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Clinical, microbiological, and salivary biomarker profiles of dental implant patients with type 2 diabetes

医学 骨保护素 牙科 糖尿病 生物标志物 唾液 牙周炎 牙密螺旋体 植入 2型糖尿病 内科学 骨整合 牙龈卟啉单胞菌 外科 内分泌学 生物 激活剂(遗传学) 受体 生物化学
作者
Nikolaos Tatarakis,Janet S. Kinney,Marita R. Inglehart,Thomas M. Braun,Charles E. Shelburne,Niklaus P. Lang,William V. Giannobile,Tae‐Ju Oh
出处
期刊:Clinical Oral Implants Research [Wiley]
卷期号:25 (7): 803-812 被引量:39
标识
DOI:10.1111/clr.12139
摘要

Abstract Objective Regulators of peri‐implant bone loss in patients with diabetes appear to involve multiple risk factors that have not been clearly elucidated. This study was conducted to explore putative local etiologic factors on implant bone loss in relation to type 2 diabetes mellitus, including clinical, microbial, salivary biomarker, and psychosocial factors. Materials and methods Thirty‐two subjects (divided into type 2 diabetes mellitus and non‐diabetic controls), having at least one functional implant and six teeth, were enrolled in a 1‐year longitudinal investigation. Analyses of clinical measurements and standardized intra‐oral radiographs, saliva and serum biomarkers (via protein arrays for 20 selected markers), and plaque biofilm (via q PCR for eight periodontal pathogens) were performed at baseline and 1 year. In addition, the subjects were asked to respond to questionnaires to assess behavioral and psychosocial variables. Results There was a significant increase from baseline to 1 year in the probing depth of implants in the diabetes group (1.95 mm to 2.35 mm, P = 0.015). The average radiographic bone loss during the study period marginally increased at dental implants compared to natural teeth over the study period (0.08 mm vs. 0.05 mm; P = 0.043). The control group harbored higher levels of T reponema denticola at their teeth at baseline ( P = 0.046), and the levels of the pathogen increased significantly over time around the implants of the same group ( P = 0.003). Salivary osteoprotegerin ( OPG ) levels were higher in the diabetes group than the control group at baseline only; in addition, the salivary levels of IL ‐4, IL ‐10, and OPG associated with host defense were significantly reduced in the diabetes group ( P = 0.010, P = 0.019, and P = 0.024), while controls showed an increase in the salivary OPG levels ( P = 0.005). For psychosocial factors, there were not many significant changes over the observation period, except for some findings related to coping behaviors at baseline. Conclusions The study suggests that the clinical, microbiological, salivary biomarker, and psychosocial profiles of dental implant patients with type 2 diabetes who are under good metabolic control and regular maintenance care are very similar to those of non‐diabetic individuals. Future studies are warranted to validate the findings in longer‐term and larger clinical trials ( ClinicalTrials.gov # NCT00933491).
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