对照样本中检查CS在MFP中的作用，并对三叉神经外和三叉神经区域的CS进行评估。CS在这两个领域的差异可能表明不同的疼痛维持机制。在这两个目标的服务中收集的数据，然后允许实现第三个目标，了解SB和CS之间的关系，在MFP，包括SB和CS的可能性，海拔可能会定义亚组中，不同的疼痛维持机制是有效的。这些目标可以实现的情况下，120 MFP患者和60人口统计学匹配的对照组的病例对照研究。追求这些目标将提供坚实的证据SB在MFP的作用，并将推进SB和CS之间的关系的理解。这种理解有望支持我们的长期目标，即通过靶向治疗潜在的疼痛维持机制来改善MFP的临床治疗。

DESCRIPTION (provided by applicant): The pathogenesis of myofascial face pain (MFP), the most prevalent type of temporomandibular disorder (TMD), remains controversial. One of the key controversies concerns the role of sleep bruxism (SB). While relatively weak measures of SB have supported a role of SB in at least some MFP patients, no laboratory based sleep study has been undertaken to resolve this issue definitively. This application proposes as its main aim the conduct of the definitive study of SB in MFP maintenance, in which the separate role of grinding and clenching would be examined. We would also explore the relationship between SB and stress induced bruxism, as well as the role of genetic anomalies in modulating the risk of pain among those with SB. A second aim would evaluate the role of central sensitization (CS) in the maintenance of MFP. Evidence supporting a role for CS in MFP has been limited by biases in the sampling of both patients and anatomic sites. Therefore, we would examine the role of CS in MFP in a more representative sample of MFP patients and controls, as well as conduct an evaluation of CS in both extratrigeminal and trigeminal regions. Differences in CS in these two areas might suggest different pain maintenance mechanisms. Data collected in the service of these two aims then allows the achievement a third aim, understanding the relationships between SB and CS in MFP, including the possibility that elevations in SB and CS may define subgroups in which different pain maintenance mechanisms are operative. These aims can be achieved in the context of a case-control study of 120 MFP patients and 60 demographically-matched controls. Pursuit of these aims will provide firm evidence regarding the role of SB in MFP and will advance understanding of the relationship between SB and CS. This understanding is expected to support our long-term goal of improving clinical treatment of MFP by targeting treatment to underlying pain-maintenance mechanisms.