Evidence map›Paper›PMID 36357677›Full record

ArticleNature medicine2022

Proteomic signatures for identification of impaired glucose tolerance.

Julia Carrasco-Zanini, Maik Pietzner, Joni V Lindbohm, Eleanor Wheeler, Erin Oerton, Nicola Kerrison, Missy Simpson, Matthew Westacott, Dan Drolet, Mika Kivimaki and 4 more

Open access · greenAbstract read
In one paragraph

Article in Nature medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 1 pooled it
5.6field-weighted citation impact, top 3% 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

41 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 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

14 authors at 5 institutions in 4 countries.

Julia Carrasco-ZaniniMRC Epidemiology Unit, Institute of Metabolic Science, University of Cambridge School of Clinical Medicine, Cambridge, UK.ORCID http://orcid.org/0000-0002-3988-7505
Maik PietznerMRC Epidemiology Unit, Institute of Metabolic Science, University of Cambridge School of Clinical Medicine, Cambridge, UK.ORCID http://orcid.org/0000-0003-3437-9963
Joni V LindbohmClinicum, Department of Public Health, University of Helsinki, Helsinki, Finland.ORCID http://orcid.org/0000-0002-9820-2692
Eleanor WheelerMRC Epidemiology Unit, Institute of Metabolic Science, University of Cambridge School of Clinical Medicine, Cambridge, UK.ORCID http://orcid.org/0000-0002-8616-6444
Erin OertonMRC Epidemiology Unit, Institute of Metabolic Science, University of Cambridge School of Clinical Medicine, Cambridge, UK.
Nicola KerrisonMRC Epidemiology Unit, Institute of Metabolic Science, University of Cambridge School of Clinical Medicine, Cambridge, UK.
Missy SimpsonSomaLogic, Inc., Boulder, CO, USA.
Matthew WestacottSomaLogic, Inc., Boulder, CO, USA.
Dan DroletSomaLogic, Inc., Boulder, CO, USA.
Mika KivimakiClinicum, Department of Public Health, University of Helsinki, Helsinki, Finland.ORCID http://orcid.org/0000-0002-4699-5627
Rachel OstroffSomaLogic, Inc., Boulder, CO, USA.
Stephen A WilliamsSomaLogic, Inc., Boulder, CO, USA.ORCID http://orcid.org/0000-0002-8661-4315
Nicholas J WarehamMRC Epidemiology Unit, Institute of Metabolic Science, University of Cambridge School of Clinical Medicine, Cambridge, UK.ORCID http://orcid.org/0000-0003-1422-2993
Claudia LangenbergMRC Epidemiology Unit, Institute of Metabolic Science, University of Cambridge School of Clinical Medicine, Cambridge, UK. claudia.langenberg@mrc-epid.cam.ac.uk.ORCID http://orcid.org/0000-0002-5017-7344
University of Cambridge · GBSomaLogic (United States) · USBroad Institute · USQueen Mary University of London · GBUniversity of Helsinki · FI

Funding

Socio-economic status and heterogeneity in agingR01AG013196 · NIA · UNIVERSITY OF LONDON INST OF NEUROLOGY · PI MARMOT, MICHAEL G, SINGH-MANOUX, ARCHANA · 1996 to 2013
$3.5M
Education, socioeconomic status and Aging: transitions from multimorbidity to functional limitations and mortalityR01AG056477 · NIA · UNIVERSITY COLLEGE LONDON · PI KIVIMAKI, MIKA J, SINGH-MANOUX, ARCHANA · 2018 to 2022
$2.8M
British Heart Foundation RG/13/2/30098Cancer Research UK C864/A14136Department of HealthMedical Research Council G0902037Medical Research Council MC_PC_13046Medical Research Council MC_UU_00006/1Medical Research Council MC_UU_12015/1Medical Research Council MR/K013351/1Medical Research Council MR/N003284/1Medical Research Council MR/N003284/1 MC-UU_12015/1Medical Research Council MR/R024227/1Medical Research Council MR/S011676/1Medical Research Council R024227NIA NIH HHS R01 AG013196NIA NIH HHS R01 AG056477Wellcome TrustWellcome Trust 220044/Z/19/ZWellcome Trust 221854/Z/20/Z
6 · The paper itself

Abstract

The implementation of recommendations for type 2 diabetes (T2D) screening and diagnosis focuses on the measurement of glycated hemoglobin (HbA1c) and fasting glucose. This approach leaves a large number of individuals with isolated impaired glucose tolerance (iIGT), who are only detectable through oral glucose tolerance tests (OGTTs), at risk of diabetes and its severe complications. We applied machine learning to the proteomic profiles of a single fasted sample from 11,546 participants of the Fenland study to test discrimination of iIGT defined using the gold-standard OGTTs. We observed significantly improved discriminative performance by adding only three proteins (RTN4R, CBPM and GHR) to the best clinical model (AUROC = 0.80 (95% confidence interval: 0.79-0.86), P = 0.004), which we validated in an external cohort. Increased plasma levels of these candidate proteins were associated with an increased risk for future T2D in an independent cohort and were also increased in individuals genetically susceptible to impaired glucose homeostasis and T2D. Assessment of a limited number of proteins can identify individuals likely to be missed by current diagnostic strategies and at high risk of T2D and its complications.

Indexed as

Diabetes Mellitus, Type 2Glucose IntoleranceBlood GlucoseFastingGlucose Tolerance TestHumansProteomicsBlood Glucose

Identifiers

PMID36357677
PMCPMC7614638
OpenAlexW4308766739

What OpenQuestion holds

Textmetadata
LicenceTDM
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.