Evidence map›Paper›PMID 27499494›Full record

ArticleEBioMedicine2016

The Ratio of Regulatory (FOXP3+) to Total (CD3+) T Cells Determined by Epigenetic Cell Counting and Cardiovascular Disease Risk: A Prospective Case-cohort Study in Non-diabetics.

Sebastian Dietmar Barth, Rudolf Kaaks, Theron Johnson, Verena Katzke, Katharina Gellhaus, Janika Josephin Schulze, Sven Olek, Tilman Kühn

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.5field-weighted citation impact, top 33% 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, 9 citations in OpenAlex.

  1. Review
  2. Review
  3. Myocardial-Treg Crosstalk: How to Tame a Wolf.Frontiers in immunology · 2022
    Review
  4. Review
  5. T cell subsets and functions in atherosclerosis.Nature reviews. Cardiology · 2020
    Review
  6. Article
  7. Article
  8. Article
  9. 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

8 authors at 2 institutions in 1 country.

Sebastian Dietmar BarthDivision of Cancer Epidemiology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 581, 69120 Heidelberg, Germany. Electronic address: s.barth@dkfz-heidelberg.de.
Rudolf KaaksDivision of Cancer Epidemiology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 581, 69120 Heidelberg, Germany. Electronic address: r.kaaks@dkfz-heidelberg.de.
Theron JohnsonDivision of Cancer Epidemiology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 581, 69120 Heidelberg, Germany. Electronic address: t.johnson@dkfz-heidelberg.de.
Verena KatzkeDivision of Cancer Epidemiology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 581, 69120 Heidelberg, Germany. Electronic address: v.katzke@dkfz-heidelberg.de.
Katharina GellhausIvana Türbachova Laboratory for Epigenetics, Epiontis GmbH, Rudower Chaussee 29, 12489 Berlin, Germany. Electronic address: katharina.gellhaus@epiontis.com.
Janika Josephin SchulzeIvana Türbachova Laboratory for Epigenetics, Epiontis GmbH, Rudower Chaussee 29, 12489 Berlin, Germany. Electronic address: janika.schulze@epiontis.com.
Sven OlekIvana Türbachova Laboratory for Epigenetics, Epiontis GmbH, Rudower Chaussee 29, 12489 Berlin, Germany. Electronic address: sven.olek@epiontis.com.
Tilman KühnDivision of Cancer Epidemiology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 581, 69120 Heidelberg, Germany. Electronic address: t.kuehn@dkfz-heidelberg.de.
Heidelberg University · DEGerman Cancer Research Center · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundExperimental and clinical evidence indicate that inflammatory processes in atherogenesis and the development of cardiovascular complications are promoted by a loss of regulatory T cell (Treg)-mediated immunological tolerance to plaque antigens. Yet, the association between alterations of systemic Treg frequency and cardiovascular disease incidence remains uncertain.

methodsA nested case-cohort study was conducted within the European Prospective Investigation into Cancer and Nutrition (EPIC)-Heidelberg, comprising a random subcohort (n=778) and primary cases of myocardial infarction (MI, n=276) and ischemic stroke (n=151). Pre-diagnostic FOXP3+ Treg and total CD3+ T-lymphocyte (tTL) frequencies in blood were measured by epigenetic-based, quantitative real-time PCR-assisted cell counting.

resultsMultivariate, Prentice-weighted Cox regression analyses revealed that lower Treg/tTL ratios were not associated with the risk of either MI (lowest vs. highest sex-specific quartile; hazard ratio: 0.72, 95% confidence interval: 0.46 to 1.13; P

conclusionsAmong middle-aged adults from the general population, imbalances in the relative frequency of Tregs within the total T cell compartment do not confer an increased risk of MI or stroke.

Indexed as

Epigenesis, GeneticLymphocyte CountAdultAgedCardiovascular DiseasesCase-Control StudiesCD3 ComplexFemaleFollow-Up StudiesForkhead Transcription FactorsHumansIncidenceMaleMiddle AgedPhenotypePopulation SurveillanceCD3 ComplexForkhead Transcription FactorsFOXP3 protein, humanCardiovascular disease riskCell-type-specific epigenetic qPCR-assaysFoxp3+ regulatory T cells (Tregs)Immune toleranceProspective study

Identifiers

PMID27499494
PMCPMC5049920
OpenAlexW2496848283

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.