2021
DOI: 10.1016/j.cyto.2021.155551
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Long-term evaluation of temporomandibular disorders in association with cytokine and autoantibody status in young women

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Cited by 11 publications
(17 citation statements)
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“…For example, local injection of cytokines [ 30 ], glutamate [ [35] , [36] , [37] , [38] ], serotonin [ 39 ], acid saline [ 40 ] and nerve growth factor [ 41 , 42 ] can cause pain and hyperalgesia in the deep craniofacial tissues. These results are consistent with the findings that TMD patients increase experimentally-induced pain sensitivity in the facial areas, in which the level of inflammatory mediators is elevated [ 24 , [27] , [28] , [29] , [30] , [31] , [32] , [33] , 43 , 44 ].…”
Section: Neural Mechanisms For Pain In the Deep Craniofacial Tissues In Humansupporting
confidence: 92%
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“…For example, local injection of cytokines [ 30 ], glutamate [ [35] , [36] , [37] , [38] ], serotonin [ 39 ], acid saline [ 40 ] and nerve growth factor [ 41 , 42 ] can cause pain and hyperalgesia in the deep craniofacial tissues. These results are consistent with the findings that TMD patients increase experimentally-induced pain sensitivity in the facial areas, in which the level of inflammatory mediators is elevated [ 24 , [27] , [28] , [29] , [30] , [31] , [32] , [33] , 43 , 44 ].…”
Section: Neural Mechanisms For Pain In the Deep Craniofacial Tissues In Humansupporting
confidence: 92%
“…IL-1 beta has been reported to play critical roles on the development and progression of TMD pain [ 22 , 24 ]. IL-2, -8 and -13 in the blood serum also indicate significant effects on generalized pain in TMD patients [ 28 ]. Besides cytokines, several mediators including prostaglandin E2, bradykinin and serotonin (5HT) are detected in the synovial fluid of TMJ in the TMD patients with internal derangements and osteoarthritis of TMJ, however, no correlation is found between each mediator and pain [ 29 ].…”
Section: Neural Mechanisms For Pain In the Deep Craniofacial Tissues In Humanmentioning
confidence: 99%
“…The accumulating evidence supports the intimate relationship between physical activity, sleep quality, and systemic inflammation which are all factors known to influence TMD symptoms in previous literature [71][72][73][74]. Through this prospective study based on objective physical activity measurements in a well-defined patient group of TMD, the resulting data will be able to support the establishment of a clinical guideline related to physical activity recommendations and the diagnostic value of such measurements in TMD prognosis.…”
Section: Discussionsupporting
confidence: 71%
“…Results of this study showed that bone morphogenetic protein (BMP) type 2 and 4, epidermal growth factor (EGF), eotaxin, granulocyte-colony stimulating factor (G-CSF), IL-1β, IL-7, IL-8, IL-10, macrophage inflammatory protein (MIP) 1β, TNF-α and TNF-β had significantly higher concentrations in patients with disc displacement without reduction. In 2021, Son et al [ 167 ] investigated the relationship between long-term clinical characteristics and different cytokine and autoimmunity levels in young female TMD patients according to pain disability. The subjects included in the study were classified in high and low disability groups, according to the Graded Chronic Pain Scale (GCPS).…”
Section: Oxygen-ozone and Temporomandibular Disordersmentioning
confidence: 99%