Please use this identifier to cite or link to this item: https://doi.org/10.1186/s12916-021-02030-4
Title: Investigating causal relationships between exposome and human longevity: a Mendelian randomization analysis
Authors: Huang, Shu-Yi
Yang, Yu-Xiang
Chen, Shi-Dong
Li, Hong-Qi
Zhang, Xue-Qing
Kuo, Kevin
Tan, Lan
Feng, Lei 
Dong, Qiang
Zhang, Can
Yu, Jin-Tai
Keywords: Exposome
Longevity
Mendelian randomization
Issue Date: 20-Jul-2021
Publisher: BioMed Central Ltd
Citation: Huang, Shu-Yi, Yang, Yu-Xiang, Chen, Shi-Dong, Li, Hong-Qi, Zhang, Xue-Qing, Kuo, Kevin, Tan, Lan, Feng, Lei, Dong, Qiang, Zhang, Can, Yu, Jin-Tai (2021-07-20). Investigating causal relationships between exposome and human longevity: a Mendelian randomization analysis. BMC Medicine 19 (1) : 150. ScholarBank@NUS Repository. https://doi.org/10.1186/s12916-021-02030-4
Rights: Attribution 4.0 International
Abstract: Background: Environmental factors are associated with human longevity, but their specificity and causality remain mostly unclear. By integrating the innovative “exposome” concept developed in the field of environmental epidemiology, this study aims to determine the components of exposome causally linked to longevity using Mendelian randomization (MR) approach. Methods: A total of 4587 environmental exposures extracting from 361,194 individuals from the UK biobank, in exogenous and endogenous domains of exposome were assessed. We examined the relationship between each environmental factor and two longevity outcomes (i.e., surviving to the 90th or 99th percentile age) from various cohorts of European ancestry. Significant results after false discovery rates correction underwent validation using an independent exposure dataset. Results: Out of all the environmental exposures, eight age-related diseases and pathological conditions were causally associated with lower odds of longevity, including coronary atherosclerosis (odds ratio = 0.77, 95% confidence interval [0.70, 0.84], P = 4.2 × 10−8), ischemic heart disease (0.66, [0.51, 0.87], P = 0.0029), angina (0.73, [0.65, 0.83], P = 5.4 × 10−7), Alzheimer’s disease (0.80, [0.72, 0.89], P = 3.0 × 10−5), hypertension (0.70, [0.64, 0.77], P = 4.5 × 10−14), type 2 diabetes (0.88 [0.80, 0.96], P = 0.004), high cholesterol (0.81, [0.72, 0.91], P = 0.0003), and venous thromboembolism (0.92, [0.87, 0.97], P = 0.0028). After adjusting for genetic correlation between different types of blood lipids, higher levels of low-density lipoprotein cholesterol (0.72 [0.64, 0.80], P = 2.3 × 10−9) was associated with lower odds of longevity, while high-density lipoprotein cholesterol (1.36 [1.13, 1.62], P = 0.001) showed the opposite. Genetically predicted sitting/standing height was unrelated to longevity, while higher comparative height size at 10 was negatively associated with longevity. Greater body fat, especially the trunk fat mass, and never eat sugar or foods/drinks containing sugar were adversely associated with longevity, while education attainment showed the opposite. Conclusions: The present study supports that some age-related diseases as well as education are causally related to longevity and highlights several new targets for achieving longevity, including management of venous thromboembolism, appropriate intake of sugar, and control of body fat. Our results warrant further studies to elucidate the underlying mechanisms of these reported causal associations. © 2021, The Author(s).
Source Title: BMC Medicine
URI: https://scholarbank.nus.edu.sg/handle/10635/231927
ISSN: 1741-7015
DOI: 10.1186/s12916-021-02030-4
Rights: Attribution 4.0 International
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