Associations of MEFV gene variants, IL-33, and sST2 with the risk of Henoch-Schönlein purpura in children

• Published in: Heliyon Vol. 10; no. 8; p. e29469
• Main Authors: Ruan, Yang, Xie, Longlong
• Format: Journal Article
• Language: English
• Published: England Elsevier Ltd 30.04.2024; Elsevier
• Subjects: alleles; C-reactive protein; Children; exons; familial Mediterranean fever; Henoch-Schönlein purpura; hospitals; Interleukin-33; MEFV; pathogenesis; pathogenicity; physical health; regression analysis; risk; Soluble ST2; vasculitis; Henoch-Schönlein purpura; Children; Soluble ST2; MEFV; Interleukin-33
• ISSN: 2405-8440; 2405-8440
• DOI: 10.1016/j.heliyon.2024.e29469

Henoch-Schönlein purpura (HSP) is the most common systemic vasculitis in children. HSP is a multifactorial inflammatory disease, but its pathogenesis is still unclear. The pathogenicity of familial Mediterranean fever gene (MEFV) variants in HSP remains controversial. The objective of this study was to evaluate relationships between MEFV variants and susceptibility to HSP and their associations with clinical outcomes. We also investigated levels of IL-33 and soluble suppression of tumorigenicity 2 (sST2) in children with HSP and their clinical significance. We selected 100 children with HSP as the case group. The control group consisted of 50 children who visited the hospital for physical health examinations. All subjects were screened for MEFV gene exon mutations, and levels of IL-33 and sST2 were measured. The frequency of MEFV variants was significantly greater in HSP patients than in healthy controls. The variant with the highest frequency was E148Q. The frequency of the C allele of the MEFV variant E148Q was 32 % in HSP patients and 18 % in controls (P-adjust = 0.04). Patients with the MEFV E148Q variant had more frequent joint involvement and recurrent purpura and higher levels of IL-33 and C-reactive protein (CRP). Levels of IL-33 and sST2 in children with HSP were significantly higher than those in the control group, and the sST2/IL-33 ratio in children with HSP was unbalanced (P-adjust <0.05). Logistic regression analysis revealed the presence of E148Q and an unbalanced sST2/IL-33 ratio to be independent risk factors for HSP. The results of this study suggest that the MEFV variant E148Q is associated with HSP susceptibility in Chinese children and that carriers of the variant may have more severe clinical manifestations and greater inflammatory responses. E148Q and the sST2/IL-33 ratio may play important roles in the pathogenesis of HSP.