No association between cataract surgery and mitochondrial DNA damage with age-related macular degeneration in human donor eyes

PLoS One. 2021 Oct 19;16(10):e0258803. doi: 10.1371/journal.pone.0258803. eCollection 2021.

Abstract

Purpose: To determine whether age-related macular degeneration (AMD) severity or the frequency of retinal pigment epithelium mitochondrial DNA lesions differ in human donor eyes that have undergone cataract surgery compared to phakic eyes.

Methods: Eyes from human donors aged ≥ 55 years were obtained from the Minnesota Lions Eye Bank. Cataract surgery status was obtained from history provided to Eye Bank personnel by family members at the time of tissue procurement. Donor eyes were graded for AMD severity using the Minnesota Grading System. Quantitative PCR was performed on DNA isolated from macular punches of retinal pigment epithelium to quantitate the frequency of mitochondrial DNA lesions in the donor tissue. Univariable and multivariable analyses were performed to evaluate for associations between (1) cataract surgery and AMD severity and (2) cataract surgery and mitochondrial DNA lesion frequency.

Results: A total of 157 subjects qualified for study inclusion. Multivariable analysis with age, sex, smoking status, and cataract surgery status showed that only age was associated with AMD grade. Multivariable analysis with age, sex, smoking status, and cataract surgery status showed that none of these factors were associated with retinal pigment epithelium mitochondrial DNA lesion frequency.

Conclusions: In this study of human donor eyes, neither retinal pigment epithelium mitochondrial DNA damage nor the stage of AMD severity are independently associated with cataract surgery after adjusting for other AMD risk factors. These new pathologic and molecular findings provide evidence against a relationship between cataract surgery and AMD progression and support the idea that cataract surgery is safe in the setting of AMD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Biological Specimen Banks
  • Cataract Extraction / adverse effects
  • Cataract Extraction / statistics & numerical data*
  • DNA Damage*
  • DNA, Mitochondrial / genetics*
  • Disease Progression
  • Female
  • Humans
  • Macular Degeneration / etiology
  • Macular Degeneration / genetics*
  • Male
  • Middle Aged
  • Multivariate Analysis
  • Retinal Pigment Epithelium / chemistry
  • Tissue Donors

Substances

  • DNA, Mitochondrial

Grants and funding

Funding was provided by the Minnesota Lions Vision Foundation, the Elaine and Robert Larson Endowed Vision Research Chair and the Helen Lindsay Family Foundation (DAF), the Knobloch Chair Professorship (SRM), an ARVO travel award (KRA), and the University of Minnesota Harry Friedman resident research award (KRA). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.