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Evidence-Based Supplement Research
Evidence-Based Supplement Research

Improvement in inner retinal function in glaucoma with nicotinamide (vitamin B3) supplementation: A crossover randomized clinical trial.

  • 2020-07-28
  • Clinical & experimental ophthalmology 48(7)
    • Flora Hui
    • Jessica Tang
    • Pete A Williams
    • Myra B McGuinness
    • Xavier Hadoux
    • Robert J Casson
    • Michael Coote
    • Ian A Trounce
    • Keith R Martin
    • Peter van Wijngaarden
    • Jonathan G Crowston

Study Design

Type
Randomized Controlled Trial (RCT)
Population
Fifty-seven participants, diagnosed and treated for glaucoma
Methods
Participants received oral placebo or nicotinamide and reviewed six-weekly. Participants commenced 6 weeks of 1.5 g/day then 6 weeks of 3.0 g/day followed by crossover without washout
Blinding
Double-blind
Duration
12 weeks (6 weeks of 1.5 g/day then 6 weeks of 3.0 g/day)
Funding
Unclear
  • Highly Cited

Importance

Retinal ganglion cells endure significant metabolic stress in glaucoma but maintain capacity to recover function. Nicotinamide, a precursor of NAD+ , is low in serum of glaucoma patients and its supplementation provides robust protection of retinal ganglion cells in preclinical models. However, the potential of nicotinamide in human glaucoma is unknown.

Background

To examine the effects of nicotinamide on inner retinal function in glaucoma, in participants receiving concurrent glaucoma therapy.

Design

Crossover, double-masked, randomized clinical trial. Participants recruited from two tertiary care centres.

Participants

Fifty-seven participants, diagnosed and treated for glaucoma.

Methods

Participants received oral placebo or nicotinamide and reviewed six-weekly. Participants commenced 6 weeks of 1.5 g/day then 6 weeks of 3.0 g/day followed by crossover without washout. Visual function measured using electroretinography and perimetry.

Main outcome measures

Change in inner retinal function, determined by photopic negative response (PhNR) parameters: saturated PhNR amplitude (Vmax), ratio of PhNR/b-wave amplitude (Vmax ratio).

Results

PhNR Vmax improved beyond 95% coefficient of repeatability in 23% of participants following nicotinamide vs 9% on placebo. Overall, Vmax improved by 14.8% [95% CI: 2.8%, 26.9%], (P = .02) on nicotinamide and 5.2% [-4.2%, 14.6%], (P = .27) on placebo. Vmax ratio improved by 12.6% [5.0%, 20.2%], (P = .002) following nicotinamide, 3.6% [-3.4%, 10.5%], (P = .30) on placebo. A trend for improved visual field mean deviation was observed with 27% improving ≥1 dB on nicotinamide and fewer deteriorating (4%) compared to placebo (P = .02).

Conclusions

Nicotinamide supplementation can improve inner retinal function in glaucoma. Further studies underway to elucidate the effects of long-term nicotinamide supplementation.

Research Insights

  • PhNR Vmax improved beyond 95% coefficient of repeatability in 23% of participants following nicotinamide vs 9% on placebo. Overall, Vmax improved by 14.8% [95% CI: 2.8%, 26.9%], (P = .02) on nicotinamide and 5.2% [-4.2%, 14.6%], (P = .27) on placebo. Vmax ratio improved by 12.6% [5.0%, 20.2%], (P = .002) following nicotinamide, 3.6% [-3.4%, 10.5%], (P = .30) on placebo.

    Effect
    Beneficial
    Effect size
    Moderate
    Dose
    1.5 g/day then 6 weeks of 3.0 g/day
  • A trend for improved visual field mean deviation was observed with 27% improving ≥1 dB on nicotinamide and fewer deteriorating (4%) compared to placebo (P = .02).

    Effect
    Beneficial
    Effect size
    Small
    Dose
    1.5 g/day then 6 weeks of 3.0 g/day
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