Section of Gastroenterology, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania; Section of Gastroenterology, VA Medical Center, Philadelphia, Pennsylvania.
Section of Gastroenterology, Drexel University College of Medicine, Philadelphia, Pennsylvania.
Clin Gastroenterol Hepatol. 2018 Dec;16(12):1919-1927.e3. doi: 10.1016/j.cgh.2017.12.052. Epub 2018 Jan 5.
BACKGROUND & AIMS: Patients with inflammatory bowel disease (IBD) might be at increased risk for herpes zoster infection. We sought to quantify the risk of herpes zoster in patients with IBD and evaluate the effects of IBD and IBD medications on the risk of herpes zoster.
We conducted 2 retrospective studies of populations of Veterans, from January 2000 through June 2016. In study 1, we compared the incidence of herpes zoster among patients with IBD receiving 5-ASA alone vs matched patients without IBD. In study 2, we compared the incidence of herpes zoster among patients with IBD treated with only 5-ASA, with thiopurines, with antagonists of tumor necrosis factor (TNF), with a combination of thiopurines and TNF antagonists, and with vedolizumab. We used multivariable Cox regression to estimate the hazard ratios and 95% CIs for herpes zoster associated with IBD in study 1 and with different treatments in study 2. We also estimated the incidence rate of herpes zoster based on age and IBD medication subgroups.
Compared to no IBD, ulcerative colitis (UC) and Crohn's disease (CD) were each associated with significantly increased risk of herpes zoster infection. In multivariable Cox regression (compared to no IBD), UC, CD, or IBD treated with 5-ASA treatment alone was associated with significantly increased risk of herpes zoster, with adjusted HRs (AHR) of 1.81 for UC (95% CI, 1.56-2.11), 1.56 for CD (95% CI, 1.28-1.91), and 1.72 for treated IBD (95% CI, 1.51-1.96). In multivariable Cox regression analysis, compared to exposure to 5-ASA alone, exposure to thiopurines (AHR, 1.47; 95% CI, 1.31-1.65) or a combination of thiopurines and TNF antagonists (AHR, 1.65; 95% CI, 1.22-2.23) was associated with increased risk of herpes zoster. However, exposure to TNF antagonists alone (AHR, 1.15; 95% CI, 0.96-1.38) was not associated with increased risk of herpes zoster. The incidence rates of herpes zoster in all age groups and all IBD medication subgroups were substantially higher than that in the oldest group of patients without IBD (older than 60 years).
In 2 retrospective studies of Veteran populations, we associated IBD and treatment with thiopurines, alone or in combination with TNF antagonists, with increased risk of herpes zoster. With the approval of a new and potentially safer vaccine for herpes zoster, the effects of immunization of patients with IBD should be investigated.
炎症性肠病(IBD)患者可能存在带状疱疹感染的风险增加。我们旨在量化 IBD 患者发生带状疱疹的风险,并评估 IBD 及其治疗药物对带状疱疹风险的影响。
我们进行了两项基于退伍军人人群的回顾性研究,时间范围为 2000 年 1 月至 2016 年 6 月。在研究 1 中,我们比较了接受 5-ASA 单药治疗的 IBD 患者与未患 IBD 的匹配患者之间带状疱疹的发病率。在研究 2 中,我们比较了仅接受 5-ASA、硫嘌呤、肿瘤坏死因子(TNF)拮抗剂、硫嘌呤和 TNF 拮抗剂联合治疗、以及维多珠单抗治疗的 IBD 患者之间带状疱疹的发病率。我们使用多变量 Cox 回归来估计与研究 1 中的 IBD 相关的带状疱疹风险的风险比(HR)和 95%置信区间(CI),并在研究 2 中估计与不同治疗方法相关的带状疱疹风险。我们还根据年龄和 IBD 药物亚组来估计带状疱疹的发病率。
与无 IBD 相比,溃疡性结肠炎(UC)和克罗恩病(CD)均与带状疱疹感染风险显著增加相关。在多变量 Cox 回归(与无 IBD 相比)中,UC、CD 或接受 5-ASA 单药治疗的 IBD 与带状疱疹风险显著增加相关,调整后的 HR(AHR)分别为 1.81(95%CI,1.56-2.11)、1.56(95%CI,1.28-1.91)和 1.72(95%CI,1.51-1.96)。在多变量 Cox 回归分析中,与单独使用 5-ASA 相比,使用硫嘌呤(AHR,1.47;95%CI,1.31-1.65)或硫嘌呤和 TNF 拮抗剂联合治疗(AHR,1.65;95%CI,1.22-2.23)与带状疱疹风险增加相关。然而,单独使用 TNF 拮抗剂(AHR,1.15;95%CI,0.96-1.38)与带状疱疹风险增加无关。所有年龄组和所有 IBD 药物亚组的带状疱疹发病率均明显高于无 IBD 患者中年龄最大的组(大于 60 岁)。
在两项基于退伍军人人群的回顾性研究中,我们发现 IBD 和单独或联合使用硫嘌呤、TNF 拮抗剂治疗与带状疱疹风险增加相关。随着一种新的、潜在更安全的带状疱疹疫苗的批准,应研究 IBD 患者免疫接种的效果。