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高剂量维生素 D 治疗 7 周可减少克罗恩病患者在一年随访期间需要进行英夫利昔单抗剂量升级的需求,并降低炎症标志物水平。

Seven Weeks of High-Dose Vitamin D Treatment Reduces the Need for Infliximab Dose-Escalation and Decreases Inflammatory Markers in Crohn's Disease during One-Year Follow-Up.

机构信息

Department of Hepatology and Gastroenterology, Aarhus University Hospital, 8200 Aarhus, Denmark.

Medical Department, Randers Regional Hospital, 8930 Randers, Denmark.

出版信息

Nutrients. 2021 Mar 26;13(4):1083. doi: 10.3390/nu13041083.

Abstract

BACKGROUND

Seven weeks of high-dose vitamin D treatment decreases intestinal IL17A and IFN-γ mRNA expression in active Crohn's disease (CD). In this follow-up study, we investigated whether seven-week vitamin D treatment affected the infliximab response in the following 45 weeks compared to placebo.

METHODS

CD patients ( = 40) were initially randomised into four groups: infliximab + vitamin-D; infliximab + placebo-vitamin-D; placebo-infliximab + vitamin-D; and placebo-infliximab + placebo-vitamin-D. Infliximab (5 mg/kg) or placebo-infliximab was administered at weeks 0, 2 and 6. Vitamin D (5 mg bolus followed by 0.5 mg/day for 7 weeks) or placebo-vitamin D was handed out. After the 7-week vitamin D period, all patients received infliximab during follow-up. Results are reported for Group D+ (infliximab + vitamin-D and placebo-infliximab + vitamin-D) and Group D- (infliximab + placebo-vitamin-D and placebo-infliximab + placebo-vitamin-D).

RESULTS

Group D- patients had greater needs for infliximab dose escalation during follow-up compared to group D+ ( = 0.05). Group D+ had lower median calprotectin levels week 15 ( = 0.02) and week 23 ( = 0.04) compared to group D-. Throughout follow-up, group D+ had 2.2 times (95% CI: 1.1-4.3) ( = 0.02) lower median CRP levels compared with group D-.

CONCLUSIONS

Seven weeks high-dose vitamin D treatment reduces the need for later infliximab dose-escalation and reduces inflammatory markers. EudraCT no. 2013-000971-34.

摘要

背景

七周高剂量维生素 D 治疗可降低活动期克罗恩病(CD)患者的肠道 IL17A 和 IFN-γ mRNA 表达。在这项随访研究中,我们研究了与安慰剂相比,七周维生素 D 治疗是否会影响随后 45 周的英夫利昔单抗反应。

方法

CD 患者(n=40)最初随机分为四组:英夫利昔单抗+维生素 D;英夫利昔单抗+安慰剂-维生素 D;安慰剂-英夫利昔单抗+维生素 D;安慰剂-英夫利昔单抗+安慰剂-维生素 D。在第 0、2 和 6 周时给予英夫利昔单抗(5mg/kg)或安慰剂-英夫利昔单抗。在第 7 周维生素 D 期结束后,所有患者在随访期间接受英夫利昔单抗治疗。报告了组 D+(英夫利昔单抗+维生素 D 和安慰剂-英夫利昔单抗+维生素 D)和组 D-(英夫利昔单抗+安慰剂-维生素 D 和安慰剂-英夫利昔单抗+安慰剂-维生素 D)的结果。

结果

与组 D+相比,组 D-患者在随访期间需要更多的英夫利昔单抗剂量升级(=0.05)。与组 D-相比,组 D+患者在第 15 周(=0.02)和第 23 周(=0.04)的中位钙卫蛋白水平更低。在整个随访期间,与组 D-相比,组 D+的 CRP 水平中位数低 2.2 倍(95%CI:1.1-4.3)(=0.02)。

结论

七周高剂量维生素 D 治疗可减少后期英夫利昔单抗剂量升级的需要,并降低炎症标志物。EudraCT 编号 2013-000971-34。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a4c/8065492/93f51b607684/nutrients-13-01083-g001.jpg

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