Evidence mapPaperPMID 24907277Full record

ReviewThe Journal of biological chemistry2014

Pathway-selective insulin resistance and metabolic disease: the importance of nutrient flux.

Yolanda F Otero, John M Stafford, Owen P McGuinness

Open access · hybridAbstract readReview
In one paragraph

Review in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 5% 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

47 citing papers in PubMed, 1 synthesis or guideline pooled it, 91 citations in OpenAlex.

  1. Pooled it
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  6. Review
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  15. Journal of diabetes and metabolic disorders · 2021
    Article
  16. Review
  17. Review
  18. Sex, Cells, and Asthma.Mayo Clinic proceedings · 2021
    Review
  19. Review
  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

3 authors at 2 institutions in 2 countries.

Yolanda F Otero
John M Stafford
Owen P McGuinness
Institute of Molecular Biology and Biophysics · RUVanderbilt University · US

Funding

REGULATION OF GLUCOSE UPTAKE DURING EXERCISE--PILOT/FEASIBILITY STUDYP60DK020593 · VANDERBILT UNIVERSITY · 1986 to 2005
$14.1M
Vanderbilt Mouse Metabolic Physiology CenterU24DK059637 · VANDERBILT UNIVERSITY · 2001 to 2005
$5.3M
NUTRITION, INFECTION AND HEPATIC CARBOHYDRATE METABOLISMR01DK043748 · VANDERBILT UNIVERSITY · 1997 to 2005
$2.1M
Vanderbilt Diabetes Research CenterP30DK020593 · VANDERBILT UNIVERSITY MEDICAL CENTER · 2025 to 2025
$1.8M
REGULATION OF HEPATIC GLUCOSE METABOLISM IN INFECTIONR29DK043748 · VANDERBILT UNIVERSITY · 1992 to 1996
BLRD VA I01 BX002223NIDDK NIH HHS DK020593NIDDK NIH HHS DK043748NIDDK NIH HHS DK059637NIDDK NIH HHS DK078188NIDDK NIH HHS P30 DK020593NIDDK NIH HHS P60 DK020593NIDDK NIH HHS R01 DK043748NIDDK NIH HHS R01 DK078188NIDDK NIH HHS R56 DK043748NIDDK NIH HHS U24 DK059637
6 · The paper itself

Abstract

Hepatic glucose and lipid metabolism are altered in metabolic disease (e.g. obesity, metabolic syndrome, and Type 2 diabetes). Insulin-dependent regulation of glucose metabolism is impaired. In contrast, lipogenesis, hypertriglyceridemia, and hepatic steatosis are increased. Because insulin promotes lipogenesis and liver fat accumulation, to explain the elevation in plasma and tissue lipids, investigators have suggested the presence of pathway-selective insulin resistance. In this model, insulin signaling to glucose metabolism is impaired, but insulin signaling to lipid metabolism is intact. We discuss the evidence for the differential regulation of hepatic lipid and glucose metabolism. We suggest that the primary phenotypic driver is altered substrate delivery to the liver, as well as the repartitioning of hepatic nutrient handling. Specific alterations in insulin signaling serve to amplify the alterations in hepatic substrate metabolism. Thus, hyperinsulinemia and its resultant increased signaling may facilitate lipogenesis, but are not the major drivers of the phenotype of pathway-selective insulin resistance.

Indexed as

Insulin ResistanceAnimalsDiabetes Mellitus, Type 2Fatty LiverGlucoseHumansHypertriglyceridemiaInsulinLipogenesisLiverMetabolic SyndromeSignal TransductionGlucoseInsulin

Identifiers

PMID24907277
PMCPMC4110258
OpenAlexW2092608666

What Socratic 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 Socratic graph.