Niacin Enhancement for Parkinson’s Disease: An Effectiveness Trial

Raymond Chong, Chandramohan Wakade, Marissa Seamon, Banabihari Giri, John Morgan, Sharad Purohit

Research output: Contribution to journalArticlepeer-review

22 Scopus citations

Abstract

We previously reported that individuals with Parkinson’s disease (PD) present with lower vitamin B3 levels compared to controls. It may be related to carbidopa interaction, defective tryptophan metabolism, and stresses of night sleep disorder. Vitamin B3 is the energy source for all cells by producing NAD+ and NADP+ in redox reactions of oxidative phosphorylation. Thus, some symptoms of PD such as fatigue, sleep dysfunction, and mood changes may be related to the deficiency of vitamin B3. Here, we conducted an effectiveness trial to determine the effect of 12 months of low-dose niacin (a vitamin B3 derivative) enhancement in PD individuals. An average of 9 ± 6-point improvement in the Unified Parkinson’s Disease Rating Scale (UPDRS) III (motor) score was observed after 12 months of daily niacin compared to the expected decline in score (effect size = 0.78, 95% CI = 7–11). Additionally, secondary outcome measures improved. Notably, handwriting size increased, fatigue perception decreased, mood improved, frontal beta rhythm during quiet stance increased, and stance postural sway amplitude and range of acceleration decreased. Set shifting, however, as measured by the Trail Making-B test, worsened from 66 to 96 s. Other measures did not change after 12 months, but it is not clear whether this represents a positive benefit of the vitamin. For example, while the quality of night sleep remained the same, there was a trend towards a decrease in the frequency of awakening episodes. These results suggest that niacin enhancement has the potential to maintain or improve quality of life in PD and slow disease progression.

Original languageEnglish (US)
Article number667032
JournalFrontiers in Aging Neuroscience
Volume13
DOIs
StatePublished - Jun 17 2021

Keywords

  • B3
  • GPR109A
  • UPDRS
  • antiinflammation
  • fatigue
  • inflammation
  • nicotinic acid

ASJC Scopus subject areas

  • Aging
  • Cognitive Neuroscience

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