Identifying Motor Resilience Proteins Associated with Motor Decline in Older Adults.

Aron S Buchman, Tianhao Wang, Katia de Paiva Lopes, Andrea R Zammit, Shahram Oveisgharan, Nicholas Seyfried, Yanling Wang, Sukriti Nag, Shinya Tasaki, Lei Yu, David A Bennett
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Abstract

Background: This study will identify cortical proteins that may provide motor resilience, the capacity to maintain motor function despite underlying ADRD pathologies.

Methods: We studied 850 decedents with postmortem indices of ten ADRD pathologies and proteome from dorsal lateral prefrontal cortex. Annual parkinsonian signs were assessed using a modified Unified Parkinson Disease Rating Scale. First, we adjusted linear models for ADRD pathologies to isolate resilience proteins, unrelated to ADRD pathologies, but that were related to linear motor decline. Next, functional mixed-effects (FME) models were used to determine if resilience proteins were related to non-linear motor decline. Exploratory functional enrichment was then used to assess pathways underlying motor resilience proteins.

Results: Mean age at death was 90 years (SD = 6.4), 69% female and 7 years follow-up. Adjusting linear models for age, sex and ADRD pathologies, we isolated thirteen proteins that may provide motor resilience (Bonferroni correction p < 5x10-6). FME models showed, that on average, progression of parkinsonian signs was non-linear from 25 years to 12 years before death, followed by accelerated linear decline until death. Five of thirteen resilience proteins were also related to non-linear decline. Motor resilience may be supported by a coordinated network of proteins that help to preserve neuronal structure, cellular transport, and synaptic integrity, functions critical for diverse aging phenotypes.

Conclusions: Cortical proteins may provide motor resilience for both linear and non-linear motor decline. Further drug discovery targeting resilience proteins may yield therapies that can reduce motor impairment even in the absence of treatments for ADRD pathologies.

识别与老年人运动能力下降相关的运动恢复蛋白。
背景:本研究将确定可能提供运动弹性的皮质蛋白,尽管存在潜在的ADRD病理,但仍能维持运动功能。方法:对850例死后ADRD 10种病理指标和背外侧前额皮质蛋白质组进行研究。使用改良的统一帕金森病评定量表评估年度帕金森症状。首先,我们调整了ADRD病理的线性模型,以分离出与ADRD病理无关但与线性运动衰退相关的弹性蛋白。接下来,使用功能混合效应(FME)模型来确定弹性蛋白是否与非线性运动衰退有关。然后使用探索性功能富集来评估运动恢复蛋白的潜在途径。结果:平均死亡年龄为90岁(SD = 6.4), 69%为女性,随访7年。通过调整年龄、性别和ADRD病理的线性模型,我们分离出13种可能提供运动恢复力的蛋白(Bonferroni校正p)。结论:皮层蛋白可能为线性和非线性运动衰退提供运动恢复力。针对弹性蛋白的进一步药物发现可能会在缺乏ADRD病理治疗的情况下产生可以减少运动损伤的治疗方法。
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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