Evidence map›Paper›PMID 34766598›Full record

Observational studyMedicine2021

Severe types of fetopathy are associated with changes in the serological proteome of diabetic mothers.

Arthur T Kopylov, Olga Papysheva, Iveta Gribova, Anna L Kaysheva, Galina Kotaysch, Lubov Kharitonova, Tatiana Mayatskaya, Malik K Nurbekov, Ekaterina Schipkova, Olga Terekhina and 1 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. Observational
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

11 authors at 3 institutions in 1 country.

Arthur T KopylovInstitute of Biomedical Chemistry, 10 Pogodinskaya str., Moscow, Russia.ORCID 0000-0002-7199-372
Olga PapyshevaS.S. Yudin 7th State Clinical Hospital, 4 Kolomenskaya str., Moscow, Russia.
Iveta GribovaN.E. Bauman 29th State Clinical Hospital, 2 Hospitalnaya sq., Moscow, Russia.
Anna L KayshevaInstitute of Biomedical Chemistry, 10 Pogodinskaya str., Moscow, Russia.
Galina KotayschN.E. Bauman 29th State Clinical Hospital, 2 Hospitalnaya sq., Moscow, Russia.
Lubov KharitonovaN.I. Pirogov Medical University, 1 Ostrovityanova st., Moscow, Russia.
Tatiana MayatskayaN.I. Pirogov Medical University, 1 Ostrovityanova st., Moscow, Russia.
Malik K NurbekovInstitute of General Pathology and Pathophysiology, 8 Baltyiskaya str., Moscow, Russia.
Ekaterina SchipkovaInstitute of General Pathology and Pathophysiology, 8 Baltyiskaya str., Moscow, Russia.
Olga TerekhinaInstitute of General Pathology and Pathophysiology, 8 Baltyiskaya str., Moscow, Russia.
Sergey G MorozovN.E. Bauman 29th State Clinical Hospital, 2 Hospitalnaya sq., Moscow, Russia.
Research Institute of General Pathology and Pathophysiology, the Russian Academy of Medical Sciences · RUInstitute of Biomedical Chemistry · RUPirogov Russian National Research Medical University · RU

Funding

russian federation fundamental research program 2021-2030
6 · The paper itself

Abstract

abstractPregestational or gestational diabetes are the main risk factors for diabetic fetopathy. There are no generalized signs of fetopathy before the late gestational age due to insufficient sensitivity of currently employed instrumental methods. In this cross-sectional observational study, we investigated several types of severe diabetic fetopathy (cardiomyopathy, central nervous system defects, and hepatomegaly) established in type 2 diabetic mothers during 30 to 35 gestational weeks and confirmed upon delivery. We examined peripheral blood plasma and determined a small proportion of proteins strongly associated with a specific type of fetopathy or anatomical malfunction. Most of the examined markers participate in critical processes at different stages of embryogenesis and regulate various phases of morphogenesis. Alterations in CDCL5 had a significant impact on mRNA splicing and DNA repair. Patients with central nervous system defects were characterized by the greatest depletion (ca. 7% of the basal level) of DFP3, a neurotrophic factor needed for the proper specialization of oligodendrocytes. Dysregulation of noncanonical wingless-related integration site signaling pathway (Wnt) signaling guided by pigment epithelium-derived factor (PEDF) and disheveled-associated activator of morphogenesis 2 (DAAM2) was also profound. In addition, deficiency in retinoic acid and thyroxine transport was exhibited by the dramatic increase of transthyretin (TTHY). The molecular interplay between the identified serological markers leads to pathologies in fetal development on the background of a diabetic condition. These warning serological markers can be quantitatively examined, and their profile may reflect different severe types of diabetic fetopathy, producing a beneficial effect on the current standard care for pregnant women and infants.

Indexed as

Diabetes, GestationalFetal DiseasesCross-Sectional StudiesFemaleHumansMothersPregnancyProteomeProteome

Identifiers

PMID34766598
PMCPMC8589259
OpenAlexW3212119266

What OpenQuestion holds

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LicenceCC BY-NC
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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 OpenQuestion graph.