Causal network between periodontitis and systemic inflammation: Triangulating evidence from Mendelian randomization and sequencing datasets

IF 4.2 2区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
Guixin Zhu, Ke Yang, Tiqian Liu, Yuhuang Chen, Ran Li, Junchi Dong, Liang Xing
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Abstract

BackgroundPeriodontitis, an inflammatory condition, results from the immune response to pathogenic microorganisms. Gingival defects from periodontitis enable these microorganisms, along with immune cells and inflammatory proteins, to enter the bloodstream, potentially causing systemic inflammation and contributing to systemic diseases. Conversely, systemic diseases can worsen periodontitis by inducing inflammation.MethodsIn this study, we investigated the connection between periodontitis and blood immune cell phenotypes/circulating inflammation‐associated proteins using bidirectional Mendelian randomization (MR). We also analyzed the interplay between immune cells, inflammation proteins, and periodontitis through a two‐step mediation analysis. Besides, we utilized sensitivity analyses, including the MR‐PRESSO outlier test, MR Egger intercept, Cochran's Q statistic, Steiger filter, and leave‐one‐out analysis. Confounder‐related instrumental variants were filtered through the Open Targets Genetics. Additionally, the results were supported by triangulation of high‐throughput sequencing dataset analyses and animal models.ResultsMR analysis identified three proteins—programmed cell death 1 ligand 1 (PD‐L1), eotaxin, and neurturin (NRTN)—with protective roles against periodontitis, alongside three proteins—protein S100‐A12 (S100A12), C‐X‐C motif chemokine ligand (CXCL) 11, and sulfotransferase 1A1 (SULT1A1)—identified as risk factors. Furthermore, our study revealed 16 immunocyte phenotypes causally linked to periodontitis. Conversely, periodontitis was associated with heightened circulating levels of CXCL 9/10/11. Notably, periodontitis influenced the characteristics of circulating immune cells, particularly regulatory T cells (Treg), maturation stages of T cells, and conventional dendritic cells (cDC). Additionally, single‐cell and bulk‐RNA sequencing and animal models verified the above results.ConclusionsThis study underscores the close connection between periodontitis and systemic inflammation, laying the groundwork for targeted immunotherapy against periodontitis and supporting the link between periodontitis and systemic diseases.Plain Language SummaryThis study explored the bidirectional causal relationship between periodontitis and systemic inflammation, demonstrating a causal relationship between periodontitis and specific circulating inflammatory proteins and immune cell phenotypes, indicating that the treatment of periodontitis needs to consider the systemic inflammatory state and that the systemic inflammatory state may be involved in the link between periodontitis and systemic diseases.
牙周炎和全身性炎症之间的因果网络:来自孟德尔随机化和测序数据集的三角测量证据
牙周炎是一种炎症性疾病,是由对病原微生物的免疫反应引起的。牙周炎引起的牙龈缺陷使这些微生物与免疫细胞和炎症蛋白一起进入血液,可能引起全身性炎症并导致全身性疾病。相反,全身性疾病会引起炎症,使牙周炎恶化。方法本研究采用双向孟德尔随机化(MR)研究了牙周炎与血液免疫细胞表型/循环炎症相关蛋白之间的关系。我们还通过两步中介分析分析了免疫细胞、炎症蛋白和牙周炎之间的相互作用。此外,我们还利用敏感性分析,包括MR - PRESSO异常值检验、MR Egger截距、Cochran’s Q统计量、Steiger滤波和留一分析。通过Open Targets Genetics筛选混杂因素相关的工具变异。此外,高通量测序数据集分析和动物模型的三角测量支持了结果。结果smr分析发现3种蛋白-程序性细胞死亡1配体1 (PD‐L1)、eotaxin和neurturin (NRTN) -对牙周炎具有保护作用,另外3种蛋白-蛋白S100‐A12 (S100A12)、C‐X‐C基序趋化因子配体(CXCL) 11和硫转移酶1A1 (SULT1A1) -被确定为危险因素。此外,我们的研究揭示了16种免疫细胞表型与牙周炎有因果关系。相反,牙周炎与循环中CXCL水平升高有关。值得注意的是,牙周炎影响了循环免疫细胞的特征,特别是调节性T细胞(Treg)、T细胞的成熟阶段和传统树突状细胞(cDC)。此外,单细胞和大RNA测序和动物模型验证了上述结果。结论本研究强调了牙周炎与全身性炎症之间的密切联系,为靶向免疫治疗牙周炎奠定了基础,支持了牙周炎与全身性疾病之间的联系。本研究探讨了牙周炎与全身性炎症之间的双向因果关系,论证了牙周炎与特定循环炎症蛋白和免疫细胞表型之间的因果关系,提示牙周炎的治疗需要考虑全身性炎症状态,全身性炎症状态可能参与了牙周炎与全身性疾病之间的联系。
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来源期刊
Journal of periodontology
Journal of periodontology 医学-牙科与口腔外科
CiteScore
9.10
自引率
7.00%
发文量
290
审稿时长
3-8 weeks
期刊介绍: The Journal of Periodontology publishes articles relevant to the science and practice of periodontics and related areas.
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