Zhongshan City People’s Hospital, Xinxiang Medical University, Xinxiang 453003, Henan, China.
Department of Radiation Oncology, Zhongshan City People’s Hospital, Zhongshan 528403, Guangdong, China.
Aging (Albany NY). 2024 Apr 24;16(8):7387-7404. doi: 10.18632/aging.205765.
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 (=-0.004, >0.05). On the contrary, upon conducting a reverse analysis, it was found that there exists a positive causal relationship (=0.054, <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.
线粒体 DNA(mtDNA)拷贝数和端粒长度(TL)是与生物体衰老过程相关的动态因素。然而,这些变量之间的因果关系尚不确定。在这项研究中,我们从公开的全基因组关联研究(GWAS)中获得了与 mtDNA 拷贝数和 TL 相关的工具变量(IVs)。通过双向孟德尔随机化(MR)分析,我们研究了这些因素之间潜在的因果关系。正向分析中,以 mtDNA 拷贝数为暴露因素,TL 为结局因素,未发现显著关联(=-0.004,>0.05)。相反,进行反向分析时,发现存在正向因果关系(=0.054,<0.05)。敏感性分析进一步证实了这些结果的可靠性。本研究的结果表明存在单向的正因果关系,提示衰老过程中端粒缩短可能导致 mtDNA 拷贝数减少,为它们的生物学机制提供了新的视角。