Department of Neurology, Brain Mapping Center, David Geffen School of Medicine at UCLA, Los Angeles, CA, USA.
Department of Psychiatry & Biobehavioral Sciences, Semel Institute for Neuroscience & Human Behavior, David Geffen School of Medicine at the University of California, Los Angeles, CA, USA.
Am J Geriatr Psychiatry. 2018 Jan;26(1):13-22. doi: 10.1016/j.jagp.2017.09.001. Epub 2017 Sep 15.
Growing evidence supports an association between increased blood pressure and: (a) poor cognitive performance in older adults, and (b) various biomarkers of increased Alzheimer's disease (AD) neuropathology. The objective of this study was to determine whether systolic blood pressure (SBP) and diastolic blood pressure (DBP) were significantly associated with cognitive functioning in non-demented adults, and to examine in vivo AD pathology as a possible mediator of this association.
Positron emission tomography (PET) scans with 2-(1-{6-[(2-[F-18]fluoroethyl)(methyl)amino]-2-naphthyl}ethylidene)malononitrile (FDDNP) provide in vivo measurements of plaque and tangle burden. A total of 101 non-demented older subjects with blood pressure data and FDDNP-PET scans were drawn from a larger study of predictors of cognitive decline. A neuropsychological test battery was used to compute "global cognitive scores" (averaged across five key domains), which served as an index of general cognitive functioning.
Higher DBP (but not SBP) was significantly associated with lower cognitive scores, controlling for age, sex, antihypertensive medication use, and ApoE genotype (η = 0.06). However, this relationship was no longer significant after introducing FDDNP-PET binding as an additional covariate in the statistical models. In vivo plaque and tangle burden accounted for over 30% of the observed association between higher DBP and poorer cognitive performance.
By suggesting a mediation of the relationship between DBP and cognitive functioning by FDDNP-PET binding, this study advances our understanding of some potential predictors of cognitive decline in non-demented adults, and underscores the importance of devising early multimodal interventions to more effectively combat degenerative brain disorders.
越来越多的证据表明,血压升高与:(a)老年人认知表现下降,以及(b)阿尔茨海默病(AD)神经病理学中各种生物标志物的增加有关。本研究的目的是确定收缩压(SBP)和舒张压(DBP)是否与非痴呆成年人的认知功能显著相关,并研究 AD 病理学是否可能是这种关联的中介。
正电子发射断层扫描(PET)扫描使用 2-(1- {6- [(2- [F-18] 氟乙基)(甲基)氨基]-2-萘基}亚乙基)丙二腈(FDDNP)提供斑块和缠结负担的体内测量。从认知衰退预测因素的更大研究中抽取了 101 名具有血压数据和 FDDNP-PET 扫描的非痴呆老年受试者。使用神经心理学测试组合来计算“总体认知评分”(平均五个关键领域),作为一般认知功能的指标。
在控制年龄、性别、抗高血压药物使用和 ApoE 基因型后,较高的 DBP(但不是 SBP)与较低的认知评分显著相关(η=0.06)。然而,在将 FDDNP-PET 结合作为附加协变量引入统计模型后,这种关系不再显著。体内斑块和缠结负担解释了 DBP 升高与认知表现较差之间观察到的关联的 30%以上。
通过表明 DBP 和认知功能之间的关系可能由 FDDNP-PET 结合介导,本研究增进了我们对非痴呆成年人认知衰退一些潜在预测因素的理解,并强调了设计早期多模态干预措施以更有效地对抗退行性脑疾病的重要性。