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Association between tumor necrosis factor-alpha polymorphisms (rs361525, rs1800629, rs1799724, 1800630, and rs1799964) and risk of psoriasis in studies following Hardy-Weinberg equilibrium: A systematic review and meta-analysis

Journal

HELIYON
Volume 9, Issue 7, Pages -

Publisher

CELL PRESS
DOI: 10.1016/j.heliyon.2023.e17552

Keywords

Psoriasis; Cytokine; Tumor necrosis factor-alpha; Polymorphism; meta-Analysis

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This study examined the relationship between tumor necrosis factor-alpha (TNF-a) polymorphisms and the risk of psoriasis. The results showed that the -238 G/A rs361525 polymorphism and the -857C/T rs1799724 polymorphism were associated with an increased risk of psoriasis. The study recommends future well-designed studies with larger sample sizes to confirm these results.
Objective: Psoriasis is a disease with an immunogenetic background in which cytokines have important effects on its prevalence and incidence. The present meta-analysis evaluated the relationship between tumor necrosis factor-alpha (TNF-a) polymorphisms (rs361525, rs1800629, rs1799724, 1800630, and rs1799964) and psoriasis risk in studies following Hardy-Weinberg equilibrium (HWE). Materials and methods: Four databases were searched to retrieve relevant studies reporting the distributions of TNF-a polymorphisms in psoriasis cases compared to controls. The effect sizes were the 95% confidence intervals (CIs) and odds ratios (ORs). Subgroup analysis, sensitivity analyses, publication bias, trial sequential analysis (TSA), and meta-regression were performed on the initial pooled results of TNF-a polymorphisms.Results: Thirty-six articles with 71 studies were included in the meta-analysis (twenty-six: rs361525, twenty-seven: rs1800629, nine: rs1799724, four: 1800630, and five: rs1799964). The pooled ORs for-238 G/A rs361525 polymorphism were 2.33 (p < 0.00001), 2.79 (p < 0.0001), 2.35 (p < 0.00001), 2.44 (p < 0.00001), and 2.45 (p < 0.00001), as well as 1.57 (p < 0.00001), 1.98 (p = 0.01), 1.61 (p < 0.00001), 1.64 (p < 0.00001), and 1.79 (p < 0.00001) for-857 C/T rs1799724 polymorphism in allelic, homozygous, heterozygous, dominant, and recessive models, respectively. Ethnicity, psoriasis type, and sample size affected the pooled results of rs361525, rs1800629, and rs1799724 polymorphisms. Based on TSA, there were just sufficient cases for-238 G/A rs361525 polymorphism in five genetic models and-857C/T rs1799724 poly-morphism in allelic, heterozygous, and dominant models.Conclusions: The A allele and GA and GG genotypes of-238 G/A rs361525 polymorphism and T allele, TT and CT genotypes of-857C/T rs1799724 polymorphism were related to increased risks in psoriasis cases. Well-designed studies (with no deviation from HWE in controls) with more cases are recommended in the future.

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