Evidence map›Paper›PMID 30599058›Full record

ArticleEuropean journal of epidemiology2019

Protein markers and risk of type 2 diabetes and prediabetes: a targeted proteomics approach in the KORA F4/FF4 study.

Cornelia Huth, Christine von Toerne, Florian Schederecker, Tonia de Las Heras Gala, Christian Herder, Florian Kronenberg, Christa Meisinger, Wolfgang Rathmann, Wolfgang Koenig, Melanie Waldenberger and 4 more

Open access · hybridAbstract read
In one paragraph

Article in European journal of epidemiology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

34 citing papers in PubMed, 58 citations in OpenAlex.

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  12. Hallmarks of the metabolic secretome.Trends in endocrinology and metabolism: TEM · 2024
    Review
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  14. Observational
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  18. Advances in multi-omics study of biomarkers of glycolipid metabolism disorder.Computational and structural biotechnology journal · 2022
    Review
  19. Article
  20. 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 2 countries.

Cornelia HuthInstitute of Epidemiology, Helmholtz Zentrum München - German Research Center for Environmental Health (GmbH), Ingolstädter Landstraße 1, 85764, Neuherberg, Germany. huth@helmholtz-muenchen.de.ORCID http://orcid.org/0000-0003-2421-433X
Christine von ToerneGerman Center for Diabetes Research (DZD), München-Neuherberg, Germany.ORCID http://orcid.org/0000-0002-4132-4322
Florian SchedereckerInstitute of Epidemiology, Helmholtz Zentrum München - German Research Center for Environmental Health (GmbH), Ingolstädter Landstraße 1, 85764, Neuherberg, Germany.
Tonia de Las Heras GalaInstitute of Epidemiology, Helmholtz Zentrum München - German Research Center for Environmental Health (GmbH), Ingolstädter Landstraße 1, 85764, Neuherberg, Germany.
Christian HerderGerman Center for Diabetes Research (DZD), München-Neuherberg, Germany.ORCID http://orcid.org/0000-0002-2050-093X
Florian KronenbergDivision of Genetic Epidemiology, Department of Medical Genetics, Molecular and Clinical Pharmacology, Medical University of Innsbruck, Innsbruck, Austria.ORCID http://orcid.org/0000-0003-2229-1120
Christa MeisingerInstitute of Epidemiology, Helmholtz Zentrum München - German Research Center for Environmental Health (GmbH), Ingolstädter Landstraße 1, 85764, Neuherberg, Germany.ORCID http://orcid.org/0000-0002-9026-6544
Wolfgang RathmannGerman Center for Diabetes Research (DZD), München-Neuherberg, Germany.
Wolfgang KoenigDepartment of Internal Medicine II - Cardiology, University of Ulm Medical Center, Ulm, Germany.
Melanie WaldenbergerInstitute of Epidemiology, Helmholtz Zentrum München - German Research Center for Environmental Health (GmbH), Ingolstädter Landstraße 1, 85764, Neuherberg, Germany.
Michael RodenGerman Center for Diabetes Research (DZD), München-Neuherberg, Germany.
Annette PetersInstitute of Epidemiology, Helmholtz Zentrum München - German Research Center for Environmental Health (GmbH), Ingolstädter Landstraße 1, 85764, Neuherberg, Germany.ORCID http://orcid.org/0000-0001-6645-0985
Stefanie M HauckGerman Center for Diabetes Research (DZD), München-Neuherberg, Germany.ORCID http://orcid.org/0000-0002-1630-6827
Barbara ThorandInstitute of Epidemiology, Helmholtz Zentrum München - German Research Center for Environmental Health (GmbH), Ingolstädter Landstraße 1, 85764, Neuherberg, Germany.ORCID http://orcid.org/0000-0002-8416-6440
Helmholtz Zentrum München · DEDeutsches Diabetes-Zentrum e.V. · DEInnsbruck Medical University · ATUniversität Ulm · DEUniversity of Augsburg · DE

Funding

Deutsche Forschungsgemeinschaft DFGDeutsche Forschungsgemeinschaft RA 459/2-1
6 · The paper itself

Abstract

The objective of the present study was to identify proteins that contribute to pathophysiology and allow prediction of incident type 2 diabetes or incident prediabetes. We quantified 14 candidate proteins using targeted mass spectrometry in plasma samples of the prospective, population-based German KORA F4/FF4 study (6.5-year follow-up). 892 participants aged 42-81 years were selected using a case-cohort design, including 123 persons with incident type 2 diabetes and 255 persons with incident WHO-defined prediabetes. Prospective associations between protein levels and diabetes, prediabetes as well as continuous fasting and 2 h glucose, fasting insulin and insulin resistance were investigated using regression models adjusted for established risk factors. The best predictive panel of proteins on top of a non-invasive risk factor model or on top of HbA1c, age, and sex was selected. Mannan-binding lectin serine peptidase (MASP) levels were positively associated with both incident type 2 diabetes and prediabetes. Adiponectin was inversely associated with incident type 2 diabetes. MASP, adiponectin, apolipoprotein A-IV, apolipoprotein C-II, C-reactive protein, and glycosylphosphatidylinositol specific phospholipase D1 were associated with individual continuous outcomes. The combination of MASP, apolipoprotein E (apoE) and adiponectin improved diabetes prediction on top of both reference models, while prediabetes prediction was improved by MASP plus CRP on top of the HbA1c model. In conclusion, our mass spectrometric approach revealed a novel association of MASP with incident type 2 diabetes and incident prediabetes. In combination, MASP, adiponectin and apoE improved type 2 diabetes prediction beyond non-invasive risk factors or HbA1c, age and sex.

Indexed as

AdiponectinAdultAgedAged, 80 and overApolipoproteins EBiomarkersDiabetes Mellitus, Type 2FemaleGermanyHumansMaleMannose-Binding Protein-Associated Serine ProteasesMiddle AgedPrediabetic StateProspective StudiesProteomicsAdiponectinApolipoproteins EBiomarkersMannose-Binding Protein-Associated Serine ProteasesBiomarkerPopulation-basedPrediabetesPredictionProteomicsType 2 diabetes

Identifiers

PMID30599058
PMCPMC6451724
OpenAlexW2907303285

What OpenQuestion holds

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Registered trials

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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.