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Investigating the Association Between Blood Metabolites and Telomere Length: A Mendelian Randomization Study

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Journal PLoS One
Date 2024 Mar 8
PMID 38457472
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Abstract

Background: Telomere length refers to the protective cap at the end of chromosomes, and it plays a crucial role in many diseases. The objective of this study is to explore the relationship between blood metabolites and telomere length, aiming to identify novel biological factors that influence telomere length.

Methods: In this study, we extracted genome-wide association study (GWAS) data for blood metabolites from a sample of 7824 Europeans. Additionally, GWAS data for telomere length were obtained from the Open GWAS database (GWAS ID: ieu-b-4879). The primary analysis of this study utilized the random inverse variance weighted (IVW) method. Complementary analyses were also conducted using the MR-Egger and weighted median approaches. Sensitivity analyses were performed to assess the robustness of the findings. These included the Cochran Q test, MR-Egger intercept test, MR-PRESSO, and leave-one-out analysis. To investigate the possibility of reverse causation, reverse MR analysis was conducted. Additionally, multivariable MR was utilized to evaluate the direct effect of metabolites on telomere length.

Results: The results suggested a potential association between 15-methylpalmitate, taurocholate, levulinate, and X-12712 and telomere length. MVMR analysis further showed that 15-methylpalmitate, taurocholate, and levulinate can directly influence telomere length, regardless of other metabolites.

Conclusions: This study suggests that 15-methylpalmitate, taurocholate, and levulinate are likely factors correlated with telomere length. These findings will contribute to the development of strategies for protecting telomeres, preventing related diseases, and establishing a new biological foundation for achieving healthy aging.

References
1.
Amin N, Liu J, Bonnechere B, Mahmoudiandehkordi S, Arnold M, Batra R . Interplay of Metabolome and Gut Microbiome in Individuals With Major Depressive Disorder vs Control Individuals. JAMA Psychiatry. 2023; 80(6):597-609. PMC: 10116384. DOI: 10.1001/jamapsychiatry.2023.0685. View

2.
Andreu-Sanchez S, Aubert G, Ripoll-Cladellas A, Henkelman S, Zhernakova D, Sinha T . Genetic, parental and lifestyle factors influence telomere length. Commun Biol. 2022; 5(1):565. PMC: 9184499. DOI: 10.1038/s42003-022-03521-7. View

3.
Guan X, Fu W, Wei W, Li G, Wu X, Bai Y . Mediation of the association between polycyclic aromatic hydrocarbons exposure and telomere attrition by oxidative stress: A prospective cohort study. J Hazard Mater. 2020; 399:123058. DOI: 10.1016/j.jhazmat.2020.123058. View

4.
Schneider C, Schneider K, Teumer A, Rudolph K, Hartmann D, Rader D . Association of Telomere Length With Risk of Disease and Mortality. JAMA Intern Med. 2022; 182(3):291-300. PMC: 8767489. DOI: 10.1001/jamainternmed.2021.7804. View

5.
Fernandez-Alvira J, Fuster V, Dorado B, Soberon N, Flores I, Gallardo M . Short Telomere Load, Telomere Length, and Subclinical Atherosclerosis: The PESA Study. J Am Coll Cardiol. 2016; 67(21):2467-76. DOI: 10.1016/j.jacc.2016.03.530. View