No evidence for cognitive improvement from oral nicotinamide adenine dinucleotide (NADH) in dementia

J Neural Transm (Vienna). 2000;107(12):1475-81. doi: 10.1007/s007020070011.

Abstract

Reduced nicotinamide adenine dinucleotide (NADH) is advertised as an over-the-counter product or dietary supplement to treat Alzheimer's disease. We performed a 3-month open-label study with oral 10 mg/day NADH with 25 patients with mild to moderate dementia of the Alzheimer, vascular, and fronto-temporal types in addition to their current cholinomimetic drug medication. In 19 patients who completed the study, we found no evidence for any cognitive effect as defined by established psychometric tests. We conclude that NADH is unlikely to achieve cognitive improvements in an extent reported earlier, and present theoretical arguments against an effectiveness of this compound in dementia disorders.

Publication types

  • Clinical Trial

MeSH terms

  • Administration, Oral
  • Aged
  • Aged, 80 and over
  • Alzheimer Disease / drug therapy
  • Alzheimer Disease / psychology*
  • Cholinesterase Inhibitors / therapeutic use
  • Cognition / drug effects
  • Cognition / physiology*
  • Dementia / drug therapy
  • Dementia / psychology*
  • Dementia, Vascular / drug therapy
  • Dementia, Vascular / psychology*
  • Drug Therapy, Combination
  • Female
  • Humans
  • Language
  • Male
  • Memory / drug effects
  • Mental Status Schedule
  • Middle Aged
  • NAD / administration & dosage
  • NAD / therapeutic use*
  • Orientation
  • Psychiatric Status Rating Scales
  • Psychological Tests
  • Treatment Failure

Substances

  • Cholinesterase Inhibitors
  • NAD