Morrow Ryan, Funk Ryan, Becker Mara, Sherman Ashley, Van Haandel Leon, Hudson Taina, Casini Rebecca, Shakhnovich Valentina
Children's Mercy Kansas City, Kansas City, MO 64108, USA.
University of Missouri Kansas City School of Medicine, Kansas City, MO 64108, USA.
Pharmaceuticals (Basel). 2021 May 14;14(5):463. doi: 10.3390/ph14050463.
Inside cells, the immunomodulator methotrexate (MTX) undergoes the addition of glutamates to form methotrexate polyglutamates (MTX-Glu)-promising biomarkers of systemic exposure and treatment response to MTX in rheumatology. MTX-Glu are underexplored in Inflammatory Bowel Disease (IBD), with no data in pediatrics. In this cross-sectional secondary analysis, we assessed the relationships between MTX-Glu and MTX dose and treatment response in pediatric IBD. Twenty-one children with IBD, receiving maintenance therapy with infliximab (IFX) and MTX, had MTX-Glu concentrations and IFX troughs/antibodies measured and disease activity assessed for comparison in remission vs. active IBD using non-parametric tests, with associations explored using Spearman's correlation (ρ) and regression analyses; SASv9.4 (α = 0.05). Total and long-chain MTX-Glu correlated with MTX dose (ρ = 0.51 and 0.56, respectively; ≤ 0.02). In children with Crohn's disease ( = 19), short-chain MTX-Glu were 2.5-fold higher in remission vs. active disease, approaching statistical significance ( = 0.066), with no statistical differences in IFX trough ( = 0.549) between groups. Our study highlights a potential role for long-chain MTX-Glu in the therapeutic drug monitoring of MTX in IBD. It is the first study in pediatric IBD and, although statistical significance was not reached, our findings also suggest that higher short-chain MTX-Glu levels may be associated with IBD treatment response to MTX in children.
在细胞内,免疫调节剂甲氨蝶呤(MTX)会添加谷氨酸形成甲氨蝶呤多聚谷氨酸盐(MTX-Glu),这有望成为风湿病学中MTX全身暴露和治疗反应的生物标志物。MTX-Glu在炎症性肠病(IBD)中的研究较少,儿科领域尚无相关数据。在这项横断面二次分析中,我们评估了儿科IBD中MTX-Glu与MTX剂量及治疗反应之间的关系。21名接受英夫利昔单抗(IFX)和MTX维持治疗的IBD患儿,测量了MTX-Glu浓度和IFX谷浓度/抗体,并使用非参数检验评估疾病活动度以比较缓解期与活动期IBD,通过Spearman相关性(ρ)和回归分析探索关联;使用SASv9.4(α = 0.05)。总MTX-Glu和长链MTX-Glu与MTX剂量相关(分别为ρ = 0.51和0.56;P≤0.02)。在克罗恩病患儿(n = 19)中,缓解期短链MTX-Glu比活动期高2.5倍,接近统计学意义(P = 0.066),两组间IFX谷浓度无统计学差异(P = 0.549)。我们的研究强调了长链MTX-Glu在IBD中MTX治疗药物监测中的潜在作用。这是儿科IBD领域的第一项研究,尽管未达到统计学意义,但我们的发现也表明,较高的短链MTX-Glu水平可能与儿童IBD对MTX的治疗反应相关。