The Effect of Cholinesterase Inhibitors on Neurodegeneration in Individuals with Amnestic Mild Cognitive Impairment.

IF 2.4 4区 医学 Q3 NEUROSCIENCES
Clinical Psychopharmacology and Neuroscience Pub Date : 2025-05-31 Epub Date: 2025-02-11 DOI:10.9758/cpn.24.1238
Gihwan Byeon, Min Soo Byun, Dahyun Yi, Hyejin Ahn, Gijung Jung, Bo Kyung Sohn, Joon Hyung Jung, Yoon Young Chang, Kyungtae Kim, Hyeji Choi, Yoon Hee Kim, Yu Kyeong Kim, Koung Mi Kang, Chul-Ho Sohn, Dong Young Lee
{"title":"The Effect of Cholinesterase Inhibitors on Neurodegeneration in Individuals with Amnestic Mild Cognitive Impairment.","authors":"Gihwan Byeon, Min Soo Byun, Dahyun Yi, Hyejin Ahn, Gijung Jung, Bo Kyung Sohn, Joon Hyung Jung, Yoon Young Chang, Kyungtae Kim, Hyeji Choi, Yoon Hee Kim, Yu Kyeong Kim, Koung Mi Kang, Chul-Ho Sohn, Dong Young Lee","doi":"10.9758/cpn.24.1238","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>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.</p><p><strong>Methods: </strong>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 [<sup>11</sup>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 [<sup>18</sup>F] fluorodeoxyglucose-PET imaging.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusion: </strong>The findings suggest that ChEIs may delay functional neurodegeneration in aMCI individuals, irrespective of the presence of amyloid pathology.</p>","PeriodicalId":10420,"journal":{"name":"Clinical Psychopharmacology and Neuroscience","volume":"23 2","pages":"256-265"},"PeriodicalIF":2.4000,"publicationDate":"2025-05-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12000676/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Psychopharmacology and Neuroscience","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.9758/cpn.24.1238","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/11 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: 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.

Methods: 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 [11C] 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 [18F] fluorodeoxyglucose-PET imaging.

Results: 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.

Conclusion: The findings suggest that ChEIs may delay functional neurodegeneration in aMCI individuals, irrespective of the presence of amyloid pathology.

胆碱酯酶抑制剂对健忘轻度认知障碍患者神经退行性变的影响。
目的:胆碱酯酶抑制剂(ChEIs)通过补偿乙酰胆碱缺乏有效治疗轻中度阿尔茨海默病(AD)痴呆。虽然它们在轻度认知障碍(MCI)中的应用缺乏强有力的试验支持,但一些研究表明它们可能延缓神经退行性变。本研究旨在利用多模态神经成像技术研究ChEIs对遗忘性MCI (aMCI)患者的神经保护作用,并确定β淀粉样蛋白(Aβ)沉积是否影响这些作用。方法:回顾性分析一项队列研究的纵向资料。共有118例aMCI患者(年龄55- 90岁)接受了基线评估,包括ChEI使用评估和[11C]匹兹堡复合b正电子发射断层扫描(PET)。所有参与者还接受了基线和2年随访磁共振成像和[18F]氟脱氧葡萄糖- pet成像。结果:与未使用ChEI组相比,使用ChEI组在2年内ad -特征区脑代谢(AD-CM)的下降明显更小(B = 0.089, 95% CI: 0.030-0.149)。然而,在ad特征区皮质厚度(AD-CT) (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)的2年变化在使用和未使用ChEI组之间没有显著差异。Aβ病理的存在并没有减缓ChEI使用对AD-CM、AD-CT或海马体积的影响。结论:研究结果表明,ChEIs可能延缓aMCI个体的功能性神经退行性变,而与淀粉样蛋白病理的存在无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Clinical Psychopharmacology and Neuroscience
Clinical Psychopharmacology and Neuroscience NEUROSCIENCESPHARMACOLOGY & PHARMACY-PHARMACOLOGY & PHARMACY
CiteScore
4.70
自引率
12.50%
发文量
81
期刊介绍: Clinical Psychopharmacology and Neuroscience (Clin Psychopharmacol Neurosci) launched in 2003, is the official journal of The Korean College of Neuropsychopharmacology (KCNP), and the associate journal for Asian College of Neuropsychopharmacology (AsCNP). This journal aims to publish evidence-based, scientifically written articles related to clinical and preclinical studies in the field of psychopharmacology and neuroscience. This journal intends to foster and encourage communications between psychiatrist, neuroscientist and all related experts in Asia as well as worldwide. It is published four times a year at the last day of February, May, August, and November.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信