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Meta-Analysis
. 2024 Feb;51(2):127-134.
doi: 10.1111/jcpe.13894. Epub 2023 Nov 5.

Complement C3 as a potential drug target in periodontitis: Evidence from the cis-Mendelian randomization approach

Affiliations
Meta-Analysis

Complement C3 as a potential drug target in periodontitis: Evidence from the cis-Mendelian randomization approach

Zoheir Alayash et al. J Clin Periodontol. 2024 Feb.

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.

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References

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