Xia Sheng-Long, Min Quan-Jia, Shao Xiao-Xiao, Lin Dao-Po, Ma Guo-Long, Wu Hao, Cao Shu-Guang, Jiang Yi
Department of Gastroenterology, The Second Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
Front Nutr. 2021 Oct 22;8:739285. doi: 10.3389/fnut.2021.739285. eCollection 2021.
It remains uncertain whether vitamin D3 (vitD3) supplementation is beneficial for remission of Crohn's disease (CD). The influence of vitD3 supplementation on Infliximab (IFX) effectiveness was analyzed in Chinese CD patients. In this retrospective cohort study, moderate-to-severe CD patients, who were bio-naïve and prescribed with IFX treatment for at least 54 weeks, were recorded from January 2014 to December 2019. VitD3 supplementation was defined as patients additionally took oral vitD3 (125 IU/d) within 3 days after the first infusion and persisted in the whole follow-up period. Disease activity was assessed using Harvey-Bradshaw Index (HBI). Serum cytokine profiles (IL-2, IL-4, IL-6, IL-10, TNF-α, and IFN-γ) were quantitatively analyzed in a subset of all patients at baseline and 54-week after intervention. Among 73 enrolled patients, 37 took vitD3 regularly (D3-patients), the others (non-D3-patients) did not. At 54-week, the mean 25-hydroxyvitaminD level increased in D3-patients (20.33 vs. 15.07 ng/mL, < 0.001). The clinical remission rate was higher in D3-patients compared to non-D3-patients (83.8 vs. 61.6%, = 0.030). The decrease of HBI from baseline to 54-week was more in D3-patients than non-D3-patients (7.41 ± 3.0 vs. 6.28 ± 2.75, = 0.023). Furthermore, vitD3 supplementation was independently related to the increase of remission rate at 54-week in D3-patients (β = -1.667, = 0.015). The benefit of vitD3 supplementation was significant only in patients with deficient vitD3 (all < 0.05), but not in non-deficient vitD3. A total of nine patients (four non-D3-patients and five D3-patients) were selected to determine serum cytokine profiles after 54-week IFX treatment. In non-D3-patients, the decreases of TNF-α and IL-6 at 54-week were more obvious than at baseline ( = 0.032, 0.022, respectively). In D3-patients, however, only IL-10 increased at 54-week compared with its baseline value ( = 0.037). VitD3 supplementation could improve IFX effectiveness in CD patients, especially for patients with vitD3 deficiency. This beneficial effect of vitD3 supplementation probably arose from the up-regulation of IL-10. NCT04606017.
维生素D3(vitD3)补充剂对克罗恩病(CD)缓解是否有益仍不确定。在中国CD患者中分析了补充vitD3对英夫利昔单抗(IFX)疗效的影响。在这项回顾性队列研究中,记录了2014年1月至2019年12月期间初治且接受IFX治疗至少54周的中重度CD患者。补充vitD3定义为患者在首次输注后3天内额外口服vitD3(125 IU/d),并在整个随访期持续服用。使用哈维-布拉德肖指数(HBI)评估疾病活动度。在所有患者的一个亚组中,于基线和干预后54周对血清细胞因子谱(IL-2、IL-4、IL-6、IL-10、TNF-α和IFN-γ)进行定量分析。在73例入组患者中,37例规律服用vitD3(D3组患者),其余患者(非D3组患者)未服用。在54周时,D3组患者的平均25-羟基维生素D水平升高(20.33对15.07 ng/mL,<0.001)。D3组患者的临床缓解率高于非D3组患者(83.8%对61.6%,=0.030)。从基线到54周,D3组患者HBI的下降幅度大于非D3组患者(7.41±3.0对6.28±2.75,=0.023)。此外,补充vitD3与D3组患者54周时缓解率的增加独立相关(β=-1.667,=0.015)。补充vitD3的益处仅在vitD3缺乏的患者中显著(均<0.05),而在非vitD3缺乏的患者中不显著。共选择9例患者(4例非D3组患者和5例D3组患者),在IFX治疗54周后测定血清细胞因子谱。在非D3组患者中,54周时TNF-α和IL-6的下降比基线时更明显(分别为=0.032,0.022)。然而,在D3组患者中,与基线值相比,仅54周时IL-10升高(=0.