Evidence map›Paper›PMID 26522807›Full record

ArticleAging cell2016

Age-associated changes in long-chain fatty acid profile during healthy aging promote pro-inflammatory monocyte polarization via PPARγ.

Chathyan Pararasa, John Ikwuobe, Shahjahan Shigdar, Alexis Boukouvalas, Ian T Nabney, James E Brown, Andrew Devitt, Clifford J Bailey, Stuart J Bennett, Helen R Griffiths

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

43 citing papers in PubMed, 77 citations in OpenAlex.

  1. Trial
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  6. Review
  7. Immunosenescence: signaling pathways, diseases and therapeutic targets.Signal transduction and targeted therapy · 2025
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  11. Reactive oxygen species in the pathogenesis of sarcopenia.Free radical biology & medicine · 2025
    Review
  12. Lipid Biochemistry and its Role in Human Diseases.Current medicinal chemistry · 2025
    Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  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

10 authors at 1 institution in 1 country.

Chathyan PararasaLife & Health Sciences, Aston University, Birmingham, B4 7ET, UK.
John IkwuobeLife & Health Sciences, Aston University, Birmingham, B4 7ET, UK.
Shahjahan ShigdarLife & Health Sciences, Aston University, Birmingham, B4 7ET, UK.
Alexis BoukouvalasEngineering & Applied Sciences, Aston University, Birmingham, B4 7ET, UK.
Ian T NabneyAston Research Centre for Healthy Ageing, Aston University, Birmingham, B4 7ET, UK.
James E BrownLife & Health Sciences, Aston University, Birmingham, B4 7ET, UK.
Andrew DevittLife & Health Sciences, Aston University, Birmingham, B4 7ET, UK.
Clifford J BaileyLife & Health Sciences, Aston University, Birmingham, B4 7ET, UK.
Stuart J BennettLife & Health Sciences, Aston University, Birmingham, B4 7ET, UK.
Helen R GriffithsLife & Health Sciences, Aston University, Birmingham, B4 7ET, UK.
Aston University · GB

Funding

Biotechnology and Biological Sciences Research Council BB/G017832/1
6 · The paper itself

Abstract

Differences in lipid metabolism associate with age-related disease development and lifespan. Inflammation is a common link between metabolic dysregulation and aging. Saturated fatty acids (FAs) initiate pro-inflammatory signalling from many cells including monocytes; however, no existing studies have quantified age-associated changes in individual FAs in relation to inflammatory phenotype. Therefore, we have determined the plasma concentrations of distinct FAs by gas chromatography in 26 healthy younger individuals (age < 30 years) and 21 healthy FA individuals (age > 50 years). Linear mixed models were used to explore the association between circulating FAs, age and cytokines. We showed that plasma saturated, poly- and mono-unsaturated FAs increase with age. Circulating TNF-α and IL-6 concentrations increased with age, whereas IL-10 and TGF-β1 concentrations decreased. Oxidation of MitoSOX Red was higher in leucocytes from FA adults, and plasma oxidized glutathione concentrations were higher. There was significant colinearity between plasma saturated FAs, indicative of their metabolic relationships. Higher levels of the saturated FAs C18:0 and C24:0 were associated with lower TGF-β1 concentrations, and higher C16:0 were associated with higher TNF-α concentrations. We further examined effects of the aging FA profile on monocyte polarization and metabolism in THP1 monocytes. Monocytes preincubated with C16:0 increased secretion of pro-inflammatory cytokines in response to phorbol myristate acetate-induced differentiation through ceramide-dependent inhibition of PPARγ activity. Conversely, C18:1 primed a pro-resolving macrophage which was PPARγ dependent and ceramide dependent and which required oxidative phosphorylation. These data suggest that a midlife adult FA profile impairs the switch from proinflammatory to lower energy, requiring anti-inflammatory macrophages through metabolic reprogramming.

Indexed as

Cell PolarityAdolescentAdultAge FactorsCell DifferentiationCeramidesCytokinesFatty AcidsHumansInflammationLipid MetabolismMacrophagesMaleMonocytesPPAR gammaTumor Necrosis Factor-alphaCeramidesCytokinesFatty AcidsPPAR gammaTumor Necrosis Factor-alphaanti-inflammatorymacrophagemitochondrial ROSoleateoxidative phosphorylationpalmitate

Identifiers

PMID26522807
PMCPMC4717269
OpenAlexW1923595707

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.