Periodontology Unit, Centre for Host Microbiome Interactions, Faculty of Dentistry, Oral & Craniofacial Sciences, King's College London, London, UK.
Dental Health Department, College of Applied Medical Sciences, King Saud University, Riyadh, Saudi Arabia.
J Periodontal Res. 2023 Dec;58(6):1272-1280. doi: 10.1111/jre.13183. Epub 2023 Oct 3.
The aim of this study was to investigate metabolomics markers in the saliva of patients with periodontal health, gingivitis and periodontitis.
The use of metabolomics for diagnosing and monitoring periodontitis is promising. Although several metabolites have been reported to be altered by inflammation, few studies have examined metabolomics in saliva collected from patients with different periodontal phenotypes.
Saliva samples collected from a total of 63 patients were analysed by nuclear magnetic resonance (NMR) followed by ELISA for interleukin (IL)-1β. The patient sample, well-characterised clinically, included periodontal health (n = 8), gingivitis (n = 19) and periodontitis (n = 36) cases, all non-smokers and not diabetic.
Periodontal diagnosis (healthy/gingivitis/periodontitis) was not associated with any salivary metabolites in this exploratory study. Periodontal staging showed nominal associations with acetoin (p = .030) and citrulline (p = .047). Among other investigated variables, the use of systemic antibiotics in the previous 3 months was associated with higher values of the amino acids taurine, glycine and ornithine (p = .002, p = .05 and p = .005, respectively, at linear regression adjusted for age, gender, ethnicity, body mass index and staging).
While periodontal staging was marginally associated with some salivary metabolites, other factors such as systemic antibiotic use may have a much more profound effect on the microbial metabolites in saliva. Metabolomics in periodontal disease is still an underresearched area that requires further observational studies on large cohorts of patients, aiming to obtain data to be used for clinical translation.
本研究旨在探讨牙周健康、牙龈炎和牙周炎患者唾液中的代谢组学标志物。
代谢组学在牙周炎的诊断和监测中具有应用前景。尽管已有报道称几种代谢物的变化与炎症有关,但很少有研究检测过来自不同牙周表型患者的唾液代谢组学。
共对 63 名患者的唾液样本进行了分析,采用核磁共振(NMR)分析,并用酶联免疫吸附法(ELISA)检测白细胞介素(IL)-1β。这些患者样本经过了全面的临床特征分析,包括牙周健康(n=8)、牙龈炎(n=19)和牙周炎(n=36),均为非吸烟者且无糖尿病。
在这项探索性研究中,牙周病诊断(健康/牙龈炎/牙周炎)与唾液中的任何代谢物均无关联。牙周病分期与乙酰丙酮(p=0.030)和瓜氨酸(p=0.047)呈名义相关。在其他研究变量中,在过去 3 个月内使用全身性抗生素与氨基酸牛磺酸、甘氨酸和精氨酸的水平升高有关(p=0.002、p=0.05 和 p=0.005,线性回归校正年龄、性别、种族、体重指数和分期后)。
虽然牙周病分期与一些唾液代谢物呈边缘相关,但其他因素,如全身性抗生素的使用,可能对唾液中的微生物代谢物产生更深远的影响。代谢组学在牙周病中的研究仍处于起步阶段,需要对大量患者进行进一步的观察性研究,以获得可用于临床转化的数据。