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High‐Intensity interval training reduces transcriptomic age: A randomized controlled trial
While the relationship between exercise and life span is well‐documented, little is known about the effects of specific exercise protocols on modern measures of biological age. Transcriptomic age (TA) predictors provide an opportunity to test the effects of high‐intensity interval training (HIIT) on...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10265161/ https://www.ncbi.nlm.nih.gov/pubmed/37078430 http://dx.doi.org/10.1111/acel.13841 |
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author | Lohman, Trevor Bains, Gurinder Cole, Steve Gharibvand, Lida Berk, Lee Lohman, Everett |
author_facet | Lohman, Trevor Bains, Gurinder Cole, Steve Gharibvand, Lida Berk, Lee Lohman, Everett |
author_sort | Lohman, Trevor |
collection | PubMed |
description | While the relationship between exercise and life span is well‐documented, little is known about the effects of specific exercise protocols on modern measures of biological age. Transcriptomic age (TA) predictors provide an opportunity to test the effects of high‐intensity interval training (HIIT) on biological age utilizing whole‐genome expression data. A single‐site, single‐blinded, randomized controlled clinical trial design was utilized. Thirty sedentary participants (aged 40–65) were assigned to either a HIIT group or a no‐exercise control group. After collecting baseline measures, HIIT participants performed three 10 × 1 HIIT sessions per week for 4 weeks. Each session lasted 23 min, and total exercise duration was 276 min over the course of the 1‐month exercise protocol. TA, PSS‐10 score, PSQI score, PHQ‐9 score, and various measures of body composition were all measured at baseline and again following the conclusion of exercise/control protocols. Transcriptomic age reduction of 3.59 years was observed in the exercise group while a 3.29‐years increase was observed in the control group. Also, PHQ‐9, PSQI, BMI, body fat mass, and visceral fat measures were all improved in the exercise group. A hypothesis‐generation gene expression analysis suggested exercise may modify autophagy, mTOR, AMPK, PI3K, neurotrophin signaling, insulin signaling, and other age‐related pathways. A low dose of HIIT can reduce an mRNA‐based measure of biological age in sedentary adults between the ages of 40 and 65 years old. Other changes in gene expression were relatively modest, which may indicate a focal effect of exercise on age‐related biological processes. |
format | Online Article Text |
id | pubmed-10265161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102651612023-06-15 High‐Intensity interval training reduces transcriptomic age: A randomized controlled trial Lohman, Trevor Bains, Gurinder Cole, Steve Gharibvand, Lida Berk, Lee Lohman, Everett Aging Cell Research Articles While the relationship between exercise and life span is well‐documented, little is known about the effects of specific exercise protocols on modern measures of biological age. Transcriptomic age (TA) predictors provide an opportunity to test the effects of high‐intensity interval training (HIIT) on biological age utilizing whole‐genome expression data. A single‐site, single‐blinded, randomized controlled clinical trial design was utilized. Thirty sedentary participants (aged 40–65) were assigned to either a HIIT group or a no‐exercise control group. After collecting baseline measures, HIIT participants performed three 10 × 1 HIIT sessions per week for 4 weeks. Each session lasted 23 min, and total exercise duration was 276 min over the course of the 1‐month exercise protocol. TA, PSS‐10 score, PSQI score, PHQ‐9 score, and various measures of body composition were all measured at baseline and again following the conclusion of exercise/control protocols. Transcriptomic age reduction of 3.59 years was observed in the exercise group while a 3.29‐years increase was observed in the control group. Also, PHQ‐9, PSQI, BMI, body fat mass, and visceral fat measures were all improved in the exercise group. A hypothesis‐generation gene expression analysis suggested exercise may modify autophagy, mTOR, AMPK, PI3K, neurotrophin signaling, insulin signaling, and other age‐related pathways. A low dose of HIIT can reduce an mRNA‐based measure of biological age in sedentary adults between the ages of 40 and 65 years old. Other changes in gene expression were relatively modest, which may indicate a focal effect of exercise on age‐related biological processes. John Wiley and Sons Inc. 2023-04-20 /pmc/articles/PMC10265161/ /pubmed/37078430 http://dx.doi.org/10.1111/acel.13841 Text en © 2023 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 Lohman, Trevor Bains, Gurinder Cole, Steve Gharibvand, Lida Berk, Lee Lohman, Everett High‐Intensity interval training reduces transcriptomic age: A randomized controlled trial |
title |
High‐Intensity interval training reduces transcriptomic age: A randomized controlled trial |
title_full |
High‐Intensity interval training reduces transcriptomic age: A randomized controlled trial |
title_fullStr |
High‐Intensity interval training reduces transcriptomic age: A randomized controlled trial |
title_full_unstemmed |
High‐Intensity interval training reduces transcriptomic age: A randomized controlled trial |
title_short |
High‐Intensity interval training reduces transcriptomic age: A randomized controlled trial |
title_sort | high‐intensity interval training reduces transcriptomic age: a randomized controlled trial |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10265161/ https://www.ncbi.nlm.nih.gov/pubmed/37078430 http://dx.doi.org/10.1111/acel.13841 |
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