4.7 Article

Anticholinergic drugs and forebrain magnetic resonance imaging changes in cognitively normal people and those with mild cognitive impairment

期刊

EUROPEAN JOURNAL OF NEUROLOGY
卷 29, 期 5, 页码 1344-1353

出版社

WILEY
DOI: 10.1111/ene.15251

关键词

anticholinergic drugs; cognition; forebrain; functional connectivity; gray matter density; nucleus basalis of Meynert

资金

  1. National Institute for Health Research Nottingham Biomedical Research Centre
  2. European Research Council [ERC/101000969]

向作者/读者索取更多资源

The use of anticholinergic medication is associated with cognitive decline and structural and functional impairment of the cholinergic nucleus basalis of Meynert. The study found that individuals on long-term anticholinergic medication have lower gray matter density and reduced functional connectivity in the nucleus basalis of Meynert, leading to cognitive impairment.
Background and purpose 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). Methods 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. Results 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. Conclusions 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.

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