Evidence map›Paper›PMID 32326243›Full record

ArticleCells2020

Association of Proteins Modulating Immune Response and Insulin Clearance During Gestation with Antenatal Complications in Patients with Gestational or Type 2 Diabetes Mellitus.

Arthur T Kopylov, Anna L Kaysheva, Olga Papysheva, Iveta Gribova, Galina Kotaysch, Lubov Kharitonova, Tatiana Mayatskaya, Anna Krasheninnikova, Sergey G Morozov

Open access · goldAbstract read
In one paragraph

Article in Cells, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.7field-weighted citation impact, top 24% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

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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

9 authors at 4 institutions in 1 country.

Arthur T KopylovDepartment of Pathology, Institute of General Pathology and Pathophysiology, 125315 Moscow, Russia.ORCID 0000-0002-7199-372X
Anna L KayshevaDepartment of Proteomic Researches, Institute of Biomedical Chemistry, 119121 Moscow, Russia.ORCID 0000-0003-4472-2016
Olga PapyshevaPerinatal Center, Sergey S. Yudin 7th State Clinical Hospital, 115446 Moscow, Russia.
Iveta GribovaNikolay E. Bauman 29th State Clinical Hospital, 110020 Moscow, Russia.
Galina KotayschNikolay E. Bauman 29th State Clinical Hospital, 110020 Moscow, Russia.
Lubov KharitonovaNikolay I. Pirogov Medical University, 117997 Moscow, Russia.
Tatiana MayatskayaNikolay I. Pirogov Medical University, 117997 Moscow, Russia.
Anna KrasheninnikovaDepartment of Pathology, Institute of General Pathology and Pathophysiology, 125315 Moscow, Russia.
Sergey G MorozovDepartment of Pathology, Institute of General Pathology and Pathophysiology, 125315 Moscow, Russia.
Research Institute of General Pathology and Pathophysiology, the Russian Academy of Medical Sciences · RUPirogov Russian National Research Medical University · RUCity Clinical Hospital · RUInstitute of Biomedical Chemistry · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe purpose of the study is to establish and quantitatively assess protein markers and their combination in association with insulin uptake that may be have value for early prospective recognition of diabetic fetopathy (DF) as a complication in patients with diabetes mellitus during gestation.

methodsProteomic surveying and accurate quantitative measurement of selected proteins from plasma samples collected from the patients with gestational diabetes mellitus (GDM) and type 2 diabetes mellitus (T2DM) who gave birth of either healthy or affected by maternal diabetes newborns was performed using mass spectrometry.

resultsWe determined and quantitatively measured several proteins, including CRP, CEACAM1, CNDP1 and Ig-family that were significantly differed in patients that gave birth of newborns with signs of DF. We found that patients with newborns associated with DF are characterized by significantly decreased CEACAM1 (113.18 ± 16.23 ng/mL and 81.09 ± 10.54 ng/mL in GDM and T2DM,

conclusionThe combination of the measured markers may assist (AUC = 0.893 (CI 95%, 0.785-0.980) in establishing the clinical finding of the developing DF especially in patients with GDM who are at the highest risk of chronic insulin resistance.

Indexed as

ImmunityAdultCalibrationCluster AnalysisDiabetes, GestationalDiabetes Mellitus, Type 2FemaleGene OntologyHumansInfant, NewbornInsulinModels, BiologicalPregnancyProteinsROC CurveInsulinProteinscarnosinediabetic fetopathygestational diabetes mellitusimmunoglobulinsinsulin resistancetype 2 diabetes mellitus

Identifiers

PMID32326243
PMCPMC7226479
OpenAlexW3019321821

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.