Ann Geriatr Med Res.  2024 Mar;28(1):116-120. 10.4235/agmr.23.0135.

Elevated Homocysteine Level and Brain Atrophy Changes as Markers to Screen the Alzheimer Disease: Case Series

Affiliations
  • 1Department of Anatomy, JSS Medical College, JSS Academy of Higher Education and Research, Mysore, India
  • 2Department of Geriatric Medicine, JSS Hospital, JSS Academy of Higher Education and Research, Mysore, India
  • 3Department of Biochemistry, Mysore Medical College and Research Institute, Mysore, India
  • 4Department of Biochemistry and Medical Genetics, JSS Medical College, JSS Academy of Higher Education and Research, Mysore, India
  • 5Department of Biochemistry, JSS Medical College, JSS Academy of Higher Education and Research, Mysore, India

Abstract

Alzheimer disease (AD) is the most common cause of dementia worldwide. Its clinical manifestations include a progressive loss of memory and other cognitive domains, as well as brain atrophy. An elevated homocysteine level (>15 µmol/L), known as hyperhomocysteinemia, is also an attributing risk factor for AD, vascular pathologies, and brain atrophy. Neuroimaging studies including T2-weighted magnetic resonance imaging scans revealed white matter hyperintensities in the periventricular and deep white matter, enlarged ventricles, widened sulci, and decreased white matter mass, which are features of aging, as well as cerebrovascular changes. This case series investigated changes in biochemical marker levels including serum homocysteine, folate, and vitamin B12, and the degree of atrophic variations in cortical-subcortical white matter in AD. The present study hypothesized that serum homocysteine levels might be used as a surrogate marker to screen for AD at an earlier stage.

Keyword

Alzheimer disease; Brain atrophy; Homocysteine; Vitamin B12
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