Evidence map›Paper›PMID 29892037›Full record

ArticleInternational journal of obesity (2005)2019

Altered tricarboxylic acid cycle flux in primary myotubes from severely obese humans.

Kai Zou, J Matthew Hinkley, Sanghee Park, Donghai Zheng, Terry E Jones, Walter J Pories, Pamela J Hornby, James Lenhard, G Lynis Dohm, Joseph A Houmard

Open access · greenAbstract read
In one paragraph

Article in International journal of obesity (2005), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

20 citing papers in PubMed, 29 citations in OpenAlex.

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  17. Plasma Lactate as a Marker for Metabolic Health.Exercise and sport sciences reviews · 2020
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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

10 authors at 2 institutions in 1 country.

Kai ZouDepartment of Exercise and Health Sciences, University of Massachusetts Boston, Boston, MA, USA. kai.zou@umb.edu.ORCID http://orcid.org/0000-0003-4164-7129
J Matthew HinkleyDepartment of Kinesiology, East Carolina University, Greenville, NC, USA.
Sanghee ParkDepartment of Kinesiology, East Carolina University, Greenville, NC, USA.
Donghai ZhengDepartment of Kinesiology, East Carolina University, Greenville, NC, USA.
Terry E JonesDepartment of Physical Therapy, East Carolina University, Greenville, NC, USA.
Walter J PoriesEast Carolina Diabetes and Obesity Institute, East Carolina University, Greenville, NC, USA.
Pamela J HornbyJanssen Research & Development LLC, Spring House, PA, USA.
James LenhardJanssen Research & Development LLC, Spring House, PA, USA.
G Lynis DohmEast Carolina Diabetes and Obesity Institute, East Carolina University, Greenville, NC, USA.
Joseph A HoumardDepartment of Kinesiology, East Carolina University, Greenville, NC, USA.
East Carolina University · USJanssen (United States) · US

Funding

TECHNOLOGY NMR SPECTROSCOPYU24DK100469 · NIDDK · MAYO CLINIC ROCHESTER · PI NAIR, K SREEKUMARAN · 2013 to 2017
$9.0M
LIPID METABOLISM IN OBESITY, WEIGHT LOSS AND EXERCISER01DK056112 · NIDDK · EAST CAROLINA UNIVERSITY · PI HOUMARD, JOSEPH A · 2000 to 2016
$4.5M
American Heart Association-American Stroke Association 15POST25080003NIDDK NIH HHS R01 DK056112NIDDK NIH HHS U24 DK100469
6 · The paper itself

Abstract

BACKGROUND/

objectiveThe partitioning of glucose toward glycolytic end products rather than glucose oxidation and glycogen storage is evident in skeletal muscle with severe obesity and type 2 diabetes. The purpose of the present study was to determine the possible mechanism by which severe obesity alters insulin-mediated glucose partitioning in human skeletal muscle. SUBJECTS/

methodsPrimary human skeletal muscle cells (HSkMC) were isolated from lean (BMI = 23.6 ± 2.6 kg/m

resultsMyotubes derived from severely obese subjects exhibited attenuated response of glycogen synthesis (20.3%; 95% CI [4.7, 28.8]; P = 0.017) and glucose oxidation (5.6%; 95% CI [0.3, 8.6]; P = 0.046) with a concomitant greater increase (23.8%; 95% CI [5.7, 47.8]; P = 0.004) in non-oxidized glycolytic end products with insulin stimulation in comparison to the lean group (34.2% [24.9, 45.1]; 13.1% [8.6, 16.4], and 2.9% [-4.1, 12.2], respectively). These obesity-related alterations in glucose partitioning appeared to be linked with reduced TCA cycle flux, as 2-[

conclusionsThese data suggest that with severe obesity the partitioning of glucose toward anaerobic glycolysis in response to insulin is a resilient characteristic of human skeletal muscle. This altered glucose partitioning appeared to be due, at least in part, to a reduction in TCA cycle flux.

Indexed as

AdultCarbohydrate MetabolismCells, CulturedCitric Acid CycleFemaleGlycogenGlycolysisHumansMaleMuscle Fibers, SkeletalObesity, MorbidPrimary Cell CultureTricarboxylic AcidsGlycogenTricarboxylic Acids

Identifiers

PMID29892037
PMCPMC13492247
OpenAlexW2807970111

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.