4.7 Article

Cholinergic and hippocampal systems facilitate cross-domain cognitive recovery after stroke

Journal

BRAIN
Volume 145, Issue 5, Pages 1698-1710

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/brain/awac070

Keywords

stroke; prognosis; neuroplasticity; hippocampus; memory

Funding

  1. Medical Research Council, UK [MR/K022113/1]
  2. European Commission [667375]
  3. University of Queensland

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A study has found that the recovery of cognitive function after stroke is related to neurotransmitter systems, learning-related networks, and brain regions that can adapt to demand. The status of the cholinergic basal forebrain, fornix, and hippocampal subfields predicted improvement in long-term memory performance. These findings provide important information for personalized therapeutic strategies after stroke.
Spontaneous recovery of motor and cognitive function occurs in many individuals after stroke. The mechanisms are incompletely understood, but may involve neurotransmitter systems that support neural plasticity, networks that are involved in learning and regions of the brain that are able to flexibly adapt to demand (such as the multiple-demand system). Forty-two patients with first symptomatic ischaemic stroke were enrolled in a longitudinal cohort study of cognitive function after stroke. High resolution volumetric, diffusion MRI and neuropsychological assessment were performed at a mean of 70 +/- 18 days after stroke. Cognitive assessment was repeated 1 year after stroke, using parallel test versions to avoid learning effects, and change scores were computed for long-term episodic, short-term, and working memory. Structural MRI features that predicted change in cognitive scores were identified by a two-stage analysis: a discovery phase used whole brain approaches in an hypothesis-free unbiased way; and an independent focused phase, where measurements were derived from regions identified in the discovery phase, using targeted volumetric measurements or tractography. Evaluation of the cholinergic basal forebrain, based on a validated atlas-based approach, was included given prior evidence of a role in neural plasticity. The status of the fornix, cholinergic basal forebrain and a set of hippocampal subfields were found to predict improvement in long-term memory performance. In contrast to prior expectation, the same pattern was found for short-term and working memory, suggesting that these regions are part of a common infrastructure that supports recovery across cognitive domains. Associations between cholinergic basal forebrain volume and cognitive recovery were found primarily in subregions associated with the nucleus basalis of Meynert, suggesting that it is the cholinergic outflow to the neocortex that enables recovery. Support vector regression models derived from baseline measurements of fornix, cholinergic basal forebrain and hippocampal subfields were able to explain 62% of change in long-term episodic and 41% of change in working memory performance over the subsequent 9 months. The results suggest that the cholinergic system and extended hippocampal network play key roles in cognitive recovery after stroke. Evaluation of these systems early after stroke may inform personalized therapeutic strategies to enhance recovery.

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