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TNF-α Antagonist and Infection in Rheumatoid Arthritis

机译:TNF-α拮抗剂与类风湿关节炎的感染

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Background: Anti-TNF treatment may increase infection risk, although this has been difficult to study because the timing of anti-TNF treatment is driven by disease activity, which may influence infection susceptibility leading to confounding that varies over time. We evaluated the association between anti-TNF initiation in rheumatoid arthritis (RA) patients on disease modifying anti-rheumatic drugs (DMARD) and infection using multiple approaches adjusting for time-varying confounding. Methods: 383 anti-TNF-na?ve RA patients on ≥ 1 non-biologic-DMARD at enrollment from the Brigham and Women’s Rheumatoid Arthritis Sequential Study (BRASS) were followed up to two years. Pooled logistic regressions estimated the association between anti-TNF and infection by including time-varying covariates in the adjusted models and inverse probability treatment weighting (IPTW). Results: Adjustment for time-varying disease activity and other suspected confounders yielded non-statistically significant positive associations between anti-TNF start and infection regardless of analytic approach (RRmvar_adj = 2.1, 95% CI: 0.8 - 5.8). Conclusions: Incorporating changing clinical status, and treatment indications and consequences, yielded consistently (though not significantly) elevated relative risks of infection associated with anti-TNF initiation. Due to limited statistical power, we cannot draw firm conclusions. However, we have illustrated multiple approaches adjusting for potential time-varying confounding in longitudinal studies and hope to replicate the approaches in larger studies.
机译:背景:抗TNF治疗可能会增加感染风险,尽管这一直很难研究,因为抗TNF治疗的时机是由疾病活动决定的,这可能会影响感染的易感性,并导致混淆现象随时间而变化。我们评估了风湿性关节炎(RA)患者的抗TNF起始之间的关系,使用多种方法调整时变混杂因素,以改善疾病的抗风湿药(DMARD)与感染之间的相关性。方法:从Brigham和女性类风湿关节炎序列研究(BRASS)入组的383例≥1例非生物DMARD的抗TNF初治RA患者被随访了两年。通过在调整后的模型中加入时变协变量和逆概率治疗权重(IPTW),汇总的logistic回归估计了抗TNF与感染之间的关联。结果:无论采用何种分析方法,对随时间变化的疾病活动和其他可疑混杂因素的调整在抗TNF起始与感染之间均产生非统计学显着的正相关性(RRmvar_adj = 2.1,95%CI:0.8-5.8)。结论:结合不断变化的临床状况以及治疗适应症和后果,与抗TNF引发相关的感染相对风险始终如一地(尽管不显着)增加。由于有限的统计能力,我们无法得出明确的结论。但是,我们已经说明了多种方法以适应纵向研究中潜在的时变混淆,并希望在较大的研究中重复使用这些方法。

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