Evidence map›Paper›PMID 27541014›Full record

ArticleDiabetologia2016

Soluble CD163, adiponectin, C-reactive protein and progression of dysglycaemia in individuals at high risk of type 2 diabetes mellitus: the ADDITION-PRO cohort.

Pia Deichgræber, Daniel R Witte, Holger J Møller, Mette V Skriver, Bjørn Richelsen, Marit E Jørgensen, Nanna B Johansen, Annelli Sandbæk

Erratum issuedOpen access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Diabetologia, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Observational
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    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 1 country.

Pia DeichgræberSection of General Practice, Department of Public Health, Aarhus University, Bartholins Allé 2, DK-8000, Aarhus, Denmark. p.deichgraeber@ph.au.dk.
Daniel R WitteDepartment of Public Health, Aarhus University, Aarhus, Denmark.
Holger J MøllerDepartment of Clinical Biochemistry, Aarhus University Hospital, Aarhus, Denmark.
Mette V SkriverSection of Health Promotion and Health Services, Department of Public Health, Aarhus University, Aarhus, Denmark.
Bjørn RichelsenDepartment of Endocrinology and Internal Medicine (MEA), Aarhus University Hospital, Aarhus, Denmark.
Marit E JørgensenSteno Diabetes Center, Gentofte, Denmark.
Nanna B JohansenDanish Diabetes Academy, Odense, Denmark.
Annelli SandbækSection of General Practice, Department of Public Health, Aarhus University, Bartholins Allé 2, DK-8000, Aarhus, Denmark.
Aarhus University · DKAarhus University Hospital · DKDanish Diabetes Academy · DKGlostrup Hospital · DKSteno Diabetes Center · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aim/hypothesisOur aim was to investigate the association between the macrophage-activation marker soluble CD163 (sCD163), adiponectin, C-reactive protein (CRP) and changes in glycaemia, insulin resistance and insulin secretion in individuals at high risk of type 2 diabetes mellitus.

methodsThis prospective study included 1014 individuals at high risk of type 2 diabetes mellitus participating in the Danish arm of the Anglo-Danish-Dutch study of Intensive Treatment In PeOple with ScreeN-detected Diabetes in Primary Care (ADDITION-Europe trial) baseline examination in 2001-2006 and follow-up examination (ADDITION-Progression [ADDITION-PRO]) in 2009-2011. Baseline serum samples were analysed for sCD163, adiponectin and CRP. The associations between sCD163, adiponectin and CRP per doubling of concentration, and changes per year in HbA1c, fasting plasma glucose, 2 h glucose, fasting insulin, HOMA-IR and HOMA-β were assessed using a mixed-effects model.

resultsA doubling of sCD163 concentration was positively associated with changes in fasting insulin (β = 1.078 per year, 95% CI 0.454, 1.702) and HOMA-β (β = 1.313 per year, 95% CI 0.537, 2.089), and a doubling of CRP concentration was positively associated with HbA 1c (β = 0.004 per year, 95% CI 0.001, 0.007) and fasting insulin (β = 0.267 per year, 95% CI 0.029, 0.504) after adjustment for age and sex. A doubling of adiponectin was inversely associated with changes in fasting glucose (β = −0.017 per year, 95% CI −0.028, −0.005), 2 h glucose (β = −0.063 per year, 95% CI −0.107, −0.019), fasting insulin (β = −1.558 per year, 95% CI −2.020, −1.096), HOMA-IR (β = −0.040 per year, 95% CI −0.062, −0.019) and HOMA-β (β = −1.009 per year, 95% CI −1.589, −0.429) after adjustment for age and sex. The associations were robust to adjustment for baseline waist circumference and smoking. Adjustment for CRP did not change the associations for sCD163 or adiponectin. CONCLUSIONS/

interpretationOur findings indicate that mechanisms related to inflammation, including macrophage activation and adipocyte metabolism, may play a role in changes in glucose homeostasis in individuals at high risk of type 2 diabetes mellitus.

Indexed as

AdipocytesAdiponectinAgedAntigens, CDAntigens, Differentiation, MyelomonocyticBlood GlucoseCD163 AntigenCholesterolC-Reactive ProteinDiabetes Mellitus, Type 2FemaleHumansInsulinMacrophagesMaleMiddle AgedAdiponectinAntigens, CDAntigens, Differentiation, MyelomonocyticBlood GlucoseCD163 AntigenCholesterolC-Reactive ProteinInsulinReceptors, Cell SurfaceAdiponectinC-reactive proteinGlycaemiaInflammationInsulin resistanceInsulin secretionProspective studysCD163Type 2 diabetes mellitus

Identifiers

PMID27541014
OpenAlexW2508933853

What OpenQuestion holds

Textmetadata
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.