The relation between C reactive protein and age related macular degeneration in the Cardiovascular Health Study

G McGwin1, T A Hall, A Xie

  • 1Department of Ophthalmology, School of Medicine, University of Alabama at Birmingham, 700 S 18th Street, Suite 609, Birmingham, AL 35294-0009, USA. mcgwin@uab.edu

Insights

This study found no significant association between C-reactive protein (CRP) levels and age-related macular degeneration (AMD). The findings do not support the theory that systemic inflammation plays a role in AMD development or progression.

Area of Science:

  • Ophthalmology
  • Immunology
  • Gerontology

Background:

  • Age-related macular degeneration (AMD) is a leading cause of vision loss in older adults.
  • Systemic inflammation has been proposed as a potential factor in the etiology and progression of AMD.
  • C-reactive protein (CRP) is a marker of systemic inflammation.

Purpose of the Study:

  • To investigate the association between C-reactive protein (CRP) levels and the presence of age-related macular degeneration (AMD).
  • To test the hypothesis that individuals with AMD have elevated CRP levels.

Main Methods:

  • Cross-sectional study using data from the Cardiovascular Health Study (CHS).
  • Identified 390 participants with AMD and 2365 without AMD using fundus photographs.
  • Compared baseline CRP levels between AMD and non-AMD groups, adjusting for demographic, lifestyle, and health factors.

Main Results:

  • Median CRP levels were similar between individuals with AMD (1.76 mg/l) and those without AMD (1.77 mg/l).
  • Adjusted odds ratios for AMD were not statistically significant across increasing CRP quartiles compared to the lowest quartile.
  • No statistically significant association was found between CRP levels and AMD.

Conclusions:

  • The Cardiovascular Health Study data do not provide evidence for an association between CRP levels and AMD.
  • These findings do not support the role of non-specific systemic inflammation in the etiology or natural history of AMD.
Abstract