Basal forebrain integrity, cholinergic innervation and cognition in idiopathic Parkinson’s disease

Abstract

Abstract Most individuals with Parkinson’s disease experience cognitive decline. Mounting evidence suggests this is partially caused by cholinergic denervation due to α-synuclein pathology in the cholinergic basal forebrain. Alpha-synuclein deposition causes inflammation, which can be measured with free water fraction, a diffusion MRI-derived metric of extracellular water. Prior studies have shown an association between basal forebrain integrity and cognition, cholinergic levels and cognition, and basal forebrain volume and acetylcholine, but no study has directly investigated whether basal forebrain physiology mediates the relationship between acetylcholine and cognition in Parkinson’s disease. We investigated the relationship between these variables in a cross-sectional analysis of 101 individuals with Parkinson’s disease. Cholinergic levels were measured using Fluorine-18 fluoroethoxybenzovesamicol PET imaging. Cholinergic innervation regions of interest included the medial, lateral capsular, and lateral perisylvian regions and the hippocampus. Brain volume and free water fraction were quantified using T1 and diffusion MRI, respectively. Cognitive measures included composites of attention/working memory, executive function, immediate memory, and delayed memory. Data were entered into parallel mediation analyses with the cholinergic projection areas as predictors, cholinergic basal forebrain volume and free water fraction as mediators, and each cognitive domain as outcomes. All mediation analyses controlled for age, years of education, levodopa equivalency dose, and systolic blood pressure. The basal forebrain integrity metrics fully mediated the relationship between lateral capsular and lateral perisylvian acetylcholine and attention/working memory, and partially mediated the relationship between medial acetylcholine and attention/working memory. Basal forebrain integrity metrics fully mediated the relationship between medial, lateral capsular, and lateral perisylvian acetylcholine and free water fraction. For all mediations in attention/working memory and executive function the free water mediation was significant, while the volume mediation was not. The basal forebrain integrity metrics fully mediated the relationship between hippocampal acetylcholine and delayed memory and partially mediated the relationship between lateral capsular and lateral perisylvian acetylcholine and delayed memory. The volume mediation was significant for the hippocampal and lateral perisylvian models, while free water fraction was not. Free water fraction in the cholinergic basal forebrain mediates the relationship between acetylcholine and attention/working memory and executive function, while cholinergic basal forebrain volume mediated the relationship between acetylcholine in temporal regions in memory. These findings suggest that these two metrics reflect different stages of neurodegenerative processes, and add additional evidence for a relationship between pathology in the basal forebrain, acetylcholine denervation, and cognitive decline in Parkinson’s disease.