Department of Periodontology, Dental School, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ, Brazil.
Departament of Periodontology, Dental School, Universidade do Estado do Rio de Janeiro, Boulevard 28 de Setembro, 157 - Vila Isabel, Rio de Janeiro, RJ, 20551-030, Brazil.
Metabolomics. 2022 Oct 25;18(11):83. doi: 10.1007/s11306-022-01940-5.
Periodontitis is resulted from a complex interaction between genetics and epigenetics, microbial factors, and the host response. Metabolomics analyses reflect both the steady-state physiological equilibrium of cells or organisms as well as their dynamic metabolic responses to environmental stimuli.
This systematic review of the literature aimed to assess which low molecular weight metabolites are more often found in biological fluids of individuals with periodontitis compared to individuals with gingivitis or periodontal health.
All the included studies employed untargeted analysis. One or more biological fluids were analyzed, including saliva (n = 14), gingival crevicular fluid (n = 6), mouthwash (n = 1), serum (n = 3) and plasma (n = 1). Fifty-six main metabolites related to periodontitis have been identified in at least two independent studies by NMR spectroscopy or MS-based metabolomics. Saliva was the main biological fluid sampled. It is noteworthy that 14 metabolites of the 56 detected were identified as main metabolites in all studies that sampled the saliva. The majority of metabolites found consistently among studies were amino acids, organic acids and derivates: acetate, alanine, butyrate, formate, GABA, lactate, propionate, phenylalanine and valine. They were either up- or down-regulated in the studies or this information was not mentioned. The main metabolic pathway was related to phenylalanine, tyrosine and tryptophan biosynthesis. Metabolites more frequently found in individuals with periodontitis were related to both the host and to microorganism responses. Future studies are needed, and they should follow some methodological standards to facilitate their comparison.
牙周炎是由遗传和表观遗传、微生物因素和宿主反应之间的复杂相互作用引起的。代谢组学分析反映了细胞或生物体的稳态生理平衡以及它们对环境刺激的动态代谢反应。
本系统文献综述旨在评估与牙龈炎或牙周健康个体相比,牙周炎个体的生物体液中更常发现哪些低分子量代谢物。
所有纳入的研究均采用非靶向分析。分析了一种或多种生物体液,包括唾液(n=14)、龈沟液(n=6)、漱口液(n=1)、血清(n=3)和血浆(n=1)。通过 NMR 光谱或基于 MS 的代谢组学,在至少两项独立研究中鉴定出与牙周炎相关的 56 种主要代谢物。唾液是主要采样的生物体液。值得注意的是,在所有采样唾液的研究中,有 14 种代谢物被鉴定为主要代谢物。在研究中一致发现的大多数代谢物是氨基酸、有机酸及其衍生物:乙酸盐、丙氨酸、丁酸盐、甲酸盐、GABA、乳酸盐、丙酸盐、苯丙氨酸和缬氨酸。它们在研究中要么上调要么下调,或者没有提到这方面的信息。主要代谢途径与苯丙氨酸、酪氨酸和色氨酸生物合成有关。在牙周炎患者中更常发现的代谢物与宿主和微生物反应都有关。需要进一步研究,并且应该遵循一些方法学标准以方便比较。