Advances in Clinical and Experimental Medicine

Title abbreviation: Adv Clin Exp Med
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ISSN 1899–5276 (print)
ISSN 2451-2680 (online)
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Advances in Clinical and Experimental Medicine

2013, vol. 22, nr 2, March-April, p. 283–288

Publication type: review article

Language: English

Initiation of Preterm Labor

Inicjacja porodu przedwczesnego

Małgorzata Pawelec1,A,B,C,D,G, Bogusław Pałczyński1,B, Joanna Krzemieniewska1,A, Mikołaj Karmowski1,B, Jerzy Koryś2,C, Krzysztof Łątkowski1,B, Andrzej Karmowski1,E,F

1 1st Department and Clinic of Gynecology and Obstetrics, Wroclaw Medical University, Wrocław, Poland

2 Non-Public Health Care Center (NZOZ), Legnickie Pole, Poland

Abstract

Preterm births are still a major problem in obstetrics. It is estimated that preterm births occur in about 12% of all pregnancies. Due to advances in medical technology and better care of fetuses and premature babies, the preterm mortality rate has been falling (as recently as 1995 the survival rate in the US for premature infants born at 34 weeks amounted to only a fraction of the corresponding rate for those born after 37 weeks). In the US in 2005, preterm births cost society approximately $26 billion, and medical care for premature babies cost more than $51 billion. Only the richest countries can afford such costly medical care. That is why it is not only the individual aspects but also the social aspects that are important when studying preterm birth mechanisms and ways of preventing them. The existing research indicates that both spontaneous mature birth and preterm birth begin and proceed in a similar manner. This is confirmed by the similar involvement in both processes of corticotropin-releasing hormone, urocortin, extracellular stress protein HSP70 (amniotic fluid heat shock protein), prostaglandins, proinflammatory cytokines or glucocorticosteroids. Apparently, at the beginning of either a preterm birth or a term birth, there is a stimulus that ends the development of the fetus or initiates birth. This stimulus works via feedback through placental hormones and through substances present in the fetal membranes, ultimately leading to functional progesterone withdrawal (FPW), thus leaving the uterus sensitive to contractive factors.

Streszczenie

Porody przedwczesne stanowią ciągle istotny problem położniczy. Szacuje się, że przedwczesnymi urodzeniami kończy się około 12% wszystkich ciąż. Dzięki rozwojowi techniki medycznej i lepszej opiece nad płodami i wcześniakami śmiertelność wcześniaków zmniejsza się (w USA jeszcze w 1995 roku współczynnik przeżycia dla wcześniaków urodzonych w 34. tygodniu ciąży stanowił zaledwie ułamek analogicznego współczynnika dla urodzonych po 37. tygodniu). W USA w 2005 roku porody przedwczesne kosztowały społeczeństwo około 26 miliardów dolarów, a ponad 51 miliardów dolarów kosztowało leczenie wcześniaków. Tylko najbogatsze kraje stać na inwestowanie w tak kosztowną opiekę medyczną, dlatego poznawanie mechanizmów porodów przedwczesnych i metod ich skutecznego leczenia ma nie tylko istotny aspekt indywidualny, ale i społeczny. Dotychczasowe badania naukowe wskazują, że samoistny poród o czasie i poród przedwczesny rozpoczynają się i przebiegają w podobny sposób, a wyrazem tego może być takie samo zaangażowanie w oba procesy między innymi: kortykoliberyny, urokortyny, pozakomórkowego białka stresu HSP70 (amniotic fluid heat shock protein), prostaglandyn, prozapalnych cytokin, czy glukokortykosteroidów. Wydaje się, że na początku porodu przedwczesnego, czy porodu o czasie, pojawia się bodziec kończący dojrzewanie płodu lub inicjujący poród przedwczesny, który drogą sprzężeń zwrotnych działa przez hormony łożyska i przez substancje obecne w błonach płodowych, w ostateczności prowadząc do czynnościowego wycofania progesteronu (FPW), a więc niejako pozostawienia macicy bezbronnej wobec czynników skurczogennych.

Key words

preterm birth, initiation of labor, urocortin, aquaporin 9, heat shock protein HSP70, glucocorticosteroids.

Słowa kluczowe

poród przedwczesny, inicjacja porodu, urokortyna, akwaporyna 9, białko stresu HSP70, glikokortykosteroidy.

References (40)

  1. ACOG Practice Bulletin. Management of preterm labor. Number 43, May 2003. Int J Gynaecol Obstet 2003, 82(1), 127–135.
  2. ACOG Practice Bulletin. Assessment of risk factors for preterm birth. Obstet Gynecol 2001, 98(4), 709–716.
  3. Iyasu S, Tomashek K, Barfield W: Infant mortality and low birth weight among black and white infants – United States, 1980–2000. MMWr Weekly 2002, 51, 589–592.
  4. Collaborative Group on Preterm Birth Prevention. Multicenter randomized, controlled trial of a preterm birth prevention program. Am J Obstet Gynecol 1993, 169(2 Pt1), 352–366.
  5. Yang J, Hartman EK, Savitz DA, Hering A, Dole N, Olshan AF, Thorp JM Jr et al.: vaginal bleeding during pregnancy and preterm birth. Am J Epidemiol 2004, 160(2), 118–125.
  6. Holtzman C, Eyster J, Kleyn M, Messer LC, Kaufman JS: Maternal weathering and risk of preterm delivery. research and Practice. Am J Public Health 2009, 99(10), 1864–1871.
  7. Love C, David RJ, Rankin KM, Collins JW Jr: Exploring weathering: effects of lifelong economic environment and maternal age on low birth weight, small for gestational age and preterm birth in African-American and white women. Am J Epidemiol 2010, 172(2), 127–134.
  8. Rooney B, Calhoun BC: Induced abortion and risk of later premature birth. J Am Phys Surg 2003, 8(2), 46–49.
  9. Hollorell J, Oakley L, Kerinczuk JJ, Brocklehury P, Gray R: The effectiveness of antenatal care programs to reduce infant mortality and preterm birth and vulnerable in socially disadvantages women in high-income countries: a systematic review. BMC Pregnancy Childbirth 2011, 11, 11–13.
  10. Westergren-Thorsson G, Norman M, Bjornsson S, Endresen U, Stjernholm Y, Ekman G et al.: Differential expression of mrNA for proteoglycans, collagens and transforming growth factor-beta in the human cervix during pregnancy and involution. Biochim Biophys Acta 1998, 1406(2), 203–223.
  11. Sennstrom MB, Lockwood CJ, Omazic B, Johansson O, Malstrom A, Ekman GE: Cervical fetal fibronectin correlates to prostaglandin E2-induced cervical ripening and can be identified in cervical tissue. Am J Obstet Gynecol 1998, 178(3), 540–545.
  12. Sennstrom MB, Brauner A, Bystrom B, Malmstrom A, Ekman G: Matrix metalloproteinase-8 correlates with cervical ripening process in humans. Acta Obstet Gynecol Scand 2003, 82(10), 904–911.
  13. Hertelendy F, Zakar T: Prostaglandins and the myometrium and cervix. Prostaglandins Leukot Essent Acids 2004, 70(2), 207–222.
  14. Sennstrom MB, Ekman G, Westergren-Thorsson G, Malmstrom A, Bystrom B, Endresen U et al.: Human cervical ripening, an inflammatory process mediated by cytokines. Mol Hum reprod 2000, 6(4), 375–381.
  15. Tornblom SA, Klimaviciute A, Bystrom B, Chromek M, Brauner A, Ekman-Ordeberg G: Non-infected preterm parturition is related to increased concentration of Il-6, Il-8 and MCP-1 in human cervix. reprod Biol Endocrinol 2005, 3, 39.
  16. Rzepka R, Torbe A, Czajka R, Kwiatkowski S, Bartoszek M, Cymbaluk A: Szybka ocena IL-6 w wydzielinie szyjkowo-pochwowej w zagrażającym porodzie przedwczesnym. Gin Pol 2009, 80, 678–683.
  17. Liggins GC: Premature parturition after infusion of corticotrophin or cortisol into foetal lambs. J Endocrinol 1968, 42(2), 323–329.
  18. Challis JR, Lye SJ, Gibb W, Whittle W, Patel F, Alfaidy N et al.: Understanding preterm labor. Ann NY Acad Sci 2001, 943, 225–234.
  19. Linton EA, Perkins AV, Woods RJ, Eben F, Wolfe CD, Behan DP et al.: Corticotropin releasing hormonebinding protein (CrH-BP): plasma levels decrease during the third trimester of normal human pregnancy. J Clin Endocrinol Matab 1993, 76(1), 260–262.
  20. Hobel Cj, Arora CP, Korst LM: Corticotrophin-releasing hormone and CrH-binding protein. Differences between patients at risk for preterm birth and hypertension. Ann NY Acad Sci 1999, 897, 54–65.
  21. Ekman G, Malmstrom A, Uldbjerg N, Ulmsten U: Cervical collagen: an important regulator of cervical function in term labor. Obstet Gynecol 1986, 67(5), 633–636.
  22. McLean M, Bisits A, Davies J: A placental clock controlling the length of human pregnancy. Nat Med 1995, 1, 460–463.
  23. Sibai B, Meis PJ, Dombrowski MP, Weiner SJ, Moawad AH, Northen A et al.: Plasma CrH measurement at 16 to 20 weeks’ gestation does not predict preterm delivery in woman at high-risk for preterm delivery. Am J Obstet Gynecol 2005, 193(3 Pt 2), 1181–1186.
  24. Hsu SY, Hsueh AJ: Human stresscopin and stresscopin releasing hormone receptor. Nat Med 2001, 7(5), 605– 611.
  25. Petraglia F, Florio P, Benedetto C, Marozio L, Di Blasio AM, Ticconi C et al.: Urocortin stimulates placental adrenocorticotropin and prostaglandin release and myometrial contractility in vitro. J Clin Endocrinol Metab 1999, 84(40), 1420–1423.
  26. Florio P, Torricelli M, Galleri L, De Falco G, Calonaci G, Picciolini E et al.: High fetal urocortin levels at term and preterm labor. J Clin Endocrinol Metab 2005, 90(9), 5361–5365.
  27. Sehringer B, Zahradnik HP, Simon M, Ziegler R, Noethling C, Schaefer WR: mrNA expression profiles for corticotrophin-releasing hormone, urocortin, CrH-binding protein and CrH-receptors in human term gestational tissues determined by real-time quantitative rT-PCr. J Mol Endocrinol 2004, 32(2), 339–348.
  28. Klimaviciute A, Calciolari J, Bertocci E, Abelin-Tornblom S, Stjernholm-Vladic Y, Bystrom B, Petraglia F et al.: Corticotropin-releasing hormone, its binding protein and receptors in human cervical tissue at preterm and term labor in comparison to non-pregnant state. reprod Biol Endocrinol 2006, 4, 29–39.
  29. Romero R, Salafia CM, Athanassiadis AP, Hanaoka S, Mazor M, Septulveda W et al.: The relationship between acute inflammatory lesions of preterm placenta and amniotic microbiology. Am J Obstet Gynecol 1992, 166, 1382–1388.
  30. Yoon BH, Jun JK, Romero R, Park KH, Gomez R, Choi JH et al.: Amniotic fluid inflammatory cytokines (interlukin-6, interleukin-1beta, and tumor necrosis factor-alpha), neonatal brain white matter lesions, and cerebral palsy. Am J Obstet Gynecol 1997, 177, 19–26.
  31. Haddad R, Tromp G, Kuivaniemi H, Chaiworapongsa T, Kim YM, Mazor M et al.: Human spontaneous labor without histologic chorioamnionitis is characterized by an acute inflammation gene expression signature. Am J Obstet Gynecol 2006, 195, 394–404.
  32. Montenegro D, Romero R, Pineles BS, Tarca AL, Kim YM, Draghici S et al.: Differential expression of microrNAs with progression of gestation and inflammation in the human chorioamniotic membranes. Am J Obstet Gynecol 2007, 197, 289–295.
  33. Mittal P, Romero R, Mazaki-Tovi S, Tromp G, Tarca AL, Kim YM et al.: Fetal membranes as an interface between inflammation and metabolism; increased aquaporin 9 expression in the presence of spontaneous labor at term and chorioamnionitis. J Matern Fetal Neonatal Med 2009, 22(12), 1167–1175.
  34. Chaiworapongsa T, Romero R, Espinoza J, Kim YM, Bujold E, Gomez R et al.: Macrophage migration inhibitory factor in patients with preterm parturition and microbial invasion of the amniotic cavity. J Matern Neonatal Med 2005, 18(6), 405–416.
  35. Chaiworapongsa T, Erez O, Kusanovic JP, Vaisbuch E, Mazaki-Tovi S, Gotsch F et al.: Amniotic fluid shock protein 70 concentration in histologic chorioamnionitis, term and preterm parturition. J Matern Neonatal Med 2008, 21(7), 449–461.
  36. Myatt L, Sun K: role of fetal membranes in signaling of fetal maturation and parturition. Int J Dev Biol 2010, 54(2–3), 545–553.
  37. Challis JR, Patel FA, Pomini F: Prostaglandin dehydrogenase and the initiation of labor. J Perinat Med 1999, 27(1), 26–34.
  38. Taylor AH, McParland PC, Taylor DJ, Bell SC: The cytoplasmic 60 kDa progesterone receptor isoform predominates in the human amniochorion and placenta at term. reprod Biol Endocronol 2009, 13(7), 22.
  39. Goldman S, Weiss A, Almalah I, Shalev E: Progesterone receptor expression in human deciduas and fetal membranes before and after contractions: possible mechanism for functional progesterone withdrawal. Mol Hum reprod 2005, 11(4), 269–277.
  40. Joffe G, Jacques D, Remis-Heys R, Burton R, Skram B, Shelburne P: Impact of fibronectin assay on admission for preterm labor. Am J Obstet Gynecol 1999, 180, 581–586.