阿尔茨海默病遗传风险会改变认知健康的中老年人的感知执行功能障碍。

IF 2.8 Q2 NEUROSCIENCES Journal of Alzheimer's disease reports Pub Date : 2024-02-16 eCollection Date: 2024-01-01 DOI:10.3233/ADR-230166
Sarah A Evans, Elizabeth R Paitel, Riya Bhasin, Kristy A Nielson
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引用次数: 0

摘要

背景:主观认知抱怨(SCC)可能是未来认知能力下降的早期指标。然而,将主观认知症状与客观认知表现进行比较的结果各不相同,尤其是在记忆领域。在非记忆领域,如执行功能领域,主观和客观主诉之间的关系就更不明确了,尽管有证据表明这些领域的变化非常早。此外,载脂蛋白-E ɛ4等位基因是阿尔茨海默病(AD)的主要遗传风险,而载脂蛋白-E ɛ4等位基因携带者在失忆和非失忆领域的早期变化尤为明显:本研究调查了ɛ4等位基因在54名健康、认知功能完好的中老年人主观和客观执行功能一致性中的作用:参与者(Mage = 64.07, SD = 9.27, range = 48-84; ɛ4+=18)完成了额叶系统行为量表(FrSBe)执行功能障碍量表(EXECDYS),以测量主观执行功能(SEF)和多项执行功能任务,这些任务被浓缩为一个单一因子:结果:在考虑年龄、抑郁和焦虑等因素后,客观执行功能表现能显著预测 SEF。重要的是ɛ4调节了这一效应。具体来说,与不携带ɛ4等位基因的人相比,携带ɛ4等位基因的人对其执行功能的自我认知准确性明显较低:采用一种将执行功能自我评估与客观神经认知评估相结合的方法,可能有助于识别即将出现的认知功能衰退的早期迹象,尤其是在那些具有 AD 遗传风险的人群中。这种方法可以在症状出现之前灵敏地确定那些最容易在未来出现认知功能衰退的人群,而此时进行干预是最有效的。
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Genetic Risk for Alzheimer's Disease Alters Perceived Executive Dysfunction in Cognitively Healthy Middle-Aged and Older Adults.

Background: Subjective cognitive complaints (SCC) may be an early indicator of future cognitive decline. However, findings comparing SCC and objective cognitive performance have varied, particularly in the memory domain. Even less well established is the relationship between subjective and objective complaints in non-amnestic domains, such as in executive functioning, despite evidence indicating very early changes in these domains. Moreover, particularly early changes in both amnestic and non-amnestic domains are apparent in those carrying the Apolipoprotein-E ɛ4 allele, a primary genetic risk for Alzheimer's disease (AD).

Objective: This study investigated the role of the ɛ4 allele in the consistency between subjective and objective executive functioning in 54 healthy, cognitively intact, middle-aged and older adults.

Methods: Participants (Mage = 64.07, SD = 9.27, range = 48-84; ɛ4+ = 18) completed the Frontal Systems Behavior Scale (FrSBe) Executive Dysfunction Scale (EXECDYS) to measure subjective executive functioning (SEF) and multiple executive functioning tasks, which were condensed into a single factor.

Results: After accounting for age, depression, and anxiety, objective executive functioning performance significantly predicted SEF. Importantly, ɛ4 moderated this effect. Specifically, those carrying the ɛ4 allele had significantly less accurate self-awareness of their executive functioning compared to ɛ4 non-carriers.

Conclusions: Utilizing an approach that integrates self-evaluation of executive functioning with objective neurocognitive assessment may help identify the earliest signs of impending cognitive decline, particularly in those with genetic risk for AD. Such an approach could sensitively determine those most prone to future cognitive decline prior to symptom onset, when interventions could be most effective.

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