Department of Psychiatry, Korea University Guro Hospital, Korea University College of Medicine, Seoul, Republic of Korea.
Department of Brain and Cognitive Engineering, Korea University, Seoul, Republic of Korea.
J Affect Disord. 2021 Feb 15;281:459-466. doi: 10.1016/j.jad.2020.12.049. Epub 2020 Dec 15.
Elderly patients with late-life depression (LLD) often report mild cognitive impairment (MCI), so Alzheimer's disease (AD) is hard to identify in these patients. We aimed to identify the structural and functional differences between prodromal AD and LLD-related MCI.
We performed voxel-based morphometry and functional connectivity (FC) analyses in elderly patients with both LLD and MCI to compare alterations between those with cerebral amyloidopathy and those without. We subdivided patients into subthreshold depression (STD) and major depressive disorder (MDD) groups. Using florbetaben positron emission tomography (PET), we compared volume and connectivity between healthy controls and four STD and MDD groups with or without amyloid deposition(A): STD-MCI-A(+), MDD-MCI-A(+), STD-MCI-A(-), and MDD-MCI-A(-).
Subjects with MDD or amyloid deposition showed greater volume reduction in the left middle temporal gyrus. MDD groups had lower FC than STD groups in the frontal, cortical, and limbic areas. The STD-MCI-A(+) group showed greater FC reduction than the MDD-MCI-A(-) and STD-MCI-A(-) groups, particularly in the hippocampus, parahippocampus, and frontal and temporal cortices. The functional differences associated with amyloid plaques were more evident in the STD group than in the MDD group.
Limitations include disproportional sex ratios, inability to determine the longitudinal effects of amyloidopathy in large populations.
Regional gray matter loss and alterations in brain networks may reflect impairments caused by amyloid deposition and depression. Such changes may facilitate the detection of prodromal AD in elderly patients with both depression and cognitive dysfunction, allowing earlier intervention and more appropriate treatment.
老年晚发性抑郁症(LLD)患者常伴有轻度认知障碍(MCI),因此这些患者的阿尔茨海默病(AD)难以识别。我们旨在确定前驱 AD 与 LLD 相关的 MCI 之间的结构和功能差异。
我们对患有 LLD 和 MCI 的老年患者进行了基于体素的形态测量和功能连接(FC)分析,以比较有脑淀粉样蛋白病和无淀粉样蛋白病的患者之间的变化。我们将患者分为亚阈抑郁(STD)和重度抑郁障碍(MDD)组。使用氟比他滨正电子发射断层扫描(PET),我们比较了健康对照组和四个 STD 和 MDD 组(有或无淀粉样蛋白沉积(A):STD-MCI-A(+)、MDD-MCI-A(+)、STD-MCI-A(-)和 MDD-MCI-A(-))之间的体积和连接。
MDD 或淀粉样蛋白沉积的患者左侧颞中回体积减少更大。MDD 组的额叶、皮质和边缘区域的 FC 低于 STD 组。与 MDD-MCI-A(-)和 STD-MCI-A(-)组相比,STD-MCI-A(+)组的 FC 减少更大,特别是在海马、海马旁回以及额叶和颞叶皮质。与淀粉样斑块相关的功能差异在 STD 组比 MDD 组更明显。
局限性包括性别比例不均,无法在大人群中确定淀粉样蛋白病的纵向影响。
区域性灰质丢失和脑网络的改变可能反映了由淀粉样蛋白沉积和抑郁引起的损伤。这些变化可能有助于在伴有抑郁和认知功能障碍的老年患者中更早地发现前驱 AD,从而进行早期干预和更适当的治疗。