C-reactive protein-to-albumin ratio and neutrophil-to-albumin ratio for predicting response and prognosis to infliximab in ulcerative colitis

被引:2
|
作者
Zhang, Yanyan [1 ]
Xu, Feng [1 ]
Li, Ya [1 ]
Chen, Bing [1 ]
机构
[1] Zhengzhou Univ, Affiliated Hosp 1, Dept Gastroenterol, Zhengzhou, Peoples R China
关键词
ulcerative colitis; inflammatory bowel disease; biomarker; C-reactive protein-to-albumin ratio; neutrophil-to-albumin ratio; drug efficacy; ANTI-SACCHAROMYCES-CEREVISIAE; LYMPHOCYTE RATIO; BIOMARKERS; DISEASE; ANTIBODIES; OUTCOMES; THERAPY; IBD;
D O I
10.3389/fmed.2024.1349070
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The C-reactive protein-to-albumin ratio (CAR) and neutrophil-to-albumin ratio (NAR) serve as established markers for inflammatory diseases. However, limited studies have investigated their potential in predicting response and prognosis following infliximab (IFX) treatment. The objective of this paper was to evaluate feasibility of CAR and NAR as biomarkers to assess response to IFX induction therapy. Additionally, we attempted to determine the capacity to predict clinical remission in ulcerative colitis (UC) after 54 weeks of IFX treatment. We enrolled a total of 157 UC patients diagnosed via endoscopic mucosal biopsy at our hospital between October 2018 and June 2023. Additionally, 199 patients presenting with gastrointestinal symptoms, who underwent physical examinations, constituted the control group. Comprehensive clinical data, laboratory indicators, and endoscopic findings were systematically collected. CAR and NAR values were computed before treatment, post-induction, and subsequently at 8-week intervals. Comparisons between two groups were analyzed using the Wilcoxon rank-sum test or the independent samples t-test, and comparisons between multiple groups were analyzed using the one-way ANOVA (analysis of variance) or the Kruskal-Wallis rank sum test. We found CAR and NAR emerged as sensitive biomarkers for assessing disease activity. Notably, our findings indicated their dual predictive capability: foreseeing response post-IFX induction therapy and prognosticating the likelihood of UC patients achieving clinical remission following 54 weeks on IFX therapy.
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页数:10
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