Relationship between serum NLRP3 along with its effector molecules and pregnancy outcomes in women with hyperglycemia

References

• Obstetrics Group, Division of Obstetrics and Gynecology, Chinese Medical Association, Division of Perinatal Medicine, China Maternal and Child Health Association. Guidelines for the diagnosis and treatment of gestational hyperglycemia. Chin J Obstet Gynecol. 2022;57(1):1–9.
   Google Scholar
• Yu XY, Wu XF, Qi HB. Interpretation of the key points of the Queensland health organization guidelines for gestational diabetes (2021 version). Chin J Pract Gynecol Obstet. 2021;37(9):933–936.
   Google Scholar
• Wei X, Xie F, Zhou X, et al. Role of pyroptosis in inflammation and cancer. Cell Mol Immunol. 2022;19(9):971–992. doi: 10.1038/s41423-022-00905-x.
   PubMed Web of Science ®Google Scholar
• Xu J, Núñez G. The NLRP3 inflammasome: activation and regulation. Trends Biochem Sci. 2023;48(4):331–344. doi: 10.1016/j.tibs.2022.10.002.
   PubMed Web of Science ®Google Scholar
• Galluzzi L, Vitale I, Abrams JM, et al. Molecular definitions of cell death subroutines: recommendations of the nomenclature committee on cell death 2012. Cell Death Differ. 2012;19(1):107–120. doi: 10.1038/cdd.2011.96.
   PubMed Web of Science ®Google Scholar
• Hu YC, Yang S. Advances in the study of cell pyroptosis. J Nanjing Med Univ Sci. 2021;41(8):1245–1251.
   Google Scholar
• Man SM, Karki R, Kanneganti TD. Molecular mechanisms and functions of pyroptosis, inflammatory caspases and inflammasomes in infectious diseases. Immunol Rev. 2017;277(1):61–75. doi: 10.1111/imr.12534.
   PubMed Web of Science ®Google Scholar
• Man SM, Karki R, Kanneganti TD. AIM2 inflammasome in infection, cancer, and autoimmunity: role in DNA sensing, inflammation, and innate immunity. Eur J Immunol. 2016;46(2):269–280. doi: 10.1002/eji.201545839.
   PubMed Web of Science ®Google Scholar
• Pragnesh M, Kaplan MJ. Cell death in the pathogenesis of systemic lupus erythematosus and lupus nephritis. Clin Immunol. 2017;185(185):59–73. doi: 10.1016/j.clim.2016.08.010.
   PubMedGoogle Scholar
• Lu F, Lan Z, Xin Z, et al. Emerging insights into molecular mechanisms underlying pyroptosis and functions of inflammasomes in diseases. J Cell Physiol. 2020;235(4):3207–3221. doi: 10.1002/jcp.29268.
   PubMed Web of Science ®Google Scholar
• Szmuilowicz ED, Josefson JL, Metzger BE. Gestational diabetes mellitus. Endocrinol Metab Clin North Am. 2019;48(3):479–493. doi: 10.1016/j.ecl.2019.05.001.
   PubMed Web of Science ®Google Scholar
• Xie X, Kong BH, Duan T. Obstetrics gynecology. Version 9. Beijing: People’s Medical Publishing House; 2018.
   Google Scholar
• Alfadul H, Sabico S, Ansari MGA, et al. Differences and associations of NLRP3 inflammasome levels with interleukins 1α, 1β, 33 and 37 in adults with prediabetes and type 2 diabetes mellitus. Biomedicines. 2023;11(5):1315. doi: 10.3390/biomedicines11051315.
   PubMed Web of Science ®Google Scholar
• Jia X, Qiu T, Yao X, et al. Arsenic induces hepatic insulin resistance via mtROS-NLRP3 inflammasome pathway. J Hazard Mater. 2020;399:123034. doi: 10.1016/j.jhazmat.2020.123034.
   PubMed Web of Science ®Google Scholar
• Jourdan T, Godlewski G, Cinar R, et al. Activation of the Nlrp3 inflammasome in infiltrating macrophages by endocannabinoids mediates beta cell loss in type 2 diabetes. Nat Med. 2013;19(9):1132–1140. doi: 10.1038/nm.3265.
   PubMed Web of Science ®Google Scholar
• Healy NP, Kirwan AM, McArdle MA, et al. A casein hydrolysate protects mice against high fat diet induced hyperglycemia by attenuating NLRP3 inflammasome-mediated inflammation and improving insulin signaling. Mol Nutr Food Res. 2016;60(11):2421–2432. doi: 10.1002/mnfr.201501054.
   PubMed Web of Science ®Google Scholar
• Youm YH, Adijiang A, Vandanmagsar B, et al. Elimination of the NLRP3-ASC inflammasome protects against chronic obesity-induced pancreatic damage. Endocrinology. 2011;152(11):4039–4045. doi: 10.1210/en.2011-1326.
   PubMed Web of Science ®Google Scholar
• Liu P, Zhang Z, Wang J, et al. Empagliflozin protects diabetic pancreatic tissue from damage by inhibiting the activation of the NLRP3/caspase-1/GSDMD pathway in pancreatic β cells: in vitro and in vivo studies. Bioengineered. 2021;12(2):9356–9366. doi: 10.1080/21655979.2021.2001240.
   PubMed Web of Science ®Google Scholar
• Zhang J, Chi H, Xiao H, et al. Interleukin 6(IL-6) and tumor necrosis factor α (TNF-α) single nucleotide polymorphisms (SNPs), inflammation and metabolism in gestational diabetes mellitus in Inner Mongolia. Med Sci Monit. 2017;23:4149–4157. doi: 10.12659/msm.903565.
   PubMed Web of Science ®Google Scholar
• Tran HT, Liong S, Lim R, et al. Resveratrol ameliorates the chemical and microbial induction of inflammation and insulin resistance in human placenta, adipose tissue and skeletal muscle. PLoS One. 2017;12(3):e0173373. doi: 10.1371/journal.pone.0173373.
   PubMed Web of Science ®Google Scholar
• Park YJ, Warnock GL, Ao Z, et al. Dual role of IL-1β in islet amyloid formation and its β-cell toxicity: implications in type 2 diabetes and islet transplantation. Diabetes Obes Metab. 2017;19(5):682–694. doi: 10.1111/dom.12873.
   PubMed Web of Science ®Google Scholar
• Chen X, Zhang D, Li Y, et al. NLRP3 inflammasome and IL-1beta pathway in type 2 diabetes and atherosclerosis: friend or foe?. Pharmacol Res. 2021;173:105885. doi: 10.1016/j.phrs.2021.105885.
   PubMed Web of Science ®Google Scholar
• Alboni S, Montanari C, Benatti C, et al. Interleukin 18 activates MAPKs and STAT3 but not NF-κB in hippocampal HT-22 cells. Brain Behav Immun. 2014;40:85–94. doi: 10.1016/j.bbi.2014.02.015.
   PubMed Web of Science ®Google Scholar
• Yang Y, Zhang H. TXNIP activates NLRP3 inflammasome in the pathogenesis of preeclampsia. J Chongqing Med Univ. 2016;41(7):658–662.
   Google Scholar
• Ingrid CW, Mariana RV, Mariana LM, et al. Increased expression of NLRP3 inflammasome in placentas from pregnant women with severe preeclampsia. J Reprod Immunol. 2017;123:40–47.
   PubMed Web of Science ®Google Scholar
• Cui SH, Shen LN, Zhi YX, et al. Expression and significance of HMGB-1 and MMP-9 in fetal membranes of patients with premature rupture of chorioamnionitis membranes. Adv Modern Obstet Gynecol. 2016;25(8):582–585.
   Google Scholar
• Xiao WX, Wang HZ, Zhou GJ, et al. Study on the correlation between premature rupture of membranes and fetal membrane cell coke death. Chinese J Reproduct Health. 2019;30(3):281–283.
   Google Scholar
• Gomez-Lopez N, Romero R, Xu Y, et al. A role for the inflammasome in spontaneous preterm labor with acute histologic chorioamnionitis. Reprod Sci. 2017;24(10):1382–1401. doi: 10.1177/1933719116687656.
   PubMed Web of Science ®Google Scholar
• Parry S, Carper BA, Grobman WA, et al. Placental protein levels in maternal serum are associated with adverse pregnancy outcomes in nulliparous patients. Am J Obstet Gynecol. 2022;227(3):497.e1–497.e13. doi: 10.1016/j.ajog.2022.03.064.
   PubMed Web of Science ®Google Scholar
• Ho YR, Wang P, Lu MC, et al. Associations of mid-pregnancy HbA1c with gestational diabetes and risk of adverse pregnancy outcomes in high-risk Taiwanese women. PLoS One. 2017;12(5):e0177563. doi: 10.1371/journal.pone.0177563.
   PubMed Web of Science ®Google Scholar
• Carlsen EØ, Harmon Q, Magnus MC, et al. Glycated haemoglobin (HbA1c) in mid-pregnancy and perinatal outcomes. Int J Epidemiol. 2022;51(3):759–768. doi: 10.1093/ije/dyab270.
   PubMed Web of Science ®Google Scholar