UFR Odontologie, Université Paris Diderot, 5, rue Garancière, 75006, Paris, France.
Groupe Hospitalier Pitie Salpêtrière Charles Foix, Paris, France.
Clin Oral Investig. 2017 Sep;21(7):2157-2164. doi: 10.1007/s00784-016-1991-0. Epub 2016 Nov 10.
Idiopathic Burning mouth syndrome (iBMS) is a poorly understood affection characterized by persistent pain in the oral cavity without any clinical or biological abnormality. Opiorphin is a natural inhibitor of enkephalin-inactivating ectopeptidases, mainly produced by salivary glands, that has demonstrated analgesic properties. The objective of the present case-control study was to test the hypothesis of a decrease in opiorphin levels in iBMS patients.
Twenty-one iBMS patients and 21 matched controls subjects were included between 2011 and 2013. Submandibular and sublingual salivary, blood, and urinary opiorphin levels of iBMS patients were compared to controls.
Results are expressed as mean values ± SD and compared using the Wilcoxon Signed Rank test. Correlations were analyzed with Spearman coefficient. The level of significance was fixed at p < 0.05. Opiorphin levels in iBMS and controls were respectively (in ng/ml) in basal saliva: 37.8 ± 42.5 and 67.6 ± 188.9 (p = NS); stimulated saliva: 28.8 ± 25.3 and 31.1 ± 29.1 (p = NS); blood: 4.6 ± 5.4 and 1.9 ± 1.4 (p < 0.05); and urines: 68.5 ± 259.8 and 8.9 ± 6.2 (p = NS).
In conclusion, the lack of significative difference in salivary opiorphin levels between iBMS and controls does not favor a direct local role for opiorphin in the etiopathogeny of iBMS. However, higher blood opiorphin levels may reflect a systemic dysregulation in iBMS. Trial registration NCT02686359 https://clinicaltrials.gov/ct2/show/NCT02686359.
特发性灼口综合征(iBMS)是一种病因不明的疾病,其特征为口腔持续性疼痛,无任何临床或生物学异常。阿片肽是一种天然的内啡肽失活外肽酶抑制剂,主要由唾液腺产生,具有镇痛作用。本病例对照研究的目的是检验 iBMS 患者阿片肽水平降低的假设。
2011 年至 2013 年期间纳入了 21 名 iBMS 患者和 21 名匹配的对照受试者。比较了 iBMS 患者的颌下腺和舌下腺唾液、血液和尿液阿片肽水平与对照组。
结果以平均值 ±标准差表示,并使用 Wilcoxon 符号秩检验进行比较。采用 Spearman 系数分析相关性。显著性水平固定在 p < 0.05。iBMS 和对照组基础唾液中的阿片肽水平分别为(ng/ml):37.8 ± 42.5 和 67.6 ± 188.9(p = NS);刺激唾液:28.8 ± 25.3 和 31.1 ± 29.1(p = NS);血液:4.6 ± 5.4 和 1.9 ± 1.4(p < 0.05);尿液:68.5 ± 259.8 和 8.9 ± 6.2(p = NS)。
总之,iBMS 和对照组之间唾液阿片肽水平无显著差异,不支持阿片肽在 iBMS 发病机制中的直接局部作用。然而,血液中较高的阿片肽水平可能反映了 iBMS 中的系统性失调。试验注册 NCT02686359 https://clinicaltrials.gov/ct2/show/NCT02686359。