Department of Biological Sciences, Bauru School of Dentistry, University of São Paulo, Bauru, Brazil.
Department of Prosthodontics, Bauru School of Dentistry, University of São Paulo, Bauru, Brazil.
J Oral Rehabil. 2023 Jan;50(1):39-53. doi: 10.1111/joor.13384. Epub 2022 Nov 11.
Previous evidence indicates significant association between genetic polymorphisms and phenotypes related to pain sensitivity in patients with temporomandibular disorders (TMD). Despite the important advances in cataloguing diverse factors such as sleep disorders, anxiety and depression, the interrelated mechanisms of painful TMD aetiopathogenesis still need investigation.
This case-control study aimed to evaluate the influence of genetic polymorphisms (rs6296, rs6295, rs1799971, rs4680, rs4633, rs4818) and psychosocial factors on the mechanical pain sensitivity and endogenous pain modulation in women with painful TMD and asymptomatic controls.
We evaluated six independent variables: anxiety levels, depression, stress, sleep quality, pain catastrophising and genetic polymorphisms, and four dependent variables: mechanical pain threshold (MPT), pressure pain threshold (PPT), wind-up ratio (WUR) and conditioned pain modulation (CPM) collected at masseter (trigeminal) and hand (spinal) areas in a sample of 95 painful TMD patients and 85 controls. A regression model was used to test the possible effect of the independent variables on dependent variables.
The regression model was significant for MPT (F = 9.772; R = .390). Painful TMD diagnoses and sleep quality were associated with trigeminal MPT (B coefficient = -.499; and B coefficient = -.211, respectively). WUR was associated with rs6295 and rs6746030, respectively, for the spinal and the trigeminal area.
Genetic polymorphisms had a slight contribution to endogenous pain modulation as indicated by the significant association with WUR but did not contribute to mechanical pain sensitivity. On the other hand, the presence of painful TMD and the sleep quality contributed significantly to mechanical pain sensitivity.
先前的证据表明,遗传多态性与颞下颌关节紊乱症(TMD)患者的疼痛敏感性相关表型之间存在显著关联。尽管在睡眠障碍、焦虑和抑郁等多种因素的分类方面取得了重要进展,但仍需研究疼痛性 TMD 发病机制的相关机制。
本病例对照研究旨在评估遗传多态性(rs6296、rs6295、rs1799971、rs4680、rs4633、rs4818)和社会心理因素对疼痛性 TMD 女性患者和无症状对照者机械性疼痛敏感性和内源性疼痛调节的影响。
我们评估了六个独立变量:焦虑水平、抑郁、压力、睡眠质量、疼痛灾难化和遗传多态性,以及四个因变量:在下颌肌(三叉神经)和手部(脊髓)区域测量的机械疼痛阈值(MPT)、压力疼痛阈值(PPT)、紧张比(WUR)和条件性疼痛调制(CPM)。在 95 名疼痛性 TMD 患者和 85 名对照者的样本中,使用回归模型来测试独立变量对因变量的可能影响。
MPT 的回归模型具有统计学意义(F=9.772;R=.390)。TMD 诊断和睡眠质量与三叉神经 MPT 相关(B 系数分别为-.499 和-.211)。WUR 与 rs6295 和 rs6746030 分别相关,分别为脊髓和三叉神经区域。
遗传多态性对内源性疼痛调节有轻微贡献,这表明与 WUR 有显著关联,但对机械性疼痛敏感性没有贡献。另一方面,疼痛性 TMD 的存在和睡眠质量对机械性疼痛敏感性有显著贡献。