Evaluation of chemerin, fetuin-A, interleukin-34, and interleukin-13 levels following periodontal treatment in diabetes mellitus.

IF 3.1 2区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
Nimet Gül Görgülü, Hatice Selin Güngörmek, Yaprak Kalkan, Başak Doğan
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引用次数: 0

Abstract

Objective: This cohort study investigated salivary and serum chemerin, fetuin-A, interleukin (IL)-34, and IL-13 changes in type 2 diabetes mellitus (T2DM) periodontitis following non-surgical periodontal therapy (NSPT).

Materials and methods: A total of 110 participants were assigned to five groups (n = 22 each): non-periodontitis, non-periodontitis with T2DM, periodontitis (P), well-controlled T2DM periodontitis (WDM-P), and poorly controlled T2DM periodontitis (PDM-P). Periodontal parameters were recorded and biological samples collected at baseline and/or 3 months post-NSPT. Biomolecule levels were measured using ELISA.

Results: All periodontitis groups improved in periodontal parameters after 3 months (p < 0.05), but the proportion of patients who responded poorly to NSPT was higher in the PDM-P group compared to the P group (p = 0.026). HbA1c decreased in WDM-P and PDM-P groups at 3 months (p < 0.05). All salivary biomolecules were individually associated with periodontitis (p < 0.05), and their combined model distinguished periodontitis (AUC: 0.94). Serum chemerin and fetuin-A were linked to T2DM (p < 0.05), and their combination predicted T2DM (AUC: 0.91). After NSPT, salivary fetuin-A increased, salivary IL-13 decreased in three periodontitis groups (p < 0.05), whereas salivary chemerin, IL-34, and serum IL-34 reduced only in P group (p < 0.05).

Conclusion: Salivary fetuin-A and IL-13 appear involved in periodontitis pathogenesis, while serum chemerin and fetuin-A in the T2DM. T2DM may hinder inflammation resolution, particularly involving chemerin and IL-34.

Clinical relevance: The distinct biomolecule changes in systemically healthy versus T2DM periodontitis patients suggests that T2DM may impair inflammation resolution, underscoring the importance of personalized periodontal treatment strategies. This study was retrospectively registered on ClinicalTrials.gov (NCT06135532) on November 11, 2023.

糖尿病患者牙周治疗后趋化素、胎蛋白a、白细胞介素34和白细胞介素13水平的评价。
目的:研究非手术牙周治疗(NSPT)后2型糖尿病(T2DM)牙周炎患者唾液和血清趋化素、胎蛋白a、白细胞介素(IL)-34和IL-13的变化。材料和方法:共有110名参与者被分为五组(n = 22):非牙周炎、非牙周炎合并T2DM、牙周炎(P)、控制良好的T2DM牙周炎(WDM-P)和控制不良的T2DM牙周炎(PDM-P)。在基线和/或nspt后3个月记录牙周参数并收集生物样本。采用ELISA法测定生物分子水平。结果:各牙周炎组3个月后牙周指标均有改善(p)。结论:唾液中胎蛋白a和IL-13参与了牙周炎的发病机制,血清趋化素和胎蛋白a参与了T2DM的发病机制。T2DM可能阻碍炎症消退,特别是与趋化素和IL-34有关。临床相关性:全身健康与T2DM牙周炎患者不同的生物分子变化表明,T2DM可能损害炎症消退,强调个性化牙周治疗策略的重要性。该研究于2023年11月11日在ClinicalTrials.gov (NCT06135532)上回顾性注册。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical Oral Investigations
Clinical Oral Investigations 医学-牙科与口腔外科
CiteScore
6.30
自引率
5.90%
发文量
484
审稿时长
3 months
期刊介绍: The journal Clinical Oral Investigations is a multidisciplinary, international forum for publication of research from all fields of oral medicine. The journal publishes original scientific articles and invited reviews which provide up-to-date results of basic and clinical studies in oral and maxillofacial science and medicine. The aim is to clarify the relevance of new results to modern practice, for an international readership. Coverage includes maxillofacial and oral surgery, prosthetics and restorative dentistry, operative dentistry, endodontics, periodontology, orthodontics, dental materials science, clinical trials, epidemiology, pedodontics, oral implant, preventive dentistiry, oral pathology, oral basic sciences and more.
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