Impact of treatment of rheumatoid arthritis on periodontal disease: A review.

IF 2.8 3区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
Molecular Oral Microbiology Pub Date : 2024-08-01 Epub Date: 2024-02-16 DOI:10.1111/omi.12454
Catherine Petit, Shauna Culshaw, Roland Weiger, Olivier Huck, Philipp Sahrmann
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引用次数: 0

Abstract

Background: Numerous studies support a bidirectional association between rheumatoid arthritis (RA), a chronic autoimmune degenerative inflammatory joint disease, and periodontitis, a chronic inflammatory disease caused by the immune reaction to bacteria organized in biofilms. RA and periodontitis are both multifactorial chronic inflammatory diseases that share common modifiable and non-modifiable risk factors. There is no cure for RA; treatment is based on lifestyle modifications and a variety of medications: nonsteroidal anti-inflammatory drugs (NSAID), glucocorticoids, and disease-modifying antirheumatic drugs (DMARDs, e.g., conventional synthetic DMARDs [csDMARDs]; biological DMARDs [bDMARD] and targeted synthetic DMARDs). There are molecular pathways of inflammation that are common to both RA and periodontitis. Thus, there is a potential effect of RA treatments on periodontitis. This systematic review aims to assess the impact of antirheumatic agents on periodontal conditions of patients suffering from both RA and periodontitis.

Methods: PubMed/MEDLINE, Cochrane Library, and Embase online databases were systematically explored, and a manual search was performed to identify relevant studies published until January 2023. This review is registered in the PROSPERO database (CRD42023409006).

Results: A total of 2827 articles were identified, and 35 fulfilled the inclusion criteria. The included studies generally show a consensus that, at normal dosage, NSAID and corticosteroids have negligible impact on periodontium. Similarly, csDMARD alone or in combination with other csDMARD demonstrated no adverse effect on periodontium. Monotherapy with bDMARD had a positive effect on periodontal pocket depths and gingival inflammation in the longitudinal studies up to 6 months but showed negligible effect on the periodontium in interventional studies with a longer follow-up (9 months and 15.1 months). However, the combination of tumor necrosis factor (TNF)-α inhibitors + methotrexate (MTX) was associated with a rise in gingival inflammation. Due to the considerable heterogeneity of the study designs, a meta-analysis could not reasonably be performed.

Conclusion: Within the limitations of the available studies, there is evidence to suggest that bDMARD monotherapy may improve the periodontal condition of RA patients with periodontal disease to a certain extent; the concomitant medication of TNF inhibitor + MTX could worsen gingival inflammation. More data are required to understand the impact of RA therapies on periodontal health.

类风湿性关节炎治疗对牙周病的影响:综述。
背景:类风湿性关节炎(RA)是一种慢性自身免疫性退行性炎症关节疾病,而牙周炎则是一种由生物膜中的细菌引起的免疫反应导致的慢性炎症疾病。关节炎和牙周炎都是多因素慢性炎症性疾病,具有共同的可改变和不可改变的风险因素。RA目前尚无根治方法,治疗主要依靠改变生活方式和多种药物:非甾体类抗炎药(NSAID)、糖皮质激素和改善病情抗风湿药(DMARDs,如传统合成DMARDs[csDMARDs]、生物DMARDs[bDMARDs]和靶向合成DMARDs)。RA和牙周炎都有共同的炎症分子途径。因此,RA治疗对牙周炎有潜在的影响。本系统综述旨在评估抗风湿药对同时患有 RA 和牙周炎的患者牙周状况的影响:方法:系统检索了 PubMed/MEDLINE、Cochrane Library 和 Embase 在线数据库,并进行了人工检索以确定 2023 年 1 月之前发表的相关研究。本综述已在 PROSPERO 数据库(CRD42023409006)中注册:结果:共发现 2827 篇文章,其中 35 篇符合纳入标准。纳入的研究普遍认为,在正常剂量下,非甾体抗炎药和皮质类固醇对牙周的影响微乎其微。同样,单用 csDMARD 或与其他 csDMARD 联用对牙周也没有不良影响。在长达 6 个月的纵向研究中,bDMARD 单药治疗对牙周袋深度和牙龈炎症有积极影响,但在随访时间较长(9 个月和 15.1 个月)的干预性研究中,bDMARD 单药治疗对牙周的影响可以忽略不计。不过,肿瘤坏死因子(TNF)-α抑制剂+甲氨蝶呤(MTX)的联合用药与牙龈炎症的上升有关。由于研究设计存在相当大的异质性,因此无法进行合理的荟萃分析:结论:在现有研究的限制下,有证据表明 bDMARD 单药治疗可在一定程度上改善患有牙周疾病的 RA 患者的牙周状况;TNF 抑制剂+MTX 的联合用药可能会加重牙龈炎症。要了解 RA 疗法对牙周健康的影响,还需要更多的数据。
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
Molecular Oral Microbiology
Molecular Oral Microbiology DENTISTRY, ORAL SURGERY & MEDICINE-MICROBIOLOGY
CiteScore
6.50
自引率
5.40%
发文量
46
审稿时长
>12 weeks
期刊介绍: Molecular Oral Microbiology publishes high quality research papers and reviews on fundamental or applied molecular studies of microorganisms of the oral cavity and respiratory tract, host-microbe interactions, cellular microbiology, molecular ecology, and immunological studies of oral and respiratory tract infections. Papers describing work in virology, or in immunology unrelated to microbial colonization or infection, will not be acceptable. Studies of the prevalence of organisms or of antimicrobials agents also are not within the scope of the journal. The journal does not publish Short Communications or Letters to the Editor. Molecular Oral Microbiology is published bimonthly.
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