Uehara Sekiko, Hirai Keita, Shirai Toshihiro, Otaki Hinako, Akamatsu Taisuke, Itoh Kunihiko
Department of Clinical Pharmacology & Genetics, School of Pharmaceutical Sciences, University of Shizuoka, 52-1 Yada, Suruga-ku, Shizuoka 422-8526, Japan.
Department of Clinical Pharmacology and Therapeutics, Shinshu University Graduate School of Medicine, 3-1-1 Asahi, Matsumoto, Nagano 390-8621, Japan.
Biol Pharm Bull. 2025;48(1):86-92. doi: 10.1248/bpb.b24-00684.
Vitamin D plays a crucial role in immune system function. Several studies have indicated that genetic variations in the vitamin D receptor (VDR) and vitamin D binding protein (VDBP, encoded by GC gene) increase the risk of developing asthma. However, the effect of these variations on the prognosis and clinical outcomes of asthma remains unclear. This study, involving 152 adult patients with asthma, aimed to assess the influence of VDR and GC polymorphisms on asthma severity and its exacerbation. Gene polymorphisms previously associated with asthma risk were analyzed, and VDR mRNA expression levels were evaluated in peripheral blood mononuclear cells. The AA genotype of the VDR rs2228570 polymorphism was associated with an elevated risk of severe asthma compared to the AG/GG genotype (odds ratio, 3.20; 95% confidence interval [CI], 1.24-8.28). Furthermore, patients with the rs2228570 AA genotype showed an elevated risk of exacerbation during the 1-year follow-up period (hazard ratio, 4.01; 95% CI, 1.75-9.15). VDR mRNA expression was significantly reduced in patients with the AA genotype. Furthermore, the mRNA expression levels of GLCCI1, HDAC2, NR3C1, and NFE2L2, which are associated with steroid response, were reduced in patients with the AA genotype. Our findings indicate that patients with the AA genotype of VDR rs2228570 are more likely to experience severe asthma and exacerbations. This polymorphism has the potential to reduce vitamin D efficacy by altering VDR function and expression, potentially resulting in increased inflammation and reduced steroid responsiveness in patients with asthma.
维生素D在免疫系统功能中起着至关重要的作用。多项研究表明,维生素D受体(VDR)和维生素D结合蛋白(VDBP,由GC基因编码)的基因变异会增加患哮喘的风险。然而,这些变异对哮喘预后和临床结局的影响仍不清楚。本研究纳入了152例成年哮喘患者,旨在评估VDR和GC基因多态性对哮喘严重程度及其加重的影响。分析了先前与哮喘风险相关的基因多态性,并评估了外周血单个核细胞中VDR mRNA表达水平。与AG/GG基因型相比,VDR rs2228570多态性的AA基因型与严重哮喘风险升高相关(优势比,3.20;95%置信区间[CI],1.24 - 8.28)。此外,rs2228570 AA基因型的患者在1年随访期内加重风险升高(风险比,4.01;95% CI,1.75 - 9.15)。AA基因型患者的VDR mRNA表达显著降低。此外,与类固醇反应相关的GLCCI1、HDAC2、NR3C1和NFE2L2的mRNA表达水平在AA基因型患者中降低。我们的研究结果表明,VDR rs2228570的AA基因型患者更易发生严重哮喘和病情加重。这种多态性可能通过改变VDR功能和表达来降低维生素D的疗效,从而可能导致哮喘患者炎症增加和类固醇反应性降低。