Evidence map›Paper›PMID 33658980›Full record

ArticleFrontiers in endocrinology2020

Signs of Deregulated Gene Expression Are Present in Both CD14

Michal Koc, Michaela Šiklová, Veronika Šrámková, Marek Štěpán, Eva Krauzová, Vladimír Štich, Lenka Rossmeislová

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03155412 (Limited Adipose Tissue Expandability as a Risk Factor for Development of Type 2 Diabetes), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 47% 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.

NCT03155412 completednot on this map

Limited Adipose Tissue Expandability as a Risk Factor for Development of Type 2 Diabetes: the Role of Preadipocytes

TypeobservationalSponsorCharles University, Czech RepublicRan2016 to 2019Enrolled44ConditionsType2 Diabetes Mellitus
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Role of Autophagy in Type 2 Diabetes Mellitus: The Metabolic Clash.Journal of cellular and molecular medicine · 2024
    Review
  5. 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

7 authors at 2 institutions in 2 countries.

Michal KocDepartment for Pathophysiology, Centre for Research on Nutrition, Metabolism and Diabetes, Third Faculty of Medicine, Charles University, Prague, Czechia.
Michaela ŠiklováDepartment for Pathophysiology, Centre for Research on Nutrition, Metabolism and Diabetes, Third Faculty of Medicine, Charles University, Prague, Czechia.
Veronika ŠrámkováDepartment for Pathophysiology, Centre for Research on Nutrition, Metabolism and Diabetes, Third Faculty of Medicine, Charles University, Prague, Czechia.
Marek ŠtěpánDepartment for Pathophysiology, Centre for Research on Nutrition, Metabolism and Diabetes, Third Faculty of Medicine, Charles University, Prague, Czechia.
Eva KrauzováDepartment for Pathophysiology, Centre for Research on Nutrition, Metabolism and Diabetes, Third Faculty of Medicine, Charles University, Prague, Czechia.
Vladimír ŠtichDepartment for Pathophysiology, Centre for Research on Nutrition, Metabolism and Diabetes, Third Faculty of Medicine, Charles University, Prague, Czechia.
Lenka RossmeislováDepartment for Pathophysiology, Centre for Research on Nutrition, Metabolism and Diabetes, Third Faculty of Medicine, Charles University, Prague, Czechia.
Charles University · CZInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aim: Development of type 2 diabetes (T2DM) is associated with disturbances in immune and metabolic status that may be reflected by an altered gene expression profile of peripheral blood mononuclear cells (PBMC). To reveal a potential family predisposition to these alterations, we investigated the regulation of gene expression profiles in circulating CD14 Materials and Methods: This work is based on the clinical study LIMEX (NCT03155412). Non-obese 12 non-diabetic (FDR), and 12 control men without family history of diabetes matched for age and BMI underwent OGTT. Blood samples taken before and at the end of OGTT were used for isolation of circulating CD14 Results: Irrespectively of the group, the majority of analyzed genes had different mRNA expression in CD14 Conclusion: This study revealed a different impact of glucose challenge on gene expression in CD14

Indexed as

Gene Expression RegulationGenetic Predisposition to DiseaseTranscriptomeAdultBiomarkersBlood GlucoseCase-Control StudiesDiabetes Mellitus, Type 2Glucose Tolerance TestHumansLeukocytes, MononuclearLipopolysaccharide ReceptorsMaleBiomarkersBlood GlucoseCD14 protein, humanLipopolysaccharide ReceptorsCD14+ cellsCD14− cellsfirst-degree relativesgene expressionoral glucose tolerance testperipheral blood mononuclear cellstype 2 diabetes mellitus

Identifiers

PMID33658980
PMCPMC7917286
OpenAlexW3133275085

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.