Evidence map›Paper›PMID 29514713›Full record

ReviewSkeletal muscle2018

A need for NAD+ in muscle development, homeostasis, and aging.

Michelle F Goody, Clarissa A Henry

Open access · goldAbstract readReview
In one paragraph

Review in Skeletal muscle, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

50 citing papers in PubMed, 75 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Protein Acetylation and NAD+ Homeostasis in Aging Muscle.Advances in experimental medicine and biology · 2025
    Review
  11. NADFrontiers in veterinary science · 2025
    Article
  12. Article
  13. Article
  14. Review
  15. Mechanisms of the NADFrontiers in cell and developmental biology · 2024
    Review
  16. Replenishing NADSkeletal muscle · 2023
    Article
  17. Article
  18. The critical role of cardiolipin in metazoan differentiation, development, and maturation.Developmental dynamics : an official publication of the American Association of Anatomists · 2023
    Review
  19. Nicotinamide Phosphoribosyltransferase-elevated NADJournal of cachexia, sarcopenia and muscle · 2023
    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

2 authors at 1 institution in 1 country.

Michelle F GoodySchool of Biology and Ecology, University of Maine, Orono, ME, 04469, USA.
Clarissa A HenrySchool of Biology and Ecology, University of Maine, Orono, ME, 04469, USA. clarissa.henry@maine.edu.
University of Maine · US

Funding

Novel Mechanisms of Extracellular Matrix Regulation During DevelopmentR15HD088217 · NICHD · UNIVERSITY OF MAINE ORONO · PI HENRY, CLARISSA A · 2016 to 2016
$355k
March of Dimes Foundation #1-FY14-284NICHD NIH HHS R15 HD088217NIH HHS R15HD088217
6 · The paper itself

Abstract

Skeletal muscle enables posture, breathing, and locomotion. Skeletal muscle also impacts systemic processes such as metabolism, thermoregulation, and immunity. Skeletal muscle is energetically expensive and is a major consumer of glucose and fatty acids. Metabolism of fatty acids and glucose requires NAD+ function as a hydrogen/electron transfer molecule. Therefore, NAD+ plays a vital role in energy production. In addition, NAD+ also functions as a cosubstrate for post-translational modifications such as deacetylation and ADP-ribosylation. Therefore, NAD+ levels influence a myriad of cellular processes including mitochondrial biogenesis, transcription, and organization of the extracellular matrix. Clearly, NAD+ is a major player in skeletal muscle development, regeneration, aging, and disease. The vast majority of studies indicate that lower NAD+ levels are deleterious for muscle health and higher NAD+ levels augment muscle health. However, the downstream mechanisms of NAD+ function throughout different cellular compartments are not well understood. The purpose of this review is to highlight recent studies investigating NAD+ function in muscle development, homeostasis, disease, and regeneration. Emerging research areas include elucidating roles for NAD+ in muscle lysosome function and calcium mobilization, mechanisms controlling fluctuations in NAD+ levels during muscle development and regeneration, and interactions between targets of NAD+ signaling (especially mitochondria and the extracellular matrix). This knowledge should facilitate identification of more precise pharmacological and activity-based interventions to raise NAD+ levels in skeletal muscle, thereby promoting human health and function in normal and disease states.

Indexed as

AgingAnimalsHomeostasisHumansIntracellular SpaceMuscle DevelopmentMuscle ProteinsMuscle, SkeletalMuscular DiseasesNADNiacinamideNicotinamide PhosphoribosyltransferasePyridinium CompoundsRegenerationSignal TransductionMuscle ProteinsNADNiacinamidenicotinamide-beta-ribosideNicotinamide PhosphoribosyltransferasePyridinium Compounds

Identifiers

PMID29514713
PMCPMC5840929
OpenAlexW2802726310

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.