Division of Paediatric Dentistry and Orthodontics, Faculty of Dentistry, The University of Hong Kong, Hong Kong, China.
Beijing Institute of Heart Lung and Blood Vessel Diseases, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Int Dent J. 2024 Dec;74(6):1258-1265. doi: 10.1016/j.identj.2024.04.019. Epub 2024 May 10.
Periodontitis is a complex and multifactorial disease and it is challenging to decipher its underlying causes and mechanisms. This study attempted to explore potential circulating proteins in connection to periodontitis through proteome-wide Mendelian randomisation (MR).
We analysed 1722 circulating proteins to identify prospective drug targets for tackling periodontitis, using the genomic dataset from the FinnGen study. Two-sample MR was conducted to evaluate the bidirectional relationship between circulating proteins and periodontitis risk. A dataset from the UK Biobank was used to validate the findings. Single-cell analysis was performed to assess the cellular expression of the identified proteins within gingival tissues.
MR analyses found that genetically predicted circulating levels of von Willebrand factor A domain-containing 1 (von Willebrand factor A domain containing 1 [VWA1], odds ratios: 0.94, 95% CI 0.92-0.97, P = 1.28 × 10) were inversely associated with periodontitis. In contrast, the level of growth differentiation factor 15 (growth differentiation factor 15 [GDF15], odds ratios: 1.05, 95% CI 1.02-1.07, P = 2.12 × 10) might be associated with an increased risk of periodontitis. Single-cell analysis indicated that VWA1 was primarily expressed in endothelial cells of healthy gingival tissues, while the main source of GDF15 was not derived from periodontal cells.
The present study suggests that certain plasma proteins like VWA1 and GDF15 may be potentially indicative of the risk and susceptibility to periodontitis. These proteins could possibly be the potential therapeutic targets for treating periodontitis, and further investigation is highly warranted.
牙周炎是一种复杂的多因素疾病,其潜在病因和机制难以破解。本研究试图通过全基因组孟德尔随机化(MR)来探索与牙周炎相关的潜在循环蛋白。
我们分析了来自 FinnGen 研究的基因组数据集,以鉴定 1722 种循环蛋白,作为治疗牙周炎的潜在药物靶点。采用两样本 MR 评估循环蛋白与牙周炎风险之间的双向关系。使用 UK Biobank 数据集验证研究结果。对牙龈组织内鉴定出的蛋白质进行单细胞分析,以评估其细胞表达。
MR 分析发现,遗传预测的循环水平 von Willebrand 因子 A 结构域包含 1(von Willebrand 因子 A 结构域包含 1 [VWA1],优势比:0.94,95%CI 0.92-0.97,P = 1.28×10)与牙周炎呈负相关。相比之下,生长分化因子 15(生长分化因子 15 [GDF15],优势比:1.05,95%CI 1.02-1.07,P = 2.12×10)的水平可能与牙周炎风险增加相关。单细胞分析表明,VWA1 主要在健康牙龈组织的内皮细胞中表达,而 GDF15 的主要来源并非来源于牙周细胞。
本研究表明,某些血浆蛋白,如 VWA1 和 GDF15,可能与牙周炎的风险和易感性有关。这些蛋白可能是治疗牙周炎的潜在治疗靶点,值得进一步研究。