Epigenetic Aging is Associated with Measures of Midlife Muscle Volume and Attenuation in CARDIA Study.

GrimAge acceleration intermuscular adipose tissue lean muscle attenuation

Journal

The journals of gerontology. Series A, Biological sciences and medical sciences
ISSN: 1758-535X
Titre abrégé: J Gerontol A Biol Sci Med Sci
Pays: United States
ID NLM: 9502837

Informations de publication

Date de publication:
13 Nov 2023
Historique:
received: 13 01 2023
medline: 13 11 2023
pubmed: 13 11 2023
entrez: 13 11 2023
Statut: aheadofprint

Résumé

GrimAge acceleration (GAA), an epigenetic marker that represents physiologic aging, is associated with age-related diseases including cancer and cardiovascular diseases. However, the associations between GAA and muscle mass and function are unknown. We estimated measures of GAA in 1118 Black and White participants from the Coronary Artery Risk Development in Young Adults (CARDIA) Study at exam years (Y) 15 (2000-01) and 20 (2005-06). Abdominal muscle composition was measured using CT scans at the year 25 (2010-11) visit. We used multivariate regression models to examine associations of GAA estimates with muscle imaging measurements. In the CARDIA study, each one-year higher GAA was associated with an average 1.1% (95% CI 0.6%, 1.5%) higher intermuscular adipose tissue [IMAT] volume for abdominal muscles. Each one-year higher GAA was associated with an average -0.089 Hounsfield unit (HU) (95% CI -0.146, -0.032) lower lean muscle attenuation and an average -0.049 HU (95% CI -0.092, -0.007) lower IMAT attenuation for abdominal muscles. Stratified analyses showed that GAA was more strongly associated with higher abdominal muscle IMAT volume in females and significantly associated with lower lean muscle attenuation for White participants only. Higher GAA is associated with higher abdominal muscle IMAT volume and lower lean muscle attenuation in a midlife population.

Sections du résumé

BACKGROUND BACKGROUND
GrimAge acceleration (GAA), an epigenetic marker that represents physiologic aging, is associated with age-related diseases including cancer and cardiovascular diseases. However, the associations between GAA and muscle mass and function are unknown.
METHODS METHODS
We estimated measures of GAA in 1118 Black and White participants from the Coronary Artery Risk Development in Young Adults (CARDIA) Study at exam years (Y) 15 (2000-01) and 20 (2005-06). Abdominal muscle composition was measured using CT scans at the year 25 (2010-11) visit. We used multivariate regression models to examine associations of GAA estimates with muscle imaging measurements.
RESULTS RESULTS
In the CARDIA study, each one-year higher GAA was associated with an average 1.1% (95% CI 0.6%, 1.5%) higher intermuscular adipose tissue [IMAT] volume for abdominal muscles. Each one-year higher GAA was associated with an average -0.089 Hounsfield unit (HU) (95% CI -0.146, -0.032) lower lean muscle attenuation and an average -0.049 HU (95% CI -0.092, -0.007) lower IMAT attenuation for abdominal muscles. Stratified analyses showed that GAA was more strongly associated with higher abdominal muscle IMAT volume in females and significantly associated with lower lean muscle attenuation for White participants only.
CONCLUSIONS CONCLUSIONS
Higher GAA is associated with higher abdominal muscle IMAT volume and lower lean muscle attenuation in a midlife population.

Identifiants

pubmed: 37956337
pii: 7416813
doi: 10.1093/gerona/glad261
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of The Gerontological Society of America. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Tao Gao (T)

Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Center for Global Oncology, Institute for Global Health, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.

Yinan Zheng (Y)

Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Center for Global Oncology, Institute for Global Health, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.

Brian T Joyce (BT)

Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Center for Global Oncology, Institute for Global Health, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.

Minjung Kho (M)

Department of Epidemiology, School of Public Health, University of Michigan, Ann Arbor, MI, USA.

James G Terry (JG)

Department of Radiology, Vanderbilt University Medicine Center, Nashville, TN, USA.

Jun Wang (J)

Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Center for Global Oncology, Institute for Global Health, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.

Drew Nannini (D)

Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Center for Global Oncology, Institute for Global Health, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.

John Jeffrey Carr (JJ)

Department of Radiology, Vanderbilt University Medicine Center, Nashville, TN, USA.

Sangeeta Nair (S)

Department of Radiology, Vanderbilt University Medicine Center, Nashville, TN, USA.

Kai Zhang (K)

Department of Environmental Health Sciences, School of Public Health, University at Albany, State University of New York, Albany, NY, USA.

Wei Zhao (W)

Department of Epidemiology, School of Public Health, University of Michigan, Ann Arbor, MI, USA.
Survey Research Center, Institute for Social Research, University of Michigan, Ann Arbor, MI, USA.

David R Jacobs (DR)

Division of Epidemiology and Community Health, University of Minnesota School of Public Health, Minneapolis, MN, USA.

Pamela J Schreiner (PJ)

Division of Epidemiology and Community Health, University of Minnesota School of Public Health, Minneapolis, MN, USA.

Philip Greenland (P)

Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.

Donald Lloyd-Jones (D)

Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.

Jennifer A Smith (JA)

Department of Epidemiology, School of Public Health, University of Michigan, Ann Arbor, MI, USA.
Survey Research Center, Institute for Social Research, University of Michigan, Ann Arbor, MI, USA.

Lifang Hou (L)

Department of Preventive Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Center for Global Oncology, Institute for Global Health, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.

Classifications MeSH