Evidence map›Paper›PMID 23443556›Full record

ArticleNature communications2013

De novo lipogenesis in human fat and liver is linked to ChREBP-β and metabolic health.

Leah Eissing, Thomas Scherer, Klaus Tödter, Uwe Knippschild, Jan Willem Greve, Wim A Buurman, Hans O Pinnschmidt, Sander S Rensen, Anna M Wolf, Alexander Bartelt and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Nature communications, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 170 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
170citing papers in PubMed, 1 pooled it
13.6field-weighted citation impact, top 1% 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

170 citing papers in PubMed, 1 synthesis or guideline pooled it, 296 citations in OpenAlex.

  1. Pooled it
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  17. Mondo family proteins in diabetes.Frontiers in endocrinology · 2025
    Review
  18. Investigating the Pathogenesis and Treatment of Type 2 Diabetes from the Perspective of Adipose Tissue.Diabetes, metabolic syndrome and obesity : targets and therapy · 2025
    Review
  19. Article
  20. Article

110 more citing papers are in PubMed but not listed here.

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

13 authors at 7 institutions in 4 countries.

Leah EissingDepartment of Biochemistry and Molecular Cell Biology, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany.
Thomas Scherer
Klaus Tödter
Uwe Knippschild
Jan Willem Greve
Wim A Buurman
Hans O Pinnschmidt
Sander S Rensen
Anna M Wolf
Alexander Bartelt
Joerg Heeren
Christoph Buettner
Ludger Scheja
Universität Hamburg · DEUniversity Medical Center Hamburg-Eppendorf · DEMaastricht University Medical Centre · NLUniversität Ulm · DEAtrium Medisch Centrum Parkstad · NLIcahn School of Medicine at Mount Sinai · USMedical University of Vienna · AT

Funding

VESICULAR LOCALIZATION AND FUNCTION OF PRESENILIN 1 FRAGMENTP50AG005138 · NIA · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI SEWELL, MARGARET · 1985 to 2019
$37.9M
Regulation of Adipose Tissue Metabolism by Central Insulin and LeptinR01DK083658 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BUETTNER, CHRISTOPH · 2009 to 2013
$1.9M
The role of Stat3 signaling in leptin's pleitropic action.K08DK074873 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BUETTNER, CHRISTOPH · 2006 to 2009
$510k
The role of the endocannabinoid system in regulating hepatic glucose fluxesR03DK082724 · NIDDK · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BUETTNER, CHRISTOPH · 2009 to 2010
$169k
NIA NIH HHS P50 AG005138NIDDK NIH HHS DK074873NIDDK NIH HHS DK082724NIDDK NIH HHS DK083568NIDDK NIH HHS K08 DK074873NIDDK NIH HHS R01 DK083658NIDDK NIH HHS R03 DK082724
6 · The paper itself

Abstract

Clinical interest in de novo lipogenesis has been sparked by recent studies in rodents demonstrating that de novo lipogenesis specifically in white adipose tissue produces the insulin-sensitizing fatty acid palmitoleate. By contrast, hepatic lipogenesis is thought to contribute to metabolic disease. How de novo lipogenesis in white adipose tissue versus liver is altered in human obesity and insulin resistance is poorly understood. Here we show that lipogenic enzymes and the glucose transporter-4 are markedly decreased in white adipose tissue of insulin-resistant obese individuals compared with non-obese controls. By contrast, lipogenic enzymes are substantially upregulated in the liver of obese subjects. Bariatric weight loss restored de novo lipogenesis and glucose transporter-4 gene expression in white adipose tissue. Notably, lipogenic gene expression in both white adipose tissue and liver was strongly linked to the expression of carbohydrate-responsive element-binding protein-β and to metabolic risk markers. Thus, de novo lipogenesis predicts metabolic health in humans in a tissue-specific manner and is likely regulated by glucose-dependent carbohydrate-responsive element-binding protein activation.

Indexed as

AdiposityHealthLipogenesisAdultBariatric SurgeryBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsBody Mass IndexFatty AcidsFatty Acid SynthasesFatty LiverFemaleGene DosageGene Expression RegulationGlucose Transporter Type 4HumansInsulin ResistanceBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsFatty AcidsFatty Acid SynthasesGlucose Transporter Type 4MLXIPL protein, humanRNA, MessengerSLC2A4 protein, humanTumor Necrosis Factor-alpha

Identifiers

PMID23443556
PMCPMC3740744
OpenAlexW1966872601

What OpenQuestion holds

Textmetadata
LicenceTDM
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.