Gerontopole of Toulouse, Institute of Ageing, Toulouse University Hospital (CHU Toulouse), Toulouse, France.
Maintain Aging Research Team, CERPOP, Inserm, Université Paul Sabatier, Toulouse, France.
J Am Geriatr Soc. 2022 Apr;70(4):1236-1243. doi: 10.1111/jgs.17604. Epub 2021 Dec 15.
In previous studies, plasma neurofilament light chain (NfL) and progranulin (PGRN) levels are associated with cognitive and physical impairment in older individuals. However, evidence of their relationships with frailty is lacking. This study aims to explore the associations of plasma NfL and PGRN levels with frailty in community-dwelling older adults.
We included 507 older adults (mean [standard deviation] age, 76.7 [4.5] years) with plasma NfL and PGRN measurements from the Multidomain Alzheimer Preventive Trial (MAPT). The timepoint of biomarker measurements, either 12 or 24 months after study enrollment, was defined as the baseline for each participant. Frailty phenotype (robust, pre-frail, and frail) was assessed at 12, 24, 36, 48, and 60 months by Fried's frailty criteria. The cross-sectional associations between plasma neurodegenerative biomarkers and frailty severity were examined using logistic regressions. We further used Cox proportional hazard models to evaluate the associations between plasma biomarkers and incident frailty among robust or pre-frail participants at baseline (n = 403).
At baseline, participants with high plasma NfL levels (>93.11 pg/ml [the upper quartile]) had a higher likelihood of pre-frailty or frailty compared to their normal NfL counterparts (odds ratio = 1.68; 95% confidence interval = 1.10-2.57); however, this association did not remain significant after controlling for covariates. Neither NfL nor PGRN levels showed prospective associations with incident frailty over 4 years.
This study failed to find associations of circulating NfL and PGRN levels with frailty among community-dwelling older adults in adjusted analyses. Whether plasma neurodegenerative markers serve as potential biomarkers of frailty requires further investigation.
在之前的研究中,血浆神经丝轻链(NfL)和颗粒体蛋白前体(PGRN)水平与老年人的认知和身体功能障碍有关。然而,缺乏它们与虚弱之间关系的证据。本研究旨在探讨社区居住的老年人中血浆 NfL 和 PGRN 水平与虚弱的关系。
我们纳入了来自多域阿尔茨海默病预防试验(MAPT)的 507 名年龄在 76.7 [4.5] 岁、有血浆 NfL 和 PGRN 测量值的老年人。每位参与者的生物标志物测量时间点(研究入组后 12 或 24 个月)被定义为基线。使用 Fried 的虚弱标准在 12、24、36、48 和 60 个月时评估虚弱表型(稳健、虚弱前期和虚弱)。使用逻辑回归检验血浆神经退行性生物标志物与虚弱严重程度的横断面关联。我们进一步使用 Cox 比例风险模型评估基线时(n=403)稳健或虚弱前期参与者中血浆生物标志物与虚弱发生的关联。
基线时,与正常 NfL 相比,高血浆 NfL 水平(>93.11pg/ml[四分位数上限])的参与者更有可能处于虚弱前期或虚弱状态(比值比=1.68;95%置信区间=1.10-2.57);然而,在控制了协变量后,这种关联不再显著。在调整分析中,NfL 和 PGRN 水平均与 4 年内发生的虚弱无前瞻性关联。
在调整分析中,本研究未发现循环 NfL 和 PGRN 水平与社区居住的老年人虚弱之间存在关联。血浆神经退行性标志物是否可作为虚弱的潜在生物标志物尚需进一步研究。