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Reverse causal relationship between periodontitis and shortened telomere length: Bidirectional two-sample Mendelian random analysis

Jiaxin Hu, Jukun Song, Zhu Chen, Jing Yang, Shi Qianhui, Fuqian Jin, Pang Qiyuan, Xingtao Chang, Yuan Tian, Yi Luo, Liming Chen

2022Frontiers in Immunology29 citationsDOIOpen Access PDF

Abstract

Background: Observational studies have demonstrated a link between shortened telomere lengths(TL) and chronic periodontitis. However, whether the shortened TL is the cause or the result of periodontitis is unknown.Therefore, our objective was to investigate a bidirectional causal relationship between periodontitis and TL using a two-sample Mendel randomized (MR) study. Methods: A two-sample bidirectional MR analysis using publicly available genome-wide association study (GWAS) data was used. As the primary analysis, inverse variance weighting (IVW) was employed. To identify pleiotropy, we used leave-one-out analysis, MR-Egger, Weighted median, Simple mode, Weighted mode, and MR pleiotropy residual sum and outlier (MR-PRESSO). Results: In reverse MR results, a genetic prediction of short TL was causally associated with a higher risk of periodontitis (IVW: odds ratio [OR]: 1.0601, 95% confidence interval [CI]: 1.0213 to 1.1002; P =0.0021) and other complementary MR methods. In the forward MR analysis, periodontitis was shown to have no significant effect on TL (IVW: p = 0.7242), with consistent results for the remaining complementary MR. No pleiotropy was detected in sensitivity analysis (all P>0.05). Conclusion: Our MR studies showed a reverse causal relationship, with shorten TL being linked to a higher risk of periodontitis, rather than periodontitis shorten that TL. Future research is needed to investigate the relationship between cell senescence and the disease.

Topics & Concepts

PeriodontitisPleiotropyOdds ratioMendelian randomizationMedicineConfidence intervalGenome-wide association studyInternal medicineBioinformaticsOncologySingle-nucleotide polymorphismGeneticsBiologyGenotypePhenotypeGenetic variantsGeneTelomeres, Telomerase, and SenescenceOral and Craniofacial LesionsEpigenetics and DNA Methylation