Placenta response of inflammation and oxidative stress in low-risk term childbirth: The implication of delivery mode

BMC Pregnancy and Childbirth

Volumn 17, Issue 1, 2017, Pages

  Hu, Yabin ^a,c   Huang, Kun ^a,c   Sun, Yuanfang ^a,c   Wang, Jianqing ^a,c   Xu, Yeqing ^b   Yan, Shuangqin ^b   Zhu, Peng ^a,c   Tao, Fangbiao ^a,c  

^a ANHUI MEDICAL UNIVERSITY   (China)

^b Ma'anshan Maternal and Child Health (MCH) Center   (China)

^c ANHUI PROVINCIAL KEY LABORATORY OF POPULATION HEALTH AND ARISTOGENICS   (China)

Author keywords

Delivery mode; Inflammation; Oxidative stress; Placenta

Indexed keywords

GAMMA INTERFERON; HEME OXYGENASE 1; INTERLEUKIN 10; INTERLEUKIN 1BETA; INTERLEUKIN 4; INTERLEUKIN 6; INTERLEUKIN 8; MESSENGER RNA; TUMOR NECROSIS FACTOR; CYTOKINE;

ADULT; ARTICLE; BODY HEIGHT; BODY MASS; BODY WEIGHT; CAESAREAN DELIVERY ON MATERNAL REQUEST; CAESAREAN DELIVERY WITH MEDICAL INDICATION; CESAREAN SECTION; CHILDBIRTH; COHORT ANALYSIS; CONTROLLED STUDY; FEMALE; FOLLOW UP; GESTATIONAL AGE; HUMAN; INFLAMMATION; INFORMED CONSENT; OXIDATIVE STRESS; PLACENTA; PREGNANT WOMAN; PROTEIN EXPRESSION; PROTEIN RNA BINDING; THIRD TRIMESTER PREGNANCY; URGENT CESAREAN DELIVERY; VAGINAL DELIVERY; CHINA; METABOLISM; NEWBORN; OBSTETRIC DELIVERY; PHYSIOLOGY; PREGNANCY; PROCEDURES; STATISTICS AND NUMERICAL DATA; TERM BIRTH; YOUNG ADULT;

ADULT; CESAREAN SECTION; CHINA; COHORT STUDIES; CYTOKINES; DELIVERY, OBSTETRIC; FEMALE; HUMANS; INFANT, NEWBORN; INFLAMMATION; OXIDATIVE STRESS; PLACENTA; PREGNANCY; TERM BIRTH; YOUNG ADULT;

EID: 85037332898     PISSN: None     EISSN: 14712393     Source Type: Journal    
DOI: 10.1186/s12884-017-1589-9     Document Type: Article

References (36)

1. Blanchette H. The rising cesarean delivery rate in America: what are the consequences? Obstet Gynecol. 2011;118(3):687-90.
2. Lumbiganon P, Laopaiboon M, Gülmezoglu AM, et al. Method of delivery and pregnancy outcomes in Asia: the WHO global survey on maternal and perinatal health 2007-08. Lancet. 2010;375(9713):490-9.
3. Vogel JP, Betrán AP, Vindevoghel N, et al. Use of the Robson classification to assess caesarean section trends in 21 countries: a secondary analysis of two WHO multicountry surveys. Lancet Glob Health. 2015;3(5):e260-70.
4. Xiong C, Zhou A, Cao Z, et al. Association of pre-pregnancy body mass index, gestational weight gain with cesarean section in term deliveries of China. Sci Rep. 2016;6:37168.
5. Zhang J, Liu Y, Meikle S, et al. Cesarean delivery on maternal request in southeast China. Obstet Gynecol. 2008;111(5):1077-82.
6. Feng XL, Wang Y, An L, et al. Cesarean section in the People's Republic of China: current perspectives. Int J Womens Health. 2014;6:59-74.
7. Wang E. Requests for cesarean deliveries: The politics of labor pain and pain relief in Shanghai, China. Soc Sci Med. 2017;173:1-8.
8. Liu X, Landon MB, Cheng W, et al. Cesarean delivery on maternal request in China: what are the risks and benefits? Am J Obstet Gynecol. 2015;212(6):817.e1-9.
9. Yu Y, Zhang X, Sun C, et al. Reducing the rate of cesarean delivery on maternal request through institutional and policy interventions in Wenzhou, China. PLoS One. 2017;12(11):e0186304.
10. Armstrong-Wells J, Donnelly M, Post MD, et al. Inflammatory predictors of neurologic disability after preterm premature rupture of membranes. Am J Obstet Gynecol. 2015;212(2):212.e1-9.
11. Joosten LA, Netea MG, Dinarello CA. Interleukin-1β in innate inflammation, autophagy and immunity. Semin Immuno. 2013;25:416-24.
12. Al-Gubory KH, Fowler PA, Garrel C. The roles of cellular reactive oxygen species, oxidative stress and antioxidants in pregnancy outcomes. Int J Biochem Cell Biol. 2010;42:1634-50.
13. Malamitsi-Puchner A, Protonotariou E, Boutsikou T, et al. The influence of the mode of delivery on circulating cytokine concentrations in the perinatal period. Early Hum Dev. 2005;81(4):387-92.
14. Gitto E, Reiter RJ, Karbownik M, et al. Causes of oxidative stress in the pre-and perinatal period. Biol Neonate. 2002;81:146-57.
15. Hung TH, Chen SF, Hsieh TT, et al. The associations between labor and delivery mode and maternal and placental oxidative stress. Reprod Toxicol. 2011;31(2):144-50.
16. Bakheit KH, Bayoumi NK, Adam I. Peripheral, placental and cord cytokines profile in spontaneous labor and elective caesarean section. Iran J Immunol. 2008;5(3):185-8.
17. Yu J, Zhou Y, Gui J, et al. Assessment of the number and function of macrophages in the placenta of gestational diabetes mellitus patients. J Huazhong Univ Sci Technolog Med Sci. 2013;33(5):725-9.
18. Radaelli T, Varastehpour A, Catalano P, et al. Gestational diabetes induces placental genes for chronic stress and inflammatory pathways. Diabetes. 2003;52(12):2951-8.
19. Bronson SL, Bale TL. Prenatal stress-induced increases in placental inflammation and offspring hyperactivity are male-specific and ameliorated by maternal antiinflammatory treatment. Endocrinology. 2014;155(7):2635-46.
20. Xiao LM, Tao FB, Zhang JL, et al. Design of pregnancy - related anxiety scale and reliability evaluation. Chin J Public Health. 2012;28(3):275-7.
21. Yadav AK, Chaudhari H, Warke H, et al. Differential expression of Collectins in human placenta and role in inflammation during spontaneous labor. PLoS One. 2014;9(10):e108815.
22. Latendresse G, Ruiz RJ, Wong B. Psychological distress and SSRI use predict variation in inflammatory cytokines during pregnancy. Open J ObstetGynecol. 2013;3(1A):184-91.
23. Girard S, Heazell AE, Derricott H, et al. Circulating cytokines and alarmins associated with placental inflammation in high-risk pregnancies. Am J Reprod Immunol. 2014;72(4):422-34.
24. Chatterjee P, Chiasson VL, Seerangan G, et al. Combined treatment with IL-4 and IL-10 modulates immune cells and prevents hypertension in pregnant mice. Am J Hypertens. 2015;28(1):135-42.
25. Lappas M. GSK3β is increased in adipose tissue and skeletal muscle from women with gestational diabetes where it regulates the inflammatory response. PLoS One. 2014;9(12):e115854.
26. Charo IF, Ransohoff RM. The many roles of chemokines and chemokine receptors in inflammation. N Engl J Med. 2006;354(6):610-21.
27. Huang K, Tao F, Faragher B, et al. A mixed-method study of factors associated with differences in caesarean section rates at community level: the case of rural China. Midwifery. 2013;29(8):911-20.
28. Zhao J, Liu XJ, Ma JW, et al. DNA damage in healthy term neonate. Early Hum Dev. 2004;77(1-2):89-98.
29. Keelan JA, Marvin KW, Sato TA, et al. Cytokine abundance in placental tissues: evidence of inflammatory activation in gestational membranes with term and preterm parturition. Am J Obstet Gynecol. 1999;181(6):1530-6.
30. Gedikbaşi A, Salihoglu Ö, Çankaya A, et al. The evaluation of cord blood interleukin-1β levels in normal and caesarean deliveries. Hum Exp Toxicol. 2014;33(12):1193-8.
31. Mutlu B, Aksoy N, Cakir H, et al. The effects of the mode of delivery on oxidative-antioxidative balance. J Matern Fetal Neonatal Med. 2011;24(11):1367-70.
32. Ozen M, Zhao H, Lewis DB, et al. Hemeoxygenase and the immune system in normal and pathological pregnancies. Front Pharmacol. 2015;6:84.
33. Zerón HM, Flores AP, Chávez AA, et al. Pregnancy weight gainlimitation by a supervised nutritional program influences placental NF-ΚB/IKK complexexpression and oxidative stress. Oman Med J. 2013;28(3):167-72.
34. Aye IL, Waddell BJ, Mark PJ, et al. Oxysterols exert proinflammatory effects in placental trophoblasts via TLR4-dependent, cholesterol-sensitive activation of NF-ΚB. Mol Hum Reprod. 2012;18(7):341-53.
35. Cindrova-Davies T, Yung HW, Johns J, et al. Oxidative stress, gene expression, and protein changes induced in the human placenta during labor. Am J Pathol. 2007;171(4):1168-79.
36. Offner H, Subramanian S, Parker SM, et al. Experimental stroke induces massive, rapid activation of the peripheral immune system. J Cereb Blood Flow Metab. 2006;26(5):654-65.