MTHFR gene polymorphisms and susceptibility to rheumatoid arthritis: a meta-analysis based on 16 studies.


Journal

Clinical rheumatology
ISSN: 1434-9949
Titre abrégé: Clin Rheumatol
Pays: Germany
ID NLM: 8211469

Informations de publication

Date de publication:
Aug 2020
Historique:
received: 02 12 2019
accepted: 05 03 2020
revised: 25 02 2020
pubmed: 15 3 2020
medline: 10 4 2021
entrez: 15 3 2020
Statut: ppublish

Résumé

Rheumatoid arthritis (RA) is the most common autoimmune rheumatic disease, in which an epigenetic implication in the disease etiopathogenesis has been noted. Here in this meta-analysis, we attempted to investigate the pooled association of methylenetetrahydrofolate reductase (MTHFR) gene C677T and A1298C polymorphisms and susceptibility to RA risk. A systematic search was performed in the main databases, including MEDLINE and Scopus to search for studies assessing the association between MTHFR gene C677T and A1298C polymorphisms and the risk of RA prior to December 2019. In this meta-analysis, 15 studies with 2165 patients and 1751 healthy controls for C677T SNP and 14 studies containing 2021 patients and 1760 healthy controls for A1298C SNP were included. A significant positive association between C677T SNP and RA risk was recognized in the dominant, recessive, and allelic model, but not TT and CT genotypes. The results indicated that the risk of RA in African population was increased under all genotype models while these results were repeated in Asian population just for recessive model, allelic model, and TT genotype. Moreover, the analysis of A1298C SNP demonstrated a significant association in overall population according to only the recessive model and CC genotype. Subgroup analysis according to the genotyping method indicated that RFLP-PCR method could impress the results of association between MTHFR gene A1298C and C677T SNPs and RA risk. The outcome of this meta-analysis indicated that MTHFR gene C677T SNP was much possibly be associated with RA risk.

Identifiants

pubmed: 32170488
doi: 10.1007/s10067-020-05031-5
pii: 10.1007/s10067-020-05031-5
doi:

Substances chimiques

MTHFR protein, human EC 1.5.1.20
Methylenetetrahydrofolate Reductase (NADPH2) EC 1.5.1.20

Types de publication

Journal Article Meta-Analysis Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

2267-2279

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Auteurs

Zahra Bagheri-Hosseinabadi (Z)

Department of Clinical Biochemistry, Faculty of Medicine, Rafsanjan University of Medical Sciences, Rafsanjan, Iran.

Danyal Imani (D)

Department of Immunology, School of Public Health, Tehran University of Medical Sciences (TUMS), Tehran, Iran.

Hassan Yousefi (H)

Department of Biochemistry and Molecular Biology, LSUHSC, School of Medicine, New Orleans, LA, USA.

Mitra Abbasifard (M)

Department of Internal Medicine, Ali-Ibn Abi-Talib Hospital, Rafsanjan University of Medical Sciences, Rafsanjan, Iran. rh.abbasi70@gmail.com.
Rheumatology Research Center, Tehran University of Medical Sciences (TUMS), Tehran, Iran. rh.abbasi70@gmail.com.

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