Abstract

BackgroundAccelerated 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).MethodsWe 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.ResultsDespite 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).ConclusionsAccelerated 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.

Highlights

  • 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

  • Accelerated long-term forgetting is a cognitive feature of presymptomatic AD

  • This memory impairment was thought to be attributed to a failure of memory consolidation process, which was primarily governed by the medial temporal lobe (MTL), especially the hippocampus [7]

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Summary

Introduction

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. The fact that AD pathological changes develop decades before visible cognitive impairments might reflect that the sensitivities of the cognitive assays currently used are not sufficient enough [3, 4] In this context, increasing evidence has suggested that accelerated long-term forgetting would be a subtle cognitive impairment in presymptomatic autosomal dominant AD (ADAD) mutation carriers [5, 6]. Initial studies in mouse models have identified pro-aging factors (monocyte chemotactic protein 1 [MCP1] and CC chemokine ligand 11 [CCL11]) [8] and rejuvenating factor (growth differentiation factor 11 [GDF11]) [9] that correlated with hippocampal neurogenesis and cognitive function Both thrombospondin-4 (THBS4) and secreted protein acidic and rich in cysteine like 1 (SPARCL1) were found to represent rejuvenation factors that enhance synaptic connectivity [10]. Few studies have examined these senescence-related blood-borne factors with respect to subtle cognitive change, especially hippocampal-dependent memory impairments, in the preclinical stage of AD

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