Evidence map›Paper›PMID 36080270›Full record

ArticleMolecules (Basel, Switzerland)2022

Exosome Proteomics Reveals the Deregulation of Coagulation, Complement and Lipid Metabolism Proteins in Gestational Diabetes Mellitus.

Elena G Bernea, Viorel I Suica, Elena Uyy, Aurel Cerveanu-Hogas, Raluca M Boteanu, Luminita Ivan, Iuliana Ceausu, Doina A Mihai, Constantin Ionescu-Tîrgoviște, Felicia Antohe

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
6.8field-weighted citation impact, top 2% 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

21 citing papers in PubMed, 35 citations in OpenAlex.

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  19. Multigenerational diabetes mellitus.Frontiers in endocrinology · 2023
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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

10 authors at 2 institutions in 2 countries.

Elena G Bernea"Prof. N. Paulescu" National Institute of Diabetes, Nutrition and Metabolic Diseases, 020474 Bucharest, Romania.
Viorel I SuicaInstitute of Cellular Biology and Pathology "Nicolae Simionescu", 050568 Bucharest, Romania.ORCID 0000-0003-2168-7182
Elena UyyInstitute of Cellular Biology and Pathology "Nicolae Simionescu", 050568 Bucharest, Romania.ORCID 0000-0003-3963-1937
Aurel Cerveanu-HogasInstitute of Cellular Biology and Pathology "Nicolae Simionescu", 050568 Bucharest, Romania.
Raluca M BoteanuInstitute of Cellular Biology and Pathology "Nicolae Simionescu", 050568 Bucharest, Romania.
Luminita IvanInstitute of Cellular Biology and Pathology "Nicolae Simionescu", 050568 Bucharest, Romania.
Iuliana CeausuUniversity of Medicine and Pharmacy "Carol Davila", 020021 Bucharest, Romania.
Doina A Mihai"Prof. N. Paulescu" National Institute of Diabetes, Nutrition and Metabolic Diseases, 020474 Bucharest, Romania.
Constantin Ionescu-Tîrgoviște"Prof. N. Paulescu" National Institute of Diabetes, Nutrition and Metabolic Diseases, 020474 Bucharest, Romania.
Felicia AntoheInstitute of Cellular Biology and Pathology "Nicolae Simionescu", 050568 Bucharest, Romania.
Carol Davila University of Medicine and Pharmacy · RONational Institute of Nutrition · IN

Funding

Romanian Academy PhD FellowshipUnitatea Executiva Pentru Finantarea Invatamantului Superior a Cercetarii Dezvoltarii si Inovarii project number PN-III-P1-1.1-TE-2021-1161 and PN-III-P4-PCE-2021-1344 within PNCDI III
6 · The paper itself

Abstract

Exosomes are small extracellular vesicles with a variable protein cargo in consonance with cell origin and pathophysiological conditions. Gestational diabetes mellitus (GDM) is characterized by different levels of chronic low-grade inflammation and vascular dysfunction; however, there are few data characterizing the serum exosomal protein cargo of GDM patients and associated signaling pathways. Eighteen pregnant women were enrolled in the study: 8 controls (CG) and 10 patients with GDM. Blood samples were collected from patients, for exosomes' concentration. Protein abundance alterations were demonstrated by relative mass spectrometric analysis and their association with clinical parameters in GDM patients was performed using Pearson's correlation analysis. The proteomics analysis revealed 78 significantly altered proteins when comparing GDM to CG, related to complement and coagulation cascades, platelet activation, prothrombotic factors and cholesterol metabolism. Down-regulation of Complement C3 (C3), Complement C5 (C5), C4-B (C4B), C4b-binding protein beta chain (C4BPB) and C4b-binding protein alpha chain (C4BPA), and up-regulation of C7, C9 and F12 were found in GDM. Our data indicated significant correlations between factors involved in the pathogenesis of GDM and clinical parameters that may improve the understanding of GDM pathophysiology. Data are available via ProteomeXchange with identifier PXD035673.

Indexed as

Diabetes, GestationalExosomesBlood ProteinsComplement C4b-Binding ProteinComplement System ProteinsFemaleHumansLipid MetabolismPregnancyProteomicsBlood ProteinsComplement C4b-Binding ProteinComplement System Proteinscomplement systemgestational diabeteslipid metabolismmass spectrometryplatelet activationproteomicsprothrombotic factors

Identifiers

PMID36080270
PMCPMC9457917
OpenAlexW4293733724

What OpenQuestion 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 OpenQuestion graph.