认知能力保持良好的非老年人的血浆神经退行性生物标志物

IF 7 2区 医学 Q1 GERIATRICS & GERONTOLOGY Aging and Disease Pub Date : 2024-11-06 DOI:10.14336/AD.2024.1260
Estrella Gómez-Tortosa, Pablo Agüero-Rabes, Alicia Ruiz-González, Sonia Wagner, Raquel Téllez, Ignacio Mahillo, Andrea Ruiz-Calvo, María José Sainz, Anna Lena Nystrom, Lucía Cremades-Jimeno, Teodoro Del Ser, Pascual Sánchez-Juan
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引用次数: 0

摘要

血浆生物标志物是筛查和诊断神经退行性疾病患者的有效工具。然而,考虑衰老对生物标志物特征的影响至关重要,尤其是在人口中最年长的群体中。此外,该样本中的生物标志物还能在体内揭示大脑衰老的生理机制,同时支持认知能力的保护。在这项研究中,我们使用单分子阵列(SIMOA)平台分析了 75 名认知能力保持良好的非老年患者的血浆阿尔茨海默病(AD)核心生物标志物、神经丝蛋白轻链(NfL)和神经胶质纤维酸蛋白(GFAP),并与 153 名在 6 年中认知能力未受损(CU)的志愿者(年龄在 70 岁以下和 71 至 85 岁之间)的基线样本以及 108 名 AD 患者进行了比较。与两个CU组相比,非老年患者几乎没有APOEε4等位基因,他们的Aß40、Aß42、p-tau181、NfL和GFAP显著较高,Aß42/40比值显著较低(P&;lt0.001)。非老年人的 NfL 和 GFAP 浓度增加了两倍。年轻组和老年 CU 组的血浆生物标志物均无差异。只有在同时分析CU对照组和非老年组时,生物标志物才与年龄密切相关。与AD病例相比,非长者的p-tau181水平较低(P=0.001),总tau水平较高(P=0.02),Aß40、Aß42和NfL水平高得多(P&;lt0.001)。非老年人的 GFAP 水平与 AD 患者相似。总之,认知能力保持良好的非老年人不会出现注意力缺失症生物标志物特征,并表现出较高的 Aß42 水平。然而,他们的 NfL 和 GFAP 增加了三倍,这证明他们衰老的大脑在某种程度上对神经变性具有抵抗力。这些数据支持根据 NfL 和 GFAP 值对临床痴呆症的预后进行谨慎判断。总体而言,CU 患者的血浆生物标志物直到八十多岁仍相当稳定。
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Plasma Neurodegenerative Biomarkers in Cognitively Preserved Nonagenarians.

Plasma biomarkers represent promising tools for the screening and diagnosis of patients with neurodegenerative conditions. However, it is crucial to account for the effects of aging on biomarker profiles, especially in the oldest segments of the population. Additionally, biomarkers in this sample can offer in vivo insights into the physiological mechanisms underlying brain aging while concomitantly supporting cognitive preservation. In this study we analyzed plasma Alzheimer's disease (AD) core biomarkers, neurofilament light chain (NfL), and glial fibrillary acid protein (GFAP) using the Single Molecule Array (SIMOA) platform in 75 cognitively preserved nonagenarians, and compared with baseline samples of 153 volunteers who were cognitively unimpaired (CU) during six years (classified in ≤ 70, and 71 to 85 years of age), and with 108 AD patients. Nonagenarians almost lack the APOEε4 allele, and had significantly higher Aß40, Aß42, p-tau181, NfL, and GFAP, along with a significantly lower Aß42/40 ratio (P&;lt0.001) compared with the two CU groups. NfL and GFAP tripled concentrations in nonagenarians. No differences were noted in any plasma biomarker between the younger and older CU groups. Biomarkers correlated strongly with age only when analyzing together CU controls and nonagenarians. Compared with AD cases, nonagenarians showed lower p-tau181 (P=0.001), higher total tau (P=0.02), and much higher Aß40, Aß42 and NfL levels (P&;lt0.001). The levels of GFAP in nonagenarians were similar to those observed in AD patients. In conclusion, cognitively preserved nonagenarians do not develop the AD biomarker signature and exhibit higher levels of Aß42. However, their threefold increase in NfL and GFAP supports their aging brains are somehow resilient to neurodegeneration. These data support caution in the prognosis of clinical dementia based on NfL and GFAP values. Overall, plasma biomarkers in CU individuals remained quite stable till the eighties.

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来源期刊
Aging and Disease
Aging and Disease GERIATRICS & GERONTOLOGY-
CiteScore
14.60
自引率
2.70%
发文量
138
审稿时长
10 weeks
期刊介绍: Aging & Disease (A&D) is an open-access online journal dedicated to publishing groundbreaking research on the biology of aging, the pathophysiology of age-related diseases, and innovative therapies for conditions affecting the elderly. The scope encompasses various diseases such as Stroke, Alzheimer's disease, Parkinson’s disease, Epilepsy, Dementia, Depression, Cardiovascular Disease, Cancer, Arthritis, Cataract, Osteoporosis, Diabetes, and Hypertension. The journal welcomes studies involving animal models as well as human tissues or cells.
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