Association of liver disease with brain volume loss, cognitive decline, and plasma neurodegenerative disease biomarkers

Neurobiol Aging. 2022 Dec:120:34-42. doi: 10.1016/j.neurobiolaging.2022.08.004. Epub 2022 Aug 17.

Abstract

Although liver dysfunction has been implicated in Alzheimer's disease (AD), it remains unknown how liver disease may influence the trajectory of brain and cognitive changes in older adults. We related self-reported liver disease to longitudinal measures of brain structure and cognition, as well as baseline measures of plasma AD/neurodegeneration biomarkers in the Baltimore Longitudinal Study of Aging. Liver disease was identified using ICD-9 classification codes. Brain volume and cognition were assessed serially using 3T-MRI and a cognitive battery. 1008, 2157, and 780 participants were included in the MRI, cognitive, and plasma biomarker analysis, respectively. After adjustment for confounders, liver disease was associated with accelerated decline in total brain and white matter volume, but not total gray matter or AD signature region volume. Although liver disease showed no relationship with domain-specific cognitive decline or plasma biomarkers, participants with a history of hepatitis demonstrated accelerated decline in verbal fluency and elevated neurofilament light. Results suggest all-cause liver disease may accelerate brain volume loss but does not appear to promote AD-specific neurocognitive changes.

Keywords: AD plasma biomarkers; Alzheimer's disease; Cognitive assessment; Liver disease; Longitudinal study; MRI.

Publication types

  • Research Support, N.I.H., Intramural
  • Research Support, N.I.H., Extramural

MeSH terms

  • Aged
  • Alzheimer Disease* / psychology
  • Amyloid beta-Peptides
  • Biomarkers
  • Brain / diagnostic imaging
  • Cognitive Dysfunction* / diagnostic imaging
  • Cognitive Dysfunction* / etiology
  • Cognitive Dysfunction* / psychology
  • Humans
  • Liver Diseases*
  • Longitudinal Studies
  • Magnetic Resonance Imaging
  • Neurodegenerative Diseases*

Substances

  • Amyloid beta-Peptides
  • Biomarkers