Eun Yong, Culpepper-Morgan Joan, Akanmode Abiodun M, Thu Myint B, Sta Lucia Aprilee A, Thearle Marie S, Trousdale Rhonda K
Department of Medicine, NYC Health + Hospitals/Harlem, New York, NY 10037, United States.
Division of Gastroenterology, Department of Medicine, NYC Health + Hospitals/Harlem, New York, NY 10037, United States.
World J Gastrointest Pharmacol Ther. 2025 Jun 5;16(2):105335. doi: 10.4292/wjgpt.v16.i2.105335.
Patients with inflammatory bowel disease (IBD) are at an increased risk of bacterial pneumonia, contributing to significant morbidity and mortality. While previous studies have identified various risk factors, including medications and comorbidities, the independent contribution of IBD to pneumonia risk remains unclear. We hypothesized that the increased pneumonia risk is primarily driven by factors other than IBD itself.
To investigate the relative contributions of IBD, comorbidities, and medications to pneumonia risk in patients with IBD.
We conducted a retrospective cohort study using the All of Us Research Program database (2010-2022). We matched 2810 participants with IBD 1:1 with controls using four propensity score models: (1) Demographics/Lifestyle only; (2) Plus comorbidities; (3) Plus medications; and (4) All factors combined. Then we used Cox proportional hazards models to assess pneumonia risk and logistic regression to evaluate risk factors.
In the primary analysis of 5620 matched participants, IBD was not independently associated with increased pneumonia risk [hazard ratio (HR) = 1.07, 95%CI: 0.84-1.35] when matched for all factors. However, participants with IBD had significantly higher risk (HR = 2.08, 95%CI: 1.56-2.78) when matched only for demographics and lifestyle factors. Within the IBD cohort, a high comorbidity burden (Charlson Comorbidity Index ≥ 10) [odds ratio (OR) = 12.20, 95%CI: 6.69-23.00] and systemic steroid use (OR = 2.26, 95%CI: 1.21-4.64) were independently associated with increased pneumonia risk.
Comorbidities and systemic steroids, rather than IBD itself, drive pneumonia risk. Management should focus on these factors and prioritize vaccination in high-risk patients.
炎症性肠病(IBD)患者发生细菌性肺炎的风险增加,这会导致显著的发病率和死亡率。虽然先前的研究已经确定了各种风险因素,包括药物和合并症,但IBD对肺炎风险的独立影响仍不清楚。我们假设肺炎风险增加主要是由IBD本身以外的因素驱动的。
研究IBD、合并症和药物对IBD患者肺炎风险的相对影响。
我们使用“我们所有人”研究计划数据库(2010 - 2022年)进行了一项回顾性队列研究。我们使用四个倾向评分模型将2810名IBD参与者与对照组进行1:1匹配:(1)仅人口统计学/生活方式;(2)加上合并症;(3)加上药物;(4)所有因素综合。然后我们使用Cox比例风险模型评估肺炎风险,并使用逻辑回归评估风险因素。
在对5620名匹配参与者的初步分析中,当对所有因素进行匹配时,IBD与肺炎风险增加无独立相关性[风险比(HR)= 1.07,95%置信区间:0.84 - 1.35]。然而,仅对人口统计学和生活方式因素进行匹配时,IBD参与者的风险显著更高(HR = 2.08,95%置信区间:1.56 - 2.78)。在IBD队列中,高合并症负担(查尔森合并症指数≥10)[比值比(OR)= 12.20,95%置信区间:6.69 - 23.00]和全身使用类固醇(OR = 2.26,95%置信区间:1.21 - 4.64)与肺炎风险增加独立相关。
驱动肺炎风险的是合并症和全身使用类固醇,而非IBD本身。管理应关注这些因素,并优先为高危患者接种疫苗。