German Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.
University of Bonn Medical Center, Department of Neurodegenerative Diseases and Geriatric Psychiatry/Psychiatry, Bonn, Germany.
J Alzheimers Dis. 2022;87(2):545-555. doi: 10.3233/JAD-215416.
It is unclear whether subjective cognitive decline (SCD) is a relevant clinical marker of incipient Alzheimer's disease (AD) and future cognitive deterioration in individuals with a family history of AD (FHAD).
To investigate the association of SCD with cross-sectional cerebrospinal fluid (CSF) AD biomarker levels and cognitive decline in cognitively normal older adults with or without a first-degree FHAD.
We analyzed data from cognitively normal individuals with first-degree FHAD (n = 82 "AD relatives"; mean age: 65.7 years (SD = 4.47); 59% female) and a similar group of n = 236 healthy controls without FHAD from the DELCODE study. We measured SCD with an in-depth structured interview from which we derived a SCD score, capturing features proposed to increase likelihood of underlying AD ("SCD-plus score"). We tested whether higher SCD-plus scores were associated with more pathological CSF AD biomarker levels and cognitive decline over time and whether this association varied by group.
AD relatives showed higher SCD-plus scores than healthy controls and more cognitive decline over time. Higher SCD-plus scores also related stronger to cognitive change and abnormal CSF AD biomarker levels in the AD relatives as compared to the healthy controls group.
Quantification of specific SCD features can provide further information on the likelihood of early AD pathology and cognitive decline among AD relatives. FHAD and SCD appear as synergistically acting enrichment strategies in AD research, the first one as a permanent indicator of genetic risk, the latter one as a correlate of disease progression.
目前尚不清楚主观认知下降(SCD)是否是具有阿尔茨海默病家族史(FHAD)的个体出现早期阿尔茨海默病(AD)和未来认知恶化的相关临床标志物。
旨在研究 SCD 与认知正常的老年个体(无论是否具有一级 FHAD)的横断面脑脊液(CSF)AD 生物标志物水平和认知下降的相关性,这些个体无认知障碍。
我们分析了来自 DELCODE 研究的认知正常的一级 FHAD 个体(n=82“AD 亲属”;平均年龄:65.7 岁(SD=4.47);59%为女性)和具有相似一级 FHAD 个体的无 FHAD 的认知正常个体(n=236 名健康对照者)的数据。我们使用深入的结构化访谈来测量 SCD,并从中得出了一个 SCD 评分,该评分捕捉了增加潜在 AD 可能性的特征(“SCD-plus 评分”)。我们检验了较高的 SCD-plus 评分是否与更高的 CSF AD 生物标志物水平和随时间的认知下降相关,以及这种相关性是否因组而异。
AD 亲属的 SCD-plus 评分高于健康对照者,且随时间推移认知下降更为明显。较高的 SCD-plus 评分与 AD 亲属的认知变化和异常 CSF AD 生物标志物水平的相关性也更强,与健康对照组相比。
对特定 SCD 特征的定量分析可以为 AD 亲属中早期 AD 病理和认知下降的可能性提供更多信息。FHAD 和 SCD 似乎是 AD 研究中协同作用的富集策略,前者是遗传风险的永久指标,后者是疾病进展的相关指标。