Evidence map›Paper›PMID 28289709›Full record

ArticleJCI insight2017

Imaging mass spectrometry demonstrates age-related decline in human adipose plasticity.

Christelle Guillermier, Pouneh K Fazeli, Soomin Kim, Mingyue Lun, Jonah P Zuflacht, Jessica Milian, Hang Lee, Hugues Francois-Saint-Cyr, Francois Horreard, David Larson and 4 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
5.0field-weighted citation impact, top 4% 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

48 citing papers in PubMed, 78 citations in OpenAlex.

  1. Review
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  7. The role of adipogenic niche resident cells in colorectal cancer progression in relation to obesity.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2025
    Review
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  16. Extract ofAntioxidants (Basel, Switzerland) · 2023
    Article
  17. Article
  18. Review
  19. Tracking cell turnover in human brain usingFrontiers in neuroscience · 2023
    Article
  20. Article
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

14 authors at 4 institutions in 2 countries.

Christelle GuillermierDepartment of Medicine, Division of Genetics, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Pouneh K FazeliHarvard Medical School, Boston, Massachusetts, USA.
Soomin KimDepartment of Medicine, Division of Genetics, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Mingyue LunDepartment of Medicine, Division of Genetics, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Jonah P ZuflachtDepartment of Medicine, Division of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Jessica MilianDepartment of Medicine, Division of Cardiovascular Medicine, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Hang LeeHarvard Medical School, Boston, Massachusetts, USA.
Hugues Francois-Saint-CyrCAMECA, Madison, Wisconsin, USA.
Francois HorreardCAMECA, Gennevilliers, France.
David LarsonCAMECA, Madison, Wisconsin, USA.
Evan D RosenHarvard Medical School, Boston, Massachusetts, USA.
Richard T LeeHarvard Medical School, Boston, Massachusetts, USA.
Claude P LecheneDepartment of Medicine, Division of Genetics, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Matthew L SteinhauserDepartment of Medicine, Division of Genetics, Brigham and Women's Hospital, Boston, Massachusetts, USA.
Brigham and Women's Hospital · USHarvard University · USMassachusetts General Hospital · USCameca (France) · FR

Funding

Harvard Clinical and Translational Science CenterUL1TR001102 · NCATS · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2013 to 2017
$106.2M
NCATS NIH HHS UL1 TR001102
6 · The paper itself

Abstract

Quantification of stable isotope tracers has revealed the dynamic state of living tissues. A new form of imaging mass spectrometry quantifies isotope ratios in domains much smaller than a cubic micron, enabling measurement of cell turnover and metabolism with stable isotope tracers at the single-cell level with a methodology we refer to as multi-isotope imaging mass spectrometry. In a first-in-human study, we utilize stable isotope tracers of DNA synthesis and de novo lipogenesis to prospectively measure cell birth and adipocyte lipid turnover. In a study of healthy adults, we elucidate an age-dependent decline in new adipocyte generation and adipocyte lipid turnover. A linear regression model suggests that the aging effect could be mediated by a decline in insulin-like growth factor-1 (IGF-1). This study therefore establishes a method for measurement of cell turnover and metabolism in humans with subcellular resolution while implicating the growth hormone/IGF-1 axis in adipose tissue aging.

Indexed as

AdipocytesAdipogenesisAdultAgingFemaleHomeostasisHuman Growth HormoneHumansInsulin-Like Growth Factor IMaleMass SpectrometryMiddle AgedSubcellular FractionsSubcutaneous FatHuman Growth HormoneIGF1 protein, humanInsulin-Like Growth Factor I

Identifiers

PMID28289709
PMCPMC5333969
OpenAlexW2594050019

What OpenQuestion holds

Textmetadata
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.