Memory and Aging Center, Department of Neurology, University of California, San Francisco.
Department of Neurology, Mayo Clinic, Rochester, Minnesota.
JAMA Neurol. 2023 Jan 1;80(1):82-90. doi: 10.1001/jamaneurol.2022.4178.
Physical activity is associated with cognitive health, even in autosomal dominant forms of dementia. Higher physical activity is associated with slowed cognitive and functional declines over time in adults carrying autosomal dominant variants for frontotemporal lobar degeneration (FTLD), but whether axonal degeneration is a potential neuroprotective target of physical activity in individuals with FTLD is unknown.
To examine the association between physical activity and longitudinal neurofilament light chain (NfL) trajectories in individuals with autosomal dominant forms of FTLD.
DESIGN, SETTING, AND PARTICIPANTS: This cohort study included individuals from the ALLFTD Consortium, which recruited patients from sites in the US and Canada. Symptomatic and asymptomatic adults with pathogenic variants in one of 3 common genes associated with FTLD (GRN, C9orf72, or MAPT) who reported baseline physical activity levels and completed annual blood draws were assessed annually for up to 4 years. Genotype, clinical measures, and blood draws were collected between December 2014 and June 2019; data were analyzed from August 2021 to January 2022. Associations between reported baseline physical activity and longitudinal plasma NfL changes were assessed using generalized linear mixed-effects models adjusting for baseline age, sex, education, functional severity, and motor symptoms.
Baseline physical activity levels reported via the Physical Activity Scale for the Elderly. To estimate effect sizes, marginal means were calculated at 3 levels of physical activity: 1 SD above the mean represented high physical activity, 0 SD represented average physical activity, and 1 SD below the mean represented low physical activity.
Annual plasma NfL concentrations were measured with single-molecule array technology.
Of 160 included FTLD variant carriers, 84 (52.5%) were female, and the mean (SD) age was 50.7 (14.7) years. A total of 51 (31.8%) were symptomatic, and 77 carried the C9orf72 variant; 39, GRN variant; and 44, MAPT variant. Higher baseline physical activity was associated with slower NfL trajectories over time. On average, NfL increased 45.8% (95% CI, 22.5 to 73.7) over 4 years in variant carriers. Variant carriers with high physical activity demonstrated 14.0% (95% CI, -22.7 to -4.3) slower NfL increases compared with those with average physical activity and 30% (95% CI, -52.2 to -8.8) slower NfL increases compared with those with low physical activity. Within genotype, C9orf72 and MAPT carriers with high physical activity evidenced 18% to 21% (95% CI, -43.4 to -7.2) attenuation in NfL, while the association between physical activity and NfL trajectory was not statistically significant in GRN carriers. Activities associated with higher cardiorespiratory and cognitive demands (sports, housework, and yardwork) were most strongly correlated with slower NfL trajectories (vs walking and strength training).
In this study, higher reported physical activity was associated with slower progression of an axonal degeneration marker in individuals with autosomal dominant FTLD. Physical activity may serve as a primary prevention target in FTLD.
即使在常染色体显性形式的痴呆症中,身体活动也与认知健康相关。在携带额颞叶变性(FTLD)常染色体显性变异的成年人中,较高的身体活动与随时间推移认知和功能下降的速度较慢有关,但身体活动是否是 FTLD 个体中轴突退化的潜在神经保护靶点尚不清楚。
研究身体活动与携带常染色体显性形式 FTLD 的个体的纵向神经丝轻链(NfL)轨迹之间的关联。
设计、地点和参与者:这项队列研究包括来自 ALLFTD 联合会的个体,该联合会从美国和加拿大的站点招募了患者。有症状和无症状的成年人携带与 FTLD 相关的 3 个常见基因(GRN、C9orf72 或 MAPT)中的一个致病性变异,他们报告了基线身体活动水平并完成了年度血液抽取,每年评估一次,最长可达 4 年。基因型、临床测量和血液抽取于 2014 年 12 月至 2019 年 6 月之间进行;数据分析于 2021 年 8 月至 2022 年 1 月进行。使用调整基线年龄、性别、教育、功能严重程度和运动症状的广义线性混合效应模型评估报告的基线身体活动与纵向血浆 NfL 变化之间的关联。
通过老年人身体活动量表报告基线身体活动水平。为了估计效应大小,在身体活动水平的 3 个水平上计算了边际均值:1 个标准差高于平均值表示高身体活动,0 个标准差表示平均身体活动,1 个标准差低于平均值表示低身体活动。
每年使用单分子阵列技术测量血浆 NfL 浓度。
在 160 名纳入的 FTLD 变异携带者中,84 名(52.5%)为女性,平均(SD)年龄为 50.7(14.7)岁。共有 51 名(31.8%)为有症状,77 名携带 C9orf72 变异;39 名携带 GRN 变异;44 名携带 MAPT 变异。较高的基线身体活动与随时间推移的 NfL 轨迹较慢有关。平均而言,变异携带者在 4 年内 NfL 增加了 45.8%(95%CI,22.5 至 73.7)。与平均身体活动相比,高身体活动的变异携带者 NfL 增加速度较慢 14.0%(95%CI,-22.7 至-4.3),与低身体活动的变异携带者 NfL 增加速度较慢 30.0%(95%CI,-52.2 至-8.8)。在基因型内,高身体活动的 C9orf72 和 MAPT 携带者的 NfL 衰减了 18%至 21%(95%CI,-43.4 至-7.2),而身体活动与 NfL 轨迹之间的关联在 GRN 携带者中没有统计学意义。与步行和力量训练相比,与更高心肺和认知需求相关的活动(运动、家务和庭院工作)与 NfL 轨迹较慢最相关。
在这项研究中,较高的报告身体活动与携带常染色体显性 FTLD 的个体中轴突退化标志物的进展较慢有关。身体活动可能是 FTLD 的主要预防目标。