Byeon Gihwan, Byun Min Soo, Yi Dahyun, Ahn Hyejin, Jung Gijung, Sohn Bo Kyung, Jung Joon Hyung, Chang Yoon Young, Kim Kyungtae, Choi Hyeji, Kim Yoon Hee, Kim Yu Kyeong, Kang Koung Mi, Sohn Chul-Ho, Lee Dong Young
Department of Psychiatry, The Catholic University of Korea, Seoul St. Mary's Hospital, Seoul, Korea.
Department of Neuropsychiatry, Seoul National University Hospital, Seoul, Korea.
Clin Psychopharmacol Neurosci. 2025 May 31;23(2):256-265. doi: 10.9758/cpn.24.1238. Epub 2025 Feb 11.
Cholinesterase inhibitors (ChEIs) are effective in treating mild to moderate Alzheimer's disease (AD) dementia by compensating for acetylcholine deficiency. While their use in mild cognitive impairment (MCI) lacks strong trial support, some studies suggest they may delay neurodegeneration. This study aims to investigate ChEIs' neuroprotective effects in individuals with amnestic MCI (aMCI) using multi-modal neuroimaging, and to determine if amyloid-beta (Aβ) deposition influences these effects.
Longitudinal data from a cohort study were retrospectively analyzed. A total of 118 aMCI patients (ages 55- 90), who underwent baseline evaluations encompassing the assessment of ChEI use and [C] Pittsburgh compound B-positron emission tomography (PET), were included in the analyses. All participants also received baseline and 2-year follow-up magnetic resonance imaging and [F] fluorodeoxyglucose-PET imaging.
The ChEI use group exhibited a significantly lesser decline in AD-signature region cerebral metabolism (AD-CM) over a 2-year period than the ChEI non-use group (B = 0.089, 95% CI: 0.030-0.149). However, there was no significant difference in the 2-year change of AD-signature region cortical thickness (AD-CT) (B = 0.032, 95% CI: -0.075 to 0.138) and hippocampal volume (B = -88.013, 95% CI: -323.900 to 147.874) between the ChEI use and non-use groups. The presence of Aβ pathology did not moderate the effect of ChEI use on AD-CM, AD-CT, or hippocampal volume.
The findings suggest that ChEIs may delay functional neurodegeneration in aMCI individuals, irrespective of the presence of amyloid pathology.
胆碱酯酶抑制剂(ChEIs)可通过弥补乙酰胆碱缺乏来有效治疗轻度至中度阿尔茨海默病(AD)痴呆。虽然其在轻度认知障碍(MCI)中的应用缺乏有力的试验支持,但一些研究表明它们可能会延缓神经退行性变。本研究旨在使用多模态神经影像学研究ChEIs对遗忘型MCI(aMCI)个体的神经保护作用,并确定β淀粉样蛋白(Aβ)沉积是否会影响这些作用。
对一项队列研究的纵向数据进行回顾性分析。分析纳入了118例aMCI患者(年龄55 - 90岁),这些患者接受了包括ChEI使用情况评估和[C]匹兹堡化合物B正电子发射断层扫描(PET)在内的基线评估。所有参与者还接受了基线和2年随访的磁共振成像以及[F]氟脱氧葡萄糖-PET成像。
在2年期间,使用ChEI的组与未使用ChEI的组相比,AD特征区域脑代谢(AD-CM)的下降显著更小(B = 0.089,95%CI:0.030 - 0.149)。然而,使用ChEI组与未使用ChEI组之间,AD特征区域皮质厚度(AD-CT)的2年变化(B = 0.032,95%CI:-0.075至0.138)和海马体积(B = -88.013,95%CI:-323.900至147.874)没有显著差异。Aβ病理的存在并未调节ChEI使用对AD-CM、AD-CT或海马体积的影响。
研究结果表明,ChEIs可能会延缓aMCI个体的功能性神经退行性变,无论是否存在淀粉样蛋白病理。