4.6 Article

Cytokine biomarkers and chronic pain: Association of genes, transcription, and circulating proteins with temporomandibular disorders and widespread palpation tenderness

期刊

PAIN
卷 152, 期 12, 页码 2802-2812

出版社

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1016/j.pain.2011.09.005

关键词

Epistasis; Gene polymorphism; Interleukin-1 receptor antagonist (IL-1ra); Interleukin-8 (IL-8); Monocyte chemotactic protein (MCP-1); Transforming growth factor beta 1 (TGF beta 1)

资金

  1. National Institutes of Health (NIH)/National Institute of Child Health & Human Development [K12 HD052191]
  2. NIH/National Institute of Dental and Craniofacial Research [R01 DE016558]
  3. NIH/National Institute of Neurological Disorders and Stroke [PO1 NS045685]

向作者/读者索取更多资源

For reasons unknown, temporomandibular disorder (TMD) can manifest as localized pain or in conjunction with widespread pain. We evaluated relationships between cytokines and TMD without or with widespread palpation tenderness (TMD-WPT or TMD+WPT, respectively) at protein, transcription factory activity, and gene levels. Additionally, we evaluated the relationship between cytokines and intermediate phenotypes characteristic of TMD and WPT. In a case-control study of 344 females, blood samples were analyzed for levels of 22 cytokines and activity of 48 transcription factors. Intermediate phenotypes were measured by quantitative sensory testing and questionnaires asking about pain, health, and psychological status. Single nucleotide polymorphisms (SNPs) coding cytokines and transcription factors were genotyped. TMD-WPT cases had elevated protein levels of proinflammatory cytokine monocyte chemotactic protein (MCP-1) and antiinflammatory cytokine interleukin (IL)-1ra, whereas TMD+WPT cases had elevated levels of proinflammatory cytokine IL-8. MCP-1, IL-1ra, and IL-8 were differentially associated with experimental pain, self-rated pain, self-rated health, and psychological phenotypes. TMD-WPT and TMD+WPT cases had inhibited transcription activity of the antiinflammatory cytokine transforming growth factor beta 1 (TGF beta 1). Interactions were observed between TGF beta 1 and IL-8 SNPs: an additional copy of the TGF beta 1 rs2241719 minor T allele was associated with twice the odds of TMD+WPT among individuals homozygous for the IL-8 rs4073 major A allele, and half the odds of TMD+WPT among individuals heterozygous for rs4073. These results demonstrate how pro-and antiinflammatory cytokines contribute to the pathophysiology of TMD and WPT in genetically susceptible people. Furthermore, they identify MCP-1, IL-1ra, IL-8, and TGF beta 1 as potential diagnostic markers and therapeutic targets for pain in patients with TMD. Published by Elsevier B. V. on behalf of International Association for the Study of Pain.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据