Bott Nicholas T, Bettcher Brianne M, Yokoyama Jennifer S, Frazier Darvis T, Wynn Matthew, Karydas Anna, Yaffe Kristine, Kramer Joel H
School of Medicine, Stanford University, StanfordCA, USA; Neurology, Memory and Aging Center, University of California San Francisco, San FranciscoCA, USA.
Neurosurgery and Neurology, School of Medicine, University of Colorado, Aurora CO, USA.
Front Aging Neurosci. 2017 Mar 10;9:55. doi: 10.3389/fnagi.2017.00055. eCollection 2017.
To examine the impact of genetic, inflammatory, cardiovascular, lifestyle, and neuroanatomical factors on cognitive processing speed (CPS) change over time in functionally intact older adults. This observational study conducted over two time points, included 120 community dwelling cognitively normal older adults between the ages of 60 and 80 from the University of California San Francisco Memory and Aging Center. Participants were followed with composite measures of CPS, calculated based on norms for 20-30 year-olds. Variables of interest were AD risk genes (APOE, CR1), markers of inflammation (interleukin 6) and cardiovascular health (BMI, LDL, HDL, mean arterial pressure, fasting insulin), self-reported physical activity, and corpus callosum (CC) volumes. The sample was divided into three groups: 17 "resilient-agers" with fast and stable processing speed; 56 "average-agers" with average and stable processing speed; and 47 "sub-agers" with average baseline speed who were slower at follow-up. Resilient-agers had larger baseline CC volumes than sub-agers ( < 0.05). Resilient-agers displayed lower levels of interleukin-6 (IL-6) and insulin (s < 0.05) than sub-agers, and reported more physical activity than both average- and sub-agers (s < 0.01). In a multinomial logistic regression, physical activity and IL-6 predicted average- and sub-ager groups. Resilient-agers displayed a higher frequency of APOE e4 and CR1 AA/AG alleles. Robust and stable CPS is associated with larger baseline CC volumes, lower levels of inflammation and insulin, and greater self-reported physical activity. These findings highlight the relevance of neuroanatomical, biological, and lifestyle factors in the identification and prediction of heterogeneous cognitive aging change over time.
为研究基因、炎症、心血管、生活方式和神经解剖学因素对功能完好的老年人认知处理速度(CPS)随时间变化的影响。这项在两个时间点进行的观察性研究,纳入了来自加州大学旧金山分校记忆与衰老中心的120名年龄在60至80岁之间、居住在社区且认知正常的老年人。参与者接受了基于20 - 30岁人群标准计算的CPS综合测量。感兴趣的变量包括AD风险基因(APOE、CR1)、炎症标志物(白细胞介素6)和心血管健康指标(BMI、低密度脂蛋白、高密度脂蛋白、平均动脉压、空腹胰岛素)、自我报告的身体活动以及胼胝体(CC)体积。样本被分为三组:17名“弹性老化者”,其处理速度快速且稳定;56名“普通老化者”,其处理速度平均且稳定;47名“亚老化者”,其基线速度平均,但随访时较慢。“弹性老化者”的基线CC体积大于“亚老化者”(<0.05)。“弹性老化者”的白细胞介素 - 6(IL - 6)和胰岛素水平低于“亚老化者”(<0.05),且报告的身体活动比“普通老化者”和“亚老化者”都多(<0.01)。在多项逻辑回归中,身体活动和IL - 6可预测“普通老化者”和“亚老化者”组。“弹性老化者”中APOE e4和CR1 AA/AG等位基因的频率较高。稳健且稳定的CPS与更大的基线CC体积、更低的炎症和胰岛素水平以及更多的自我报告身体活动相关。这些发现凸显了神经解剖学、生物学和生活方式因素在识别和预测随时间变化的异质性认知老化中的相关性。