Evidence map›Paper›PMID 32992039›Full record

ArticleMolecular metabolism2020

Prolonged fasting drives a program of metabolic inflammation in human adipose tissue.

Pouneh K Fazeli, Yang Zhang, John O'Keefe, Tristan Pesaresi, Mingyue Lun, Brian Lawney, Matthew L Steinhauser

Open access · goldAbstract read
In one paragraph

Article in Molecular metabolism, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

39 citing papers in PubMed, 54 citations in OpenAlex.

  1. Trial
  2. Review
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  6. TNF/TNFR1 is a Key Regulator of Prolonged Fasting-Induced Decrease in Adipose Tissue.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  7. Article
  8. Review
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  10. Article
  11. Article
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  14. Mechanisms of Lipid-Associated Macrophage Accrual in Metabolically Stressed Adipose Tissue.BioEssays : news and reviews in molecular, cellular and developmental biology · 2025
    Review
  15. Article
  16. Review
  17. Article
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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 4 institutions in 1 country.

Pouneh K FazeliDepartment of Medicine, Neuroendocrine Unit, Massachusetts General Hospital, Boston, MA, USA; Harvard Medical School, Boston, MA, USA; Department of Medicine, Division of Endocrinology, Neuroendocrinology Unit, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA; Center for Human Integrative Physiology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA. Electronic address: pkfazeli@pitt.edu.
Yang ZhangDepartment of Medicine, Division of Genetics, Brigham and Women's Hospital, Boston, MA, USA; Aging Institute, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
John O'KeefeDepartment of Medicine, Division of Genetics, Brigham and Women's Hospital, Boston, MA, USA.
Tristan PesaresiCenter for Human Integrative Physiology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA; Aging Institute, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA.
Mingyue LunDepartment of Medicine, Division of Genetics, Brigham and Women's Hospital, Boston, MA, USA.
Brian LawneyQuantitative Biomedical Research Center, Department of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Matthew L SteinhauserHarvard Medical School, Boston, MA, USA; Center for Human Integrative Physiology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA; Department of Medicine, Division of Genetics, Brigham and Women's Hospital, Boston, MA, USA; Aging Institute, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA. Electronic address: msteinhauser@pitt.edu.
Brigham and Women's Hospital · USHarvard University · USQuantitative BioSciences · USUniversity of Pittsburgh · US

Funding

Institutional Career Development CoreKL2TR002542 · NCATS · HARVARD MEDICAL SCHOOL · PI BREDELLA, MIRIAM ANTOINETTE, RUTKOVE, SEWARD B. · 2018 to 2022
$8.7M
NCATS NIH HHS KL2 TR002542
6 · The paper itself

Abstract

objectiveThe human adaptive fasting response enables survival during periods of caloric deprivation. A crucial component of the fasting response is the shift from glucose metabolism to utilization of lipids, underscoring the importance of adipose tissue as the central lipid-storing organ. The objective of this study was to investigate the response of adipose tissue to a prolonged fast in humans.

methodsWe performed RNA sequencing of subcutaneous adipose tissue samples longitudinally collected during a 10-day, 0-calorie fast in humans. We further investigated observed transcriptional signatures utilizing cultured human monocytes and Thp1 cells. We examined the cellularity of adipose tissue biopsies with transmission electron microscopy and tested for associated changes in relevant inflammatory mediators in the systemic circulation by ELISA assays of longitudinally collected blood samples.

resultsCoincident with the expected shift away from glucose utilization and lipid storage, we demonstrated downregulation of pathways related to glycolysis, oxidative phosphorylation, and lipogenesis. The canonical lipolysis pathway was also downregulated, whereas fasting drove alternative lysosomal paths to lipid digestion. Unexpectedly, the dominant induced pathways were associated with immunity and inflammation, although this only became evident at the 10-day time point. Among the most augmented transcripts were those associated with macrophage identity and function, such as members of the erythroblast transformation-specific (ETS) transcription factor family. Key components of the macrophage transcriptional signal in fasting adipose tissue were recapitulated with induced expression of two of the ETS transcription factors via cultured macrophages, SPIC and SPI1. The inflammatory signal was further reflected by an increase in systemic inflammatory mediators.

conclusionsCollectively, this study demonstrates an unexpected role of metabolic inflammation in the human adaptive fasting response.

Indexed as

Adipose TissueAdultDNA-Binding ProteinsFastingFemaleGene ExpressionGene Expression RegulationHumansInflammationInsulinInsulin ResistanceLipid MetabolismLipogenesisLipolysisMacrophagesMaleDNA-Binding ProteinsInsulinSPIC protein, humanTranscription FactorsAdipose tissueFastingHumanInflammationMacrophageSPIC

Identifiers

PMID32992039
PMCPMC7554650
OpenAlexW3090856552

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.