Prevalence was calculated as the ratio of the number of individuals with a given level of myopia to the total number of individuals whose myopia status was known, using a given definition (worse eye, better eye, or right eye). Data were stratified by age, gender, and selected variables identified as risk indicators. Myopia risk indicators were explored using univariate and multiple logistic regression. Sociodemographic factors evaluated included age, gender, birth country (United States, other), education level (0–6, 7–11, ≥12 years), marital status (married/with stable partner, never married, widowed, separated/divorced), working status (used, retired, unemployed), annual income (<$20,000, $20,000–$40,000, >$40,000), acculturation (low, ≤1.9, high, >1.9), smoking and alcohol history (none, former, current), healthcare utilization (visit within past year), and health-vision insurance. Clinical factors included hypertension (by history, or LALES evaluation), diabetes (determined by history, by hemoglobin A1c ≥6.5%, or by random blood glucose ≥200 mg/dL), body mass index (normal, ≤24.9, overweight, 24.0 to 29.9; obese >29.9), self-reported comorbid nonocular conditions (0, 1, ≥2), and self-reported history of ocular disease (diabetic retinopathy, cataract, age-related macular degeneration or glaucoma). Univariate logistic regression analyses were first performed for all of these sociodemographic and clinical risk indicators. Variables showing at least marginally significant associations (P < 0.1) in univariate regression were considered candidates for subsequent forward stepwise multiple logistic regression. Odds ratios are reported for the significant independent risk indicators included in the final model. To further control for confounding by nuclear lens opacification (NO) of associations of age and ocular disease with myopia, age/gender-stratified myopia prevalence and risk indicators were also assessed in a cohort from which all participants with NO (LOCS II grade ≥2 either eye) were excluded. All analyses were conducted on computer (SAS software; SAS Institute, Cary, NC) and a significance level of P < 0.05.