Evidence map›Paper›PMID 37005925›Full record

ArticleMetabolomics : Official journal of the Metabolomic Society2023

Metabolomic profiling of glucose homeostasis in African Americans: the Insulin Resistance Atherosclerosis Family Study (IRAS-FS).

Hayrettin Okut, Yingchang Lu, Nicholette D Palmer, Yii-Der Ida Chen, Kent D Taylor, Jill M Norris, Carlos Lorenzo, Jerome I Rotter, Carl D Langefeld, Lynne E Wagenknecht and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Metabolomics : Official journal of the Metabolomic Society, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Metaboepigenetic regulation of gene expression in obesity and insulin resistance.Metabolomics : Official journal of the Metabolomic Society · 2024
    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

12 authors at 6 institutions in 1 country.

Hayrettin Okut *Center for Precision Medicine, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Yingchang Lu *Division of Genetic Medicine, Vanderbilt Genetics Institute, Vanderbilt University Medical Center, Nashville, TN, 37232, USA.
Nicholette D PalmerCenter for Precision Medicine, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Yii-Der Ida ChenDepartment of Pediatrics, The Institute for Translational Genomics and Population Sciences, The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, USA.
Kent D TaylorDepartment of Pediatrics, The Institute for Translational Genomics and Population Sciences, The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, USA.
Jill M NorrisDepartments of Epidemiology, Colorado School of Public Health, University of Colorado Denver, Aurora, CO, USA.
Carlos LorenzoDepartment of Medicine, University of Texas Health Science Center, San Antonio, TX, USA.
Jerome I RotterDepartment of Pediatrics, The Institute for Translational Genomics and Population Sciences, The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, USA.
Carl D LangefeldDepartment of Biostatistical Sciences, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Lynne E WagenknechtDivision of Public Health Sciences, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Donald W BowdenCenter for Precision Medicine, Wake Forest School of Medicine, Winston-Salem, NC, USA.
Maggie C Y NgCenter for Precision Medicine, Wake Forest School of Medicine, Winston-Salem, NC, USA. maggie.ng@vumc.org.
Wake Forest University · USUCLA Medical Center · USVanderbilt University Medical Center · USColorado School of Public Health · USThe University of Texas Health Science Center at San Antonio · USUniversity of Kansas · US

Funding

UCLA Clinical Translational Science InstituteUL1TR001881 · NCATS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ARLEEN F. BROWN, ARASH NAEIM · 2016 to 2026
$118.1M
Transgenic & Knock-out MouseP30DK063491 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Andrea L Hevener · 2003 to 2026
$40.4M
Genetics of African American Type 2 DiabetesR01DK066358 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI NG, MAGGIE · 2003 to 2019
$6.2M
IRAS FAMILY STUDY--GENETICS OF INSULIN RESISTANCER01HL060944 · NHLBI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI WAGENKNECHT, LYNNE E · 1999 to 2009
$5.5M
IRAS FAMILY STUDY: GENETICS OF INSULIN RESISTANCER01HL060919 · NHLBI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI LORENZO, CARLOS · 1999 to 2008
$2.7M
IRAS FAMILY STUDY--GENETICS OF INSULIN RESISTANCER01HL061019 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI NORRIS, JILL M · 1999 to 2009
$2.6M
Genome-wide association study of coronary artery diseases in individuals of African ancestryR56HL150186 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI LU, YINGCHANG · 2020 to 2020
$935k
NCATS NIH HHS UL1 TR001881NHLBI NIH HHS R01 HL060919NHLBI NIH HHS R01 HL060944NHLBI NIH HHS R01 HL061019NHLBI NIH HHS R56 HL150186NIDDK NIH HHS P30 DK063491NIDDK NIH HHS R01 DK066358
6 · The paper itself

Abstract

introductionAfrican Americans are at increased risk for type 2 diabetes.

objectivesThis work aimed to examine metabolomic signature of glucose homeostasis in African Americans.

methodsWe used an untargeted liquid chromatography-mass spectrometry metabolomic approach to comprehensively profile 727 plasma metabolites among 571 African Americans from the Insulin Resistance Atherosclerosis Family Study (IRAS-FS) and investigate the associations between these metabolites and both the dynamic (S

resultsWe confirmed increased plasma metabolite levels of branched-chain amino acids and their metabolic derivatives, 2-aminoadipate, 2-hydroxybutyrate, glutamate, arginine and its metabolic derivatives, carbohydrate metabolites, and medium- and long-chain fatty acids were associated with insulin resistance, while increased plasma metabolite levels in the glycine, serine and threonine metabolic pathway were associated with insulin sensitivity. We also observed a differential ancestral effect of glutamate on glucose homeostasis with significantly stronger effects observed in African Americans than those previously observed in Mexican Americans.

conclusionWe extended the observations that metabolites are useful biomarkers in the identification of prediabetes in individuals at risk of type 2 diabetes in African Americans. We revealed, for the first time, differential ancestral effect of certain metabolites (i.e., glutamate) on glucose homeostasis traits. Our study highlights the need for additional comprehensive metabolomic studies in well-characterized multiethnic cohorts.

Indexed as

AtherosclerosisDiabetes Mellitus, Type 2Insulin ResistanceBlack or African AmericanGlucoseGlutamatesHomeostasisHumansMetabolomicsGlucoseGlutamatesAfrican AmericansGlucose homeostasisMetabolomics

Identifiers

PMID37005925
PMCPMC10068644
OpenAlexW4362521181

What OpenQuestion holds

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LicenceCC BY
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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.