Department of Hepatology and Gastroenterology, Aarhus University Hospital, 8200 Aarhus, Denmark.
Medical Department, Randers Regional Hospital, 8930 Randers, Denmark.
Nutrients. 2021 Mar 26;13(4):1083. doi: 10.3390/nu13041083.
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.
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).
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-.
Seven weeks high-dose vitamin D treatment reduces the need for later infliximab dose-escalation and reduces inflammatory markers. EudraCT no. 2013-000971-34.
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。
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。
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)。
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。