University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.
Division of Gastroenterology, Washington University School of Medicine, St. Louis, Missouri, USA.
Inflamm Bowel Dis. 2022 Jan 5;28(1):70-78. doi: 10.1093/ibd/izab031.
Inflammatory bowel disease (IBD) is associated with alterations of the innate and adaptive immune systems. Monocytes respond to inflammation and infection, yet the relationship between monocytosis and IBD severity is not fully understood. We aimed to characterize the prevalence of monocytosis in IBD and the association between monocytosis and disease severity and IBD-related health care utilization.
We used a multiyear, prospectively collected natural history registry to compare patients with IBD with monocytosis to those without monocytosis, among all patients and by disease type.
A total of 1290 patients with IBD (64.1% with Crohn disease; 35.9% with ulcerative colitis) were included (mean age 46.4 years; 52.6% female). Monocytosis was found in 399 (30.9%) of patients with IBD (29.3% with Crohn disease; 33.9% with ulcerative colitis). Monocytosis was significantly associated with abnormal C-reactive protein level and erythrocyte sedimentation rate, anemia, worse quality of life, active disease, and increased exposure to biologics (all P < 0.001). Compared with patients without monocytosis, patients with monocytosis had a 3-fold increase in annual financial health care charges (median: $127,013 vs. $32,925, P < 0.001) and an increased likelihood of hospitalization (adjusted odds ratio [AOR], 4.5; P < 0.001), IBD-related surgery (AOR, 1.9; P = 0.002), and emergency department (ED) use (AOR, 2.8; P < 0.001). Patients with monocytosis had a shorter time to surgery, hospitalization, and ED visit after stratifying by disease activity (all P < 0.05).
Patients with IBD with monocytosis, regardless of disease type, are at increased risk for worse clinical outcomes, hospitalization, surgery, and ED use. Peripheral monocytosis may represent a routinely available biomarker of a distinct subgroup with severe disease.
炎症性肠病(IBD)与先天和适应性免疫系统的改变有关。单核细胞对炎症和感染作出反应,但单核细胞增多症与 IBD 严重程度之间的关系尚不完全清楚。我们旨在描述 IBD 中单核细胞增多症的患病率,以及单核细胞增多症与疾病严重程度和 IBD 相关医疗保健利用之间的关系。
我们使用了一个多年的前瞻性自然史登记处,比较了所有患者和不同疾病类型患者中 IBD 伴单核细胞增多症患者与不伴单核细胞增多症患者。
共纳入 1290 例 IBD 患者(64.1%为克罗恩病;35.9%为溃疡性结肠炎)(平均年龄 46.4 岁;52.6%为女性)。IBD 患者中有 399 例(30.9%)存在单核细胞增多症(29.3%为克罗恩病;33.9%为溃疡性结肠炎)。单核细胞增多症与异常 C 反应蛋白水平和红细胞沉降率、贫血、生活质量下降、疾病活动期和生物制剂暴露增加显著相关(均 P < 0.001)。与无单核细胞增多症的患者相比,有单核细胞增多症的患者每年的医疗保健费用增加了 3 倍(中位数:$127013 与$32925,P < 0.001),住院(校正优势比 [AOR],4.5;P < 0.001)、IBD 相关手术(AOR,1.9;P = 0.002)和急诊就诊(AOR,2.8;P < 0.001)的可能性增加。在按疾病活动分层后,单核细胞增多症患者的手术、住院和急诊就诊时间更短(均 P < 0.05)。
无论疾病类型如何,IBD 伴单核细胞增多症的患者发生更差的临床结局、住院、手术和急诊就诊的风险增加。外周血单核细胞增多症可能代表了一种可用于严重疾病的特定亚群的常规生物标志物。