Pain Research & Intervention Center of Excellence, University of Florida, Gainesville, FL, United States of America; Department of Community Dentistry and Behavioral Science, University of Florida, Gainesville, FL, United States of America.
Department of Biostatistics, University of Florida, Gainesville, FL, United States of America.
Exp Gerontol. 2022 Sep;166:111861. doi: 10.1016/j.exger.2022.111861. Epub 2022 May 29.
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 pain-free 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.
膝关节疼痛是导致老龄化人口残疾的主要原因,并且可能间接加速生物衰老过程。随着年龄的增长,患膝关节疼痛的风险增加,而膝关节疼痛会降低身体机能;然而,关于表观遗传衰老如何影响这种关系的数据有限,因为表观遗传衰老是生物衰老的一个已知标志,被证明可以预测健康寿命和死亡率。本研究的目的是研究与膝关节疼痛相关的身体机能下降是否与表观遗传衰老标志物有关。参与者(57.91±8.04 岁)分为低冲击膝关节疼痛组(n=95)、高冲击膝关节疼痛组(n=53)和无痛对照组(n=26),完成了自我报告的疼痛、血液采集和短体适能电池测试(SPPB),其中包括平衡、行走和坐站任务。我们使用了以前与膝关节疼痛相关并被证明可以预测总体死亡率风险的表观遗传钟(DNAmGrimAge)。采用bootstrap 中介分析来确定 DNAmGrimAge 和 SPPB 之间在疼痛组中的相关性。高冲击和低冲击疼痛组的生物表观遗传年龄更大(5.14y±5.66 和 1.32y±5.41)。然而,尽管疼痛对整体身体机能有直接影响,但这些影响不能用表观遗传衰老来解释。表观遗传衰老仅介导了疼痛对平衡表现的影响。未来需要进一步研究疼痛对生物衰老过程(包括表观遗传衰老)的影响及其对已知预测健康寿命和死亡率的身体机能测量的最终影响。