Aug 2026· International Journal of Molecular Sciences· Vol 27· 0 citations· 46 references
Medicine
TL;DR
IL1RN rs4251961 may represent a novel genetic marker for PD, with clinical relevance given its inflammatory role and therapeutic use of recombinant IL-1RA in chronic inflammatory diseases, and supports validation in larger European cohorts.
Abstract
Periodontitis (PD), the second most prevalent oral disease, contributes to systemic health issues and results from a complex interaction between microbial dysbiosis and host immune responses, strongly shaped by genetic background. This pilot case–control study evaluated associations between five inflammation-related variants (IL1A rs1800587, IL1B rs1143634, IL1B rs16944, IL1RN rs4251961, TNFA rs1800629) and PD susceptibility in Portuguese postpartum women. Eighty-eight women (33 PD patients and 55 controls) were genotyped using iPLEX Gold technology. Associations were tested using logistic regression models, with multiple-testing correction applied to adjust significance thresholds. TNFA rs1800629 was associated with PD in the collapsed model (GA+AA vs. GG; OR = 3.3, p < 0.05). IL1RN rs4251961 showed strong associations across all models. In the codominant model, heterozygotes had increased PD odds (OR = 3.52, adjusted p < 0.05), while CC homozygotes showed 8-fold odds (OR = 8.1, adjusted p < 0.05). The collapsed model was also significant (p < 0.05). The remaining variants were not associated with PD. IL1RN rs4251961 may represent a novel genetic marker for PD, with clinical relevance given its inflammatory role and therapeutic use of recombinant IL-1RA in chronic inflammatory diseases. This first report linking IL1RN rs4251961 to PD supports validation in larger European cohorts.
Endometriosis is a chronic inflammatory disorder with a complex genetic etiology. The interleukin-17 (IL-17) family, particularly IL-17 A and IL-17 F, plays a critical role in driving pro-inflammatory responses within the peritoneal cavity. This case-control study investigated the association of IL17A rs2275913 and IL1...
D. Jahantigh, M. Taheri, F. Forghani et al.· Bratislava Medical Journal· 0 citations
Asthma is a chronic inflammatory airway disease strongly influenced by genetic factors. Interleukin-33 (IL-33), a key mediator of type 2 immune responses, has been implicated in airway inflammation and remodeling. However, the effects of IL-33 polymorphisms on asthma susceptibility and severity remain unclear, particul...
T. Hsia, Liang-Wen Hang, Te-Chun Shen et al.· Life· 0 citations
BACKGROUND
Ankylosing spondylitis (AS) is an inflammatory disorder exacerbated by the innate immune response. A 23-bp ins/del polymorphism at the 5'-untranslated region of the TLR-2 gene (rs111200466) is linked to varying expression levels of inflammatory cytokines, crucial in AS pathogenesis. This study examined the a...
V. Gopalaswamy, Subrat Pradhan, S. Tripathy et al.· Human Immunology· 0 citations
The A allele of the VDR ApaI (rs7975232) gene polymorphism was associated with increased susceptibility to psoriasis in Iraqi patients and AA carriers showed the lowest mean vitamin D3 and zinc levels and the highest mean ferritin level; however, genotype-related differences in these biochemical parameters were not sta...
Safana S. Dardouh, M. Mohammed, Mohammad M. F. Al-Halbosiy· Adolescência e Saúde· 0 citations
Our study examined the impact of IL6 −174 G/C (rs1800795) and IL18 −607 C/A (rs1946518) promoter polymorphisms on susceptibility to rheumatoid arthritis (RA) and protein/mRNA levels. RA patients had significantly higher serum IL-6 and IL-18 levels than controls; healthy men had higher IL-18 than women (p < 0.001). Conv...
V. Vasileva, G. Vasilev, M. Ivanova et al.· International Journal of Mol...· 0 citations
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