Objective
To describe how retinal venular diameter changes over time for an individual and to examine differences in these changes among people with different risk profiles.
Design
Population-based cohort study.
Participants
4600 persons aged 43–86 years from the Beaver Dam Eye Study who participated in at least 1 examination and had venular diameter measured in the right eye.
Methods
Data from 4 examinations over 15 years were analyzed. Retinal venular diameter was measured from photographs at each examination by computer-assisted methods and summarized as the central retinal venular equivalent (CRVE). Associations of risk factors to concurrent CRVE measurements and changes in CRVE over time were determined using multivariate analyses.
Main Outcome Measure
CRVE.
Results
CRVE tended to narrow with age. Mean CRVE was about 5 µm smaller (225 vs. 230 µm) for the average 70-year-old compared to the average 50-year-old, and was about 13 µm smaller (217 vs. 230 µm) for the average 85-year-old compared to the average 50-year-old. Male sex (beta estimate [β]=5.34; 95% confidence interval [CI] 3.58, 6.90), current smoking (β=9.38; 95% CI 8.26, 10.49), and higher white blood cell count (per 1000/µL: β=0.95; 95% CI 0.74, 1.16) were independently associated with larger concurrent CRVE while higher mean arterial blood pressure (per 5 mmHg: β=−0.36; 95% CI −0.50, −0.23) and higher high-density lipoprotein cholesterol (per 10 mg/dL: β=−0.89; 95% CI −1.15, −0.63) were independently associated with smaller concurrent CRVE. History of cardiovascular disease (β=−0.16; 95% CI −0.26, −0.06) and presence of chronic kidney disease (β=−0.20; 95% CI −0.34, −0.05) were associated with a greater decrease in CRVE over time.
Conclusions
These data show that retinal venular diameter tended to narrow with age, and that concurrent venular diameter is independently associated with sex, blood pressure, high-density lipoprotein cholesterol, white blood cell count, and current smoking, and change in CRVE is independently associated with a history of cardiovascular disease and presence of chronic kidney disease. The different independent effects of these interrelated factors on CRVE highlight the complex relationship between systemic diseases and conditions and CRVE, and the difficulty in determining specific causes of change in CRVE over time.