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家族性常染色体显性阿尔茨海默病无症状个体中加速的长期遗忘与衰老相关的血源性因素的关联。

Association of accelerated long-term forgetting and senescence-related blood-borne factors in asymptomatic individuals from families with autosomal dominant Alzheimer's disease.

机构信息

Innovation Center for Neurological Disorders and Department of Neurology, Xuanwu Hospital, Capital Medical University, National Clinical Research Center for Geriatric Diseases, 45 Changchun St, Beijing, China.

Beijing Key Laboratory of Geriatric Cognitive Disorders, Beijing, China.

出版信息

Alzheimers Res Ther. 2021 May 27;13(1):107. doi: 10.1186/s13195-021-00845-0.

Abstract

BACKGROUND

Accelerated long-term forgetting has been identified in preclinical Alzheimer's disease (AD) and is attributed to a selective impairment of memory consolidation in which the hippocampus plays a key role. As blood may contain multiple senescence-related factors that involved in neurogenesis and synaptic plasticity in the hippocampus, we tested whether there is an association between blood-borne factors and accelerated long-term forgetting in asymptomatic individuals from families with autosomal dominant AD (ADAD).

METHODS

We analyzed data of 39 asymptomatic participants (n = 18 ADAD mutation carriers, n = 21 non-carriers) from the Chinese Familial Alzheimer's Disease Network (CFAN) study. Long-term forgetting rates were calculated based on recall or recognition of two materials (word list and complex figure) at three delays comprising immediate, 30 min, and 7 days. Peripheral blood concentrations of candidate pro-aging factors (CC chemokine ligand 11 [CCL11] and monocyte chemotactic protein 1 [MCP1]) and rejuvenation factors (growth differentiation factor 11 [GDF11], thrombospondin-4 [THBS4], and secreted protein acidic and rich in cysteine like 1 [SPARCL1]) were evaluated in all participants.

RESULTS

Despite normal performance on standard 30-min delayed testing, mutation carriers exhibited accelerated forgetting of verbal and visual material over 7 days in comparison with matched non-carriers. In the whole sample, lower plasma THBS4 was associated with accelerated long-term forgetting in list recall (β = -0.46, p = 0.002), figure recall (β = -0.44, p = 0.004), and list recognition (β = -0.37, p = 0.010). Additionally, higher plasma GDF11 and CCL11 were both associated with accelerated long-term forgetting (GDF11 versus figure recall: β = 0.39, p = 0.007; CCL11 versus list recognition: β = 0.44, p = 0.002).

CONCLUSIONS

Accelerated long-term forgetting is a cognitive feature of presymptomatic AD. Senescence-related blood-borne factors, especially THBS4, GDF11, and CCL11, may be promising biomarkers for the prediction of accelerated long-term forgetting.

摘要

背景

在临床前阿尔茨海默病(AD)中已经发现了加速的长期遗忘,这归因于记忆巩固的选择性损伤,其中海马体起着关键作用。由于血液中可能含有多种与衰老相关的因子,这些因子参与海马体中的神经发生和突触可塑性,因此我们测试了血液来源的因子与无症状个体中是否存在关联家族性 AD(ADAD)。

方法

我们分析了来自中国家族性阿尔茨海默病网络(CFAN)研究的 39 名无症状参与者的数据(n = 18 名 ADAD 基因突变携带者,n = 21 名非携带者)。根据两个材料(单词列表和复杂图形)在三个延迟时间(即时、30 分钟和 7 天)的回忆或识别,计算长期遗忘率。在所有参与者中评估了候选衰老前因子(趋化因子配体 11 [CCL11]和单核细胞趋化蛋白 1 [MCP1])和恢复活力因子(生长分化因子 11 [GDF11]、血栓素-4 [THBS4]和富含半胱氨酸的分泌蛋白酸性和丰富 1 [SPARCL1])的外周血浓度。

结果

尽管标准的 30 分钟延迟测试表现正常,但与匹配的非携带者相比,突变携带者在 7 天内表现出言语和视觉材料的遗忘速度加快。在整个样本中,较低的血浆 THBS4 与列表回忆(β = -0.46,p = 0.002)、图形回忆(β = -0.44,p = 0.004)和列表识别(β = -0.37,p = 0.010)的长期遗忘加快相关。此外,较高的血浆 GDF11 和 CCL11 均与长期遗忘加速相关(GDF11 与图形回忆:β = 0.39,p = 0.007;CCL11 与列表识别:β = 0.44,p = 0.002)。

结论

加速的长期遗忘是无症状 AD 的认知特征。衰老相关的血液来源因子,尤其是 THBS4、GDF11 和 CCL11,可能是预测加速长期遗忘的有希望的生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/448e/8157428/8205587545ce/13195_2021_845_Fig1_HTML.jpg

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