Salivarni i inflamatorni medijatori plazme i sekretorni status prevremeno porođenih žena sa periodontitisom – studija preseka

  • Ljubinka Nikolić Clinical Center of Serbia, Clinic for Ginecology and Obstetrics, Department for Hematology and Transfusion Laboratory, Belgrade, Serbia
  • Saša Čakić University of Belgrade, Faculty of Dental Medicine, Serbia
  • Neda Perunović University of Belgrade, Faculty of Dental Medicine, Serbia
  • Emina Čolak Clinical Center of Serbia, Clinic for Ginecology and Obstetrics, Institute of Medical Biohemistry, Belgrade, Serbia
  • Jelena Kotur-Stevuljević Faculty of Pharmacy, Department for Medical Biochemistry Belgrade, Serbia
  • Saša Janković University of Belgrade, Faculty of Dental Medicine, Belgrade, Serbia
  • Milanko Djurić University of Novi Sad, Faculty of Medicine, Novi Sad, Serbia
  • Darko Plećaš Clinical Center of Serbia, Clinic for Ginecology and Obstetrics, Department for Hematology and Transfusion Laboratory, Belgrade, Serbia
Ključne reči: porođaj, prevremeni, periodontitis, interleukin-1beta, dinoproston, pljuvačka, plazma

Sažetak


Uvod/Cilj. Prevremeni porođaj se definiše kao porođaj pre navršene 37 nedelje gestacije. Podaci iz literature govore u prilog tome da periodontalni procesi mogu uticati na fetoplacentalnu jedinicu i indukovati preterminski porođaj. Sekretorni status može uticati na stepen periodontalne bolesti. Proinflamatorni citokini imaju uticaj na periodontitis kao i na porođaj. Kombinovani uticaj ovih faktora rizika za prevremeni porođaj nije dovoljno istražen. Cilj ove studije je bio da istraži povezanost između periodontalne bolesti, sekretornog statusa, nivoa interleukina 1-β (IL1-ß) i prostaglandina E2 (PGE2) kod žena koje su imale prevremeni porođaj. Metode. Studijom je bilo obuhvaćeno 56 žena, koje su imale prevremen porođaj i 56 žena u kontrolnoj grupi koje su se porodile u terminu, starosti između 17 i 41 godine. Periodontalni pregled, uzorkovanje krvi i salive je izvršeno u prvih 48 sati po porođaju. Sekretorni status je određen metodom inhibicije hemaglutinacije. Koncentracije IL1-ß i PGE2 su merene visoko senzivinim Enzyme-linked Immunosorbent Assay (ELISA) testom. Rezultati. U grupi prevremenih porođaja bilo je 66,1% žena sa periodontitisom, a u kontrolnoj grupi 12,5% (p < 0.01). Prevremeno porođene žena, nesekretori sa periodontitisom imale su u plazmi značajno više vrednosti IL 1-ß i PGE 2 u odnosu na ostale grupe (p < 0,01). U grupi prevremeno porođenih žena postojala je značajna korelacija između salivarnih i plazmatskih koncentracija PGE2 i IL1-ß (R = 0.416, p = 0.017 i R = -0,592, p < 0,001, redom). Ove korelacije nisu postojale kod žena koje su imale terminski porođaj. Zaključak. Naši rezultati podržavaju hipotezu da su sekretorni status i periodontitis, bar delimično, odgovorni za patogenezu preterminskog porođaja. Verovatnoća negativnog uticaja nesekretornog statusa se ne sme ignorisati. Ovi zaključci ukazuju na potrebu za dodatnim istraživanjima porođaja.

Reference

Blencowe H, Cousens S, Oestergaard MZ, Chou D, Moller AB, Narwal R, et al. National, regional, and worldwide estimates of preterm birth rates in the year 2010 with time trends since 1990 for selected countries: a systematic analysis and implica-tions. Lancet 2012; 379(9832): 2162–72.

Beck S, Wojdyla D, Say L, Betran AP, Merialdi M, Requejo JH, et al. The worldwide incidence of preterm birth: a systematic re-view of maternal mortality and morbidity. Bull World Health Organ 2010; 88(1): 31–8.

Shiozaki A, Yoneda S, Nakabayashi M, Takeda Y, Takeda S, Sugimura M, et al. Multiple pregnancy, short cervix, part-time worker, steroid use, low educational level and male fetus are risk factors for preterm birth in Japan: a multicenter, prospec-tive study. J Obstet Gynaecol Res 2014; 40(1): 53–61.

Romero R, Miranda J, Chaemsaithong P, Chaiworapongsa T, Kusa-novic JP, Dong Z, et al. Sterile and microbialassociated intra-amniotic inflammation in preterm prelabor rupture of mem-branes. J Matern Fetal Neonatal Med 2015; 28: 1394–409.

Miller WD. The human mouth as a focus of infection. Dent Cosmos 1891; 33(9): 689–713.

Stadelmann PF, Eick S, Salvi GE, Surbek D, Mohr S, Bürgin W, et al. Increased periodontal inflammation in women with pre-term premature rupture of membranes. Clin Oral Investig 2015; 19(6): 1537–46.

Oliveira Costa F, Soares Dutra Oliveira AM, Miranda Cota LO. Interrelation Between Periodontal Disease and Preterm Birth, In: Erez O, editor. Preterm Birth. Rijeka: InTech; 2013; p. 3–39.

Armitage GC. Periodontal disease and pregnancy: discussion, conclusions and recommendations. Ann Periodontol 2001; 6(1): 189–92.

Robinson P, Schmerman M. Influence of Pregnancy on the Oral Cavity. Glob libr women's med 2015; ISSN: 1756–2228; [about 5 p]. Available from: https://www.glowm.com [cited 2017 Jun 19].

Chukkapalli SS, Rivera-Kweh MF, Velsko IM, Chen H, Zheng D, Bhattacharyya I, et al. Chronic oral infection with major perio-dontal bacteria Tannerella forsythia modulates systemic ather-osclerosis risk factors and inflammatory markers. Pathog Dis 2015; 73(3): pii: ftv009.

Roth-Isigkeit A, Hasselbach L, Ocklitz E, Brückner S, Ros A, Gehring H, et al. Inter-individual differences in cytokine re-lease in patients undergoing cardiac surgery with cardiopulmo-nary bypass. Clin Exp Immunol 2001; 125(1): 80–8.

Abati S, Villa A, Cetin I. Oral environment, inflammation and preterm birth. J Pediatr Neonat Individual Med 2015; 4(2): e040239.

Saini R, Saini S, Saini SR. Periodontitis: A risk for delivery of premature labor and low-birth-weight infants. J Nat Sci Biol Med 2010; 1(1): 40–2.

Chaemsaithong P, Romero R, Korzeniewski SJ, Dong Z, Yeo L, Hassan SS, et al. A point of care test for the determination of amniotic fluid interleukin-6 and the chemokine CXCL-10/IP-10. J Matern Fetal Neonatal Med 2015; 28(13): 1510–9.

Rathnayake N, Akerman S, Klinge B, Lundegren N, Jansson H, Tryselius Y, et al. Salivary biomarkers of oral health: a cross-sectional study. J Clin Periodontol 2013; 40(2): 140–7.

Rocha Dde M, Zenóbio EG, Van Dyke T, Silva KS, Costa FO, Soares RV. Differential expression of salivary glycoproteins in aggressive and chronic periodontitis. J Appl Oral Sci 2012; 20(2): 180–5.

Nikolić Lj, Janković Lj, Čakić S, Movsesijan A. Secretory status and periodontal disease. Bilt Transf 1996; 42(1): 23–6. (Serbi-an)

Nurjadi D, Lependu J, Kremsner PG, Zanger P. Staphylococcus aureus throat carriage is associated with ABO-/secretor status. J Infect 2012; 65(4): 310–7.

Gunput ST, Ligtenberg AJ, Terlouw B, Brouwer M, Veerman EC, Wouters D. Complement activation by salivary agglutinin is se-cretor status dependent. Biol Chem 2015; 396(1): 35–43.

Armitage GC. Development of a classification system for peri-odontal diseases and conditions. Ann Periodontol 1999; 4(1): 1–6.

Blood grouping and typing. In: Walker RH, editor. Technical manual. 11th ed. Bethesda: American Association of Blood Banks; 1993. p. 621–38.

Ferrero DM, Larson J, Jacobsson B, Di Renzo GC, Norman JE, Martin JN Jr, et al. Cross-Country Individual Participant Analysis of 4.1 Million Singleton Births in 5 Countries with Very High Human Development Index Confirms Known As-sociations but Provides No Biologic Explanation for 2/3 of All Preterm Births. PLoS One. 2016; 11(9): e0162506.

Gümüş P, Öztürk VÖ, Bozkurt E, Emingil G. Evaluation of the gingival inflammation in pregnancy and postpartum via 25-hydroxy-vitamin D3, prostaglandin E2 and TNF-α levels in saliva. Arch Oral Biol 2016; 63: 1–6.

Corbella S, Taschieri S, Del Fabbro M, Francetti L, Weinstein R, Ferrazzi E. Adverse pregnancy outcomes and periodontitis: A systematic review and meta-analysis exploring potential asso-ciation. Quintessence Int 2016; 47(3): 193–204.

Walia M, Saini N.Relationship between periodontal diseases and preterm birth: Recent epidemiological and biological data. Int J Appl Basic Med Res 2015; 5(1): 2–6.

Boggess KA, Moss K, Madianos P, Murtha AP, Beck J, Offenbacher S. Fetal immune response to oral pathogens and risk of pre-term birth. Am J Obstet Gynecol 2005; 193(3 Pt 2): 1121–6.

Madianos PN, Bobetsis YA, Offenbacher S. Adverse pregnancy outcomes (APOs) and periodontal disease: pathogenic mecha-nisms. J Periodontol 2013; 84(4 Suppl): S170–80.

Kamei H, Ishihara Y, Fuma D, Niwa T, Kamiya Y, Yokoi T, et al. Interleukin-1 receptor gene variants are associated with ag-gressive periodontitis in the Japanese. Arch Oral Biol 2014; 59(7): 756–63.

Dörtbudak O, Eberhardt R, Ulm M, Persson GR. Periodontitis, a marker of risk in pregnancy for preterm birth. J Clin Perio-dontol 2005; 32(1): 45–52.

Jarjoura K, Devine PC, Prez-Delboy A, Herrera-Abreu M, D’Alton M, Papapanou PN. Markers of periodontal infection and pre-term birth. Am J Obstet Gynecol 2005; 192(2): 513–9.

Lieff S, Boggess KA, Murtha AP, Jared H, Madianos PN, Moss K, et al. The oral conditions and pregnancy study: periodontal status of a cohort of pregnant women. J Periodontol 2004; 75(1): 116–26.

Soucy-Giguère L, Tétu A, Gauthier S, Morand M, Chandad F, Giguère Y, et al. Periodontal Disease and Adverse Pregnancy Outcomes: A Prospective Study in a Low-Risk Population. J Obstet Gynaecol Can 2016; 38(4): 346–50.

Gringhuis SI, Kaptein TM, Wevers BA, Theelen B, van der Vlist M, Boekhout T, et al. Dectin-1 is an extracellular pathogen sen-sor for the induction and processing of IL-1β via a noncanoni-cal caspase-8 inflammasome. Nat Immunol 2012; 13(3): 246–54.

Romero R, Xu Y, Plazyo O, Chaemsaithong P, Chaiworapongsa T, Unkel R, et al. A Role for the Inflammasome in Spontaneous Labor at Term. Am J Reprod Immunol 2018; 79(6): e124403

Zhumakanova K, Abeuova B, Kuzgibekova A, Kenzhebayeva K, Er-emicheva G. Some clinical and immunological aspects of pre-term birth. Georgian Med News 2016; (253): 17–25. (Rus-sian)

Kinney JS, Morelli T, Braun T, Ramseier CA, Herr AE, Sugai JV, et al. Saliva/pathogen biomarker signatures and periodontal disease progression. J Dent Res 2011; 90(6): 752–8.

Karjalainen MK, Huusko JM, Ulvila J, Sotkasiira J, Luukkonen A, Teramo K, et al. A Potential Novel Spontaneous Preterm Birth Gene, AR, Identified by Linkage and Association Analysis of X Chromosomal Markers, PLoS One 2012; 7(12): e51378.

Amirisetty R, Patel RP, Das S, Saraf J, Jyothy A, Munshi A. In-terleukin 1β (+3954, -511 and -31) polymorphism in chronic periodontitis patients from North India. Acta Odontol Scand 2015; 73(5): 343–7.

Vamvakopoulos JE, Taylor CJ, Green C, McNeil K, Wallwork J, Goodman R, et al. Interleukin 1 and chronic rejection: possible genetic links in human heart allografts. Am J Transplant 2002; 2(1): 76–83.

Medawar PB. Some immunological and endocrinological prob-lems raised by the evolution of viviparity in vertebrates. Symp Soc Exp Biol 1953; 7: 320–38.

Kedzierska-Markowicz A, Krekora M, Biesiada L, Głowacka E, Krasomski G. Evaluation of the correlation between IL-1β, IL-8, IFN-γ cytokine concentration in cervico-vaginal fluid and the risk of preterm delivery. Ginekol Pol 2015; 86(11): 821–6. (Polish)

Michalowicz BS, Novak MJ, Hodges JS, DiAngelis A, Buchanan W, Papapanou PN, et al. Serum inflammatory mediators in preg-nancy: changes after periodontal treatment and association with pregnancy outcomes. J Periodontol 2009; 80(11): 1731–41.

Lopez-Castejon G, Brough D. Understanding the mechanism of IL-1β secretion. Cytokine Growth Factor Rev 2011; 22(4): 189–95.

Gloria-Bottini F, Magrini A, Cozzoli E, Neri A, Pietroiusti A, Amante A, et al. ABH secretor genetic polymorphism: evi-dence of intrauterine selection. Eur J Obstet Gynecol Reprod Biol 2011; 154(1): 20–3.

Lewis ZT, Totten SM, Smilowitz JT, Popovic M, Parker E, Lemay DG, et al. Maternal fucosyltransferase 2 status affects the gut bifidobacterial communities of breastfed infants, Microbiome 2015; 3: 13.

Tabasum ST, Nayak RP. Salivary blood group antigens and mi-crobial flora. Int J Dent Hyg 2011; 9(2): 117–21.

Objavljeno
2021/08/04
Rubrika
Originalni članak