口腔医学 ›› 2026, Vol. 46 ›› Issue (6): 422-426.

• 基础与临床研究 • 上一篇    下一篇

生物抗菌多肽对牙周炎症因子及骨代谢指标的影响研究

王春晓1, 黄优2, 刘燕2()   

  1. 1 苏州口腔医院钻石分部, 江苏苏州 (215000)
    2 苏州口腔医院星海分部, 江苏苏州 (215000)
  • 收稿日期:2025-03-29 出版日期:2026-06-28 发布日期:2026-06-17
  • 通讯作者: 刘燕 E-mail:935486693@qq.com
  • 基金资助:
    苏州口腔医院院级科研基金(SZKQYY20B007)

Study on the effects of biological antimicrobial peptides on periodontitis factors and bone metabolism indicators

WANG Chunxiao1, HUANG You2, LIU Yan2()   

  1. Department of Zuanshi, Suzhou Stomatological Hospital, Suzhou 215000, China
  • Received:2025-03-29 Online:2026-06-28 Published:2026-06-17

摘要:

目的 探究生物抗菌多肽对牙周炎患者龈沟液炎症因子和骨代谢因子水平变化的影响。方法 选取苏州口腔医院星海分部108例Ⅲ期牙周炎患者,随机分为对照组、米诺环素组和抗菌多肽组,每组36例。对照组在常规刮治后即刻及1周进行全口牙周袋袋内碘甘油给药,米诺环素组进行盐酸米诺环素给药,抗菌多肽组进行生物抗菌多肽给药。通过临床检查比较各组刮治前及刮治后30 d牙周指数(出血指数(bleeding index,BI)、探诊深度(probing depth,PD)、附着丧失(attachment loss,AL));利用酶联免疫吸附法(enzyme-linked immunosorbent assay,ELISA)检测治疗前后3组患者龈沟液中炎症因子(肿瘤坏死因子-α(tumor necrosis factor-α,TNF-α)、白细胞介素-1β(interleukin-1β,IL-1β)、基质金属蛋白酶-9(matrix metalloproteinase-9,MMP-9))和骨代谢指标(碱性磷酸酶(alkaline phosphatase,ALP)、骨钙素(bone γ-carboxyglutamic acid-containing protein,BGP)、骨保护素(osteoprotegerin,OPG)、SP7)。结果 治疗前,3组牙周指数(BI、PD、AL)、炎症因子(MMP-9、IL-1β、TNF-α)及骨代谢指标(ALP、SP7、BGP、OPG)水平差异均无统计学意义(P>0.05)。刮治后30 d,①3组各项指标均较刮治前有显著改善(P<0.05),米诺环素组和抗菌多肽组各项指标均优于对照组(P<0.05);②与米诺环素组相比,抗菌多肽组患者的牙周指数BI、PD、AL明显改善(P<0.05),MMP-9、IL-1β水平明显降低(P<0.05),ALP、SP7、BGP、OPG骨代谢指标均明显升高(P<0.05),但两组间TNF-α水平未见明显差异(P>0.05)。结论 生物抗菌多肽在减轻牙周炎症反应、改善骨代谢方面显著优于盐酸米诺环素,有作为牙周炎患者口腔局部用药的应用潜力。

关键词: 生物抗菌多肽, 牙周炎, 骨代谢

Abstract:

Objective To explore the effects of antimicrobial peptides on the levels of periodontal inflammatory factors and bone metabolism factors in gingival crevicular fluid of patients with periodontitis. Methods A total of 108 patients with stage Ⅲ periodontitis in Department of Xinghai, Suzhou Stomatological Hospital were randomly divided into a control group, a minocycline group and an antimicrobial peptide group, with 36 patients in each group. The control group was given iodine glycerol in the periodontal pocket immediately and one week after scaling and root planing; the minocycline group was given minocycline hydrochloride, and the antimicrobial peptide group was given biological antimicrobial peptides. The differences in periodontal status (bleeding index (BI), probing depth (PD), attachment loss (AL)) between groups before and 30 d after treatment were compared through clinical examination. The inflammatory factors (matrix metalloproteinase-9 (MMP-9), interleukin-1β (IL-1β), tumor necrosis factor-α (TNF-α)) and bone metabolism indicators (alkaline phosphatase (ALP), bone γ-carboxyglutamic acid-containing protein (BGP), osteoprotegerin (OPG), SP7) in gingival crevicular fluid between three groups before and after treatment were compared through enzyme-linked immunosorbent assay (ELISA) detection. Results Before treatment, there were no statistically significant differences in periodontal indices (BI, PD, AL), inflammatory factors (MMP-9, IL-1β, TNF-α), and bone metabolism factors (ALP, SP7, BGP, OPG) among the three groups (P>0.05). Thirty days after treatment, all three groups showed significant improvement in various indicators compared to before treatment (P<0.05), and the indicators of the minocycline group and antimicrobial peptide group were better than those of the control group (P<0.05). In addition, the improvement of periodontal index BI, PD, and AL in the antimicrobial peptide group was better than that in the minocycline group (P<0.05); MMP-9, IL-1β were significantly lower in the antimicrobial group than in the minocycline group (P<0.05); ALP, SP7, BGP and OPG bone metabolism indicators were significantly higher than those in the minocycline group (P<0.05), but there was no significant difference in TNF-α levels between the two groups (P>0.05). Conclusion Biological antimicrobial peptides are significantly superior to minocycline hydrochloride in reducing periodontal inflammation and improving bone metabolism, and have potential for application as oral topical drugs for the treatment of periodontitis.

Key words: antimicrobial peptides, periodontitis, bone metabolism

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