Homocysteine and Age-Related Central Nervous System Diseases: Role of Inflammation

Amany Tawfik1,2,3,4,5, Nehal M Elsherbiny1,2,6, Yusra Zaidi1,2

  • 1Department of Oral Biology and Diagnostic Sciences, Dental College of Georgia, Augusta University, Augusta, GA 30912, USA.

Insights

High homocysteine levels (HHcy) are common in older adults and linked to neurodegenerative diseases like Alzheimer's (AD) and eye conditions. Inflammation disrupts blood-brain and blood-retinal barriers, contributing to these HHcy-related aging diseases.

Area of Science:

  • Neuroscience
  • Ophthalmology
  • Gerontology

Background:

  • Hyperhomocysteinemia (HHcy) is prevalent in the aging population.
  • HHcy is associated with neurodegenerative diseases like Alzheimer's disease (AD) and ocular conditions such as age-related macular degeneration (AMD) and diabetic retinopathy (DR).
  • Disruption of blood-brain and blood-retinal barrier integrity is a key mechanism in HHcy-related disorders.

Purpose of the Study:

  • To review the role of inflammation in HHcy-induced barrier dysfunction.
  • To explore the link between HHcy, barrier impairment, and neurovascular injury in aging diseases.
  • To focus on the implications for Alzheimer's disease (AD).

Main Methods:

  • Literature review of studies on HHcy, neurodegenerative diseases, and eye diseases.
  • Analysis of mechanisms underlying blood-brain and blood-retinal barrier disruption.
  • Examination of the role of inflammation in HHcy-associated pathology.

Main Results:

  • HHcy contributes to neurodegenerative and retinal disorders by impairing barrier function.
  • Impaired barrier function triggers inflammatory responses, exacerbating disease.
  • AD patients frequently exhibit visual impairments, suggesting retinal involvement.

Conclusions:

  • Inflammation is a likely mechanism driving HHcy-induced barrier dysfunction and neurovascular injury in aging.
  • The retina may be a significant site for AD pathology, linked to HHcy.
  • Targeting inflammation could be crucial for managing HHcy-related aging diseases.

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