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Genetic trade‐offs between complex diseases and longevity
Longevity was influenced by many complex diseases and traits. However, the relationships between human longevity and genetic risks of complex diseases were not broadly studied. Here, we constructed polygenic risk scores (PRSs) for 225 complex diseases/traits and evaluated their relationships with hu...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9282840/ https://www.ncbi.nlm.nih.gov/pubmed/35754110 http://dx.doi.org/10.1111/acel.13654 |
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author | Hu, Dingxue Li, Yan Zhang, Detao Ding, Jiahong Song, Zijun Min, Junxia Zeng, Yi Nie, Chao |
author_facet | Hu, Dingxue Li, Yan Zhang, Detao Ding, Jiahong Song, Zijun Min, Junxia Zeng, Yi Nie, Chao |
author_sort | Hu, Dingxue |
collection | PubMed |
description | Longevity was influenced by many complex diseases and traits. However, the relationships between human longevity and genetic risks of complex diseases were not broadly studied. Here, we constructed polygenic risk scores (PRSs) for 225 complex diseases/traits and evaluated their relationships with human longevity in a cohort with 2178 centenarians and 2299 middle‐aged individuals. Lower genetic risks of stroke and hypotension were observed in centenarians, while higher genetic risks of schizophrenia (SCZ) and type 2 diabetes (T2D) were detected in long‐lived individuals. We further stratified PRSs into cell‐type groups and significance‐level groups. The results showed that the immune component of SCZ genetic risk was positively linked to longevity, and the renal component of T2D genetic risk was the most deleterious. Additionally, SNPs with very small p‐values (p ≤ 1x10(‐5)) for SCZ and T2D were negatively correlated with longevity. While for the less significant SNPs (1x10(‐5) < p ≤ 0.05), their effects on disease and longevity were positively correlated. Overall, we identified genetically informed positive and negative factors for human longevity, gained more insights on the accumulation of disease risk alleles during evolution, and provided evidence for the theory of genetic trade‐offs between complex diseases and longevity. |
format | Online Article Text |
id | pubmed-9282840 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92828402022-07-15 Genetic trade‐offs between complex diseases and longevity Hu, Dingxue Li, Yan Zhang, Detao Ding, Jiahong Song, Zijun Min, Junxia Zeng, Yi Nie, Chao Aging Cell Research Articles Longevity was influenced by many complex diseases and traits. However, the relationships between human longevity and genetic risks of complex diseases were not broadly studied. Here, we constructed polygenic risk scores (PRSs) for 225 complex diseases/traits and evaluated their relationships with human longevity in a cohort with 2178 centenarians and 2299 middle‐aged individuals. Lower genetic risks of stroke and hypotension were observed in centenarians, while higher genetic risks of schizophrenia (SCZ) and type 2 diabetes (T2D) were detected in long‐lived individuals. We further stratified PRSs into cell‐type groups and significance‐level groups. The results showed that the immune component of SCZ genetic risk was positively linked to longevity, and the renal component of T2D genetic risk was the most deleterious. Additionally, SNPs with very small p‐values (p ≤ 1x10(‐5)) for SCZ and T2D were negatively correlated with longevity. While for the less significant SNPs (1x10(‐5) < p ≤ 0.05), their effects on disease and longevity were positively correlated. Overall, we identified genetically informed positive and negative factors for human longevity, gained more insights on the accumulation of disease risk alleles during evolution, and provided evidence for the theory of genetic trade‐offs between complex diseases and longevity. John Wiley and Sons Inc. 2022-06-26 2022-07 /pmc/articles/PMC9282840/ /pubmed/35754110 http://dx.doi.org/10.1111/acel.13654 Text en © 2022 The Authors. Aging Cell published by Anatomical Society and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Hu, Dingxue Li, Yan Zhang, Detao Ding, Jiahong Song, Zijun Min, Junxia Zeng, Yi Nie, Chao Genetic trade‐offs between complex diseases and longevity |
title | Genetic trade‐offs between complex diseases and longevity |
title_full | Genetic trade‐offs between complex diseases and longevity |
title_fullStr | Genetic trade‐offs between complex diseases and longevity |
title_full_unstemmed | Genetic trade‐offs between complex diseases and longevity |
title_short | Genetic trade‐offs between complex diseases and longevity |
title_sort | genetic trade‐offs between complex diseases and longevity |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9282840/ https://www.ncbi.nlm.nih.gov/pubmed/35754110 http://dx.doi.org/10.1111/acel.13654 |
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