Complement C3 as a potential drug target in periodontitis: Evidence from the cis-Mendelian randomization approach
- PMID: 37926509
- DOI: 10.1111/jcpe.13894
Complement C3 as a potential drug target in periodontitis: Evidence from the cis-Mendelian randomization approach
Abstract
Aim: Evidence from a Phase IIa trial showed that a complement C3-targeted drug reduced gingival inflammation in patients with gingivitis. Using drug-target Mendelian randomization (MR), we investigated whether genetically proxied C3 inhibition alters the risk of periodontitis.
Materials and methods: We used multiple 'cis' instruments from the vicinity of the encoding loci of C3. Instrument selection was restricted to the drug target encoding loci (chromosome 19; 6,677,715-6,730,573 (GRCh37/hg19)). We selected three uncorrelated single-nucleotide polymorphisms (rs141552034, rs145406915, rs11569479) that were associated with serum C3 levels (p value <1 × 10-4 ) from a genome-wide association study (GWAS) of 5368 European descent individuals. We extracted association statistics from a GWAS of 17,353 clinical periodontitis cases and 28,210 European controls. Wald ratios were combined using inverse-variance weighted meta-analysis to estimate the odds ratio (OR) of the genetically proxied inhibition of C3 in relation to periodontitis.
Results: MR analysis revealed that the inhibition of C3 reduces the odds of periodontitis (OR 0.91 per 1 standard deviation reduction in C3; 95% confidence interval 0.87-0.96, p value = .0003).
Conclusions: Findings from our MR analysis suggest a potential protective effect of C3 blockade against periodontitis.
Keywords: Mendelian randomization analysis; complement C3; drug discovery; immunomodulation; periodontitis.
© 2023 The Authors. Journal of Clinical Periodontology published by John Wiley & Sons Ltd.
Comment in
-
Complement C3 as a drug target in periodontitis.Br Dent J. 2023 Dec;235(12):965. doi: 10.1038/s41415-023-6670-3. Br Dent J. 2023. PMID: 38102271 No abstract available.
References
REFERENCES
-
- Balta, M. G., Papathanasiou, E., Blix, I. J., & van Dyke, T. E. (2021). Host modulation and treatment of periodontal disease. Journal of Dental Research, 100(8), 798-809. https://doi.org/10.1177/0022034521995157
-
- Burgess, S., Davey Smith, G., Davies, N. M., Dudbridge, F., Gill, D., Glymour, M. M., Hartwig, F. P., Holmes, M. V., Minelli, C., Relton, C. L., & Theodoratou, E. (2019). Guidelines for performing Mendelian randomization investigations. Wellcome Open Research, 4, 186. https://doi.org/10.12688/wellcomeopenres.15555.2
-
- Burgess, S., Foley, C. N., & Zuber, V. (2018). Inferring causal relationships between risk factors and outcomes from genome-wide association study data. Annual Review of Genomics and Human Genetics, 19, 303-327. https://doi.org/10.1146/annurev-genom-083117-021731
-
- Chapple, I. L. C. (2014). Time to take periodontitis seriously. BMJ (Clinical Research Ed.), 348, g2645. https://doi.org/10.1136/bmj.g2645
-
- Eke, P. I., Dye, B. A., Wei, L., Slade, G. D., Thornton-Evans, G. O., Borgnakke, W. S., Taylor, G. W., Page, R. C., Beck, J. D., & Genco, R. J. (2015). Update on prevalence of periodontitis in adults in the United States: NHANES 2009 to 2012. Journal of Periodontology, 86(5), 611-622. https://doi.org/10.1902/jop.2015.140520
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous