Muhammad Ridho Fiki, Julyanto Syachputra Andika, Dias Nur'aini Anisa, Ulfah Kamailiya, Faqih Muhamad, Nurhuda Andang
Dental Profession Program, Faculty of Dental Medicine, Universitas Airlangga. Surabaya, Indonesia.
Department of Biology, Faculty of Biology, Universitas Gadjah Mada. Yogyakarta, Indonesia.
Rev Cient Odontol (Lima). 2024 Nov 23;12(4):e222. doi: 10.21142/2523-2754-1204-2024-222. eCollection 2024 Oct-Dec.
There is ongoing exploration into herbal treatments to identify adjunct therapies with minimal side effects. One such treatment involves curcumin from turmeric (). This study aims to review the efficacy of curcumin as an anti-inflammatory agent for periodontitis along with the mechanisms of action involved.
A systematic review of pre-clinical and clinical studies published on Scopus, PubMed, ScienceDirect, and Google Scholar up to May 2024 was employed following the PRISMA guidelines. Three tools were used for risk of bias assessment, namely the QUIN tool for studies, the SYRCLE's RoB for studies, and the Cochrane RoB 2 for RCTs. Finally, nineteen studies were included for review.
This study highlights curcumin's efficacy in addressing periodontitis through diverse mechanisms. Curcumin demonstrated efficacy in attenuating inflammation within periodontal tissue by inhibiting several pro-inflammatory cytokines and mediators such as interleukin (IL)-1, IL-6, tumor necrosis factor (TNF)-α, matrix metalloproteinases (MMPs), prostaglandin E2 (PGE2), cyclooxygenase (COX)-2, while concurrently increasing IL-4 and IL-10. In addition, several transcription factors such as nuclear factor-kappa B (NF-κB) and signal transducer and activator of transcription 1 (STAT1) were also inhibited by curcumin. Administration of curcumin has additionally been demonstrated to reduce other biomarkers of periodontitis, including C-reactive protein (CRP), alkaline phosphatase (ALP), and procalcitonin (PCT).
Curcumin has been shown to be effective as an adjunct therapeutic agent for periodontitis due to its anti-inflammatory effects by reducing the inflammatory response through a diverse range of mechanisms of action.
目前正在探索草药治疗方法,以确定副作用最小的辅助疗法。其中一种治疗方法涉及姜黄中的姜黄素()。本研究旨在综述姜黄素作为牙周炎抗炎剂的疗效及其作用机制。
按照PRISMA指南,对截至2024年5月在Scopus、PubMed、ScienceDirect和谷歌学术上发表的临床前和临床研究进行系统综述。使用了三种工具进行偏倚风险评估,即用于 研究的QUIN工具、用于 研究的SYRCLE's RoB工具以及用于随机对照试验的Cochrane RoB 2工具。最后,纳入了19项研究进行综述。
本研究强调了姜黄素通过多种机制治疗牙周炎的疗效。姜黄素通过抑制几种促炎细胞因子和介质,如白细胞介素(IL)-1、IL-6、肿瘤坏死因子(TNF)-α、基质金属蛋白酶(MMPs)、前列腺素E2(PGE2)、环氧化酶(COX)-2,同时增加IL-4和IL-10,从而在减轻牙周组织炎症方面显示出疗效。此外,姜黄素还抑制了几种转录因子,如核因子-κB(NF-κB)和信号转导及转录激活因子1(STAT1)。姜黄素的给药还被证明可以降低牙周炎的其他生物标志物水平,包括C反应蛋白(CRP)、碱性磷酸酶(ALP)和降钙素原(PCT)。
姜黄素已被证明是一种有效的牙周炎辅助治疗剂,因为它通过多种作用机制减轻炎症反应,从而发挥抗炎作用。