Diagnostic significance of determining the expression of energy metabolism genes in fetal growth retardation
- Autores: Kan N.E.1, Soldatova E.E.1, Tyutyunnik V.L.1, Volochaeva M.V.1, Sadekova A.A.1, Krasnyi A.M.1
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Afiliações:
- Academician V.I. Kulakov National Medical Research Centre for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia
- Edição: Nº 8 (2023)
- Páginas: 48-55
- Seção: Original Articles
- URL: https://journals.eco-vector.com/0300-9092/article/view/585242
- DOI: https://doi.org/10.18565/aig.2023.93
- ID: 585242
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Resumo
Objective: To determine the level of expression of energy metabolism genes, namely visfatin (NAMPT), ghrelin (GHRL) and leptin (LEP) in maternal and umbilical cord blood and in the placenta in case of fetal growth retardation.
Materials and methods: The study included 52 pregnant women: the main group consisted of 27 patients diagnosed with fetal growth retardation postnatally; the control group included 25 women with normal course of pregnancy. Real-time PCR was used to determine the expression level of energy metabolism genes.
Results: The level of expression of the NAMPT and GHRL genes in maternal blood was found to be statistically significantly reduced in fetal growth retardation (p=0.012 and p=0.019, respectively). The level of expression of the NAMPT and GHRL genes in umbilical cord blood was also reduced in comparison with the control group, but it was not statistically significant (p=0.30 and p=0.23, respectively). LEP gene expression in maternal and umbilical cord blood was not found. The level of leptin expression in the placenta was found to be statistically significantly increased in the main group (p=0.045), though these differences were not associated with gestational age at the time of delivery.
Conclusion: The decreased levels of expression of the NAMPT and GHRL genes in maternal blood can become an objective marker for diagnosing fetal growth retardation during pregnancy. The increased expression of LEP in the placenta in fetal growth retardation may give a better understanding of its pathogenesis and new opportunities for its diagnosis.
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Sobre autores
Natalia Kan
Academician V.I. Kulakov National Medical Research Centre for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia
Email: kan-med@mail.ru
ORCID ID: 0000-0001-5087-5946
Código SPIN: 5378-8437
Scopus Author ID: 57008835600
Researcher ID: B-2370-2015
Dr. Med. Sci., Professor, MD, PhD, Deputy Director of Science
Rússia, MoscowEkaterina Soldatova
Academician V.I. Kulakov National Medical Research Centre for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia
Autor responsável pela correspondência
Email: katerina.soldatova95@bk.ru
ORCID ID: 0000-0001-6463-3403
Postgraduate Student
Rússia, MoscowVictor Tyutyunnik
Academician V.I. Kulakov National Medical Research Centre for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia
Email: tioutiounnik@mail.ru
ORCID ID: 0000-0002-5830-5099
Código SPIN: 1963-1359
Scopus Author ID: 56190621500
Researcher ID: B-2364-2015
Professor, MD, PhD, Leading Researcher of Center of Scientific and Clinical Researches
Rússia, MoscowMaria Volochaeva
Academician V.I. Kulakov National Medical Research Centre for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia
Email: m_volochaeva@oparina4.ru
ORCID ID: 0000-0001-8953-7952
PhD, Senior Researcher, Department of Regional Cooperation and Integration, Physician at the 1st Maternity Department
Rússia, MoscowAlsu Sadekova
Academician V.I. Kulakov National Medical Research Centre for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia
Email: a_sadekova@oparina4.ru
ORCID ID: 0000-0003-4726-7477
PhD, Researcher at the Cytology Laboratory
Rússia, MoscowAleksey Krasnyi
Academician V.I. Kulakov National Medical Research Centre for Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia
Email: alexred@list.ru
ORCID ID: 0000-0001-7883-2702
PhD (Bio), Head of the Cytology Laboratory
Rússia, MoscowBibliografia
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