Evidence map›Paper›PMID 27007651›Full record

ArticleBrazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica2016

Cytokine profile and lymphocyte subsets in type 2 diabetes.

C O Francisco, A M Catai, S C G Moura-Tonello, L C M Arruda, S L B Lopes, B G Benze, A M Del Vale, K C R Malmegrim, A M O Leal

Open access · goldAbstract read
In one paragraph

Article in Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

11 citing papers in PubMed, 33 citations in OpenAlex.

  1. Article
  2. Review
  3. The immunomodulator effect ofFood science & nutrition · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. Transcriptome of CD8Cancer immunology, immunotherapy : CII · 2021
    Article
  8. Review
  9. Article
  10. Review
  11. Review
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

9 authors at 3 institutions in 1 country.

C O FranciscoDepartamento de Fisioterapia, Universidade Federal de São Carlos, São Carlos, SP, Brasil.
A M CataiDepartamento de Fisioterapia, Universidade Federal de São Carlos, São Carlos, SP, Brasil.
S C G Moura-TonelloDepartamento de Fisioterapia, Universidade Federal de São Carlos, São Carlos, SP, Brasil.
L C M ArrudaCentro de Terapia Celular, Fundação de Amparo è Pesquisa do Estado de São Paulo, Ribeirão Preto, SP, Brasil.
S L B LopesDepartamento de Medicina, Universidade Federal de São Carlos, São Carlos, SP, Brasil.
B G BenzeDepartamento de Estatística, Universidade Federal de São Carlos, São Carlos, SP, Brasil.
A M Del ValeDepartamento de Medicina, Universidade Federal de São Carlos, São Carlos, SP, Brasil.
K C R MalmegrimDepartamento de Análises Clínicas, Toxicológicas e Bromatológicas, Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, SP, Brasil.
A M O LealDepartamento de Medicina, Universidade Federal de São Carlos, São Carlos, SP, Brasil.
Universidade Federal de São Carlos · BRFundação de Amparo à Pesquisa do Estado de São Paulo · BRUniversidade Brasil · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type 2 diabetes mellitus (T2D) is a metabolic disease with inflammation as an important pathogenic background. However, the pattern of immune cell subsets and the cytokine profile associated with development of T2D are unclear. The objective of this study was to evaluate different components of the immune system in T2D patients' peripheral blood by quantifying the frequency of lymphocyte subsets and intracellular pro- and anti-inflammatory cytokine production by T cells. Clinical data and blood samples were collected from 22 men (51.6±6.3 years old) with T2D and 20 nonsmoking men (49.4±7.6 years old) who were matched for age and sex as control subjects. Glycated hemoglobin, high-sensitivity C-reactive protein concentrations, and the lipid profile were measured by a commercially available automated system. Frequencies of lymphocyte subsets in peripheral blood and intracellular production of interleukin (IL)-4, IL-10, IL-17, tumor necrosis factor-α, and interferon-γ cytokines by CD3+ T cells were assessed by flow cytometry. No differences were observed in the frequency of CD19+ B cells, CD3+CD8+ and CD3+CD4+ T cells, CD16+56+ NK cells, and CD4+CD25+Foxp3+ T regulatory cells in patients with T2D compared with controls. The numbers of IL-10- and IL-17-producing CD3+ T cells were significantly higher in patients with T2D than in controls (P<0.05). The frequency of interferon-γ-producing CD3+ T cells was positively correlated with body mass index (r=0.59; P=0.01). In conclusion, this study shows increased numbers of circulating IL-10- and IL-17-producing CD3+ T cells in patients with T2D, suggesting that these cytokines are involved in the immune pathology of this disease.

Indexed as

AdultCase-Control StudiesC-Reactive ProteinCytokinesDiabetes Mellitus, Type 2Flow CytometryHumansImmunity, CellularLymphocyte CountMaleMiddle AgedReference ValuesStatistics, NonparametricT-LymphocytesT-Lymphocyte SubsetsC-Reactive ProteinCytokines

Identifiers

PMID27007651
PMCPMC4819407
OpenAlexW2306927750

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.