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New insights from bidirectional Mendelian randomization: causal relationships between telomere length and mitochondrial DNA copy number in aging biomarkers

Xinyu Yan, Peixuan Yang, Yani Li, Ting Liu, Yawen Zha, Ting Wang, Jingjing Zhang, Zhijun Feng, Min-Ying Li

2024Aging17 citationsDOIOpen Access PDF

Abstract

Mitochondrial DNA (mtDNA) copy number and telomere length (TL) are dynamic factors that have been linked to the aging process in organisms.However, the causal relationship between these variables remains uncertain.In this research, instrumental variables (IVs) related to mtDNA copy number and TL were obtained from publicly available genome-wide association studies (GWAS).Through bidirectional Mendelian randomization (MR) analysis, we examined the potential causal relationship between these factors.The forward analysis, with mtDNA copy number as the exposure and TL as the outcome, did not reveal a significant effect (B=-0.004,P>0.05).On the contrary, upon conducting a reverse analysis, it was found that there exists a positive causal relationship (B=0.054,P<0.05).Sensitivity analyses further confirmed the reliability of these results.The outcomes of this study indicate a one-way positive causal relationship, indicating that telomere shortening in the aging process may lead to a decrease in mtDNA copy number, providing new perspectives on their biological mechanisms.

Topics & Concepts

Mendelian randomizationTelomereBiologyMitochondrial DNAGeneticsCopy-number variationComputational biologyNon-Mendelian inheritanceCellular AgingEvolutionary biologyDNAGenomeGeneGenotypeGenetic variantsTelomeres, Telomerase, and SenescenceMitochondrial Function and PathologyGenetics, Aging, and Longevity in Model Organisms
New insights from bidirectional Mendelian randomization: causal relationships between telomere length and mitochondrial DNA copy number in aging biomarkers | Litcius