AI Article Synopsis

  • Mild cognitive impairment (MCI) is identified as a possible precursor to Alzheimer’s disease and vascular dementia, with white matter lesions (WML) potentially linked to hippocampal shrinkage.
  • In a study involving 166 participants (including MCI patients and healthy controls), it was found that those progressing from MCI to dementia had smaller hippocampal volumes and more WML compared to stable MCI patients and controls.
  • The correlation between hippocampal volume and WML was significant only for patients with the highest WML volumes, indicating that a certain threshold of WML is needed for noticeable hippocampal atrophy.

Article Abstract

Background: Mild cognitive impairment (MCI) is a heterogeneous condition suggested as a prodromal state of Alzheimer's disease (AD) and subcortical vascular dementia (SVD). Recent findings suggest that white matter lesions (WML) may be associated with hippocampal atrophy. The objective of the study was to examine hippocampal and WML volumes in MCI patients and to examine if WML were linked to hippocampal atrophy.

Methods: The Gothenburg MCI study is a clinically based longitudinal study with biennial clinical assessments. The participants (n = 166) consist of 92 patients with stable MCI, 30 patients with converting MCI, and 44 healthy controls. WML volumes was measured manually using MRIcron. Automated segmentation of hippocampal and total white matter volumes was performed using FreeSurfer.

Results: The patients converting from MCI to dementia had reduced hippocampal volume. Stable MCI patients had fewer WML and converting MCI patients had more WML compared to controls. Hippocampal volume was only correlated to WML volume (ρ = 0.57; p < 0.01) in the quartile (n = 42) with the most WML.

Conclusions: Hippocampal atrophy is present in both AD and SVD. Hippocampal volume was associated with WML volume only in the high WML quartile, suggesting that the WML volume must reach a threshold before hippocampal atrophy is seen.

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Source
http://dx.doi.org/10.1159/000323014DOI Listing

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