Institute for Inflammation Research, Center for Rheumatology and Spine Disease, Section 7521, Copenhagen University Hospital Rigshospitalet, 2200 Copenhagen, Denmark.
Department of Cardiology, Herlev-Gentofte Hospital, 2900 Hellerup, Denmark.
Int J Mol Sci. 2022 Aug 23;23(17):9536. doi: 10.3390/ijms23179536.
Epidemiologic studies have shown associations between periodontitis and rheumatoid arthritis (RA), but a causal relationship has not been established. Citrullination of gingival proteins by human peptidylarginine deiminases (PADs) or PAD from has been proposed to generate autoantigens in anti-CCP-positive RA. This study investigated whether the association between periodontitis and RA is influenced by single nucleotide polymorphisms (SNPs) in the genes encoding PAD2 and PAD4 that catalyze aberrant citrullination in RA and often are overexpressed in inflamed gingival connective tissue in subjects with periodontitis. The study included 137 RA patients and 161 controls with self-reported periodontitis. Periodontitis onset preceded RA onset by 13 years on average and was not associated with any of the SNPs investigated. In subjects with periodontitis, carriage of the minor alleles of rs2057094 and rs2235912 in significantly increased the risk of RA (odds ratios 1.42 [ = 0.03] and 1.48 [ = 0.02], respectively), and this effect was driven by the anti-CCP-negative RA patients. The minor alleles of these SNPs only increased risk of anti-CCP-positive RA in individuals with periodontitis and a history of smoking. These data suggest that individuals with periodontitis carrying the minor alleles of SNPs rs2057094, rs2076616 and rs2235912 in may be at increased risk of RA.
流行病学研究表明,牙周炎与类风湿关节炎(RA)之间存在关联,但尚未确定因果关系。有人提出,人类肽基精氨酸脱亚氨酶(PADs)或 中的 PAD 使牙龈蛋白瓜氨酸化,从而产生抗 CCP 阳性 RA 中的自身抗原。本研究旨在探讨编码 PAD2 和 PAD4 的基因中的单核苷酸多态性(SNPs)是否会影响牙周炎和 RA 之间的关联,这些基因编码的酶可催化 RA 中的异常瓜氨酸化,并且在牙周炎患者的炎症性牙龈结缔组织中常常过度表达。该研究纳入了 137 名 RA 患者和 161 名自述患有牙周炎的对照者。牙周炎的发病平均比 RA 早 13 年,与所研究的任何 SNP 均无关。在患有牙周炎的患者中,rs2057094 和 rs2235912 的次要等位基因携带者显著增加了 RA 的发病风险(比值比 1.42 [ = 0.03] 和 1.48 [ = 0.02]),这种效应是由抗 CCP 阴性 RA 患者驱动的。这些 SNP 的次要等位基因仅增加了牙周炎且有吸烟史的个体发生抗 CCP 阳性 RA 的风险。这些数据表明,携带 SNP rs2057094、rs2076616 和 rs2235912 的次要等位基因的牙周炎患者可能会增加患 RA 的风险。