EARLY AND LATE PREECLAMPSY: MATERNAL, PERINATAL OUTCOMES AND PATHOMORPHOLOGICAL CHANGES OF THE PLACENTA
Introduction: Preeclampsia (PE) is one of the important causes of maternal and perinatal morbidity and mortality worldwide, with a prevalence of 4–6%. To date, the exact pathogenesis of PE has not been established, but its occurrence is associated with impaired trophoblast invasion, incomplete transformation of the spiral arteries, impaired immune system and an increase in the level of markers of endothelial dysfunction. Recently, more and more researchers believe that, despite the similarity of the diagnostic criteria for PE, the pathogenesis of preeclampsia with early - onset (up to 34 weeks) differs from PE with late - onset (after 34 weeks). Maternal and perinatal morbidity and mortality rates are much higher in early preeclampsia than in late preeclampsia. With early preeclampsia, morphohistological changes in the placenta are more often observed than with late preeclampsia. Objective: to compare maternal, perinatal outcomes and pathomorphological changes of the placenta in early –onset and late - onset preeclampsia. Materials and methods: Study design: a cross-sectional retrospective study. We carried out a retrospective analysis of the birth histories of 308 pregnant women with preeclampsia at the Semey Perinatal Center and the accounting and reporting documentation of the Semey Pathological Anatomical Bureau from January 2017 to November 2019. Statistical analysis was performed using SPSS software (version IBM SPSS Statistics 20). When comparing quantitative features with a normal distribution, we used t - Student's test for unrelated samples, if the distribution differed from normal, we used the U - Mann-Whitney test. When comparing the relative performance between the two groups, depending on the value of the expected event, we used the Pearson test (χ2) with Yates's correction for continuity and Pearson's (χ2). The critical level of significance p when testing statistical hypotheses was taken equal to 0.05. Results: During the study birth histories with preeclampsia were analyzed: with early -onset PE (up to 34 weeks) - 128 (41.5%), with late -onset PE - 180 (58.5%). Surgical delivery for early preeclampsia was performed in 69 cases (53.9%), with late PE in 34 (18.8%). Perinatal mortality with early PE was 4.7%, with late PE - 1.7%. Placental abruption with early -onset PE was 1.6%, with late - onset PE - 0.5%. When assessing the morphohistological characteristics of these placentas in early PE, more pronounced morphological changes were noted, in the form of a decrease in the size of the placenta in comparison with gestational age, chronic focal abnormalities in the placenta (calcifications and petrification), thinning of the placenta, and a decrease in its weight were revealed. Conclusions: our study showed that, despite the similarity of clinical and laboratory data for early and late preeclampsia, maternal, perinatal outcomes and pathological changes have statistically significant differences. Further research is needed in this direction, because dividing preeclampsia into subtypes will help to understand the underlying pathophysiology in order to further develop effective prevention and treatment.
Ayaulym N. Nurgaliyeva2, https://orcid.org/0000-0002-7262-1768 Gulnara T. Nurgaliyeva1, https://orcid.org/0000-0002-2161-105X Madina K. Kadyrgazina2, https://orcid.org/0000-0001-6079-4146 Nargiz Bakytzhankyzy2, https://orcid.org/0000-0003-1344-8675 Alma M. Zhexenayeva2, https://orcid.org/0000-0002-4378-9799 Aruzhan A. Kurabay2, https://orcid.org/0000-0002-2420-9429 Gulshat K. Manabaeva3, https://orcid.org/0000-0002-8217-7680 1 NCJSC "Semey Medical University", Department of Clinic, Semey, Republic of Kazakhstan; 2 NCJSC "Semey Medical University", 5th year student, group 501 of the specialty "General Medicine", Semey, Republic of Kazakhstan; 3 NCJSC "Semey Medical University", Department of Perinatology named after A.A. Kozbagarov, Semey, Republic of Kazakhstan.
1. Abalos E. et al. Global and regional estimates of preeclampsia and eclampsia: a systematic review // European Journal of Obstetrics Gynecology and Reproductive Biology. 2013. Vol. 170.1. P. 1–7. 2. Aksornphusitaphong A., Phupong V. Risk factors of early and late onset pre-eclampsia // J Obstet Gynaecol.2013. Vol. 39.3. P. 627–631. 3. Alpoim P. et al. Oxidative stress markers and thrombomodulin plasma levels in women with early and late severe preeclampsia // Clinica Chimica Acta. 2018. Vol. 483. P. 234–238. 4. Broekhuijsen K. et al. Immediate delivery versus expectant monitoring for hypertensive disorders of pregnancy between 34 and 37 weeks of gestation (HYPITAT-II): an open-label, randomised controlled trial // The Lancet. 2015. Vol. 385.9886. P. 2492–2501. 5. Brosens I., Pijnenborg R., Benagiano D. Defective myometrial spiral artery remodelling as a cause of major obstetrical syndromes in endometriosis and adenomyosis // Placenta. 2013 Vol. 34.2. P. 100–105. 6. Brown M.A. et al. Hypertensive disorders of pregnancy: ISSHP classification, diagnosis, and management recommendations for international practice // Hypertension. 2018. Vol. 72.1. P. 24–43. 7. Brownfoot F. et al. Different corticosteroids and regimens for accelerating fetal lung maturation for women at risk of preterm birth (Review) // Cochrane Database of Systematic Reviews. 2013. Vol.8. P.1-36. 8. Dadelszen P., Magee L., Roberts J. Subclassification of Preeclampsia // Hypertension in Pregnancy. 2003. Vol. 22.2. P. 143–148. 9. Deepak A., Reena P., Anirudhan D. Fetal and maternal outcome following expectant management of severe pre-eclampsia remote from term // International Journal of Reproduction, Contraception, Obstetrics and Gynecology. 2017. Vol. 6.12. P. 5420–5424. 10. Dolgushina V., Syundyukova U, Fartukina Yu. Features history, pregnancy and childbirth in early and late preeclampsia // Journal of the International Scientific School. 2015. Vol. 7. P. 90–99. 11. Falco M. et al. Placental histopathology associated with pre-eclampsia: systematic review and meta-analysis // Ultrasound in Obstetrics and Gynecology. 2017. Vol. 50.3. P. 295–301. 12. Fisher S. Why is placentation abnormal in preeclampsia? // American Journal of Obstetrics and Gynecology. 2015. P. 152-157. 13. Gomathy E, Akurati L., Radhika K. Early onset and late onset preeclampsia-maternal and perinatal outcomes in a Rural teritiary health center // International Journal of Reproduction, Contraception, Obstetrics and Gynecology. 2018. Vol. 7.6. P. 2266–2269. 14. Herzog E. et al. Impact of early- and late-onset preeclampsia on features of placental and newborn vascular health // Placenta. 2017. Vol. 49. P.72–79. 15. Iacobelli S., Bonsante F., Robillard P.Y. Comparison of risk factors and perinatal outcomes in early onset and late onset preeclampsia: a cohort based study in reunion island // Journal of Reproductive Immunology. 2017. Vol. 123. P. 12–16. 16. Kaufmann P., Black S., Huppertz B. Endovascular trophoblast invasion: implications for the pathogenesis of intrauterine growth retardation and preeclampsia // Biology of Reproduction – 2003- Vol. 69.1. P. 1–7. 17. Khodzhaeva Z. S. et al. Clinical and pathogenetic features of early and late onset preeclampsia // The Journal of Maternal-Fetal & Neonatal Medicine – 2015- Vol. 7058. 18. Khong T.Y. et al. Sampling and definitions of placental lesions Amsterdam placental workshop group consensus statement // Archives of Pathology and Laboratory Medicine. 2016. Vol. 140.7. P. 698–713. 19. Khong Y., Brosens I. Defective deep placentation // Best Practice and Research: Clinical Obstetrics and Gynaecology. 2011. Vol. 25.3. P. 301–311. 20. Kleinrouweler C.E. et al. Accuracy of circulating placental growth factor, vascular endothelial growth factor, soluble fms-like tyrosine kinase 1 and soluble endoglin in the prediction of pre-eclampsia: a systematic review and meta-analysis // BJOG: An International Journal of Obstetrics and Gynaecology. 2012. Vol. 119.7. P. 778–787. 21. Li X.L. et al. An analysis of the differences between early and late preeclampsia with severe hypertension // Pregnancy Hypertension. 2016. Vol. 6.1. P. 47–52. 22. Lisonkova S. et al. Maternal morbidity associated with early-onset and late-onset preeclampsia // Obstetrics and Gynecology – 2014- Vol. 124.4. P. 771–781. 23. Lisonkova S., Joseph. K. Incidence of preeclampsia: risk factors and outcomes associated with early- versus late-onset disease // The American Journal of Obstetrics & Gynecology – 2013- Vol. 209.6. P. 1–12. 24. Liu X. et al. Maternal preeclampsia and childhood asthma in the offspring // pediatric allergy and immunology – 2015- Vol. 26.2. P. 181–185. 25. Lo J. et al. Hypertensive disease of pregnancy and maternal mortality // Current Opinion in Obstetrics and Gynecology – 2013- Vol. 25.2. P. 124–132. 26. Lu Ch. et al. Pregnancy induced hypertension and outcomes in early and moderate preterm infants. // Pregnancy Hypertension – 2018- Vol. 14. P. 68–71 27. 27. Madazli R. et al. Comparison of clinical and perinatal outcomes in early- and late-onset preeclampsia // Archives of Gynecology and Obstetrics. 2014. Vol.290. 1. P.53–57. 28. Mol B. et al. Pre-Eclampsia // The Lancet. 2016. Vol. 387.10022. P. 999–1011. 29. Nguefack Ch. et al. Comparison of materno-fetal predictors and short-term outcomes between early and late onset pre-eclampsia in the low-income setting of Douala, Cameroon // International Federation of Gynecology and Obstetrics. 2018. Vol. 142.2. P. 228–234. 30. Nurgaliyeva G. et al. Epidemiology of pre-eclampsia in the republic of Kazakhstan: maternal and neonatal outcomes // Pregnancy Hypertension. 2020. P.1–6. 31. Pettit F. et al. Pre-Eclampsia causes adverse maternal outcomes across the gestational spectrum // Pregnancy Hypertension. 2015. Vol. 5.2. P.198–204. 32. Phipps E. et al. Preeclampsia: updates in pathogenesis, definitions, and guidelines // Clinical Journal of the American Society of Nephrology. 2016. Vol. 6. P.1–12. 33. Roberts J., Escudero С. The Placenta in Preeclampsia // Pregnancy Hypertens. 2012. Vol. 2.2. P.72–83. 34. Sibai B., Barton J. Expectant management of severe preeclampsia remote from term: patient selection, treatment, and delivery indications // American Journal of Obstetrics and Gynecology. 2017. Vol. 196.6. P. 215-221. 35. Sircar M., Thadhani R., Karumanchi S.A. Pathogenesis of Preeclampsia // Current Opinion in Nephrology and Hypertension. 2015. Vol. 24.2. P. 131–138. 36. Steegers E. et al. Pre-Eclampsia // Lancet. 2010. Vol. 7. P. 12 -19. 37. Stubert J. et al. Clinical differences between early- and late-onset severe preeclampsia and analysis of predictors for perinatal outcome // J. Perinat. Med. 2014. Vol. 42.5. P. 617–627. 38. Tranquilli A.L. et al. The definition of severe and early-onset preeclampsia . statements from the international society for the study of hypertension in pregnancy (ISSHP) // Pregnancy Hypertension: An International Journal of Women’s Cardiovascular Health. 2013. Vol. 3.1. P. 44–47. 39. Tranquilli A.L. et al. The classification, diagnosis and management of the hypertensive disorders of pregnancy: a revised statement from the ISSHP // Pregnancy Hypertension. 2014. Vol. 4.2. P. 97–104. 40. Viswanathan M., Suja D. The study of maternal outcome of early onset severe preeclampsia with expectant management // International Journal of Reproduction, Contraception, Obstetrics and Gynecology. 2014. Vol. 3.1. P. 92–97. 41. Woelkers D. et al. The revised 2013 ACOG definitions of hypertensive disorders of pregnancy significantly increase the diagnostic prevalence of preeclampsia // Pregnancy Hypertension: An International Journal of Women’s Cardiovascular Health. 2015. Vol. 5.1. P. 38–40.
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Nurgaliyeva A.N., Nurgaliyeva G.T., Kadyrgazina M.K., Bakytzhankyzy N., Zheksenayeva A.M., Kurabay A.A., Manabaeva G.K. Early and late preeclampsy: maternal, perinatal outcomes and pathomorphological changes of the placenta // Nauka i Zdravookhranenie [Science & Healthcare]. 2021, (Vol.23) 5, pp. 40-48. doi 10.34689/SH.2021.23.5.005

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