4.7 Article

Higher glucose levels associated with lower memory and reduced hippocampal microstructure

Journal

NEUROLOGY
Volume 81, Issue 20, Pages 1746-1752

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/01.wnl.0000435561.00234.ee

Keywords

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Funding

  1. Deutsche Forschungsgemeinschaft [Fl 379-8/1, Fl 379-10/1, Fl 379-11/1, DFG-Exc 257]
  2. Else-Kroner Fresenius Stiftung [2009-141, 2011-119]
  3. Bundesministerium fur Bildung und Forschung [FKZ 0315673A, 01EO0801, 01GY1144]

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Objectives: For this cross-sectional study, we aimed to elucidate whether higher glycosylated hemoglobin (HbA1c) and glucose levels exert a negative impact on memory performance and hippocampal volume and microstructure in a cohort of healthy, older, nondiabetic individuals without dementia. Methods: In 141 individuals (72 women, mean age 63.1 years +/- 6.9 SD), memory was tested using the Rey Auditory Verbal Learning Test. Peripheral levels of fasting HbA1c, glucose, and insulin and 3-tesla MRI scans were acquired to assess hippocampal volume and microstructure, as indicated by gray matter barrier density. Linear regression and simple mediation models were calculated to examine associations among memory, glucose metabolism, and hippocampal parameters. Results: Lower HbA1c and glucose levels were significantly associated with better scores in delayed recall, learning ability, and memory consolidation. In multiple regression models, HbA1c remained strongly associated with memory performance. Moreover, mediation analyses indicated that beneficial effects of lower HbA1c on memory are in part mediated by hippocampal volume and microstructure. Conclusions: Our results indicate that even in the absence of manifest type 2 diabetes mellitus or impaired glucose tolerance, chronically higher blood glucose levels exert a negative influence on cognition, possibly mediated by structural changes in learning-relevant brain areas. Therefore, strategies aimed at lowering glucose levels even in the normal range may beneficially influence cognition in the older population, a hypothesis to be examined in future interventional trials.

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