Are gene polymorphisms related to adverse events of methotrexate in patients with rheumatoid arthritis? A retrospective cohort study based on an updated meta-analysis

Author:

Huang Jing12,Fan Huizhen3,Qiu Qi4,Liu Kunpeng5,Lv Shuang67,Li Jiang8,Yang Hui8,Shu Xiaoming9,Xu Yuan10,Lu Xiangchen67,Lu Cheng11,Zhang Yunnan4,Xiao Cheng167ORCID

Affiliation:

1. Department of Emergency, China-Japan Friendship Hospital, Beijing, China

2. School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing, China

3. Department of Gastroenterology, People’s Hospital of Yichun, Jiangxi Yichun, China

4. Institute of Clinical Pharmacology, Beijing An Zhen Hospital, Capital Medical University, Beijing, China

5. Department of Anesthesiology, Peking University International Hospital, Beijing, China

6. Institute of Clinical Medicine, China-Japan Friendship Hospital, Beijing, China

7. Beijing University of Chinese Medicine, Beijing, China

8. Department of Laboratory Medicine, China-Japan Friendship Hospital, Beijing, China

9. Department of Rheumatology, China-Japan Friendship Hospital, Beijing, China

10. Department of TCM Rheumatology, China-Japan Friendship Hospital, Beijing, China

11. Institute of Basic Research in Clinical Medicine, China Academy of Chinese Medical Sciences, Beijing, China

Abstract

Aims: We performed an updated meta-analysis to verify correlations between gene polymorphisms and adverse events in methotrexate (MTX)-treated rheumatoid arthritis (RA) patients. Then, we conducted a retrospective cohort study of Han Chinese in China. Methods: Relevant studies were collected from the PubMed database and the EMBASE database until December 2017. Pre-allele, dominant, recessive, codominant, and homozygotic models were applied. In addition, a retrospective cohort study enrolling 162 RA patients treated with MTX was conducted. Single nucleotide polymorphism (SNP) genotyping was analyzed by PCR and product sequencing. Results: A total of 39 studies were included in 20 meta-analyses; meta-analysis showed a significant association between MTX-related toxicity and 5,10-methylenetetrahydrofolate reductase (MTHFR) 677C>T(rs1801133) polymorphism in East Asian RA patients, and significant associations were observed between MTX-related toxicity and 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase (ATIC) 347C>G (rs2372536), reduced folate carrier 1 (RFC-1) 80G>A (rs1051266), and adenosine triphosphate-binding cassette B1 (ABCB1) 3435C>T(rs1045642) polymorphisms in European RA patients but not in East Asian RA patients. Moreover, in our retrospective cohort study, ATIC 347C>G(rs2372536) and ABCB1 3435C>T(rs1045642) polymorphisms were not associated with MTX-related toxicity. However, a significant association was observed between MTX-related toxicity and RFC-1 80G>A (rs1051266) polymorphism in Chinese Han RA patients. Conclusion: Evidence-based results suggest that the MTHFR 677C>T(rs1801133), ATIC 347C>G(rs2372536), RFC-1 80G>A (rs1051266), ABCB1 3435C>T(rs1045642) polymorphisms are associated with MTX-related toxicity. Larger and more stringent study designs may provide more accurate findings for the effects of these SNPs on MTX-related toxicity, and larger sample-size studies of the Chinese Han population should be conducted for further validation.

Funder

International Cooperation Project of the Ministry of Science and Technology

Publisher

SAGE Publications

Subject

Medicine (miscellaneous)

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