Evidence map›Paper›PMID 31572171›Full record

ArticleFrontiers in aging neuroscience2019

A Pilot Study Investigating Changes in the Human Plasma and Urine NAD+ Metabolome During a 6 Hour Intravenous Infusion of NAD.

Ross Grant, Jade Berg, Richard Mestayer, Nady Braidy, James Bennett, Susan Broom, James Watson

Open access · goldAbstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.3field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 45 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Review
  5. Narrative review of intravenous NADFrontiers in aging · 2026
    Review
  6. Article
  7. NADNature metabolism · 2025
    Review
  8. The role of NADnpj metabolic health and disease · 2025
    Review
  9. NADSub-cellular biochemistry · 2024
    Review
  10. Review
  11. Review
  12. Nicotinamide Riboside, a Promising Vitamin BMolecules (Basel, Switzerland) · 2023
    Review
  13. Article
  14. Article
  15. Article
  16. Supplementation with NADNutrients · 2022
    Review
  17. NADMetabolites · 2022
    Review
  18. Review
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 6 institutions in 2 countries.

Ross GrantAustralasian Research Institute, Sydney Adventist Hospital, Wahroonga, NSW, Australia.
Jade BergAustralasian Research Institute, Sydney Adventist Hospital, Wahroonga, NSW, Australia.
Richard MestayerNAD+ Research Inc., Springfield, LA, United States.
Nady BraidySchool of Psychiatry, University of New South Wales, NPI, Euroa Centre, Randwick, NSW, Australia.
James BennettSpringfield Wellness Center, Springfield, LA, United States.
Susan BroomSchool of Natural and Behavioural Sciences, William Carey University, Hattiesburg, MS, United States.
James WatsonDivision of Plastic Surgery, Clinical Faculty, David Geffen School of Medicine, University of California, Los Angeles, Los Angeles, CA, United States.
Springfield Clinic · USSydney Adventist Hospital · AUUniversity of California, Los Angeles · USUniversity of Sydney · AUUNSW Sydney · AUWilliam Carey University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Accumulating evidence suggests that active maintenance of optimal levels of the essential pyridine nucleotide, nicotinamide adenine dinucleotide (NAD+) is beneficial in conditions of either increased NAD+ turnover or inadequate synthesis, including Alzheimer's disease and other neurodegenerative disorders and the aging process. While studies have documented the efficacy of some NAD+ precursors such as nicotinamide riboside (NR) in raising plasma NAD+, no data are currently available on the fate of directly infused NAD+ in a human cohort. This study, therefore, documented changes in plasma and urine levels of NAD+ and its metabolites during and after a 6 h 3 μmol/min NAD+ intravenous (IV) infusion. Surprisingly, no change in plasma (NAD+) or metabolites [nicotinamide, methylnicotinamide, adenosine phosphoribose ribose (ADPR) and nicotinamide mononucleotide (NMN)] were observed until after 2 h. Increased urinary excretion of methylnicotinamide and NAD+ were detected at 6 h, however, no significant rise in urinary nicotinamide was observed. This study revealed for the first time that: (i) at an infusion rate of 3 μmol/min NAD+ is rapidly and completely removed from the plasma for at least the first 2 h; (ii) the profile of metabolites is consistent with NAD+ glycohydrolase and NAD+ pyrophosphatase activity; and (iii) urinary excretion products arising from an NAD+ infusion include NAD+ itself and methyl nicotinamide (meNAM) but not NAM.

Indexed as

ADP ribosemethyl nicotinamideNAD+nicotinamide mononucleotidenicotinamide (NAM)

Identifiers

PMID31572171
PMCPMC6751327
OpenAlexW2970474168

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.