Department of Periodontology, Faculty of Dentistry, Sakarya University, Sakarya, Turkey.
Private Practice, Ankara, Turkey.
Acta Odontol Scand. 2020 Jul;78(5):327-331. doi: 10.1080/00016357.2020.1715471. Epub 2020 Jan 24.
Type 2 diabetes mellitus (T2DM) is a well-defined risk factor of periodontitis and it can affect expression of human beta-defensins (hBDs) and cathelicidin (LL-37) as well. The aim of the present study was to evaluate the impact of periodontitis and T2DM on salivary concentrations of these antimicrobial peptides. Unstimulated saliva samples, together with full-mouth periodontal recordings were collected from 92 individuals with periodontitis (63 with T2DM and 21 smokers) and 86 periodontally healthy controls (58 with T2DM and 21 smokers). Salivary hBD-1, -2, -3, LL-37, and advanced glycalization end products (AGE) concentrations were measured by enzyme-linked immunosorbent assay. Among the periodontitis patients, T2DM group demonstrated lower levels of hBD-1 ( = .006), hBD-2 ( < .001) and hBD-3 ( < .001), and higher levels of LL-37 ( < .001) compared to systemically healthy controls. When only periodontally healthy controls were included into the analysis, higher hBD-1 ( = .002) and LL-37 ( < .001) levels were found in T2DM patients in comparison to systemically healthy controls. Salivary LL-37 levels were associated with HbA1c and periodontitis, while hBD-2, hBD-3 and levels associated only with HbA1c. In the limits of this study, hyperglycaemia can be proposed as a regulator of salivary hBD and cathelicidin levels. Periodontitis, on the other hand, affects only salivary LL-37 levels.
2 型糖尿病(T2DM)是牙周炎的明确危险因素,它也会影响人β防御素(hBDs)和抗菌肽(LL-37)的表达。本研究旨在评估牙周炎和 T2DM 对这些抗菌肽唾液浓度的影响。从 92 名牙周炎患者(63 名患有 T2DM 和 21 名吸烟者)和 86 名牙周健康对照者(58 名患有 T2DM 和 21 名吸烟者)中采集非刺激性唾液样本和全口牙周记录。通过酶联免疫吸附试验测量唾液 hBD-1、-2、-3、LL-37 和晚期糖基化终产物(AGE)浓度。在牙周炎患者中,与系统性健康对照组相比,T2DM 组 hBD-1( = .006)、hBD-2( < .001)和 hBD-3( < .001)水平较低,LL-37( < .001)水平较高。当仅将牙周健康对照者纳入分析时,与系统性健康对照组相比,T2DM 患者的 hBD-1( = .002)和 LL-37( < .001)水平更高。唾液 LL-37 水平与 HbA1c 和牙周炎相关,而 hBD-2、hBD-3 仅与 HbA1c 相关。在本研究范围内,可以提出高血糖症可作为唾液 hBD 和抗菌肽水平的调节剂。另一方面,牙周炎仅影响唾液 LL-37 水平。