Goud Veera Krishna, Goud Alladi Charanraj, Ramassamy Sivaranjini, Jayanthi M, Medha R, Chandrashekar Laxmisha
Department of Dermatology, JIPMER, Puducherry, 06 India.
Institute of Molecular and Translational Medicine, University of Palacky, Olomouc, Czech Republic.
Indian J Clin Biochem. 2025 Jan;40(1):89-96. doi: 10.1007/s12291-024-01269-x. Epub 2024 Sep 18.
Methotrexate is used to manage moderate to severe psoriasis and psoriatic arthritis. Methotrexate acts by inhibiting the enzymes involved in nucleotide synthesis. Methotrexate polyglutamates (MTXPGs) have a higher potency to inhibit Dihydrofolate reductase (DHFR), 5-aminoimidazole-4-carboxamide ribonucleotide transformylase (ATIC), and thymidylate synthase (TS), compared to naïve methotrexate. Among all the MTXPGs, methotrexate polyglutamate three (MTXPG-3) is a more potent inhibitor of DHFR, ATIC, and TS enzymes. MTXPG-3 is anticipated to allow therapeutic drug monitoring in immune-mediated inflammatory diseases. We aim to study MTXPG-3 levels as a biomarker for both efficacy and adverse events among psoriatic patients treated with methotrexate monotherapy. We used the LC-MS/MS (Liquid Chromatography Mass Spectrophotometry) system for measuring erythrocyte MTXPG-3. We recruited 106 patients with psoriasis who were treated with methotrexate. Sixty-one of them had psoriatic arthritis (concomitant or in the past). The mean age was 45.08 ± 13.04 years. After twenty-four weeks of methotrexate treatment, 73(69%) were responders, and 33(31%) were non-responders. Thirty-nine (36%) experienced adverse effects, and 67(64%) did not experience any adverse effects. We observed a significant positive correlation between erythrocyte MTXPG-3 and methotrexate dose per week at weeks 12 and 16 but not at week 24. Erythrocyte MTXPG-3 did not correlate with response or adverse effects. It can be used as a marker of compliance.
The online version contains supplementary material available at 10.1007/s12291-024-01269-x.
甲氨蝶呤用于治疗中度至重度银屑病和银屑病关节炎。甲氨蝶呤通过抑制参与核苷酸合成的酶发挥作用。与单纯的甲氨蝶呤相比,甲氨蝶呤多聚谷氨酸盐(MTXPGs)对二氢叶酸还原酶(DHFR)、5-氨基咪唑-4-甲酰胺核糖核苷酸转甲酰酶(ATIC)和胸苷酸合成酶(TS)具有更高的抑制效力。在所有的MTXPGs中,甲氨蝶呤三聚谷氨酸盐(MTXPG-3)是DHFR、ATIC和TS酶更有效的抑制剂。预计MTXPG-3可用于免疫介导性炎症疾病的治疗药物监测。我们旨在研究MTXPG-3水平作为接受甲氨蝶呤单药治疗的银屑病患者疗效和不良事件生物标志物的情况。我们使用液相色谱-串联质谱(LC-MS/MS)系统测量红细胞MTXPG-3。我们招募了106例接受甲氨蝶呤治疗的银屑病患者。其中61例患有银屑病关节炎(同时患有或既往有过)。平均年龄为45.08±13.04岁。甲氨蝶呤治疗24周后,73例(69%)为反应者,33例(31%)为无反应者。39例(36%)出现不良反应,67例(64%)未出现任何不良反应。我们观察到在第12周和第16周时红细胞MTXPG-3与每周甲氨蝶呤剂量之间存在显著正相关,但在第24周时无此相关性。红细胞MTXPG-3与反应或不良反应无关。它可作为依从性的标志物。
在线版本包含可在10.1007/s12291-024-01269-x获取的补充材料。