Radiological Sciences, Mental Health & Clinical Neurosciences, School of Medicine, University of Nottingham, Nottingham, UK.
Sir Peter Mansfield Imaging Centre, School of Medicine, University of Nottingham, Nottingham, UK.
Eur J Neurol. 2022 May;29(5):1344-1353. doi: 10.1111/ene.15251. Epub 2022 Feb 7.
Anticholinergic (AC) medication use is associated with cognitive decline and dementia, which may be related to an AC-induced central hypocholinergic state, but the exact mechanisms remain to be understood. We aimed to further elucidate the putative link between AC drug prescription, cognition, and structural and functional impairment of the forebrain cholinergic nucleus basalis of Meynert (NBM).
Cognitively normal (CN; n = 344) and mildly cognitively impaired (MCI; n = 224) Alzheimer's Disease Neuroimaging Initiative Phase 3 participants with good quality 3-T magnetic resonance imaging were included. Structural (regional gray matter [GM] density) and functional NBM integrity (functional connectivity [FC]) were compared between those on AC medication for > 1 year (AC ) and those without (AC ) in each condition. AC burden was classed as mild, moderate, or severe.
MCI AC participants (0.55 ± 0.03) showed lower NBM GM density compared to MCI AC participants (0.56 ± 0.03, p = 0.002), but there was no structural AC effect in CN. NBM FC was lower in CN AC versus CN AC (3.6 ± 0.5 vs. 3.9 ± 0.6, p = 0.001), and in MCI AC versus MCI AC (3.3 ± 0.2 vs. 3.7 ± 0.5, p < 0.001), with larger effect size in MCI. NBM FC partially mediated the association between AC medication burden and cognition.
Our findings provide novel support for a detrimental effect of mild AC medication on the forebrain cholinergic system characterized as functional central hypocholinergic that partially mediated AC-related cognitive impairment. Moreover, structural tissue damage suggests neurodegeneration, and larger effect sizes in MCI point to enhanced susceptibility for AC medication in those at risk of dementia.
抗胆碱能(AC)药物的使用与认知能力下降和痴呆有关,这可能与 AC 引起的中枢拟胆碱能状态有关,但确切机制仍不清楚。我们旨在进一步阐明 AC 药物处方、认知以及前脑胆碱能核基底核(NBM)的结构和功能损伤之间的潜在联系。
我们纳入了认知正常(CN;n=344)和轻度认知障碍(MCI;n=224)阿尔茨海默病神经影像学倡议第三阶段有高质量 3-T 磁共振成像的参与者。在每种情况下,我们比较了服用 AC 药物>1 年(AC+)和未服用 AC 药物(AC-)的参与者之间的结构(区域灰质[GM]密度)和 NBM 完整性(功能连接[FC])。AC 负担分为轻度、中度或重度。
与 MCI AC-参与者(0.56±0.03)相比,MCI AC 参与者(0.55±0.03)的 NBM GM 密度较低(p=0.002),但 CN 中没有结构 AC 效应。与 CN AC-相比,CN AC 的 NBM FC 较低(3.6±0.5 对 3.9±0.6,p=0.001),与 MCI AC-相比,MCI AC 的 NBM FC 较低(3.3±0.2 对 3.7±0.5,p<0.001),MCI 的效应大小更大。NBM FC 部分介导了 AC 药物负担与认知之间的关联。
我们的研究结果为轻度 AC 药物对以功能性中枢拟胆碱能为特征的前脑胆碱能系统的有害影响提供了新的支持,这种影响部分解释了 AC 相关的认知障碍。此外,结构组织损伤表明神经退行性变,并且 MCI 中更大的效应大小表明在痴呆风险人群中,AC 药物更容易产生副作用。