Effective connectivity in the default mode network is distinctively disrupted in Alzheimer's disease—A simultaneous resting‐state FDG‐PET/fMRI study

默认模式网络 神经科学 海马体 前额叶皮质 静息状态功能磁共振成像 阿尔茨海默病 心理学 后扣带 后顶叶皮质 皮质(解剖学) 认知 医学 疾病 病理
作者
Martin Scherr,Lukas Utz,Masoud Tahmasian,Lorenzo Pasquini,Michel J. Grothe,Josef P. Rauschecker,Timo Grimmer,Alexander Drzezga,Christian Sorg,Valentin Riedl
出处
期刊:Human Brain Mapping [Wiley]
卷期号:42 (13): 4134-4143 被引量:58
标识
DOI:10.1002/hbm.24517
摘要

Abstract A prominent finding of postmortem and molecular imaging studies on Alzheimer's disease (AD) is the accumulation of neuropathological proteins in brain regions of the default mode network (DMN). Molecular models suggest that the progression of disease proteins depends on the directionality of signaling pathways. At network level, effective connectivity (EC) reflects directionality of signaling pathways. We hypothesized a specific pattern of EC in the DMN of patients with AD, related to cognitive impairment. Metabolic connectivity mapping is a novel measure of EC identifying regions of signaling input based on neuroenergetics. We simultaneously acquired resting‐state functional MRI and FDG‐PET data from patients with early AD ( n = 35) and healthy subjects ( n = 18) on an integrated PET/MR scanner. We identified two distinct subnetworks of EC in the DMN of healthy subjects: an anterior part with bidirectional EC between hippocampus and medial prefrontal cortex and a posterior part with predominant input into medial parietal cortex. Patients had reduced input into the medial parietal system and absent input from hippocampus into medial prefrontal cortex ( p < 0.05, corrected). In a multiple linear regression with unimodal imaging and EC measures ( F 4,25 = 5.63, p = 0.002, r 2 = 0.47), we found that EC ( β = 0.45, p = 0.012) was stronger associated with cognitive deficits in patients than any of the PET and fMRI measures alone. Our approach indicates specific disruptions of EC in the DMN of patients with AD and might be suitable to test molecular theories about downstream and upstream spreading of neuropathology in AD.
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