Genetic Markers of Methotrexate Treatment Failure in Psoriasis

<b>Background:</b> Pharmacogenetic markers associated with the need to switch patients from methotrexate (MTX) to biologic agents in moderate-to-severe psoriasis remain insufficiently studied. The pharmacokinetics of MTX depend on the individual characteristics of the patient, as well as on the function of specific transporters and enzymes involved in its absorption, distribution, metabolism, and elimination; therefore, polymorphisms in genes encoding these proteins may be considered pharmacogenetic predictors of MTX intolerance or insufficient efficacy. This study aimed to investigate genetic variants associated with MTX intolerance or insufficient efficacy leading to therapy switch. <b>Methods:</b> A total of 80 patients with moderate-to-severe psoriasis were included: 43 who required switching from MTX to biologics and 37 who continued MTX therapy. Twelve polymorphisms in transporter and metabolism-related genes (<i>ABCB1</i> (rs1045642), <i>MTHFR</i> (rs1801133), <i>ABCB1</i> (rs1128503), <i>ABCC2</i> (rs3740066), <i>ABCC2</i> (rs717620), <i>ABCG2</i> (rs2231137), <i>GSTP1</i> (rs1695), <i>SLC19A1</i> (rs1051266), <i>COL18A1</i> (rs9977268), <i>SLCO1B1</i> (rs2306283), <i>SLCO1B1</i> (rs4149056), and <i>ABCB1</i> (rs2229109)) were analyzed using next-generation sequencing. <b>Results:</b> Significant differences in genotype frequencies were observed for <i>SLC19A1</i> rs1051266 (<i>p</i> = 0.03) and <i>COL18A1</i> rs9977268 (<i>p</i> = 0.02). Carriers of the T allele in both genes were more frequent among patients requiring biologic therapy, suggesting a possible association with MTX intolerance or reduced efficacy. <b>Conclusions:</b> The study revealed an association between polymorphisms in the <i>SLC19A1</i> rs1051266 and <i>COL18A1</i> rs9977268 genes and the need to switch from MTX to biologic therapy in patients with moderate-to-severe psoriasis. These findings suggest that carriers of the C allele in these genes may have an increased risk of methotrexate intolerance.

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Journal
Journal of Personalized Medicine
Published
2025-12-25
DOI
https://doi.org/10.3390/jpm16010005
Primary Topic
Psoriasis: Treatment and Pathogenesis
Type
article
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article

Genetic Markers of Methotrexate Treatment Failure in Psoriasis

Sh. P. Abdullaev, Тучкова Светлана Николаевна, Karin Badavievich Mirzaev, Oleg S. Glotov et al.
Journal of Personalized Medicine
Psoriasis: Treatment and Pathogenesis
article

Genetic Markers of Methotrexate Treatment Failure in Psoriasis

Sh. P. Abdullaev, Тучкова Светлана Николаевна, Karin Badavievich Mirzaev, Oleg S. Glotov, Dmitry Alekseevich Sychev, P. A. Suchko, Andrey Sergeevich Glotov, Maria N. Vikhreva, Andrey A. Martynov, Olga A. Levashova
article en

Abstract

<b>Background:</b> Pharmacogenetic markers associated with the need to switch patients from methotrexate (MTX) to biologic agents in moderate-to-severe psoriasis remain insufficiently studied. The pharmacokinetics of MTX depend on the individual characteristics of the patient, as well as on the function of specific transporters and enzymes involved in its absorption, distribution, metabolism, and elimination; therefore, polymorphisms in genes encoding these proteins may be considered pharmacogenetic predictors of MTX intolerance or insufficient efficacy. This study aimed to investigate genetic variants associated with MTX intolerance or insufficient efficacy leading to therapy switch. <b>Methods:</b> A total of 80 patients with moderate-to-severe psoriasis were included: 43 who required switching from MTX to biologics and 37 who continued MTX therapy. Twelve polymorphisms in transporter and metabolism-related genes (<i>ABCB1</i> (rs1045642), <i>MTHFR</i> (rs1801133), <i>ABCB1</i> (rs1128503), <i>ABCC2</i> (rs3740066), <i>ABCC2</i> (rs717620), <i>ABCG2</i> (rs2231137), <i>GSTP1</i> (rs1695), <i>SLC19A1</i> (rs1051266), <i>COL18A1</i> (rs9977268), <i>SLCO1B1</i> (rs2306283), <i>SLCO1B1</i> (rs4149056), and <i>ABCB1</i> (rs2229109)) were analyzed using next-generation sequencing. <b>Results:</b> Significant differences in genotype frequencies were observed for <i>SLC19A1</i> rs1051266 (<i>p</i> = 0.03) and <i>COL18A1</i> rs9977268 (<i>p</i> = 0.02). Carriers of the T allele in both genes were more frequent among patients requiring biologic therapy, suggesting a possible association with MTX intolerance or reduced efficacy. <b>Conclusions:</b> The study revealed an association between polymorphisms in the <i>SLC19A1</i> rs1051266 and <i>COL18A1</i> rs9977268 genes and the need to switch from MTX to biologic therapy in patients with moderate-to-severe psoriasis. These findings suggest that carriers of the C allele in these genes may have an increased risk of methotrexate intolerance.

Journal of Personalized MedicineVol. 16(1)
St Petersburg University (RU), Research Institute of Obstetrics and Gynecology named after D.O. Ott (RU), Children's Scientific and Clinical Center for Infectious Diseases of the Federal Medical and Biological Agency (RU), Russian Medical Academy of Continuous Professional Education (RU), Scientific Research Institute of Healthcare Organization and Medical Management (RU), Russian Scientific Center of Surgery (RU), Federal Medical-Biological Agency (RU)
Good health and well-being
Openalex Percentile: Top 36%
Psoriasis: Treatment and Pathogenesis
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