The impacts of gene polymorphisms on methotrexate in Chinese psoriatic patients.


Journal

Journal of the European Academy of Dermatology and Venereology : JEADV
ISSN: 1468-3083
Titre abrégé: J Eur Acad Dermatol Venereol
Pays: England
ID NLM: 9216037

Informations de publication

Date de publication:
Sep 2020
Historique:
received: 23 10 2019
accepted: 24 03 2020
pubmed: 10 4 2020
medline: 15 5 2021
entrez: 10 4 2020
Statut: ppublish

Résumé

Methotrexate (MTX) is the first-line treatment for psoriasis in China. The metabolic processes of MTX include various proteins and genes. Previous studies have shown that gene polymorphisms had significant impacts on the efficacy of MTX. However, the influence of gene polymorphisms has not been reported in the Chinese psoriatic patients. The aim of this study was to verify the impacts of candidate genes polymorphisms on the effectiveness of MTX in a Chinese psoriatic population. In this study, we enrolled 259 psoriasis patients from two clinical centres. Each of them received MTX treatment at 7.5-15 mg/week for at least 8 weeks. Patients were stratified as responders and non-responders according to whether the Psoriasis Area and Severity Index score declined more than 75% (PASI75). According to previous reports, 16 single nucleotide polymorphisms (SNPs) were selected and genotyped for each patient using the Sequenom platform. Fisher's exact test, the chi-square test, Mann-Whitney tests and ANOVA analyses were used for statistical analysis. Among 259 patients, there were 182 males and 77 females, 63 patients with psoriatic arthritis and 196 patients without arthritis phenotype, and the age of all patients ranged from 19 to 70 years (49.7 ± 13.6). The baseline PASI value of patients was 13.8 ± 8.5, and 33.2% of patients achieved a PASI75 response after MTX treatment. Patients carrying the ATP-binding cassette subfamily B member 1 gene (ABCB1) rs1045642 TT genotype were associated with more severe psoriasis skin lesion (P = 0.032). Furthermore, the ABCB1 rs1045642 TT genotype was found to be more frequent in non-responders (P = 0.017), especially in moderate-to-severe patients (P = 0.002) and patients without psoriatic arthritis (P = 0.026) after MTX treatment. We have demonstrated for the first time that polymorphism of the ABCB1 rs1045642 TT genotype is predictive of a worse clinical response of skin lesions to MTX therapy in a Chinese psoriatic population.

Sections du résumé

BACKGROUND BACKGROUND
Methotrexate (MTX) is the first-line treatment for psoriasis in China. The metabolic processes of MTX include various proteins and genes. Previous studies have shown that gene polymorphisms had significant impacts on the efficacy of MTX. However, the influence of gene polymorphisms has not been reported in the Chinese psoriatic patients.
OBJECTIVE OBJECTIVE
The aim of this study was to verify the impacts of candidate genes polymorphisms on the effectiveness of MTX in a Chinese psoriatic population.
METHODS METHODS
In this study, we enrolled 259 psoriasis patients from two clinical centres. Each of them received MTX treatment at 7.5-15 mg/week for at least 8 weeks. Patients were stratified as responders and non-responders according to whether the Psoriasis Area and Severity Index score declined more than 75% (PASI75). According to previous reports, 16 single nucleotide polymorphisms (SNPs) were selected and genotyped for each patient using the Sequenom platform. Fisher's exact test, the chi-square test, Mann-Whitney tests and ANOVA analyses were used for statistical analysis.
RESULTS RESULTS
Among 259 patients, there were 182 males and 77 females, 63 patients with psoriatic arthritis and 196 patients without arthritis phenotype, and the age of all patients ranged from 19 to 70 years (49.7 ± 13.6). The baseline PASI value of patients was 13.8 ± 8.5, and 33.2% of patients achieved a PASI75 response after MTX treatment. Patients carrying the ATP-binding cassette subfamily B member 1 gene (ABCB1) rs1045642 TT genotype were associated with more severe psoriasis skin lesion (P = 0.032). Furthermore, the ABCB1 rs1045642 TT genotype was found to be more frequent in non-responders (P = 0.017), especially in moderate-to-severe patients (P = 0.002) and patients without psoriatic arthritis (P = 0.026) after MTX treatment.
CONCLUSION CONCLUSIONS
We have demonstrated for the first time that polymorphism of the ABCB1 rs1045642 TT genotype is predictive of a worse clinical response of skin lesions to MTX therapy in a Chinese psoriatic population.

Identifiants

pubmed: 32271961
doi: 10.1111/jdv.16440
doi:

Substances chimiques

Methotrexate YL5FZ2Y5U1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2059-2065

Subventions

Organisme : Central South University
ID : 2016GL03
Organisme : National Natural Science Foundation of China
ID : 81573049
Organisme : National Natural Science Foundation of China
ID : 81773329
Organisme : National Natural Science Foundation of China
ID : 81803118
Organisme : National Natural Science Foundation of China
ID : 81830096
Organisme : National Natural Science Foundation of China
ID : 81974479
Organisme : Science and Technology Innovation Foundation of Dalian, China
ID : 2019J13SN93
Organisme : Management Research Foundation of Xiangya Hospital

Informations de copyright

© 2020 European Academy of Dermatology and Venereology.

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Auteurs

M Chen (M)

The Department of Dermatology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Hunan Key Laboratory of Skin Cancer and Psoriasis, Changsha, Hunan, China.
Hunan Engineering Research Center of Skin Health and Disease, Changsha, Hunan, China.
Department of Dermatology, Hua Shan Hospital, Fu dan University, Shanghai, China.

W Chen (W)

The Department of Dermatology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Hunan Key Laboratory of Skin Cancer and Psoriasis, Changsha, Hunan, China.
Hunan Engineering Research Center of Skin Health and Disease, Changsha, Hunan, China.
Department of Dermatology, Hua Shan Hospital, Fu dan University, Shanghai, China.

P Liu (P)

The Department of Dermatology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Hunan Key Laboratory of Skin Cancer and Psoriasis, Changsha, Hunan, China.
Hunan Engineering Research Center of Skin Health and Disease, Changsha, Hunan, China.
Department of Dermatology, Hua Shan Hospital, Fu dan University, Shanghai, China.

K Yan (K)

Department of Dermatology, Dalian Dermatosis Hospital, Dalian, Liaoning, China.

C Lv (C)

Gerontology Center of Xiangya Hospital, Central South University, Changsha, Hunan, China.

M Zhang (M)

The Department of Dermatology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Hunan Key Laboratory of Skin Cancer and Psoriasis, Changsha, Hunan, China.
Hunan Engineering Research Center of Skin Health and Disease, Changsha, Hunan, China.
Department of Dermatology, Hua Shan Hospital, Fu dan University, Shanghai, China.

Y Lu (Y)

The Department of Dermatology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Hunan Key Laboratory of Skin Cancer and Psoriasis, Changsha, Hunan, China.
Hunan Engineering Research Center of Skin Health and Disease, Changsha, Hunan, China.
Department of Dermatology, Hua Shan Hospital, Fu dan University, Shanghai, China.

Q Qin (Q)

The Department of Dermatology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Hunan Key Laboratory of Skin Cancer and Psoriasis, Changsha, Hunan, China.
Hunan Engineering Research Center of Skin Health and Disease, Changsha, Hunan, China.
Department of Dermatology, Hua Shan Hospital, Fu dan University, Shanghai, China.

Y Kuang (Y)

The Department of Dermatology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Hunan Key Laboratory of Skin Cancer and Psoriasis, Changsha, Hunan, China.
Hunan Engineering Research Center of Skin Health and Disease, Changsha, Hunan, China.
Department of Dermatology, Hua Shan Hospital, Fu dan University, Shanghai, China.

W Zhu (W)

The Department of Dermatology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Hunan Key Laboratory of Skin Cancer and Psoriasis, Changsha, Hunan, China.
Hunan Engineering Research Center of Skin Health and Disease, Changsha, Hunan, China.
Department of Dermatology, Hua Shan Hospital, Fu dan University, Shanghai, China.

X Chen (X)

The Department of Dermatology, Xiangya Hospital, Central South University, Changsha, Hunan, China.
Hunan Key Laboratory of Skin Cancer and Psoriasis, Changsha, Hunan, China.
Hunan Engineering Research Center of Skin Health and Disease, Changsha, Hunan, China.
Department of Dermatology, Hua Shan Hospital, Fu dan University, Shanghai, China.

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