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Lifestyle weight-loss intervention may attenuate methylation aging: the CENTRAL MRI randomized controlled trial

BACKGROUND: DNA methylation age (mAge), a methylation biomarker for the aging process, might serve as a more accurate predictor of morbidity and aging status than chronological age. We evaluated the role of multiple factors, including fat deposition, cardiometabolic risk factors and lifestyle weight...

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Autores principales: Yaskolka Meir, Anat, Keller, Maria, Bernhart, Stephan H., Rinott, Ehud, Tsaban, Gal, Zelicha, Hila, Kaplan, Alon, Schwarzfuchs, Dan, Shelef, Ilan, Gepner, Yftach, Li, Jun, Lin, Yifei, Blüher, Matthias, Ceglarek, Uta, Stumvoll, Michael, Stadler, Peter F., Stampfer, Meir J., Kovacs, Peter, Liang, Liming, Shai, Iris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7934393/
https://www.ncbi.nlm.nih.gov/pubmed/33663610
http://dx.doi.org/10.1186/s13148-021-01038-0
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author Yaskolka Meir, Anat
Keller, Maria
Bernhart, Stephan H.
Rinott, Ehud
Tsaban, Gal
Zelicha, Hila
Kaplan, Alon
Schwarzfuchs, Dan
Shelef, Ilan
Gepner, Yftach
Li, Jun
Lin, Yifei
Blüher, Matthias
Ceglarek, Uta
Stumvoll, Michael
Stadler, Peter F.
Stampfer, Meir J.
Kovacs, Peter
Liang, Liming
Shai, Iris
author_facet Yaskolka Meir, Anat
Keller, Maria
Bernhart, Stephan H.
Rinott, Ehud
Tsaban, Gal
Zelicha, Hila
Kaplan, Alon
Schwarzfuchs, Dan
Shelef, Ilan
Gepner, Yftach
Li, Jun
Lin, Yifei
Blüher, Matthias
Ceglarek, Uta
Stumvoll, Michael
Stadler, Peter F.
Stampfer, Meir J.
Kovacs, Peter
Liang, Liming
Shai, Iris
author_sort Yaskolka Meir, Anat
collection PubMed
description BACKGROUND: DNA methylation age (mAge), a methylation biomarker for the aging process, might serve as a more accurate predictor of morbidity and aging status than chronological age. We evaluated the role of multiple factors, including fat deposition, cardiometabolic risk factors and lifestyle weight-loss intervention, on the deviation of mAge from chronological age (mAge deviation) or 18-month change in mAge (∆mAge). In this sub-study of the CENTRAL magnetic resonance imaging weight-loss trial, we evaluated mAge by a validated 240-CpG-based prediction formula at baseline and after 18-month intervention of either low fat (LF) or mediterranean/low carbohydrate (MED/LC) diets. RESULTS: Among 120 CENTRAL participants with abdominal obesity or dyslipidemia, mAge (mean ± SD: 60.3 ± 7.5 years) was higher than the chronological age (48.6 ± 9.3 years) but strongly correlated (r = 0.93; p = 3.1 × 10(–53)). Participants in the lowest tertile of mAge deviation from their chronological age had significantly lower waist-circumference, visceral adipose tissue, intrahepatic fat (IHF) content, fasting-glucose and HOMA-IR, as compared with participants in the highest sex-specific residual tertile (p < 0.05 for all). IHF% remained associated with greater mAge deviation after further adjustments (β = 0.23; p = 0.02). After 18-month weight-loss lifestyle intervention, mAge remained significantly correlated with chronological age (r = 0.94, p = 1.5 × 10(–55)). mAging occurred, with no difference between lifestyle intervention groups (∆ = 0.9 ± 1.9 years in MED/LC vs. ∆ = 1.3 ± 1.9 years in LF; p = 0.2); however, we observed a mAging attenuation in successful weight losers (> 5% weight loss) vs. weight-loss failures ( ∆ = 0.6 years vs. ∆ = 1.1 years; p = 0.04), and in participants who completed the trial with healthy liver fat content (< 5% IHF) vs. participants with fatty liver (∆ = 0.6 years vs. ∆ = 1.8 years; p = 0.003). Overall, 18 months of weight-loss lifestyle intervention attenuated the mAging of the men, mainly the older, by 7.1 months than the expected (p < 0.05). CONCLUSIONS: Lifestyle weight-loss intervention may attenuate mAging. Deviation of mAge from chronological age might be related to body fat distribution and glycemic control and could indicate biological age, health status and the risk for premature cardiometabolic diseases. Trial registration: ClinicalTrials.gov NCT01530724. Registered 10 February 2012, https://clinicaltrials.gov/ct2/show/study/NCT01530724. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13148-021-01038-0.
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spelling pubmed-79343932021-03-08 Lifestyle weight-loss intervention may attenuate methylation aging: the CENTRAL MRI randomized controlled trial Yaskolka Meir, Anat Keller, Maria Bernhart, Stephan H. Rinott, Ehud Tsaban, Gal Zelicha, Hila Kaplan, Alon Schwarzfuchs, Dan Shelef, Ilan Gepner, Yftach Li, Jun Lin, Yifei Blüher, Matthias Ceglarek, Uta Stumvoll, Michael Stadler, Peter F. Stampfer, Meir J. Kovacs, Peter Liang, Liming Shai, Iris Clin Epigenetics Research BACKGROUND: DNA methylation age (mAge), a methylation biomarker for the aging process, might serve as a more accurate predictor of morbidity and aging status than chronological age. We evaluated the role of multiple factors, including fat deposition, cardiometabolic risk factors and lifestyle weight-loss intervention, on the deviation of mAge from chronological age (mAge deviation) or 18-month change in mAge (∆mAge). In this sub-study of the CENTRAL magnetic resonance imaging weight-loss trial, we evaluated mAge by a validated 240-CpG-based prediction formula at baseline and after 18-month intervention of either low fat (LF) or mediterranean/low carbohydrate (MED/LC) diets. RESULTS: Among 120 CENTRAL participants with abdominal obesity or dyslipidemia, mAge (mean ± SD: 60.3 ± 7.5 years) was higher than the chronological age (48.6 ± 9.3 years) but strongly correlated (r = 0.93; p = 3.1 × 10(–53)). Participants in the lowest tertile of mAge deviation from their chronological age had significantly lower waist-circumference, visceral adipose tissue, intrahepatic fat (IHF) content, fasting-glucose and HOMA-IR, as compared with participants in the highest sex-specific residual tertile (p < 0.05 for all). IHF% remained associated with greater mAge deviation after further adjustments (β = 0.23; p = 0.02). After 18-month weight-loss lifestyle intervention, mAge remained significantly correlated with chronological age (r = 0.94, p = 1.5 × 10(–55)). mAging occurred, with no difference between lifestyle intervention groups (∆ = 0.9 ± 1.9 years in MED/LC vs. ∆ = 1.3 ± 1.9 years in LF; p = 0.2); however, we observed a mAging attenuation in successful weight losers (> 5% weight loss) vs. weight-loss failures ( ∆ = 0.6 years vs. ∆ = 1.1 years; p = 0.04), and in participants who completed the trial with healthy liver fat content (< 5% IHF) vs. participants with fatty liver (∆ = 0.6 years vs. ∆ = 1.8 years; p = 0.003). Overall, 18 months of weight-loss lifestyle intervention attenuated the mAging of the men, mainly the older, by 7.1 months than the expected (p < 0.05). CONCLUSIONS: Lifestyle weight-loss intervention may attenuate mAging. Deviation of mAge from chronological age might be related to body fat distribution and glycemic control and could indicate biological age, health status and the risk for premature cardiometabolic diseases. Trial registration: ClinicalTrials.gov NCT01530724. Registered 10 February 2012, https://clinicaltrials.gov/ct2/show/study/NCT01530724. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13148-021-01038-0. BioMed Central 2021-03-04 /pmc/articles/PMC7934393/ /pubmed/33663610 http://dx.doi.org/10.1186/s13148-021-01038-0 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Yaskolka Meir, Anat
Keller, Maria
Bernhart, Stephan H.
Rinott, Ehud
Tsaban, Gal
Zelicha, Hila
Kaplan, Alon
Schwarzfuchs, Dan
Shelef, Ilan
Gepner, Yftach
Li, Jun
Lin, Yifei
Blüher, Matthias
Ceglarek, Uta
Stumvoll, Michael
Stadler, Peter F.
Stampfer, Meir J.
Kovacs, Peter
Liang, Liming
Shai, Iris
Lifestyle weight-loss intervention may attenuate methylation aging: the CENTRAL MRI randomized controlled trial
title Lifestyle weight-loss intervention may attenuate methylation aging: the CENTRAL MRI randomized controlled trial
title_full Lifestyle weight-loss intervention may attenuate methylation aging: the CENTRAL MRI randomized controlled trial
title_fullStr Lifestyle weight-loss intervention may attenuate methylation aging: the CENTRAL MRI randomized controlled trial
title_full_unstemmed Lifestyle weight-loss intervention may attenuate methylation aging: the CENTRAL MRI randomized controlled trial
title_short Lifestyle weight-loss intervention may attenuate methylation aging: the CENTRAL MRI randomized controlled trial
title_sort lifestyle weight-loss intervention may attenuate methylation aging: the central mri randomized controlled trial
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7934393/
https://www.ncbi.nlm.nih.gov/pubmed/33663610
http://dx.doi.org/10.1186/s13148-021-01038-0
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