Aller au contenu principal
Accès ouvert déclaré 2025 article

A Phase-II Randomized Controlled Pilot and Feasibility Study of Nicotinamide Riboside Supplementation in Older Adults With Amnestic Mild Cognitive Impairment

0Citations signalées, ce qui n’est pas une note de qualité
0Institutions déclarées
0Pays d’affiliation déclarés

Le résumé fourni par la source

Abstract Background The decline of nicotinamide adenine dinucleotide (NAD+) with aging may elevate risk of Alzheimer’s disease and related neurocognitive disorders (ADRD) by impairing cellular energy metabolism and reducing cerebral blood flow. Method We conducted a 12-week double-blind, randomized, placebo-controlled pilot study to evaluate the safety, tolerability, and preliminary efficacy of the NAD+ precursor, nicotinamide riboside (NR; 500 mg b.i.d.), for enhancing cognitive function and cerebral perfusion in older adults with mild cognitive impairment (MCI). Result 52 participants (33 females, 19 males) were randomized and 42 completed the trial (NR = 22, placebo = 20). Adherence was similar between groups (NR = 85 ± 20% vs. placebo = 91 ± 5%), with no serious adverse effects and comparable side effects. Blood NAD+ increased with NR (pre: 23.36 ± 1.94; post: 48.52 ± 4.12 µM) compared with placebo (pre: 24.12 ± 1.70; post: 25.14 ± 1.58 µM) with a significant treatment by time interaction (p < 0.001). Cognitive function did not significantly improve, however, there was a modest increase in delayed recall memory from the WMS-IV in the NR group (interaction p = 0.062). Perfusion of the left hippocampus increased with NR (pre: 51.7 ± 3.3; post: 58.0 ± 3.8 ml/min/100g) compared with placebo (pre: 55.6 ± 2.8; post: 51.7 ± 2.3 ml/min/100g; interaction p = 0.033); however, this was not associated with the change in memory performance. These outcomes were not strongly influenced by baseline plasma pTau-217. Conclusion NR is well-tolerated in older adults with MCI and may enhance perfusion of the hippocampus regardless of underlying AD pathology. However, this was not associated with improved memory performance in this short-duration trial. A larger phase-III trial over a longer treatment duration is warranted to determine the efficacy of NR for delaying cognitive impairment due to ADRD.

Ce résumé expose les affirmations des auteurs. BNTIC ne l’interprète pas comme une validation indépendante des résultats.

Le contrôle bibliographique ouvert

Aucun DOI disponible pour le contrôle Crossref.

Les sujets associés

PARP inhibition in cancer therapySirtuins and Resveratrol in MedicineCalcium signaling and nucleotide metabolism

BNTIC News n’est pas le producteur de ces données. Les publications sont interrogées à la demande dans Crossref, OpenAIRE, DOAJ, Europe PMC, HAL, DataCite, AfricArXiv, ROR et la Banque mondiale, sans clé d’accès. OpenAlex reste optionnel. Aucun service payant n’est nécessaire et aucune donnée externe n’est enregistrée en base. Consulter les sources et leurs limites.