Altered functional connectivity between primary visual cortex and cerebellum in Alzheimer's disease

小脑 神经科学 功能磁共振成像 视皮层 阿尔茨海默病 正电子发射断层摄影术 显著性(神经科学) 心理学 认知 认知障碍 功能连接 磁共振成像 听力学 医学 疾病 病理 放射科
作者
Chang Cai,Takashi Kato,Yutaka Arahata,Akinori Takeda,Takashi Nihashi,Keita Sakurai,Emi Tanaka,Kersten Diers,Kosuke Fujita,Taiki Sugimoto,Takashi Sakurai,Kengo Ito,Akinori Nakamura
出处
期刊:Journal of Alzheimer's Disease [IOS Press]
标识
DOI:10.1177/13872877241303849
摘要

Background It is known that eyes-open (EO) and eyes-closed (EC) conditions invoke different organizations of brain functional networks, such as sensorimotor, attention, and salience networks in healthy participants. Functional connectivity (FC) extracted from resting-state functional magnetic resonance imaging data, under either EO or EC conditions, has been widely applied to explore the neural substrates of Alzheimer's disease (AD). However, the impact of eye conditions on FC within the AD continuum remains not fully understood. Objective This study aims to investigate the effects of eye conditions on FC across the AD continuum. Methods FC with the primary visual cortex (V1) seed was analyzed for both EO and EC conditions in 59 amyloid-β (Aβ)-positron emission tomography (PET)-negative cognitively normal (CN−), 14 Aβ-PET-positive CN+, 24 mild cognitive impairment (MCI+), and 15 AD individuals. Results EO and EC differently modulated FC between the V1 and cerebellum, especially the posterior vermis, in all groups. In CN−, CN+, and MCI+ groups, EO significantly facilitated FC between V1 and the cerebellum compared with the EC condition. However, the AD group showed the reverse pattern. Moreover, a sub-analysis demonstrated that the FC significantly correlated with a truncal balance measure under EO, but not EC, in participants with MCI+ and AD. Conclusions The results show that the FC between the V1 and cerebellum changed in AD. This finding may partially explain the impaired truncal balance and tendency to fall down in AD. This study suggests that analyzing FC under EO and EC conditions may provide a new functional biomarker for AD.
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