Evidence map›Paper›PMID 32990346›Full record

ArticleAging cell2020

Metabolic dysfunction in human skin: Restoration of mitochondrial integrity and metabolic output by nicotinamide (niacinamide) in primary dermal fibroblasts from older aged donors.

John E Oblong, Amy Bowman, Holly A Rovito, Bradley B Jarrold, Joseph D Sherrill, Markaisa R Black, Glyn Nelson, Alexa B Kimball, Mark A Birch-Machin

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

20 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Skin Cancer Prevention and Antiaging: Role of Nicotinamide.International journal of molecular sciences · 2026
    Review
  3. Review
  4. Article
  5. Benefits and risks of hair, skin, and nail supplements in older adults.International journal of women's dermatology · 2025
    Review
  6. Review
  7. Review
  8. Autophagy-Enhancing Properties ofMolecules (Basel, Switzerland) · 2025
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Skin Aging, Cellular Senescence and Natural Polyphenols.International journal of molecular sciences · 2021
    Review
  18. Article
  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

9 authors at 3 institutions in 2 countries.

John E OblongThe Procter & Gamble Company, Cincinnati, OH, USA.ORCID 0000-0001-7628-6242
Amy BowmanDermatological Sciences, Translational and Clinical Research Institute, Medical School, Newcastle University, Newcastle upon Tyne, UK.ORCID 0000-0001-9263-8180
Holly A RovitoThe Procter & Gamble Company, Cincinnati, OH, USA.ORCID 0000-0003-2352-1477
Bradley B JarroldThe Procter & Gamble Company, Cincinnati, OH, USA.ORCID 0000-0001-5948-2276
Joseph D SherrillThe Procter & Gamble Company, Cincinnati, OH, USA.ORCID 0000-0003-0502-2252
Markaisa R BlackThe Procter & Gamble Company, Cincinnati, OH, USA.ORCID 0000-0001-8901-7789
Glyn NelsonThe Bioimaging Unit, William Leech Building, Newcastle University, Newcastle upon Tyne, UK.ORCID 0000-0002-1895-4772
Alexa B KimballHarvard Medical School, Boston, MA, USA.ORCID 0000-0001-9405-0479
Mark A Birch-MachinDermatological Sciences, Translational and Clinical Research Institute, Medical School, Newcastle University, Newcastle upon Tyne, UK.ORCID 0000-0002-2668-2623
Procter & Gamble (United States) · USNewcastle University · GBHarvard University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alterations in metabolism in skin are accelerated by environmental stressors such as solar radiation, leading to premature aging. The impact of aging on mitochondria is of interest given their critical role for metabolic output and the finding that environmental stressors cause lowered energy output, particularly in fibroblasts where damage accumulates. To better understand these metabolic changes with aging, we performed an in-depth profiling of the expression patterns of dermal genes in face, forearm, and buttock biopsies from females of 20-70 years of age that encode for all subunits comprising complexes I-V of the mitochondrial electron transport chain. This complements previous preliminary analyses of these changes. "Oxidative phosphorylation" was the top canonical pathway associated with aging in the face, and genes encoding for numerous subunits had decreased expression patterns with age. Investigations on fibroblasts from older aged donors also showed decreased gene expression of numerous subunits from complexes I-V, oxidative phosphorylation rates, spare respiratory capacity, and mitochondrial number and membrane potential compared to younger cells. Treatment of older fibroblasts with nicotinamide (Nam) restored these measures to younger cell levels. Nam increased complexes I, IV, and V activity and gene expression of representative subunits. Elevated mt-Keima staining suggests a possible mechanism of action for these restorative effects via mitophagy. Nam also improved mitochondrial number and membrane potential in younger fibroblasts. These findings show there are significant changes in mitochondrial functionality with aging and that Nam treatment can restore bioenergetic efficiency and capacity in older fibroblasts with an amplifying effect in younger cells.

Indexed as

AdultAgedCells, CulturedFibroblastsHumansMiddle AgedMitochondriaNiacinamideSkinTissue DonorsYoung AdultNiacinamide

Identifiers

PMID32990346
PMCPMC7576238
OpenAlexW3089994865

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.