Evidence map›Paper›PMID 26290049›Full record

ArticleDiabetologia2015

Elevated HbA(1c) levels and the accumulation of differentiated T cells in CMV(+) individuals.

Jerrald L Rector, G Neil Thomas, Victoria E Burns, Jennifer B Dowd, Raphael M Herr, Paul A Moss, Marc N Jarczok, Kristina Hoffman, Joachim E Fischer, Jos A Bosch

Open access · hybridAbstract read
In one paragraph

Article in Diabetologia, 2015. 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
1.0field-weighted citation impact, top 21% 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, 19 citations in OpenAlex.

  1. Article
  2. Article
  3. Observational
  4. Overweight, obesity, and risk of hospitalization for COVID-19: A community-based cohort study of adults in the United Kingdom.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  5. Article
  6. Article
  7. Review
  8. The silent war of CMV in aging and HIV infection.Mechanisms of ageing and development · 2016
    Review
  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

10 authors at 5 institutions in 4 countries.

Jerrald L RectorSchool of Sport, Exercise, and Rehabilitation Sciences, University of Birmingham, Birmingham, UK.
G Neil ThomasSchool of Health and Population Sciences, College of Medical and Dental Sciences, University of Birmingham, Birmingham, UK.
Victoria E BurnsSchool of Sport, Exercise, and Rehabilitation Sciences, University of Birmingham, Birmingham, UK.
Jennifer B DowdCUNY School of Public Health, New York, NY, USA.
Raphael M HerrMannheim Institute of Public Health, Social and Preventive Medicine, Mannheim Medical Faculty, University of Heidelberg, Mannheim, Germany.
Paul A MossCancer Research UK Centre, University of Birmingham, Birmingham, UK.
Marc N JarczokMannheim Institute of Public Health, Social and Preventive Medicine, Mannheim Medical Faculty, University of Heidelberg, Mannheim, Germany.
Kristina HoffmanMannheim Institute of Public Health, Social and Preventive Medicine, Mannheim Medical Faculty, University of Heidelberg, Mannheim, Germany.
Joachim E FischerMannheim Institute of Public Health, Social and Preventive Medicine, Mannheim Medical Faculty, University of Heidelberg, Mannheim, Germany.
Jos A BoschMannheim Institute of Public Health, Social and Preventive Medicine, Mannheim Medical Faculty, University of Heidelberg, Mannheim, Germany. j.a.bosch@uva.nl.
University of Birmingham · GBUniversity of Mannheim · DEUniversity Hospital Heidelberg · DECUNY School of Law · USHeidelberg University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aims/hypothesisBiological ageing of the immune system, or immunosenescence, predicts poor health and increased mortality. A hallmark of immunosenescence is the accumulation of differentiated cytotoxic T cells (CD27(-)CD45RA(+/-); or dCTLs), partially driven by infection with the cytomegalovirus (CMV). Immune impairments reminiscent of immunosenescence are also observed in hyperglycaemia, and in vitro studies have illustrated mechanisms by which elevated glucose can lead to increased dCTLs. This study explored associations between glucose dysregulation and markers of immunosenescence in CMV(+) and CMV(-) individuals.

methodsA cross-sectional sample of participants from an occupational cohort study (n = 1,103, mean age 40 years, 88% male) were assessed for HbA(1c) and fasting glucose levels, diabetes, cardiovascular risk factors (e.g. lipids), numbers of circulating effector memory (EM; CD27(-)CD45RA(-)) and CD45RA re-expressing effector memory (EMRA; CD27(-)CD45RA(+)) T cells, and CMV infection status. Self-report and physical examination assessed anthropometric, sociodemographic and lifestyle factors.

resultsAmong CMV(+) individuals (n = 400), elevated HbA(1c) was associated with increased numbers of EM (B = 2.75, p < 0.01) and EMRA (B = 2.90, p < 0.01) T cells, which was robust to adjustment for age, sex, sociodemographic variables and lifestyle factors. Elevated EM T cells were also positively associated with total cholesterol (B = 0.04, p < 0.05) after applying similar adjustments. No associations were observed in CMV(-) individuals. CONCLUSIONS/

interpretationThe present study identified consistent associations of unfavourable glucose and lipid profiles with accumulation of dCTLs in CMV(+) individuals. These results provide evidence that the impact of metabolic risk factors on immunity and health can be co-determined by infectious factors, and provide a novel pathway linking metabolic risk factors with accelerated immunosenescence.

Indexed as

AdolescentAdultCohort StudiesCytomegalovirusCytomegalovirus InfectionsFemaleGlycated HemoglobinHumansImmunosenescenceLymphocyte ActivationMaleMiddle AgedRisk FactorsT-LymphocytesT-Lymphocyte SubsetsYoung AdultGlycated Hemoglobinhemoglobin A1c protein, humanCholesterolCMVCytomegalovirusDiabetesGlucoseHaemoglobin A1cHbA1cImmune ageingMetabolic syndromeT cell

Identifiers

PMID26290049
PMCPMC4589544
OpenAlexW1754950289

What OpenQuestion holds

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LicenceCC BY
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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.