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三阳性患者和其他类风湿因子阳性患者在吸烟与类风湿关节炎相关联中的主要作用。

A predominant involvement of the triple seropositive patients and others with rheumatoid factor in the association of smoking with rheumatoid arthritis.

机构信息

Experimental and Observational Rheumatology and Rheumatology Unit, Instituto de Investigacion Sanitaria, Hospital Clínico Universitario de Santiago (IDIS), Santiago de Compostela, Spain.

Rheumatology Department, Hospital Clínico San Carlos, Instituto Investigación Sanitaria San Carlos (IdISSC), Madrid, Spain.

出版信息

Sci Rep. 2020 Feb 25;10(1):3355. doi: 10.1038/s41598-020-60305-x.

DOI:10.1038/s41598-020-60305-x
PMID:32098994
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7042270/
Abstract

The major environmental risk factor for rheumatoid arthritis (RA) is smoking, which according to a widely accepted model induces protein citrullination in the lungs, triggering the production of anti-citrullinated protein antibodies (ACPA) and RA development. Nevertheless, some research findings do not fit this model. Therefore, we obtained six independent cohorts with 2253 RA patients for a detailed analysis of the association between smoking and RA autoantibodies. Our results showed a predominant association of smoking with the concurrent presence of the three antibodies: rheumatoid factor (RF), ACPA and anti-carbamylated protein antibodies (ACarPA) (3 Ab vs. 0 Ab: OR = 1.99, p = 2.5 × 10). Meta-analysis with previous data (4491 patients) confirmed the predominant association with the concurrent presence of the three antibodies (3 Ab vs. 0 Ab: OR = 2.00, p = 4.4 ×10) and revealed that smoking was exclusively associated with the presence of RF in patients with one or two antibodies (RF vs. RF: OR = 1.32, p = 0.0002). In contrast, no specific association with ACPA or ACarPA was found. Therefore, these results showed the need to understand how smoking favors the concordance of RA specific antibodies and RF triggering, perhaps involving smoking-induced epitope spreading and other hypothesized mechanisms.

摘要

吸烟是类风湿关节炎(RA)的主要环境风险因素,这一观点基于一个被广泛接受的模型,即吸烟可导致肺部蛋白质瓜氨酸化,从而触发抗瓜氨酸化蛋白抗体(ACPA)的产生,并引发 RA 的发生。然而,一些研究结果并不符合这一模型。因此,我们收集了六个独立的队列,共 2253 名 RA 患者,以详细分析吸烟与 RA 自身抗体之间的关系。我们的研究结果表明,吸烟与同时存在三种抗体(类风湿因子 [RF]、ACPA 和抗氨甲酰化蛋白抗体 [ACarPA])具有显著相关性(3 种抗体阳性与 0 种抗体阳性相比:OR=1.99,p=2.5×10)。与先前数据(4491 名患者)的荟萃分析进一步证实了这种与三种抗体同时存在的显著相关性(3 种抗体阳性与 0 种抗体阳性相比:OR=2.00,p=4.4×10),并表明吸烟仅与同时存在 RF 的患者存在一种或两种抗体(RF 阳性与 RF 阳性相比:OR=1.32,p=0.0002)有关。相反,吸烟与 ACPA 或 ACarPA 无特异性关联。因此,这些结果表明,需要深入了解吸烟如何促进 RA 特异性抗体和 RF 同时发生的机制,这可能涉及吸烟诱导的表位扩展和其他假设的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/737d/7042270/33f57c02ec19/41598_2020_60305_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/737d/7042270/71bb0db032ef/41598_2020_60305_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/737d/7042270/6d67f4cbaf7a/41598_2020_60305_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/737d/7042270/357cefebef79/41598_2020_60305_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/737d/7042270/33f57c02ec19/41598_2020_60305_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/737d/7042270/71bb0db032ef/41598_2020_60305_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/737d/7042270/6d67f4cbaf7a/41598_2020_60305_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/737d/7042270/357cefebef79/41598_2020_60305_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/737d/7042270/33f57c02ec19/41598_2020_60305_Fig4_HTML.jpg

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