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Epigenetic aging, knee pain and physical performance in community-dwelling middle-to-older age adults
被引:13
|作者:
Peterson, Jessica A.
[1
,2
]
Meng, Lingsong
[3
]
Rani, Asha
[4
]
Sinha, Puja
[4
]
Johnson, Alisa J.
[1
,2
]
Huo, Zhiguang
[3
]
Foster, Thomas C.
[4
,5
]
Fillingim, Roger B.
[1
,2
]
Cruz-Almeida, Yenisel
[1
,2
,4
,6
]
机构:
[1] Univ Florida, Pain Res & Intervent Ctr Excellence, Gainesville, FL USA
[2] Univ Florida, Dept Community Dent & Behav Sci, Gainesville, FL USA
[3] Univ Florida, Dept Biostat, Gainesville, FL USA
[4] Univ Florida, McKnight Brain Inst, Dept Neurosci, Gainesville, FL USA
[5] Univ Florida, Genet & Genom Program, Gainesville, FL USA
[6] Univ Florida, Dept Community Dent & Behav Sci & Neurosci, Gainesville, FL 32610 USA
关键词:
Knee pain;
Epigenetic aging;
Biological clocks;
Aging;
Physical performance;
Balance;
LOWER-EXTREMITY FUNCTION;
DNA METHYLATION;
MUSCULOSKELETAL PAIN;
UNITED-STATES;
MUSCLE MASS;
DISABILITY;
MORTALITY;
SEVERITY;
HEALTH;
IMPACT;
D O I:
10.1016/j.exger.2022.111861
中图分类号:
R592 [老年病学];
C [社会科学总论];
学科分类号:
03 ;
0303 ;
100203 ;
摘要:
Knee pain is a leading cause of disability in the aging population and may indirectly accelerate biological aging processes. Chronological aging increases the risk of developing of knee pain and knee pain reduces physical function; however, limited data exist on how epigenetic aging, a known hallmark of biological aging shown to predict health span and mortality, may influence this relationship. The purpose of this study was to examine whether decreased physical performance associated with knee pain is mediated by markers of epigenetic aging. Participants (57.91 +/- 8.04 years) with low impact knee pain (n = 95), high impact knee pain (n = 53) and painfree controls (n = 26) completed self-reported pain, a blood draw and a short physical performance battery (SPPB) that included balance, walking, and sit to stand tasks. We employed an epigenetic clock previously associated with knee pain and shown to predict overall mortality risk (DNAmGrimAge). Bootstrapped-mediation analyses were used to determine associations of DNAmGrimAge and SPPB between pain groups. Those with high impact and low impact pain had a biologically older epigenetic age (5.14y +/- 5.66 and 1.32y +/- 5.41, respectively). However, while there were direct effects of pain on overall physical performance, these were not explained by epigenetic aging. Epigenetic aging only mediated the effect of pain on balance performance. Future work is needed to examine pain's impact on biological aging processes including epigenetic aging and its ultimate effect on physical function measures known to predict health span and mortality.
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