Evidence map›Paper›PMID 24584551›Full record

ArticleDiabetes2014

Increased interaction with insulin receptor substrate 1, a novel abnormality in insulin resistance and type 2 diabetes.

Michael Caruso, Danjun Ma, Zaher Msallaty, Monique Lewis, Berhane Seyoum, Wissam Al-janabi, Michael Diamond, Abdul B Abou-Samra, Kurt Højlund, Rebecca Tagett and 4 more

Open access · hybridAbstract readComparative Study
In one paragraph

Article in Diabetes, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

38 citing papers in PubMed, 65 citations in OpenAlex.

  1. Review
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  5. NovelFrontiers in genetics · 2024
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  20. Skeletal muscle DNA methylation modifications and psychopharmacologic treatment in bipolar disorder.European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology · 2019
    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 5 institutions in 3 countries.

Michael CarusoDepartment of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy/Health Sciences, Wayne State University, Detroit, MI.
Danjun MaDepartment of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy/Health Sciences, Wayne State University, Detroit, MI.
Zaher MsallatyDivision of Endocrinology, Wayne State University School of Medicine, Wayne State University, Detroit, MI.
Monique LewisDepartment of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy/Health Sciences, Wayne State University, Detroit, MI.
Berhane SeyoumDivision of Endocrinology, Wayne State University School of Medicine, Wayne State University, Detroit, MI.
Wissam Al-janabiDepartment of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy/Health Sciences, Wayne State University, Detroit, MI.
Michael DiamondDepartment of Obstetrics and Gynecology, Wayne State University, Detroit, MIDepartment of Obstetrics and Gynecology, Georgia Regents University, Augusta, GA.
Abdul B Abou-SamraDivision of Endocrinology, Wayne State University School of Medicine, Wayne State University, Detroit, MIDepartment of Medicine, Hamad Medical Corporation, Doha, Qatar.
Kurt HøjlundDiabetes Research Centre, Department of Endocrinology, Odense University Hospital, Odense, Denmark.
Rebecca TagettDepartment of Computer Science, College of Engineering, Wayne State University, Detroit, MI.
Sorin DraghiciDepartment of Computer Science, College of Engineering, Wayne State University, Detroit, MI.
Xiangmin ZhangDepartment of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy/Health Sciences, Wayne State University, Detroit, MI.
Jeffrey F HorowitzSchool of Kinesiology, University of Michigan, Ann Arbor, MI.
Zhengping YiDepartment of Pharmaceutical Sciences, Eugene Applebaum College of Pharmacy/Health Sciences, Wayne State University, Detroit, MI zhengping.yi@wayne.edu.
Wayne State University · USEugene Applebaum College of Pharmacy and Health Sciences · USAugusta University · USOdense University Hospital · DKUniversity of Michigan–Ann Arbor · US

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
Human Skeletal Muscle Proteome and Phosphoproteome in Obesity and Type 2 DiabetesR01DK081750 · NIDDK · WAYNE STATE UNIVERSITY · PI YI, ZHENGPING · 2009 to 2017
$3.0M
Training Program in Endocrine and Diabetes ResearchT32DK080657 · NIDDK · WAYNE STATE UNIVERSITY · PI GRANNEMAN, JAMES G · 2010 to 2014
$851k
NIDDK NIH HHS P30 DK020572NIDDK NIH HHS R01 DK081750NIDDK NIH HHS R01-DK-081750NIDDK NIH HHS R01-DK-081750-04S1NIDDK NIH HHS T32 DK080657NIDDK NIH HHS T32-DK-080657
6 · The paper itself

Abstract

Insulin receptor substrate 1 (IRS1) is a key mediator of insulin signal transduction. Perturbations involving IRS1 complexes may lead to the development of insulin resistance and type 2 diabetes (T2D). Surprisingly little is known about the proteins that interact with IRS1 in humans under health and disease conditions. We used a proteomic approach to assess IRS1 interaction partners in skeletal muscle from lean healthy control subjects (LCs), obese insulin-resistant nondiabetic control subjects (OCs), and participants with T2D before and after insulin infusion. We identified 113 novel endogenous IRS1 interaction partners, which represents the largest IRS1 interactome in humans and provides new targets for studies of IRS1 complexes in various diseases. Furthermore, we generated the first global picture of IRS1 interaction partners in LCs, and how they differ in OCs and T2D patients. Interestingly, dozens of proteins in OCs and/or T2D patients exhibited increased associations with IRS1 compared with LCs under the basal and/or insulin-stimulated conditions, revealing multiple new dysfunctional IRS1 pathways in OCs and T2D patients. This novel abnormality, increased interaction of multiple proteins with IRS1 in obesity and T2D in humans, provides new insights into the molecular mechanism of insulin resistance and identifies new targets for T2D drug development.

Indexed as

Blood GlucoseBody Mass IndexDiabetes Mellitus, Type 2FemaleGenetic Predisposition to DiseaseGenetic VariationGlucose Clamp TechniqueHumansInsulinInsulin Receptor Substrate ProteinsInsulin ResistanceLinkage DisequilibriumMaleMiddle AgedMuscle, SkeletalObesityBlood GlucoseInsulinInsulin Receptor Substrate ProteinsIRS1 protein, humanRNA, Messenger

Identifiers

PMID24584551
PMCPMC4030113
OpenAlexW2104346018

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.