Investigative Ophthalmology & Visual Science Cover Image for Volume 65, Issue 7
June 2024
Volume 65, Issue 7
Open Access
ARVO Annual Meeting Abstract  |   June 2024
The relation between leukocyte telomere length and glaucoma traits in the UK Biobank
Author Affiliations & Notes
  • Timing Liu
    NIHR Biomedical Research Centre at Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology, London, United Kingdom
    Reading Centre, Moorfields Eye Hospital NHS Foundation Trust, London, London, United Kingdom
  • Jae H Kang
    Brigham and Women's Hospital, Boston, Massachusetts, United States
  • Kelsey Vernon Stuart
    NIHR Biomedical Research Centre at Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology, London, United Kingdom
  • Robert Luben
    NIHR Biomedical Research Centre at Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology, London, United Kingdom
  • Paul J Foster
    NIHR Biomedical Research Centre at Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology, London, United Kingdom
  • Peng Tee Khaw
    NIHR Biomedical Research Centre at Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology, London, United Kingdom
  • Louis R Pasquale
    Icahn School of Medicine at Mount Sinai, New York, New York, United States
  • Anthony P Khawaja
    NIHR Biomedical Research Centre at Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology, London, United Kingdom
  • Rachel H. Lee
    Icahn School of Medicine at Mount Sinai, New York, New York, United States
  • Footnotes
    Commercial Relationships   Timing Liu None; Jae Kang None; Kelsey Stuart None; Robert Luben None; Paul Foster Alphasights, GLG, Google Health, Guidepoint, PwC, and Santen, Code C (Consultant/Contractor); Peng Khaw Aerie, Alcon, Allergan, Novartis, Pfizer, and Sanofi-Aventis, Code C (Consultant/Contractor); Louis Pasquale Eyenovia, Twenty, Skye Biosciences, and Character Biosciences , Code C (Consultant/Contractor); Anthony Khawaja AbbVie, Aerie, Allergan, Google Health, Heidelberg Novartis, Reichert, Santen, and Thea, Code C (Consultant/Contractor); Rachel Lee None
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science June 2024, Vol.65, 4063. doi:
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      Timing Liu, Jae H Kang, Kelsey Vernon Stuart, Robert Luben, Paul J Foster, Peng Tee Khaw, Louis R Pasquale, Anthony P Khawaja, Rachel H. Lee; The relation between leukocyte telomere length and glaucoma traits in the UK Biobank. Invest. Ophthalmol. Vis. Sci. 2024;65(7):4063.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : This study examines the potential link between leukocyte telomere length (LTL) and glaucoma traits, based on the hypothesis that shortened LTL can induce cellular apoptosis, a process implicated in glaucoma.

Methods : This cross-sectional analysis involved 164,250 participants with glaucoma traits and standardized LTL measurements in the UK Biobank cohort. Primary analysis examined LTL length as an independent risk factor for glaucoma prevalence. Secondary analyses examined associations with intraocular pressure (IOP), macular retinal nerve fiber layer (mRNFL), and ganglion cell inner plexiform layer (mGCIPL) thicknesses after controlling for age, sex, ethnicity, deprivation, diabetes, body mass index, systolic blood pressure, physical activity, alcohol, smoking, obesity, and IOP polygenic risk score. Mediation analysis further investigated the relationship between age, LTL, and primary and secondary endpoints.

Results :
Participants were age-stratified (<50 years, 50-60 years, 60-70 years) due to the strong correlation between age and LTL. After adjusting for multiple covariates, there was no significant association between LTL and glaucoma (<50 years: P=0.52; 50-60 years: P=0.81; 60-70 years: P=0.29). Similarly, there was no significant association between LTL and IOP (<50 years: P=0.05; 50-60 years: P=0.07; 60-70 years: P=0.82); mRNFL thickness (<50 years: P= 0.32; 50-60 years: P=0.49; 60-70 years: P=0.23); nor mGCIPL thickness (<50 years: P= 0.64; 50-60 years: P=0.60; 60-70 years: P=0.56).

The mediation analysis indicated that LTL did not mediate the relationship between older age and increasing risk of glaucoma (P=0.47), or the relationship between age and mGCIPL thickness (P=0.40). Interestingly, longer LTL showed a minor suppression effect on the relationship between age and IOP (-1.3% suppression; P=0.01). Furthermore, LTL modestly mediates the relationship between increasing age and thinner mRNFL thickness (2.4% mediation; P=0.005).

Conclusions : LTL was not associated with prevalent glaucoma or glaucoma-related measures independently of age and other covariates. LTL may partly mediate the relationship between age and mRNFL thickness. This warrants future investigation into how glaucoma-related variables might be modified by known lifestyle factors influencing LTL.

This abstract was presented at the 2024 ARVO Annual Meeting, held in Seattle, WA, May 5-9, 2024.

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