Citation Information :
Sayeed G. Pathophysiological Mechanisms of Periodontitis in Pregnant Women with Metabolic Syndrome Leading to Adverse Pregnancy Outcomes. World J Dent 2023; 14 (2):192-199.
Aim: To review the current data on the association between problems in a pregnant woman with metabolic syndrome (MetS) and periodontitis and to discuss the mechanisms underlying this association.
Background: Periodontitis, according to some studies, has been linked to pregnancy complications such as preterm (PT) labor, reduced weight at birth, and preeclampsia (PE). MetS is a group of health factors that includes physiological, circulatory, and immunological markers. The physiologic perturbations that support MetS are constant and also include thrombotic dyslipidemia, hypertension blood pressure (BP), resistance against insulin, overweight, and prothrombotic and proinflammatory states, despite the fact that there were many interpretations used to characterize and classify MetS.
Review results: Premature deliveries and other prenatal difficulties associated with MetS are linked to periodontitis. Periodontal bacteria may play a role in this process, either directly generating fetal anomalies or indirectly stimulating the inflammatory reaction and myocyte contraction, resulting in PT birth. However, there is yet no information on the effects of diverse oral microbial populations. Furthermore, current data did not provide definite answers about the effectiveness of periodontal therapy in preventing PT births and other prenatal problems associated with MetS, and definitive intervention strategies have not been created.
Conclusion: Premature deliveries and other prenatal difficulties associated with MetS are linked to periodontitis, which may damage the subject throughout their life. Periodontal bacteria may play a role in this process, either directly generating fetal anomalies or indirectly stimulating the inflammatory reaction and myocyte contraction, resulting in PT. However, there is yet no information on the effects of diverse oral microbial populations.
Clinical significance: Pregnant women with MetS should be encouraged to get regular dental checkups throughout their pregnancy to assess their oral health and receive periodontal disease therapy. They should be informed that such therapy during the course of gestation is effective in lowering the probability of premature delivery or newborns with low weight at birth.
WHO. (2013). Available from: http://whqlibdoc.who.int/publications/2004/9280638327.pdf?ua=1
WHO. Global Health Observatory Data Repository (2014). Available from: http://apps.who.int/gho/data/view.main.1730?lang=en
Romero R, Dey SK, Fisher SJ. Preterm labor: one syndrome, many causes. Science 2014;345(6198):760–765. DOI: 10.1126/science.1251816
Wardlaw T, Blanc A, Zupan J, et al. Low birthweight: country regional and global estimates. WHO 2004.
Mikolajczyk RT, Zhang J, Betran AP, et al. A global reference for fetal-weight and birthweight percentiles. Lancet 2011;377(9780): 1855–1861. DOI: 10.1016/S0140-6736(11)60364-4
Lee AC, Katz J, Blencowe H, et al. National and regional estimates of term and preterm babies born small for gestational age in 138 low-income and middle-income countries in 2010. Lancet Glob Health 2013;1(1):e26–e36. DOI: 10.1016/S2214-109X(13)70006-8
Figueras F, Figueras J, Meler E, et al. Customised birthweight standards accurately predict perinatal morbidity. Arch Dis Child Fetal Neonatal Ed 2007;92(4):F277–F280. DOI: 10.1136/adc. 2006.108621
Katz J, Lee AC, Kozuki N, et al. Mortality risk in preterm and small-for-gestational-age infants in low-income and middle-income countries: a pooled country analysis. Lancet 2013;382(9890):417–425. DOI: 10.1016/S0140-6736(13)60993-9
Klimova RR, Malinovskaia VV, Parshina OV, et al. The effect of viral infections on the cytokine profile in pregnant women with obstetric complications and immunotherapy with human alpha2b interferon. Vopr Virusol 2013;58(1):18–23.
Peoples MD, Siegel E. Measuring the impact of programs for mothers and infants on prenatal care and low birth weight: the value of refined analyses. Med Care 1983;21(6):586–608. DOI: 10.1097/00005650-198306000-00002
Huck O, Tenenbaum H, Davideau JL. Relationship between periodontal diseases and preterm birth: recent epidemiological and biological data. J Pregnancy 2011;2011:164654. DOI: 10.1155/2011/164654
Raghupathy R. Cytokines as key players in the pathophysiology of preeclampsia. Med Princ Pract 2013;22(Suppl. 1):8–19 DOI: 10.1159/000354200
Zenclussen AC. Adaptive immune responses during pregnancy. Am J Reprod Immunol 2013;69(4):291–303. DOI: 10.1111/aji.12097
Piccinni MP, Scaletti C, Maggi E, et al. Role of hormone-controlled Th1- and Th2-type cytokines in successful pregnancy. J Neuroimmunol 2000;109(1):30–33. DOI: 10.1016/s0165-5728(00)00299-x
Chaouat G, Zourbas S, Ostojic S, et al. A brief review of recent data on some cytokine expressions at the materno-foetal interface which might challenge the classical Th1/Th2 dichotomy. J Reprod Immunol 2002;53(1–2):241–256. DOI: 10.1016/s0165-0378(01)00119-x
Hayashi C, Gudino CV, Gibson FC 3rd, et al. Review: pathogen-induced inflammation at sites distant from oral infection: bacterial persistence and induction of cell-specific innate immune inflammatory pathways. Mol Oral Microbiol 2010;25(5):305–316. DOI: 10.1111/j.2041-1014.2010.00582.x
Saito S, Nakashima A, Myojo-Higuma S, et al. The balance between cytotoxic NK cells and regulatory NK cells in human pregnancy. J Reprod Immunol 2008;77(1):14–22. DOI: 10.1016/j.jri.2007.04.007
Challis JR, Lockwood CJ, Myatt L, et al. Inflammation and pregnancy. Reprod Sci 2009;16(2):206–215. DOI: 10.1177/1933719108329095
Raghupathy R. Pregnancy: success and failure within the Th1/Th2/Th3 paradigm. Semin Immunol 2001;13(4):219–227. DOI: 10.1006/smim.2001.0316
Liu YS, Wu L, Tong XH, et al. Study on the relationship between Th17 cells and unexplained recurrent spontaneous abortion. Am J Reprod Immunol 2011;65(5):503–511. DOI: 10.1111/j.1600-0897.2010.00921.x
Robertson SA, Prins JR, Sharkey DJ, et al. Seminal fluid and the generation of regulatory T cells for embryo implantation. Am J Reprod Immunol 2013;69(4):315–330. DOI: 10.1111/aji.12107
Du M, Piao H, Li D. The 3rd international conference on reproductive immunology in Shanghai: September 27-29, 2013. Am J Reprod Immunol 2014;71(3):203–209. DOI: 10.1111/aji.12187
Laird SM, Tuckerman EM, Cork BA, et al. A review of immune cells and molecules in women with recurrent miscarriage. Hum Reprod Update 2003;9(2):163–174. DOI: 10.1093/humupd/dmg013
Adams Waldorf KM, McAdams RM. Influence of infection during pregnancy on fetal development. Reproduction 2013;146(5):R151–R162. DOI: 10.1530/REP-13-0232
Sobel JD. Gynecologic infections in human immunodeficiency virus-infected women. Clin Infect Dis 2000;31(5):1225–3310. DOI: 10.1086/317436
Gibbs RS. The relationship between infections and adverse pregnancy outcomes: an overview. Ann Periodontol 2001;6(1):153–163. DOI: 10.1902/annals.2001.6.1.153
Stout MJ, Conlon B, Landeau M, et al. Identification of intracellular bacteria in the basal plate of the human placenta in term and preterm gestations. Am J Obstet Gynecol 2013;208(3):226.e1–226.e7. DOI: 10.1016/j.ajog.2013.01.018
Aagaard K, Ma J, Antony KM, et al. The placenta harbors a unique microbiome. Sci Transl Med 2014;6(237):287–293. DOI: 10.1126/scitranslmed.3008599
Xiong X, Buekens P, Fraser WD, et al. Periodontal disease and adverse pregnancy outcomes: a systematic review. BJOG 2006;113(2):135–143. DOI: 10.1111/j.1471-0528.2005.00827.x
Armitage GC. Development of a classification system for periodontal diseases and conditions. Ann Periodontol 1999;4(1):1–6. DOI: 10.1902/annals.1999.4.1.1
Darveau RP. Periodontitis: a polymicrobial disruption of host homeostasis. Nat Rev Microbiol 2010;8(7):481–490. DOI: 10.1038/nrmicro2337
Kolenbrander PE, Palmer RJ Jr, Periasamy S, et al. Oral multispecies biofilm development and the key role of cell-cell distance. Nat Rev Microbiol 2010:8(7):471–480. DOI: 10.1038/nrmicro2381
Nibali L, Farias BC, Vajgel A, et al. Tooth loss in aggressive periodontitis: a systematic review. J Dent Res 2013;92(10):868–875. DOI: 10.1177/0022034513501878
Tonetti MS, Mombelli A. Early-onset periodontitis. Ann Periodontol 1999;4(1):39–53. DOI: 10.1902/annals.1999.4.1.39
Socransky SS, Haffajee AD, Cugini MA, et al. Microbial complexes in subgingival plaque. J Clin Periodontol 1998;25(2):134–144. DOI: 10.1111/j.1600-051x.1998.tb02419.x
Faveri M, Figueiredo LC, Duarte PM, et al. Microbiological profile of untreated subjects with localized aggressive periodontitis. J Clin Periodontol 2009;36(9):739–749. DOI: 10.1111/j.1600-051X.2009.01449.x
Ando ES, De-Gennaro LA, Faveri M, et al. Immune response to cytolethal distending toxin of Aggregatibacter actinomycetemcomitans in periodontitis patients. J Periodontal Res 2010;45(4):471–480. DOI: 10.1111/j.1600-0765.2009.01260.x
Saraiva L, Rebeis ES, Martins ED, et al. IgG sera levels against a subset of periodontopathogens and severity of disease in aggressive periodontitis patients: a cross-sectional study of selected pocket sites. J Clin Periodontol 2014;41(10):943–951. DOI: 10.1111/jcpe.12296
Pérez-Chaparro PJ, Gonçalves C, Figueiredo LC, et al. Newly identified pathogens associated with periodontitis: a systematic review. J Dent Res 2014;93(9):846–858. DOI: 10.1177/0022034514542468
Hajishengallis G, Lambris JD. Complement and dysbiosis in periodontal disease. Immunobiology 2012;217(11):1111–1116. DOI: 10.1016/j.imbio.2012.07.007
Finoti LS, Anovazzi G, Pigossi SC, et al. Periodontopathogens levels and clinical response to periodontal therapy in individuals with the interleukin-4 haplotype associated with susceptibility to chronic periodontitis. Eur J Clin Microbiol Infect Dis 2013;32(12):1501–1509. DOI: 10.1007/s10096-013-1903-z
Gonçalves PF, Klepac-Ceraj V, Huang H, et al. Correlation of Aggregatibacter actinomycetemcomitans detection with clinical/immunoinflammatory profile of localized aggressive periodontitis using a 16S rRNA microarray method: a cross-sectional study. PLoS One 2013;8(12):e85066. DOI: 10.1371/journal.pone.0085066
Cairo F, Nieri M, Gori AM, et al. Markers of systemic inflammation in periodontal patients: chronic versus aggressive periodontitis. An explorative cross-sectional study. Eur J Oral Implantol 2010;3(2): 147–153.
Garlet GP, Martins W Jr, Ferreira BR, et al. Patterns of chemokines and chemokine receptors expression in different forms of human periodontal disease. J Periodontal Res 2003;38(2):210–217. DOI: 10.1034/j.1600-0765.2003.02012.x
Lima PM, Souza PE, Costa JE, et al. Aggressive and chronic periodontitis correlate with distinct cellular sources of key immunoregulatory cytokines. J Periodontol 2011;82(1):86–95. DOI: 10.1902/jop.2010.100248
Shaker OG, Ghallab NA. IL-17 and IL-11 GCF levels in aggressive and chronic periodontitis patients: relation to PCR bacterial detection. Mediators Inflamm 2012;2012:174764. DOI: 10.1155/2012/174764
Lubberts E, van den Bersselaar L, Oppers-Walgreen B, et al. IL-17 promotes bone erosion in murine collagen-induced arthritis through loss of the receptor activator of NF-kappa B ligand/osteoprotegerin balance. J Immunol 2003;170(5):2655–2662. DOI: 10.4049/jimmunol.170.5.2655
Suga K, Saitoh M, Kokubo S, et al. Synergism between interleukin-11 and bone morphogenetic protein-2 in the healing of segmental bone defects in a rabbit model. J Interferon Cytokine Res 2004;24(6): 343–349. DOI: 10.1089/107999004323142204
Carrillo-de-Albornoz A, Figuero E, Herrera D, et al. Gingival changes during pregnancy: II. Influence of hormonal variations on the subgingival biofilm. J Clin Periodontol 2010;37(3):230–240. DOI: 10.1111/j.1600-051X.2009.01514.x
Gürsoy M, Pajukanta R, Sorsa T, et al. Clinical changes in periodontium during pregnancy and post-partum. J Clin Periodontol 2008;35(7): 576–583. DOI: 10.1111/j.1600-051X.2008.01236.x
Kornman KS, Loesche WJ. Effects of estradiol and progesterone on Bacteroides melaninogenicus and Bacteroides gingivalis. Infect Immun 1982;35(1):256–263. DOI: 10.1128/iai.35.1.256-263.1982
Adriaens LM, Alessandri R, Spörri S, et al. Does pregnancy have an impact on the subgingival microbiota. J Periodontol 2009;80(1): 72–81. DOI: 10.1902/jop.2009.080012
Lin D, Moss K, Beck JD, et al. Persistently high levels of periodontal pathogens associated with preterm pregnancy outcome. J Periodontol 2007;78(5):833–841. DOI: 10.1902/jop.2007.060201
Koren O, Goodrich JK, Cullender TC, et al. Host remodeling of the gut microbiome and metabolic changes during pregnancy. Cell 2012;150(3):470–480. DOI: 10.1016/j.cell.2012.07.008
Lunardelli AN, Peres MA. Is there an association between periodontal disease, prematurity and low birth weight? A population-based study. J Clin Periodontol 2005;32(9):938–946. DOI: 10.1111/j.1600-051X.2005.00759.x
Siqueira FM, Cota LO, Costa JE, et al. Intrauterine growth restriction, low birth weight, and preterm birth: adverse pregnancy outcomes and their association with maternal periodontitis. J Periodontol 2007;78(12):2266–2276. DOI: 10.1902/jop.2007.070196
Moutsopoulos NM, Madianos PN. Low-grade inflammation in chronic infectious diseases: paradigm of periodontal infections. Ann N Y Acad Sci 2006;1088:251–264. DOI: 10.1196/annals.1366.032
Govindasamy R, Periyasamy S, Narayanan M, et al. The influence of nonsurgical periodontal therapy on the occurrence of adverse pregnancy outcomes: a systematic review of the current evidence. J Indian Soc Periodontol 2020;24(1):7–14. DOI: 10.4103/jisp.jisp_228_19
Lavigne SE, Forrest JL. An umbrella review of systematic reviews of the evidence of a causal relationship between periodontal disease and adverse pregnancy outcomes: a position paper from the Canadian Dental Hygienists Association. Can J Dent Hyg 2020;54(2):92–100.
Jain P, Hassan N, Khatoon K, et al. Periodontitis and systemic disorder-an overview of relation and novel treatment modalities. Pharmaceutics 2021;13(8):1175. DOI: 10.3390/pharmaceutics13081175
Zi MY, Longo PL, Bueno-Silva B, et al. Mechanisms involved in the association between periodontitis and complications in pregnancy. Front Public Health 2015;2:290. DOI: 10.3389/fpubh.2014.00290
Uwambaye P, Munyanshongore C, Rulisa S, et al. Assessing the association between periodontitis and premature birth: a case-control study. BMC Pregnancy Childbirth 2021;21(1):204. DOI: 10.1186/s12884-021-03700-0