Evidence map›Paper›PMID 34093556›Full record

ArticleFrontiers in immunology2021

In Patients With Obesity, the Number of Adipose Tissue Mast Cells Is Significantly Lower in Subjects With Type 2 Diabetes.

David Lopez-Perez, Anaïs Redruello-Romero, Jesús Garcia-Rubio, Carlos Arana, Luis A Garcia-Escudero, Francisco Tamayo, Jose D Puentes-Pardo, Sara Moreno-SanJuan, Javier Salmeron, Armando Blanco and 3 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Impact ofFrontiers in gastroenterology (Lausanne, Switzerland) · 2024
    Review
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  7. Article
  8. Article
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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

13 authors.

David Lopez-PerezDepartment of Pharmacology, Faculty of Pharmacy, University of Granada, Granada, Spain.
Anaïs Redruello-RomeroResearch Unit, Instituto de Investigación Biosanitaria de Granada (ibs.GRANADA), Granada, Spain.
Jesús Garcia-RubioSurgery Unit, San Cecilio University Hospital, Granada, Spain.
Carlos AranaEndocrinology and Nutrition Unit, Virgen de las Nieves University Hospital, Granada, Spain.
Luis A Garcia-EscuderoDepartment of Statistics and Operative Research, Faculty of Sciences, University of Valladolid, Valladolid, Spain.
Francisco TamayoSurgery Unit, San Cecilio University Hospital, Granada, Spain.
Jose D Puentes-PardoDepartment of Pharmacology, Faculty of Pharmacy, University of Granada, Granada, Spain.
Sara Moreno-SanJuanCytometry and Microscopy Research Service, Instituto de Investigación Biosanitaria de Granada (ibs.GRANADA), Granada, Spain.
Javier SalmeronGastroenterology Unit, San Cecilio University Hospital, Granada, Spain.
Armando BlancoDepartment of Computer Science and Artificial Intelligence, University of Granada, Granada, Spain.
Julio GalvezDepartment of Pharmacology, Faculty of Pharmacy, University of Granada, Granada, Spain.
Josefa LeonResearch Unit, Instituto de Investigación Biosanitaria de Granada (ibs.GRANADA), Granada, Spain.
Ángel CarazoResearch Unit, Instituto de Investigación Biosanitaria de Granada (ibs.GRANADA), Granada, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Type 2 diabetes (T2D) is a rising global health problem mainly caused by obesity and a sedentary lifestyle. In healthy individuals, white adipose tissue (WAT) has a relevant homeostatic role in glucose metabolism, energy storage, and endocrine signaling. Mast cells contribute to these functions promoting WAT angiogenesis and adipogenesis. In patients with T2D, inflammation dramatically impacts WAT functioning, which results in the recruitment of several leukocytes, including monocytes, that enhance this inflammation. Accordingly, the macrophages population rises as the WAT inflammation increases during the T2D status worsening. Since mast cell progenitors cannot arrive at WAT, the amount of WAT mast cells depends on how the new microenvironment affects progenitor and differentiated mast cells. Here, we employed a flow cytometry-based approach to analyze the number of mast cells from omental white adipose tissue (o-WAT) and subcutaneous white adipose tissue (s-WAT) in a cohort of 100 patients with obesity. Additionally, we measured the number of mast cell progenitors in a subcohort of 15 patients. The cohort was divided in three groups: non-T2D, pre-T2D, and T2D. Importantly, patients with T2D have a mild condition (HbA1c <7%). The number of mast cells and mast cell progenitors was lower in patients with T2D in both o-WAT and s-WAT in comparison to subjects from the pre-T2D and non-T2D groups. In the case of mast cells in o-WAT, there were statistically significant differences between non-T2D and T2D groups (p = 0.0031), together with pre-T2D and T2D groups (p=0.0097). However, in s-WAT, the differences are only between non-T2D and T2D groups (p=0.047). These differences have been obtained with patients with a mild T2D condition. Therefore, little changes in T2D status have a huge impact on the number of mast cells in WAT, especially in o-WAT. Due to the importance of mast cells in WAT physiology, their decrease can reduce the capacity of WAT, especially o-WAT, to store lipids and cause hypoxic cell deaths that will trigger inflammation.

Indexed as

Cell CountAdipogenesisAdipose TissueAdipose Tissue, WhiteBiomarkersDiabetes Mellitus, Type 2HumansImmunophenotypingIntestinal MucosaMast CellsNeovascularization, PhysiologicObesityBiomarkersadipogenesisadipose tissueangiogenesisflow cytometryinflammationmast cellobesityT2D

Identifiers

PMID34093556
PMCPMC8177010

What Socratic 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 Socratic graph.