Evidence map›Paper›PMID 37329449›Full record

ArticleDiabetologia2023

Plasma proteomic signatures of a direct measure of insulin sensitivity in two population cohorts.

Daniela Zanetti, Laurel Stell, Stefan Gustafsson, Fahim Abbasi, Philip S Tsao, Joshua W Knowles, RISC Investigators, Björn Zethelius, Johan Ärnlöv, Beverley Balkau and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Diabetologia, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.0field-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

11 citing papers in PubMed, 13 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

15 authors at 8 institutions in 4 countries.

Daniela ZanettiDepartment of Medicine, Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA, USA.ORCID http://orcid.org/0000-0002-1225-1021
Laurel StellVA Palo Alto Health Care System, Palo Alto, CA, USA.ORCID http://orcid.org/0000-0003-2971-4317
Stefan GustafssonDepartment of Medical Sciences, Uppsala University, Uppsala, Sweden.ORCID http://orcid.org/0000-0001-5894-0351
Fahim AbbasiDepartment of Medicine, Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA, USA.ORCID http://orcid.org/0000-0002-3932-8375
Philip S TsaoDepartment of Medicine, Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA, USA.ORCID http://orcid.org/0000-0001-7274-9318
Joshua W KnowlesDepartment of Medicine, Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA, USA.ORCID http://orcid.org/0000-0003-1922-7240
RISC Investigators
Björn ZetheliusDepartment of Public Health/Geriatrics, Uppsala University, Uppsala, Sweden.ORCID http://orcid.org/0000-0002-1738-0834
Johan ÄrnlövDivision of Family Medicine and Primary Care, Department of Neurobiology, Care Sciences and Society, Karolinska Institute, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-6933-4637
Beverley BalkauClinical Epidemiology, Centre for Research in Epidemiology and Population Health, Inserm U1018, Villejuif, France.ORCID http://orcid.org/0000-0003-2021-413X
Mark WalkerTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, UK.ORCID http://orcid.org/0000-0002-2526-9810
Laura C LazzeroniDepartment of Biomedical Data Science, Stanford University School of Medicine, Stanford, CA, USA.ORCID http://orcid.org/0000-0002-1846-6920
Lars LindDepartment of Medical Sciences, Uppsala University, Uppsala, Sweden. lars.lind@medsci.uu.se.ORCID http://orcid.org/0000-0003-2335-8542
John R PetrieSchool of Health and Wellbeing, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK. John.Petrie@glasgow.ac.uk.ORCID http://orcid.org/0000-0002-4894-9819
Themistocles L AssimesDepartment of Medicine, Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA, USA. tassimes@stanford.edu.ORCID http://orcid.org/0000-0003-2349-0009
University of Glasgow · GBUppsala University · SEVA Palo Alto Health Care System · USInserm · FRNewcastle University · GBDalarna University · SECardiovascular Institute of the South · USStanford University · US

Funding

Stanford Islet Research CoreP30DK116074 · NIDDK · STANFORD UNIVERSITY · PI Seung K Kim · 2017 to 2026
$19.5M
Proteomic determinants of direct measures of insulin sensitivityR01DK114183 · NIDDK · STANFORD UNIVERSITY · PI ASSIMES, THEMISTOCLES LEONARD · 2018 to 2022
$3.5M
Characterization of novel insulin resistance genes by gene editing, high-throughput phenotyping and in vivo studiesR01DK120565 · NIDDK · STANFORD UNIVERSITY · PI KNOWLES, JOSHUA WILEY · 2019 to 2023
$3.2M
Mechanisms of NAT2 Regulation of Insulin Resistance and Mitochondrial DysfunctionR01DK116750 · NIDDK · STANFORD UNIVERSITY · PI KNOWLES, JOSHUA WILEY · 2019 to 2023
$2.4M
Beyond GWAS of insulin resistance: An integrated approach to translate genetic association to functionR01DK106236 · NIDDK · STANFORD UNIVERSITY · PI KNOWLES, JOSHUA WILEY · 2016 to 2020
$2.4M
Molecular Mechanisms of Insulin Resistance Associated LociR01DK107437 · NIDDK · STANFORD UNIVERSITY · PI QUERTERMOUS, THOMAS · 2016 to 2019
$2.2M
NIDDK NIH HHS R01 DK106236NIDDK NIH HHS R01 DK107437NIDDK NIH HHS R01 DK114183NIDDK NIH HHS R01 DK116750NIDDK NIH HHS R01 DK120565NIH HHS 1R01DK114183
6 · The paper itself

Abstract

aims/hypothesisThe euglycaemic-hyperinsulinaemic clamp (EIC) is the reference standard for the measurement of whole-body insulin sensitivity but is laborious and expensive to perform. We aimed to assess the incremental value of high-throughput plasma proteomic profiling in developing signatures correlating with the M value derived from the EIC.

methodsWe measured 828 proteins in the fasting plasma of 966 participants from the Relationship between Insulin Sensitivity and Cardiovascular disease (RISC) study and 745 participants from the Uppsala Longitudinal Study of Adult Men (ULSAM) using a high-throughput proximity extension assay. We used the least absolute shrinkage and selection operator (LASSO) approach using clinical variables and protein measures as features. Models were tested within and across cohorts. Our primary model performance metric was the proportion of the M value variance explained (R

resultsA standard LASSO model incorporating 53 proteins in addition to routinely available clinical variables increased the M value R CONCLUSIONS/

interpretationA plasma proteomic signature identified using a standard LASSO approach improves the cross-sectional estimation of the M value over routine clinical variables. However, a small subset of these proteins identified using a stability selection algorithm affords much of this improvement, especially when considering cross-cohort analyses. Our approach provides opportunities to improve the identification of insulin-resistant individuals at risk of insulin resistance-related adverse health consequences.

Indexed as

Cardiovascular DiseasesInsulin ResistanceAdultCross-Sectional StudiesHumansInsulinLongitudinal StudiesMaleProteomicsInsulinEuglycaemic–hyperinsulinaemic clampInsulin resistanceInsulin sensitivityLASSOPlasma proteomicsPopulation studyStability selection

Identifiers

PMID37329449
PMCPMC10390625
OpenAlexW4381095111

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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.