Risk Factors of Optic Neuropathy in Ethambutol Users: Interaction with Isoniazid and Other Associated Conditions of Toxic Optic Neuropathy

• Published in: Toxics (Basel) Vol. 12; no. 8; p. 549
• Main Authors: Kim, Jiyeong, Ahn, Seong Joon
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 30-07-2024; MDPI
• Subjects: Age; Alcohol; Codes; Confounding (Statistics); Diabetes; Diabetes mellitus; Diabetic neuropathy; Drug dosages; Ethambutol; Hyperlipidemia; Hypertension; Isoniazid; Kidney diseases; Liver diseases; Malnutrition; Metabolism; Multivariate analysis; Neurotoxicity; Nutrient deficiency; Optic neuropathy; Peripheral neuropathy; Regression analysis; Risk factors; Statistical analysis; Systemic diseases; Tobacco; Toxicity; Tuberculosis; Visual aspects; Visual impairment; Vitamin deficiency; South Korea; optic neuropathy; risk factors; ethambutol
• DOI: 10.3390/toxics12080549
• EISSN: 2305-6304

(1) Background: To investigate the risk factors associated with optic neuropathy (ON) and validate the hypothesis that concomitant isoniazid use and other causes of toxic ON affect the development of ON in ethambutol users. (2) Methods: This cohort study identified ethambutol users who initiated ethambutol therapy between January 2015 and December 2021 and had no ON prior to ethambutol therapy. ON incidence up to 31 December 2022 was evaluated. The users were grouped on the basis of the presence of ON. Demographic and clinical characteristics were investigated for risk factor analyses of ON. Odds ratios (ORs) were calculated using multivariate logistic regression analyses. (3) Results: Among 204,598 ethambutol users, 5277 (2.6%) patients developed ON over the study period. Patients with ON included a higher percentage of women and had a higher mean age than patients without ON. In the multivariate analyses, the risk factors for ON and visual impairment included sex, age, cumulative dose, extrapulmonary indications for ethambutol use, and systemic conditions such as diabetes, hypertension, hyperlipidemia, diabetes, kidney disease, and liver disease. Malnutrition or nutritional disorders significantly increased the risk of ON (OR = 1.27, 95% confidence interval [CI] = 1.19-1.34), whereas concomitant isoniazid use decreased the risk (OR = 0.78, 95% CI = 0.72-0.86). (4) Conclusion: An increased risk of ON in patients with systemic diseases and nutritional deficiency was identified, whereas concomitant isoniazid use was associated with a decreased risk of ON. Patients with these risk factors should be carefully monitored to minimize the vision-threatening ON.