Ontology highlight
ABSTRACT: Aim
To investigate the effect of genetically proxied inhibition of tumor necrosis factor receptor 1 (TNFR1) on the risk of periodontitis.Materials and methods
Genetic instruments were selected from the vicinity of TNFR superfamily member 1A (TNFRSF1A) gene (chromosome 12; base pairs 6,437,923-6,451,280 as per GRCh37 assembly) based on their association with C-reactive protein (N= 575,531). Summary statistics of these variants were obtained from a genome-wide association study (GWAS) of 17,353 periodontitis cases and 28,210 controls to estimate the effect of TNFR1 inhibition on periodontitis using a fixed-effects inverse method.Results
Considering rs1800693 as an instrument, we found no effect of TNFR1 inhibition on periodontitis risk (Odds ratio (OR) scaled per standard deviation increment in CRP: 1.57, 95% confidence interval (CI): 0.38;6.46). Similar results were derived from a secondary analysis that used three variants (rs767455, rs4149570, and rs4149577) to index TNFR1 inhibition.Conclusions
We found no evidence of a potential efficacy of TNFR1 inhibition on periodontitis risk.
SUBMITTER: Alayash Z
PROVIDER: S-EPMC9949605 | biostudies-literature | 2023
REPOSITORIES: biostudies-literature
Alayash Zoheir Z Baumeister Sebastian-Edgar SE Holtfreter Birte B Kocher Thomas T Baurecht Hansjörg H Ehmke Benjamin B Reckelkamm Stefan Lars SL Nolde Michael M
Frontiers in immunology 20230209
<h4>Aim</h4>To investigate the effect of genetically proxied inhibition of tumor necrosis factor receptor 1 (TNFR1) on the risk of periodontitis.<h4>Materials and methods</h4>Genetic instruments were selected from the vicinity of TNFR superfamily member 1A (TNFRSF1A) gene (chromosome 12; base pairs 6,437,923-6,451,280 as per GRCh37 assembly) based on their association with C-reactive protein (N= 575,531). Summary statistics of these variants were obtained from a genome-wide association study (GW ...[more]