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

Aging (Albany NY). 2024 Apr 24;16(8):7387-7404. doi: 10.18632/aging.205765. Epub 2024 Apr 24.

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.

Keywords: bidirectional two-sample Mendelian randomization; causal relationship; mitochondrial DNA copy number; telomere length.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging* / genetics
  • Biomarkers
  • DNA Copy Number Variations*
  • DNA, Mitochondrial* / genetics
  • Genome-Wide Association Study*
  • Humans
  • Mendelian Randomization Analysis*
  • Telomere Homeostasis / genetics
  • Telomere Shortening / genetics
  • Telomere* / genetics

Substances

  • DNA, Mitochondrial
  • Biomarkers