Ahmed Zunirah, Lysek Michael, Zhang Nan, Malik Talha A
Department of Medicine, University of Alabama at Birmingham Montgomery, AL 36116, USA.
Department of Medicine, University of South Alabama, Mobile, AL 36617, USA.
J Clin Med Res. 2020 Jan;12(1):6-12. doi: 10.14740/jocmr4016. Epub 2020 Jan 6.
The aim was to study the association between six serological markers and Crohn's disease (CD) activity at an inflammatory bowel disease (IBD) referral center.
We designed a retrospective cohort study using adults (> 18 years) with CD followed for at least 1 year at University of Alabama at Birmingham. Baseline serological markers ASCA-IgA, ASCA-IgG, anti-OmpC IgA, anti-CBir1 IgG, anti-A4Fla2 IgG and anti-FlaX IgG were drawn at initial visit. Poisson regression was used to assess the longitudinal relationship between these markers drawn at baseline and rate of active clinical disease during follow-up.
Each marker, from 135 patients, was categorized into high vs. low. A Poisson regression model adjusted for age, gender, race, duration of disease, obesity, proton pump inhibitor; steroid and thiopurine use, and disease location demonstrated that CD patients with high anti-CBir1 IgG at baseline were approximately twice more likely to have active clinical disease (incidence rate ratio (IRR) 2.06, 95% confidence interval (CI) 1.28 - 3.33, P = 0.0032). The unadjusted Poisson regression model for A4Fla2 IgG antibody level did suggest that a high A4Fla2 IgG at baseline was associated with a higher likelihood of active CD (IRR 1.64, 95% CI 1.07, 2.53, P = 0.0238) which however, upon adjustment based on effect size, was not significant. The other four antibodies did not appear to predict clinical course.
High levels of anti-CBir1 IgG appear to be associated with a greater likelihood of active CD. Whether routine baseline testing for anti-CBir1 IgG to predict a more active clinical course is warranted needs more research.
本研究旨在探讨在一家炎症性肠病(IBD)转诊中心,六种血清学标志物与克罗恩病(CD)活动度之间的关联。
我们设计了一项回顾性队列研究,纳入了阿拉巴马大学伯明翰分校随访至少1年的成年(>18岁)CD患者。在初次就诊时检测基线血清学标志物抗酿酒酵母抗体IgA(ASCA-IgA)、抗酿酒酵母抗体IgG(ASCA-IgG)、抗OmpC IgA、抗CBir1 IgG、抗A4Fla2 IgG和抗FlaX IgG。采用泊松回归分析评估这些基线标志物与随访期间活动性临床疾病发生率之间的纵向关系。
对135例患者的每种标志物进行高值与低值分类。在调整了年龄、性别、种族、病程、肥胖、质子泵抑制剂使用情况、类固醇和硫唑嘌呤使用情况以及疾病部位的泊松回归模型中,基线抗CBir1 IgG水平高的CD患者出现活动性临床疾病的可能性约为两倍(发病率比(IRR)2.06,95%置信区间(CI)1.28 - 3.33,P = 0.0032)。抗A4Fla2 IgG抗体水平的未调整泊松回归模型表明,基线抗A4Fla2 IgG水平高与活动性CD的可能性较高相关(IRR 1.64,95%CI 1.07,2.53,P = 0.0238),然而,根据效应量进行调整后并不显著。其他四种抗体似乎无法预测临床病程。
抗CBir1 IgG水平高似乎与活动性CD的可能性更大相关。是否有必要进行抗CBir1 IgG的常规基线检测以预测更活跃的临床病程,还需要更多研究。