Structural and morphological changes of the human umbilical cord in complicated pregnancy

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Abstract

The close interaction between two circulatory systems separated by the placental barrier determines the sensitivity of the fetoplacental circulation to critical disturbances of maternal blood flow within the intervillous space of the placental cotyledon and to activation of hemostatic processes on the surface of chorionic villi. Maternal somatic diseases manifesting as by hypertension and metabolic disorders during pregnancy affect the development and function of the placenta and umbilical cord. Because structural alterations in the umbilical cord vessel walls appear earlier than in fetal vessels and are associated with placental vascular resistance, detailed morphological assessment of the umbilical cord may improve prediction of neonatal health outcomes.

The aim of this study is to review published data describing the morphological and functional features of the umbilical cord in infants born to mothers with complicated obstetric histories.

Studies of umbilical cords from infants born to mothers with preeclampsia have demonstrated narrowed umbilical artery lumen associated with thickening or edema of the vascular smooth muscle layer. Reduced Wharton jelly has not been consistently observed; in only one study was it accompanied by thickening of the vascular muscular layer. In contrast, another study reported an increased volume of Wharton jelly. No morphological changes in the umbilical vein wall were detected in all studies. Thickening of the umbilical vein wall may have compensatory significance, whereas thinning appears to be pathological. Morphological changes of the umbilical vein in fetuses with intrauterine growth restriction and in preterm infants have not been described. Furthermore, detailed investigation is required to clarify the role of tissue factors, including matrix metalloproteinases and vascular endothelial growth factor, in shaping the morphological characteristics of the umbilical cord.

Comprehensive evaluation of morphological and structural alterations of the umbilical cord and its components in large cohorts of pregnant women with various somatic diseases may improve the predictive accuracy of neonatal health outcomes and the risk of fetal developmental abnormalities.

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About the authors

Albina A. Kondratenko

Saint Petersburg State Pediatric Medical University; Kirov Military Medical Academy

Author for correspondence.
Email: kondraa24@gmail.com
ORCID iD: 0000-0002-8511-5864
SPIN-code: 1668-3497

Cand. Sci. (Biology)

Russian Federation, Saint Petersburg; Saint Petersburg

Anna O. Drobintseva

Saint Petersburg State Pediatric Medical University

Email: ao.drobintseva@gpmu.org
ORCID iD: 0000-0002-6833-6243
SPIN-code: 4277-0122

Cand. Sci. (Biology), Assistant Professor

Russian Federation, Saint Petersburg

Saulesh A. Apbasova

Semey State Medical University

Email: saulesh.apbasova@smu.edu.kz
ORCID iD: 0000-0001-6650-4971

MD, Cand. Sci. (Medicine)

Kazakhstan, Semey

Ruslan A. Nasyrov

Saint Petersburg State Pediatric Medical University

Email: rrmd99@mail.ru
ORCID iD: 0000-0001-8120-2816
SPIN-code: 5446-0950

MD, Dr. Sci. (Medicine), Professor

Russian Federation, Saint Petersburg

Maria A. Kalinina

Saint Petersburg State Pediatric Medical University

Email: mariakalinina0044@gmail.com
ORCID iD: 0009-0009-4922-1422
SPIN-code: 1953-3453
Russian Federation, Saint Petersburg

References

  1. Popova IG, Protsenko EV, Sitnikova OG, et al. Pathomorphological and biochemical features of the endothelium of the umbilical cord vessels during pregnancy complicated by preeclampsia. Russian Journal of Human Reproduction. 2022;28(6):44–52. doi: 10.17116/repro20222806144 EDN: DQPTIZ
  2. Hasegawa J. Ultrasound screening of umbilical cord abnormalities and delivery management. Placenta. 2018;62:66–78. doi: 10.1016/j.placenta.2017.12.003
  3. Milovanov AP, Ozhiganova IN. Embryochorionic insufficiency: anatomic and physiologic prerequisites, rationale, definitions and pathogenetic mechanisms. Russia Journal of Archive of Pathology. 2014;76(3):4–8. EDN: STSGPX
  4. Zampieri F, Thiene G, Basso C, Zanatta A. The three fetal shunts: A story of wrong eponyms. J Anat. 2021;238(4):1028–1035. doi: 10.1111/joa.13357 EDN: TRQDYO
  5. Krasnopolskiy VI, editor. Placenta: formation and pathology. Moscow: Meditsina; 2007. (In Russ) EDN: QLOXMN
  6. Shahbazi MN. Mechanisms of human embryo development: from cell fate to tissue shape and back. Development. 2020;147(14):dev.190629. doi: 10.1242/dev.190629 EDN: QRSEIU
  7. Hopwood N. Species choice and model use: reviving research on human development. J Hist Biol. 2024;57(2):231–279. doi: 10.1007/s10739-024-09775-7 EDN: IJGQVC
  8. Tonni G, Lituania M, Cecchi A, et al. Umbilical cord diseases affecting obstetric and perinatal outcomes. Healthcare (Basel). 2023;11(19):2634. doi: 10.3390/healthcare11192634 EDN: REMVKN
  9. Conrad MS, Gardner ML, Miguel C, et al. Proteomic analysis of the umbilical cord in fetal growth restriction and preeclampsia. PLoS One. 2022;17(2):e0262041. doi: 10.1371/journal.pone.0262041 EDN: JAHDLP
  10. Sánchez-Trujillo L, García-Montero C, Fraile-Martinez O, et al. Considering the effects and maternofoetal implications of vascular disorders and the umbilical cord. Medicina (Kaunas). 2022;58(12):1754. doi: 10.3390/medicina58121754 EDN: YRXMBW
  11. Santana EFM, Castello RG, Rizzo G, et al. Placental and umbilical cord anomalies diagnosed by two- and three-dimensional ultrasound. Diagnostics (Basel). 2022;12(11):2810. doi: 10.3390/diagnostics12112810 EDN: EKSXQH
  12. Volkov AE. Prenatal diagnosis of cord pathology. Medical Herald of the South of Russia. 2011;(2):38–45. EDN: OOKNAD
  13. Dubetskyi BI, Makarchuk OM, Zhurakivska OY, et al. Pregnancy and umbilical cord pathology: structural and functional parameters of the umbilical cord. J Med Life. 2023;16(8):1282–1291. doi: 10.25122/jml-2023-0025 EDN: OPJCUH
  14. Ebbing C, Kessler J, Moster D, Rasmussen S. Isolated single umbilical artery and the risk of adverse perinatal outcome and third stage of labor complications: A population-based study. Acta Obstet Gynecol Scand. 2020;99(3):374–380. doi: 10.1111/aogs.13747
  15. Botezatu R, Raduteanu S, Ciobanu AM, et al. Absence of Wharton’s Jelly at the abdominal site of the umbilical cord insertion. Rare case report and review of the literature. Medicina (Kaunas). 2021;57(11):1268. doi: 10.3390/medicina57111268 EDN: XWLBFQ
  16. Murphy SJ, Deegan N, O’Leary BD, McParland P. Absence of Wharton’s jelly. BMJ Case Reports. 2020;13(11):e237222. doi: 10.1136/bcr-2020–237222 EDN: XLFQXS
  17. Kalluru PKR, Kalluru HR, Allagadda TR, et al. Abnormal umbilical cord coiling and association with pregnancy factors. J Turk Ger Gynecol Assoc. 2024;25(1):44–52. doi: 10.4274/jtgga.galenos.2023.2023-3-3 EDN: KXMIAQ
  18. Agarwal I, Singh S. Adverse perinatal outcomes of true knot of the umbilical cord: a case series and review of literature. Cureus. 2022;14(7):e26992. doi: 10.7759/cureus.26992 EDN: ZOVFIS
  19. Mishin AV, Bortnovskaya NP, Martemyanova LA, et al. Ultrasound and morphological diagnosis of anomaliesin the development of the body stem. Health and Ecology Issues. 2022;19(3):120–129. (In Russ). doi: 10.51523/2708-6011.2022-19-3-17 EDN: LEYKHG
  20. Shchegolev AI, Tumanova UN, Lyapin VM. Umbilical cord coiling: definition, classification, clinical significance. Akusherstvo i Ginekologiya. 2019;(2):42–50. doi: 10.18565/aig.2019.2.42-50 EDN: YYXPOH
  21. Iupatov EIu, Kurmanbaev TE, Galimova IR, et al. Umbilical cord vascular thrombosis: literature review and two clinical cases. Obstetrics, Gynecology and Reproduction. 2022;16(1):81–89. doi: 10.17749/2313-7347/ob.gyn.rep.2021.260 EDN: DLJYEV
  22. Yue T, Guo Y, Qi X, et al. Sex-biased regulatory changes in the placenta of native highlanders contribute to adaptive fetal development. Elife. 2024;12:RP89004. doi: 10.7554/eLife.89004 EDN: VWFXMM
  23. Debebe SK, Cahill LS, Kingdom JC, et al. Wharton’s jelly area and its association with placental morphometry and pathology. Placenta. 2020;94:34–38. doi: 10.1016/j.placenta.2020.03.008 EDN: GHDLHQ
  24. Thomas MR, Bhatia JK, Kumar S, Boruah D. The histology and histomorphometry of umbilical cord cross section in preeclampsia and normal pregnancies: a comparative study. J Histotechnol. 2020;43(3):109–117. doi: 10.1080/01478885.2020.1734741 EDN: JPXFTP
  25. Zarina KZ, Pilmane M. Characterization of angiogenic,matrix remodeling, and antimicrobial factors in preterm and full-term human umbilical cords. J Dev Biol. 2024;12(2):13. doi: 10.3390/jdb12020013 EDN: CHPRQJ
  26. Chen J, Liu FX, Tao RX. Relationship between ultrasound parameters of the umbilical and middle cerebral arteries and intrauterine fetal distress. World J Clin Cases. 2024;12(16):2745–2750. doi: 10.12998/wjcc.v12.i16.2745 EDN: RGYWZI
  27. Colson A, Sonveaux P, Debiève F, Sferruzzi-Perri AN. Adaptations of the human placenta to hypoxia: opportunities for interventions in fetal growth restriction. Hum Reprod Update. 2021;27(3):531–569. doi: 10.1093/humupd/dmaa053 EDN: LEDBKE
  28. Akolekar R, Ciobanu A, Zingler E, et al. Routine assessment of cerebroplacental ratio at 35-37 weeks’ gestation in the prediction of adverse perinatal outcome. Am J Obstet Gynecol. 2019;221(1):65.e1–65.e18. doi: 10.1016/j.ajog.2019.03.002
  29. Najafi L, Honardoost M, Khajavi A, et al. The association of umbilical coiling and angiogenesis markers: Impact assessment of gestational diabetes. Placenta. 2022;129:70–76. doi: 10.1016/j.placenta.2022.09.006 EDN: FGYWWE
  30. Tenaw Goshu B. Histopathologic impacts of diabetes mellitus on umbilical cord during pregnancy. Pediatric Health, Med Ther. 2022;13:37–41. doi: 10.2147/PHMT.S323812 EDN: VQGVTN
  31. Chillakuru S, Velichety SD, Rajagopalan V. Human umbilical cord and its vessels: a histomorphometric study in difference severity of hypertensive disorders of pregnancy. Anat Cell Biol. 2020;53(1):68–75. doi: 10.5115/acb.19.158 EDN: VWVGTR
  32. Dzugkoev SG, Dzugkoeva FS, Margieva OI, et al. Experimental participation of pharmacological substances in mechanisms of lead acetate toxicity. Pharmacy & Pharmacology. 2022;10(6):589–600. doi: 10.19163/2307-9266-2022-10-6-589-600 EDN: TEPJNE
  33. Nguyen TPH, Patrick CJ, Parry LJ, Familari M. Using proteomics to advance the search for potential biomarkers for preeclampsia: A systematic review and meta-analysis. PLoS One. 2019;14(4):e0214671. doi: 10.1371/journal.pone.0214671
  34. Gęca T, Stupak A, Nawrot R, et al. Placental proteome in late-onset of fetal growth restriction. Mol Med Rep. 2022;26(6):356. doi: 10.3892/mmr.2022.12872 EDN: MDLVXR
  35. Saw SN, Dai Y, Yap CH. A review of biomechanics analysis of the umbilical-placenta system with regards to diseases. Front Physiol. 2021;12:587635. doi: 10.3389/fphys.2021.587635 EDN: HCVLIQ
  36. Shi JW, Lai ZZ, Yang HL, et al. Collagen at the maternal-fetal interface in human pregnancy. Int J Biol Sci. 2020;16(12):2220–2234. doi: 10.7150/ijbs.45586 EDN: JWSXYP
  37. Rizzo G, Mappa I, Bitsadze V, et al. Role of Doppler ultrasound at time of diagnosis of late-onset fetal growth restriction in predicting adverse perinatal outcome: prospective cohort study. Ultrasound Obstet Gynecol. 2020;55(6):793–798. doi: 10.1002/uog.20406 EDN: HSLNVF

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