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淀粉样蛋白-β调节阿尔茨海默病中神经丝轻链与脑萎缩的关联。

Amyloid-beta modulates the association between neurofilament light chain and brain atrophy in Alzheimer's disease.

机构信息

Translational Neuroimaging Laboratory, McGill University Research Centre for Studying in Aging, Montreal, QC, Canada.

Cerebral Imaging Centre, Douglas Research Centre, Montreal, QC, Canada.

出版信息

Mol Psychiatry. 2021 Oct;26(10):5989-6001. doi: 10.1038/s41380-020-0818-1. Epub 2020 Jun 26.

Abstract

Neurofilament light chain (NFL) measurement has been gaining strong support as a clinically useful neuronal injury biomarker for various neurodegenerative conditions. However, in Alzheimer's disease (AD), its reflection on regional neuronal injury in the context of amyloid pathology remains unclear. This study included 83 cognitively normal (CN), 160 mild cognitive impairment (MCI), and 73 AD subjects who were further classified based on amyloid-beta (Aβ) status as positive or negative (Aβ+ vs Aβ-). In addition, 13 rats (5 wild type and 8 McGill-R-Thy1-APP transgenic (Tg)) were examined. In the clinical study, reduced precuneus/posterior cingulate cortex and hippocampal grey matter density were significantly associated with increased NFL concentrations in cerebrospinal fluid (CSF) or plasma in MCI Aβ+ and AD Aβ+. Moreover, AD Aβ+ showed a significant association between the reduced grey matter density in the AD-vulnerable regions and increased NFL concentrations in CSF or plasma. Congruently, Tg rats recapitulated and validated the association between CSF NFL and grey matter density in the parietotemporal cortex, entorhinal cortex, and hippocampus in the presence of amyloid pathology. In conclusion, reduced grey matter density and elevated NFL concentrations in CSF and plasma are associated in AD-vulnerable regions in the presence of amyloid positivity in the AD clinical spectrum and amyloid Tg rat model. These findings further support the NFL as a neuronal injury biomarker in the research framework of AD biomarker classification and for the evaluation of therapeutic efficacy in clinical trials.

摘要

神经丝轻链(NFL)的测量作为各种神经退行性疾病的有用的神经元损伤生物标志物,已得到越来越多的支持。然而,在阿尔茨海默病(AD)中,其在淀粉样蛋白病理学背景下对区域性神经元损伤的反映仍不清楚。本研究纳入了 83 名认知正常(CN)、160 名轻度认知障碍(MCI)和 73 名 AD 患者,这些患者根据淀粉样蛋白-β(Aβ)状态进一步分为阳性(Aβ+)或阴性(Aβ-)。此外,还检查了 13 只大鼠(5 只野生型和 8 只 McGill-R-Thy1-APP 转基因(Tg))。在临床研究中,MCI Aβ+和 AD Aβ+患者脑脊液(CSF)或血浆中 NFL 浓度升高与楔前叶/后扣带回皮质和海马灰质密度降低显著相关。此外,AD Aβ+患者在 AD 易损区灰质密度降低与 CSF 或血浆中 NFL 浓度升高之间存在显著相关性。一致地,Tg 大鼠在淀粉样蛋白病理学存在的情况下,重现并验证了 CSF NFL 与颞顶叶皮质、内嗅皮质和海马灰质密度之间的相关性。总之,在 AD 临床谱中存在淀粉样蛋白阳性和淀粉样蛋白 Tg 大鼠模型中,AD 易损区灰质密度降低和 CSF 及血浆中 NFL 浓度升高相关。这些发现进一步支持 NFL 作为 AD 生物标志物分类研究框架中的神经元损伤生物标志物,以及在临床试验中评估治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d25d/8758474/a1e9ed63964e/41380_2020_818_Fig1_HTML.jpg

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