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Abstract
Pregnant women with chronic genital and non-genital infections are at a high risk of infections pregnancy and postpartum complications. Preterm birth is one of the leading causes of obstetric and neonatal complications and occurs in one in nine women. Forty per cent of preterm births are considered to be caused by abnormal vaginal flora, and there is currently no consensus on the contribution of combined bacterial and viral infection.
Aim – to assess the course of pregnancy and delivery in women with a high risk of infection and/or inflammatory conditions in pregnancy.
Materials and methods. We performed a prospective controlled observational two-phase study in 417 pregnant women with a high risk of infectious pregnancy complications. In Phase 1, we evaluated the medical history, pregnancy and delivery course in 355 women with a high risk of infectious pregnancy complications. In Phase 2, we evaluated 62 women with a high risk of infectious pregnancy complications and preterm birth. The control group for immunological parameters included 18 healthy women with uncomplicated term delivery.
Results. In women with a high risk of infectious complications, pregnancy was associated with recurrent threatened pregnancy loss (49.8 %), preterm premature rupture of foetal membranes (64.3 %), followed by prolonged oligohydramnios. Almost in one in two women (47.9 %), pregnancy resulted in the delivery of preterm, low-birth-weight neonates. One in three women (30 %) experienced uterine hypotony and bleeding after vaginal and Caesarean delivery. Almost a third of women (32.1 %) developed inflammatory complications postpartum, and more than half of complications (54.4 %) was observed in women giving birth prematurely. Vaginal and cervical cultures in women who experienced preterm birth were dominated by non-obligate pathogens. We observed persistence of the Herpesviridae family both in the cervical canal and uterine cavity, specifically the Epstein-Barr virus (17.2 %; 95% CI: 10 %; 26.8 %). Preterm birth was associated with a significant increase in the CD16+/CD56+ cells and reduction of the CD3+/CD8+ cells, increase of the pro-inflammatory cytokine levels and reduction in anti-inflammatory cytokines.
Conclusions. Pregnancies in women with a high risk of infections and/or inflammatory conditions were associated with high rates of recurrent threatened pregnancy loss, preterm rupture of membranes and preterm delivery.
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Veresova AA, Tyutyunnik VL, Kan NE, Balushkina AA. Modern ideas about the development of postpartum infectious and inflammatory complications. Questions of Gynecology, Obstetrics and Perinatology. 2013; 12(4): 30-37. Russian (Вересова А.А., Тютюнник В.Л., Кан Н.Е., Балушкина А.А. Современные представления о развитии послеродовых инфекционно-воспалительных осложнений //Вопросы гинекологии, акушерства и перинатологии. 2013; 12(4): 30-37)
Silasi M, Cardenas I, Kwon JY, Racicot K, Aldo P, Mor G. Viral infections during pregnancy. Am J Reprod Immunol. 2015; 73(3): 199-213
Cappelletti M, Della Bella S, Ferrazzi E, Mavilio D, Divanovic S. Inflammation and preterm birth. J Leukoc Biol. 2016; 99(1): 67-78
Woodd SL, Montoya A, Barreix M, Pi L, Calvert C, Rehman AM et al. Incidence of maternal peripartum infection: A systematic review and meta-analysis. PLoS Med. 2019; 16(12): e1002984
Krasnyj AM, Kan NE, Tyutyunnik VL, Sadekova AA, Saribekova AG, Kokoeva DN et al. Predicting preterm birth by combined detection of cytokines and extracellular DNA. Obstetrics and Gynecology. 2019; 1: 86-91. Russian (Красный А.М., Кан Н.Е., Тютюнник В.Л., Садекова А.А., Сарибекова А.Г., Кокоева Д.Н. и др. Прогнозирование преждевременных родов путем комбинированного определения цитокинов и внеклеточной ДНК //Акушерство и гинекология. 2019. № 1. С. 86-91)
Dunn AB, Dunlop AL, Hogue CJ, Miller A, Corwin EJ. The microbiome and complement activation: a mechanistic model for preterm birth. Biol Res Nurs. 2017; 19(3): 295-307
Helmo FR, Alves EAR, Moreira RAA, Severino VO, Rocha LP, Monteiro MLGDR et al. Intrauterine infection, immune system and premature birth. J Matern Fetal Neonatal Med. 2018; 31(9): 1227-1233
Freitas AC, Bocking A, Hill JE, Money DM. VOGUE Research Group. Increased richness and diversity of the vaginal microbiota and spontaneous preterm birth. Microbiome. 2018; 6(1): 117
Romero R, Espinoza J, Kusanovic JP, Gotsch F, Hassan S, Erez O et al. The preterm parturition syndrome. BJOG. 2006;113 Suppl 3: 17-42
Racicot K, Mor G. Risks associated with viral infections during pregnancy. J Clin Invest. 2017; 127(5): 1591-1599
Capoccia R, Greub G, Baud D. Ureaplasma urealyticum, Mycoplasma hominis and adverse pregnancy outcomes. Curr Opin Infect Dis. 2013; 26(3): 231-240
Rittenschober-Böhm J, Waldhoer T, Schulz SM, Pimpel B, Goeral K, Kasper DC et al. Vaginal Ureaplasma parvum serovars and spontaneous preterm birth. Am J Obstet Gynecol. 2019; 220(6): 594.e1-594.e9. doi: 10.1016/j.ajog.2019.01.237
Payne MS, Ireland DJ, Watts R, Nathan EA, Furfaro LL, Kemp MW et al. Ureaplasma parvum genotype, combined vaginal colonisation with Candida albicans, and spontaneous preterm birth in an Australian cohort of pregnant women. BMC Pregnancy Childbirth. 2016; 16(1): 312
Shi TL, Huang LJ, Xiong YQ, Zhong YY, Yang JJ, Fu T et al. The risk of herpes simplex virus and human cytomegalovirus infection during pregnancy upon adverse pregnancy outcomes: A meta-analysis. J Clin Virol. 2018; 104: 48-55
McGee D, Smith A, Poncil S, Patterson A, Bernstein AI, Racicot K. Cervical HSV-2 infection causes cervical remodeling and increases risk for ascending infection and preterm birth. PLoS One. 2017; 12(11): e0188645
