Evidence map›Paper›PMID 28080219›Full record

ArticleMetabolic syndrome and related disorders2017

Adipose Tissue Insulin Resistance in Gestational Diabetes.

Batbayar Tumurbaatar, Aaron T Poole, Gayle Olson, Michel Makhlouf, Hanaa S Sallam, Shwetha Thukuntla, Sucharitha Kankanala, Obos Ekhaese, Guillermo Gomez, Manisha Chandalia and 1 more

Abstract read
In one paragraph

Article in Metabolic syndrome and related disorders, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

21 citing papers in PubMed, 60 citations in OpenAlex.

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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

11 authors at 1 institution in 1 country.

Batbayar Tumurbaatar1 Division of Endocrinology, Department of Internal Medicine, University of Texas Medical Branch , Galveston, Texas.
Aaron T Poole2 Department of Obstetrics and Gynecology, Maternal and Fetal Medicine, University of Texas Medical Branch , Galveston, Texas.
Gayle Olson2 Department of Obstetrics and Gynecology, Maternal and Fetal Medicine, University of Texas Medical Branch , Galveston, Texas.
Michel Makhlouf2 Department of Obstetrics and Gynecology, Maternal and Fetal Medicine, University of Texas Medical Branch , Galveston, Texas.
Hanaa S Sallam1 Division of Endocrinology, Department of Internal Medicine, University of Texas Medical Branch , Galveston, Texas.
Shwetha Thukuntla1 Division of Endocrinology, Department of Internal Medicine, University of Texas Medical Branch , Galveston, Texas.
Sucharitha Kankanala1 Division of Endocrinology, Department of Internal Medicine, University of Texas Medical Branch , Galveston, Texas.
Obos Ekhaese3 Department of General Surgery, University of Texas Medical Branch , Galveston, Texas.
Guillermo Gomez3 Department of General Surgery, University of Texas Medical Branch , Galveston, Texas.
Manisha Chandalia4 Bay Area Metabolic Health, Houston, Texas.
Nicola Abate1 Division of Endocrinology, Department of Internal Medicine, University of Texas Medical Branch , Galveston, Texas.
The University of Texas Medical Branch at Galveston · US

Funding

UTMB CLINICAL AND TRANSLATIONAL SCIENCE AWARD: NASA BED REST STUDIESUL1RR029876 · NCRR · UNIVERSITY OF TEXAS MED BR GALVESTON · PI BRASIER, ALLAN R. · 2009 to 2011
$17.7M
NCRR NIH HHS UL1 RR029876
6 · The paper itself

Abstract

backgroundGestational diabetes mellitus (GDM) is a metabolic disorder characterized by insulin resistance (IR) and altered glucose-lipid metabolism. We propose that ectonucleotide pyrophosphate phosphodiesterase-1 (ENPP1), a protein known to induce adipocyte IR, is a determinant of GDM. Our objective was to study ENPP1 expression in adipose tissue (AT) of obese pregnant women with or without GDM, as well as glucose tolerance in pregnant transgenic (Tg) mice with AT-specific overexpression of human ENPP1.

methodsAT biopsies and blood were collected from body mass index-matched obese pregnant women non-GDM (n = 6), GDM (n = 7), and nonpregnant controls (n = 6) undergoing cesarian section or elective surgeries, respectively. We measured the following: (1) Expression of key molecules involved in insulin signaling and glucose-lipid metabolism in AT; (2) Plasma glucose and insulin levels and calculation of homeostasis model assessment of IR (HOMA-IR); (3) Intraperitoneal glucose tolerance test in AtENPP1 Tg pregnant mice.

resultsWe found that: (1) Obese GDM patients have higher AT ENPP1 expression than obese non-GDM patients, or controls (P = 0.01-ANOVA). (2) ENPP1 expression level correlated negatively with glucose transporter 4 (GLUT4) and positively with insulin receptor substrate-1 (IRS-1) serine phosphorylation, and to other adipocyte functional proteins involved in glucose and lipid metabolism (P < 0.05 each), (3) AT ENPP1 expression levels were positively correlated with HOMA-IR (P = 0.01-ANOVA). (4) Pregnant AT ENPP1 Tg mice showed higher plasma glucose than wild type animals (P = 0.046-t test on area under curve [AUC]

conclusionsOur results provide evidence of a causative link between ENPP1 and alterations in insulin signaling, glucose uptake, and lipid metabolism in subcutaneous abdominal AT of GDM, which may mediate IR and hyperglycemia in GDM.

Indexed as

Adipose TissueAdultAnimalsCase-Control StudiesCross-Sectional StudiesDiabetes, GestationalFemaleHumansInsulin ResistanceLipid MetabolismMaleMiceMice, Inbred C57BLMice, TransgenicPhosphoric Diester HydrolasesPregnancyectonucleotide pyrophosphatase phosphodiesterase 1Phosphoric Diester HydrolasesPyrophosphatasesENPP1gestational diabetesinsulin signalingpregnancy

Identifiers

PMID28080219
PMCPMC5333579
OpenAlexW2588364541

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.