Changes in Quality of Life Among Glaucoma Patients Following Six Months of Niacinamide Supplementation.
- 2025-08-27
- Nutrients 17(17)
- Constantin Alin Nicola
- Maria Cristina Marinescu
- Anne Marie Firan
- Georgica Tartea
- Mihaela Simona Naidin
- Radu Constantin Ciuluvica
- Marina Daniela Dimulescu
- Nicoleta Mirela Voicu
- Carmen Marinela Mihailescu
- Andreea-Daniela Meca
- Maria Bogdan
- Adina Turcu-Stiolica
- PubMed: 40944166
- DOI: 10.3390/nu17172775
Study Design
- Type
- Clinical Trial
- Population
- 58 patients diagnosed with primary open angle glaucoma, under topical hypotensive treatment
- Methods
- prospective, non-randomized, single-arm clinical trial; 6 months of daily administration of 500 mg of oral niacinamide
- Blinding
- Open-label
- Duration
- 6 months
- Funding
- Unclear
- Rigorous Journal
Background/Objectives: Glaucoma is the primary cause of irreversible blindness worldwide, with enormous impact on quality of life and activities of daily living. Since one pathogenic mechanism of glaucoma is mitochondrial dysfunction at the retinal ganglion cell level, niacin has been proposed as an adjuvant treatment, with encouraging results. The objective of this prospective, non-randomized, single-arm clinical trial was to investigate the effect of oral supplementation with niacin on the quality of life of a cohort of glaucoma patients in Romania. Methods: Fifty-eight patients diagnosed with primary open angle glaucoma, under topical hypotensive treatment, were evaluated before and after a 6-month period of daily administration of 500 mg of oral niacinamide. Evaluation involved a complete ophthalmological exam and QoL quantification using the Glaucoma Quality of Life-15 (GQL-15) Questionnaire. Results: We found strong evidence that niacin supplementation for 6 months led to a statistically significant improvement in QoL scores among glaucoma patients (mean difference = -2.10, 95% CI: [-2.89, -1.32], p < 0.0001), including central and near vision (mean difference = -2.16, 95% CI: [-3.91, -0.4], p = 0.017), peripheral vision (mean difference = -2.66, 95% CI: [-0.23, -0.08], p < 0.001), and the glare and dark adaptation (mean difference = -5.24, 95% CI: [-0.33, -0.14], p < 0.001). In addition, B3 treatment resulted in a significant reduction in intraocular pressure in both eyes over 6 months (mean difference = 0.53, 95% CI: [0.21, 0.86] in the left eye and mean difference = 0.36, 95% CI: [0.04, 0.68] in the right eye), indicating potential clinical benefits. Conclusions: The observed GQL-15 score reductions suggest that B3 may be of benefit in glaucoma management. Further research with larger sample sizes and placebo-controlled designs is needed to confirm B3 potential impact on disease progression and quality of life. Trial Registration at clinicaltrials.gov: NCT07007260.
Research Insights
glare and dark adaptation (mean difference = -5.24, 95% CI: [-0.33, -0.14], p < 0.001)
- Effect
- Beneficial
- Effect size
- Small
- Dose
- 500 mg daily
peripheral vision (mean difference = -2.66, 95% CI: [-0.23, -0.08], p < 0.001)
- Effect
- Beneficial
- Effect size
- Small
- Dose
- 500 mg daily
niacin supplementation for 6 months led to a statistically significant improvement in QoL scores among glaucoma patients (mean difference = -2.10, 95% CI: [-2.89, -1.32], p < 0.0001)
- Effect
- Beneficial
- Effect size
- Small
- Dose
- 500 mg daily
central and near vision (mean difference = -2.16, 95% CI: [-3.91, -0.4], p = 0.017)
- Effect
- Beneficial
- Effect size
- Small
- Dose
- 500 mg daily
B3 treatment resulted in a significant reduction in intraocular pressure in both eyes over 6 months (mean difference = 0.53, 95% CI: [0.21, 0.86] in the left eye and mean difference = 0.36, 95% CI: [0.04, 0.68] in the right eye)
- Effect
- Beneficial
- Effect size
- Small
- Dose
- 500 mg daily