Evaluating the predictive effect of vitamin D on clinical outcomes of infliximab-treated Crohn's disease patients

评估维生素D对英夫利昔单抗治疗的克罗恩病患者临床结局的预测作用

阅读:1

Abstract

BACKGROUNDS: The aim of this study was to examine the clinical predictors of Infliximab (IFX) in Crohn's disease (CD) patients in eastern China and to support further research on the vitamin D remission rate compared to CD patients. METHODS: Patients with CD who were hospitalized at Xuzhou First People's Hospital between January 2020 and December 2023 were included in our retrospective analysis. Clinical information was gathered from CD patients at baseline and the endpoint (7th IFX therapy, 38 weeks). To determine the baseline variable [Crohn's Disease Activity Index (CDAI) < 150] for endpoint clinical remission in patients receiving IFX, and to examine the relationship between blood vitamin D (VIT-D) levels before starting IFX medication and CDAI at Week 38. The potential risk variables were then investigated using univariate, multivariate, and LASSO regression models. RESULTS: Included were 158 individuals with CD treated with IFX. At baseline, 18.35% of patients had a VIT-D deficit; 64.19% of patients experienced a decrease in VIT-D, and 63.29% of patients achieved clinical remission. The high Vitamin D levels at baseline were independent predictors of clinical remission after IFX therapy, according to univariate, multivariate, and LASSO regression analysis (P < 0.05). Receiver operating characteristic curve analysis revealed that AUC (95%CI) 0.56(0.25-0.95) was the endpoint CDAI (= 150) diagnostic value when the Vit-D level was 19.35 ng/ml. The corresponding sensitivity and specificity were 75.02% and 79.6%. Endpoint CDAI was independently predicted by male sex, age, BMI, and VIT-D levels <30 ng/ml (P < 0.05). CONCLUSION: After receiving IFX therapy, CD patients in eastern China with higher VIT-D levels were more likely to achieve clinical remission, particularly those who were male, older, had a higher BMI, and had VIT-D levels below 30 ng/ml.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。