Pain and Nutrition in Dementia and Alzheimer's Phase 1: a cross-sectional, observational study design.

Frontiers in dementia Pub Date : 2026-03-31 eCollection Date: 2026-01-01 DOI:10.3389/frdem.2026.1789761
Taylor C Judkins, Hailey J Andrews, Qianqian Song, Edward I Clark, Camesha Tate, Joshua I Wais, Roger Fillingim, Zhiguang Huo, Steven T DeKosky, Barabara Gower, Ronald A Cohen, Natalie C Ebner, Yenisel Cruz-Almeida, Larissa J Strath
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Abstract

Background: Neurodegenerative diseases such as Alzheimer's Disease and related dementias (ADRDs) as well as chronic pain have increased in prevalence as the population ages. In fact, recent epidemiological research suggests that having chronic pain may increase one's risk of all-cause dementia. There are mechanistic factors that overlap in both ADRD and chronic pain progression, including epigenetic dysregulation that could lead to increased inflammation. Previously, our group presented evidence that dietary patterns impact inflammatory potential and epigenetic modifications, and accelerate epigenetic aging. Here, we hypothesize that diet- induced inflammation and epigenetic alterations may be underexplored mechanistic pathways connecting chronic pain and ADRD risk.

Methods: The Pain and Nutrition in Dementia and Alzheimer's Phase 1 (PANDA-1) study is a cross-sectional, observational study, which will recruit 90 individuals ≥55 years of age with and without painful knee osteoarthritis (OA). Biological samples will be collected to assess study eligibility, blood-based inflammatory markers, and epigenetic age using the epigenetic clock DNAmGrimAge. A 24-h dietary recall will be completed to determine nutrition status via the Dietary Inflammation Index (DII). Pain and psychosocial questionnaires will be employed to determine pain phenotypes. Quantitative Sensory Testing will be conducted to determine responses to noxious mechanical and thermal stimuli. Lower-extremity function and mobility measures will also be obtained. Finally, height, weight, pain history, medical history, medication use, and demographic variables will be collected as covariates. Hierarchical regression, mediation and moderation analyses, as well as ANOVAs will be conducted to evaluate relationships among the DII, epigenetic aging, cognition status, and pain.

Conclusion: This study will integrate dietary, epigenetic, and cognitive assessments in a chronic pain population, to lay the groundwork of a possible associations linking chronic pain and ADRDs. PANDA-1 aims to determine potential relationships of dietary patterns on interindividual variability of cognitive status and pain outcomes in older adults deemed cognitively intact. Subsequent phases of this study will include individuals with mild cognitive impairment and ADRDs. Findings from this work will inform future studies targeting dietary intervention approaches to mitigate overlapping neurodegenerative and pain-related aging processes.

痴呆和阿尔茨海默病的疼痛和营养1期:一项横断面观察性研究设计。
背景:随着人口老龄化,神经退行性疾病如阿尔茨海默病和相关痴呆(ADRDs)以及慢性疼痛的患病率增加。事实上,最近的流行病学研究表明,慢性疼痛可能会增加患全因痴呆的风险。在ADRD和慢性疼痛进展中存在重叠的机制因素,包括可能导致炎症增加的表观遗传失调。之前,我们的研究小组提出了饮食模式影响炎症潜力和表观遗传修饰,并加速表观遗传衰老的证据。在这里,我们假设饮食诱导的炎症和表观遗传改变可能是连接慢性疼痛和ADRD风险的未充分探索的机制途径。方法:痴呆和阿尔茨海默病的疼痛和营养1期(PANDA-1)研究是一项横断面观察性研究,将招募90名年龄≥55 的患有或不患有疼痛性膝骨关节炎(OA)的个体。将收集生物样本,使用表观遗传时钟DNAmGrimAge评估研究资格、血液炎症标志物和表观遗传年龄。将完成24小时饮食召回,通过饮食炎症指数(DII)确定营养状况。疼痛和社会心理问卷将被用来确定疼痛的表型。将进行定量感官测试,以确定对有害机械和热刺激的反应。还将获得下肢功能和活动措施。最后,身高、体重、疼痛史、病史、药物使用和人口统计学变量将被收集为协变量。通过层次回归、中介和调节分析以及方差分析来评估DII、表观遗传老化、认知状态和疼痛之间的关系。结论:本研究将整合慢性疼痛人群的饮食、表观遗传和认知评估,为慢性疼痛和不良反应之间可能的关联奠定基础。PANDA-1旨在确定饮食模式与认知状态和疼痛结局的个体差异之间的潜在关系。该研究的后续阶段将包括患有轻度认知障碍和不良反应的个体。这项工作的发现将为未来针对饮食干预方法的研究提供信息,以减轻重叠的神经退行性和疼痛相关的衰老过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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