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Associations of triglyceride levels with longevity and frailty: A Mendelian randomization analysis
Observational studies suggest associations of triglyceride levels with longevity and frailty. This study aimed to test whether the associations are causal. We used data from the Rugao Longevity and Ageing Study, a population-based cohort study performed in Rugao, China. A variant in the APOA5 gene r...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5278549/ https://www.ncbi.nlm.nih.gov/pubmed/28134330 http://dx.doi.org/10.1038/srep41579 |
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author | Liu, Zuyun Burgess, Stephen Wang, Zhengdong Deng, Wan Chu, Xuefeng Cai, Jian Zhu, Yinsheng Shi, Jianming Xie, Xuejuan Wang, Yong Jin, Li Wang, Xiaofeng |
author_facet | Liu, Zuyun Burgess, Stephen Wang, Zhengdong Deng, Wan Chu, Xuefeng Cai, Jian Zhu, Yinsheng Shi, Jianming Xie, Xuejuan Wang, Yong Jin, Li Wang, Xiaofeng |
author_sort | Liu, Zuyun |
collection | PubMed |
description | Observational studies suggest associations of triglyceride levels with longevity and frailty. This study aimed to test whether the associations are causal. We used data from the Rugao Longevity and Ageing Study, a population-based cohort study performed in Rugao, China. A variant in the APOA5 gene region (rs662799) was used as the genetic instrument. Mendelian randomization (MR) analyses were performed to examine the associations of genetically predicted triglycerides with two ageing phenotypes – longevity ( ≥95 years) and frailty (modified Fried frailty phenotype and Rockwood frailty index). C allele of rs662799 was robustly associated with higher triglyceride levels in the comparison group (β = 0.301 mmol/L per allele, p < 0.001), with an F statistic of 95.3 and R(2) = 0.040. However MR analysis did not provide strong evidence for an association between genetically predicted triglyceride levels and probability of longevity (OR: 0.61; 95% CI: 0.35, 1.07 per 1 mmol/L increase in triglycerides). In the ageing arm (70–84 years), genetically predicted triglyceride levels were not associated with the frailty index (β = 0.008; 95% CI: −0.013, 0.029) or the frailty phenotype (OR: 1.91; 95% CI: 0.84, 4.37). In conclusion, there is currently a lack of sufficient evidence to support causal associations of triglyceride levels with longevity and frailty in elderly populations. |
format | Online Article Text |
id | pubmed-5278549 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52785492017-02-03 Associations of triglyceride levels with longevity and frailty: A Mendelian randomization analysis Liu, Zuyun Burgess, Stephen Wang, Zhengdong Deng, Wan Chu, Xuefeng Cai, Jian Zhu, Yinsheng Shi, Jianming Xie, Xuejuan Wang, Yong Jin, Li Wang, Xiaofeng Sci Rep Article Observational studies suggest associations of triglyceride levels with longevity and frailty. This study aimed to test whether the associations are causal. We used data from the Rugao Longevity and Ageing Study, a population-based cohort study performed in Rugao, China. A variant in the APOA5 gene region (rs662799) was used as the genetic instrument. Mendelian randomization (MR) analyses were performed to examine the associations of genetically predicted triglycerides with two ageing phenotypes – longevity ( ≥95 years) and frailty (modified Fried frailty phenotype and Rockwood frailty index). C allele of rs662799 was robustly associated with higher triglyceride levels in the comparison group (β = 0.301 mmol/L per allele, p < 0.001), with an F statistic of 95.3 and R(2) = 0.040. However MR analysis did not provide strong evidence for an association between genetically predicted triglyceride levels and probability of longevity (OR: 0.61; 95% CI: 0.35, 1.07 per 1 mmol/L increase in triglycerides). In the ageing arm (70–84 years), genetically predicted triglyceride levels were not associated with the frailty index (β = 0.008; 95% CI: −0.013, 0.029) or the frailty phenotype (OR: 1.91; 95% CI: 0.84, 4.37). In conclusion, there is currently a lack of sufficient evidence to support causal associations of triglyceride levels with longevity and frailty in elderly populations. Nature Publishing Group 2017-01-30 /pmc/articles/PMC5278549/ /pubmed/28134330 http://dx.doi.org/10.1038/srep41579 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Liu, Zuyun Burgess, Stephen Wang, Zhengdong Deng, Wan Chu, Xuefeng Cai, Jian Zhu, Yinsheng Shi, Jianming Xie, Xuejuan Wang, Yong Jin, Li Wang, Xiaofeng Associations of triglyceride levels with longevity and frailty: A Mendelian randomization analysis |
title | Associations of triglyceride levels with longevity and frailty: A Mendelian randomization analysis |
title_full | Associations of triglyceride levels with longevity and frailty: A Mendelian randomization analysis |
title_fullStr | Associations of triglyceride levels with longevity and frailty: A Mendelian randomization analysis |
title_full_unstemmed | Associations of triglyceride levels with longevity and frailty: A Mendelian randomization analysis |
title_short | Associations of triglyceride levels with longevity and frailty: A Mendelian randomization analysis |
title_sort | associations of triglyceride levels with longevity and frailty: a mendelian randomization analysis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5278549/ https://www.ncbi.nlm.nih.gov/pubmed/28134330 http://dx.doi.org/10.1038/srep41579 |
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