izpis_h1_title_alt

Polymorphism in gene for ABCC2 transporter predicts methotrexate drug survival in patients with psoriasis
ID Grželj, Jasna (Author), ID Marovt, Maruška (Author), ID Marko, Pij B. (Author), ID Mlinarič-Raščan, Irena (Author), ID Gmeiner, Tanja (Author), ID Šmid, Alenka (Author)

.pdfPDF - Presentation file, Download (865,71 KB)
MD5: 5A9A29310574538A3648B28EE2CDEF85
URLURL - Source URL, Visit https://www.mdpi.com/1648-9144/57/10/1050 This link opens in a new window

Abstract
Background and Objectives: Methotrexate is widely prescribed for the treatment of moderateto-severe psoriasis. As drug survival encompasses efficacy, safety, and treatment satisfaction, such studies provide insights into successful drug treatments in the real-life scenario. The objective was to define methotrexate drug survival and reasons for discontinuation, along with factors associated with drug survival, in a cohort of adult patients with moderate-to-severe plaque psoriasis. Materials and Methods: Data on methotrexate treatment were extracted from our institutional registry. Drug survival was estimated by Kaplan–Meier analysis, and predictors of drug survival were analyzed by Cox proportional hazards regression. Results: We included 133 patients treated with methotrexate. Due to significant effects of the year of treatment initiation, drug survival analysis was performed for 117 patients who started methotrexate in 2010 or later. Median methotrexate drug survival was 11.0 months. Overall, 89% of patients discontinued treatment, with over half of these (51%) due to lack of efficacy. Significantly longer drug survival was seen for patients who discontinued treatment due to lack of efficacy versus drug safety (p = 0.049); when stratified by sex, this remained significant only for women (p = 0.002). The patient ABCC2 rs717620 genotype was significantly associated with drug survival in both univariate log-rank and multivariate Cox regression analyses, with variant T allele associated with longer drug survival (hazard ratio, 0.606; 95% confidence interval, 0.380–0.967; p = 0.036). Conclusions: We have identified the novel association of patient ABCC2 rs717620 genotype with methotrexate drug survival. This pharmacogenetic marker might thus help in the management of psoriasis patients in daily practice.

Language:English
Keywords:psoriasis, drug survival, methotrexate, pharmacogenetics
Work type:Article
Typology:1.01 - Original Scientific Article
Organization:FFA - Faculty of Pharmacy
Publication status:Published
Publication version:Version of Record
Year:2021
Number of pages:12 str.
Numbering:Vol. 57, iss. 10, art. 1050
PID:20.500.12556/RUL-136272 This link opens in a new window
UDC:616.517-085
ISSN on article:1648-9144
DOI:10.3390/medicina57101050 This link opens in a new window
COBISS.SI-ID:79774723 This link opens in a new window
Publication date in RUL:21.04.2022
Views:754
Downloads:112
Metadata:XML DC-XML DC-RDF
:
Copy citation
Share:Bookmark and Share

Record is a part of a journal

Title:Medicina
Publisher:MDPI
ISSN:1648-9144
COBISS.SI-ID:6754623 This link opens in a new window

Licences

License:CC BY 4.0, Creative Commons Attribution 4.0 International
Link:http://creativecommons.org/licenses/by/4.0/
Description:This is the standard Creative Commons license that gives others maximum freedom to do what they want with the work as long as they credit the author.
Licensing start date:01.10.2021

Secondary language

Language:Slovenian
Keywords:metotreksat, zdravljenje luskavice, psoriaza, farmakogenetika

Projects

Funder:ARRS - Slovenian Research Agency
Project number:P1-0208
Name:Farmacevtska kemija: načrtovanje, sinteza in vrednotenje učinkovin

Funder:EC - European Commission
Funding programme:European Regional Development Fund
Project number:C333-19-952061
Acronym:EATRIS-TRI.SI

Similar documents

Similar works from RUL:
Similar works from other Slovenian collections:

Back