Relationship between air pollutants and spontaneous abortion in a coal resource valley city: a retrospective cohort study

References

• Yin P, Brauer M, Cohen AJ, et al. The effect of air pollution on deaths, disease burden, and life expectancy across China and its provinces, 1990-2017: an analysis for the global burden of disease study 2017. Lancet Planet Health. 2020;4(9):e386–e398. doi: 10.1016/S2542-5196(20)30161-3.PubMed PMID: 32818429; PubMed Central PMCID: PMCPMC7487771.
   PubMedGoogle Scholar
• Verhoeven JI, Allach Y, Vaartjes ICH, et al. Ambient air pollution and the risk of ischaemic and haemorrhagic stroke. Lancet Planet Health. 2021;5(8):e542–e552. doi: 10.1016/S2542-5196(21)00145-5.
   PubMedGoogle Scholar
• Schraufnagel DE, Balmes JR, Cowl CT, et al. Air pollution and noncommunicable diseases: a review by the forum of international respiratory societies’ environmental committee, part 2: air pollution and organ systems. Chest. 2019;155(2):417–426. doi: 10.1016/j.chest.2018.10.041.
   PubMed Web of Science ®Google Scholar
• Li Y, Yuan X, Wei J, et al. Long-term exposure to ambient air pollution and serum liver enzymes in older adults: a population-based longitudinal study. Ann Epidemiol. 2022;74:1–7. doi: 10.1016/j.annepidem.2022.05.011.
   PubMed Web of Science ®Google Scholar
• Ha S, Martinez V, Chan-Golston AM. Air pollution and preterm birth: a time-stratified case-crossover study in the san joaquin valley of California. Paediatr Perinat Epidemiol. 2022;36(1):80–89. doi: 10.1111/ppe.12836.
   PubMed Web of Science ®Google Scholar
• Chu C, Zhu Y, Liu C, et al. Ambient fine particulate matter air pollution and the risk of preterm birth: a multicenter birth cohort study in China. Environ Pollut. 2021;287:117629. doi: 10.1016/j.envpol.2021.117629.
   PubMed Web of Science ®Google Scholar
• Zhou W, Ming X, Chen Q, et al. The acute effect and lag effect analysis between exposures to ambient air pollutants and spontaneous abortion: a case-crossover study in China, 2017-2019. Environ Sci Pollut Res Int. 2022;29(44):67380–67389. doi: 10.1007/s11356-022-20379-8.
   PubMed Web of Science ®Google Scholar
• Leiser CL, Hanson HA, Sawyer K, et al. Acute effects of air pollutants on spontaneous pregnancy loss: a case-crossover study. Fertil Steril. 2019;111(2):341–347. doi: 10.1016/j.fertnstert.2018.10.028.
   PubMed Web of Science ®Google Scholar
• Zhang Q, Sun S, Sui X, et al. Associations between weekly air pollution exposure and congenital heart disease. Sci Total Environ. 2021;757:143821. doi: 10.1016/j.scitotenv.2020.143821.
   PubMed Web of Science ®Google Scholar
• Wright CY, Kapwata T, Wernecke B, et al. The risk of orofacial cleft lip/palate due to maternal ambient air pollution exposure: a call for further research in South Africa. Ann Glob Health. 2023;89(1):6. doi: 10.5334/aogh.4007.
   PubMedGoogle Scholar
• Luo D, Kuang T, Chen YX, et al. Air pollution and pregnancy outcomes based on exposure evaluation using a land use regression model: a systematic review. Taiwan J Obstet Gynecol. 2021;60(2):193–215. doi: 10.1016/j.tjog.2021.01.004.
   PubMed Web of Science ®Google Scholar
• Walter CM, Schneider-Futschik EK, Lansbury NL, et al. The health impacts of ambient air pollution in Australia: a systematic literature review. Intern Med J. 2021;51(10):1567–1579. doi: 10.1111/imj.15415.
   PubMed Web of Science ®Google Scholar
• Edwards L, Wilkinson P, Rutter G, et al. Health effects in people relocating between environments of differing ambient air pollution concentrations: a literature review. Environ Pollut. 2022;292(Pt A):118314. doi: 10.1016/j.envpol.2021.118314.
   PubMedGoogle Scholar
• Zhou W, Ming X, Yang Y, et al. Association between maternal exposure to ambient air pollution and the risk of preterm birth: a birth cohort study in chongqing, China, 2015-2020. Int J Environ Res Public Health. 2022;19(4):2211. doi: 10.3390/ijerph19042211.
   Web of Science ®Google Scholar
• Wang L, Fang L, Fang Z, et al. Assessment of the association between prenatal exposure to multiple ambient pollutants and preterm birth: a prospective cohort study in jinan, east China. Ecotoxicol Environ Saf. 2022;232:113297. doi: 10.1016/j.ecoenv.2022.113297.
   PubMed Web of Science ®Google Scholar
• Bravo MA, Miranda ML. A longitudinal study of exposure to fine particulate matter during pregnancy, small-for-gestational age births, and birthweight percentile for gestational age in a statewide birth cohort. Environ Health. 2022;21(1):9. doi: 10.1186/s12940-021-00823-x.
   PubMed Web of Science ®Google Scholar
• Quenby S, Gallos ID, Dhillon-Smith RK, et al. Miscarriage matters: the epidemiological, physical, psychological, and economic costs of early pregnancy loss. Lancet. 2021;397(10285):1658–1667. doi: 10.1016/S0140-6736(21)00682-6.
   PubMed Web of Science ®Google Scholar
• Hu CY, Yang XJ, Hua XG, et al. Risk factors for spontaneous abortion from a prevention perspective in rural China: a population-based follow-up study. J Matern Fetal Neonatal Med. 2021;34(16):2583–2591. doi: 10.1080/14767058.2019.1670160.
   PubMed Web of Science ®Google Scholar
• Miao ZY, Liu XY, Wu H, et al. Cytogenetic analysis of 2959 couples with spontaneous abortion and detailed analysis of rare karyotypes. J Genet. 2022;101:10.
   PubMed Web of Science ®Google Scholar
• Park SJ, Min JY, Kang JS, et al. Chromosomal abnormalities of 19,000 couples with recurrent spontaneous abortions: a multicenter study. Fertil Steril. 2022;117(5):1015–1025. doi: 10.1016/j.fertnstert.2022.01.011.
   PubMed Web of Science ®Google Scholar
• Xu Q, Chan Y, Feng Y, et al. Factors associated with fetal karyotype in spontaneous abortion: a case-case study. BMC Pregnancy Childbirth. 2022;22(1):320. doi: 10.1186/s12884-022-04491-8.
   PubMed Web of Science ®Google Scholar
• Kalantari N, Gorgani-Firouzjaee T, Moulana Z, et al. Toxoplasma gondii infection and spontaneous abortion: a systematic review and meta-analysis. Microb Pathog. 2021;158:105070. doi: 10.1016/j.micpath.2021.105070.
   PubMed Web of Science ®Google Scholar
• Chen W, Xiong S, Shen X, et al. The association between genital mycoplasma infection and spontaneous abortion: a systematic review and meta-analysis. Reprod Toxicol. 2023;116:108334. doi: 10.1016/j.reprotox.2023.108334.
   PubMed Web of Science ®Google Scholar
• Li J, Wang L, Ding J, et al. Multiomics studies investigating recurrent pregnancy loss: an effective tool for mechanism exploration. Front Immunol. 2022;13:826198. doi: 10.3389/fimmu.2022.826198.
   PubMed Web of Science ®Google Scholar
• Ramandeep K, Kapil G, Harkiran K. Correlation of enhanced oxidative stress with altered thyroid profile: Probable role in spontaneous abortion. Int J Appl Basic Med Res. 2017;7(1):20–25. doi: 10.4103/2229-516X.198514.
   PubMedGoogle Scholar
• Wang L, Luo D, Liu X, et al. Effects of PM2.5 exposure on reproductive system and its mechanisms. Chemosphere. 2021;264(Pt 1):128436. doi: 10.1016/j.chemosphere.2020.128436.
   PubMedGoogle Scholar
• Li Z, Tang Y, Song X, et al. Impact of ambient PM2.5 on adverse birth outcome and potential molecular mechanism. Ecotoxicol Environ Saf. 2019;169:248–254. doi: 10.1016/j.ecoenv.2018.10.109.
   PubMed Web of Science ®Google Scholar
• Hunter A, Tussis L, MacBeth A. The presence of anxiety, depression and stress in women and their partners during pregnancies following perinatal loss: a meta-analysis. J Affect Disord. 2017;223:153–164. doi: 10.1016/j.jad.2017.07.004.
   PubMed Web of Science ®Google Scholar
• Weng SC, Chang JC, Yeh MK, et al. Do stillbirth, miscarriage, and termination of pregnancy increase risks of attempted and completed suicide within a year? A population-based nested case-control study. BJOG. 2018;125(8):983–990. doi: 10.1111/1471-0528.15105.
   PubMed Web of Science ®Google Scholar
• Kyriacou H, Al-Mohammad A, Muehlschlegel C, et al. The risk of cardiovascular diseases after miscarriage, stillbirth, and induced abortion: a systematic review and meta-analysis. Eur Heart J Open. 2022;2(5):oeac065. doi: 10.1093/ehjopen/oeac065.
   PubMedGoogle Scholar
• Peters SAE, Yang L, Guo Y, et al. Pregnancy, pregnancy loss, and the risk of cardiovascular disease in chinese women: findings from the China kadoorie biobank. BMC Med. 2017;15(1):148. doi: 10.1186/s12916-017-0912-7.
   PubMedGoogle Scholar
• Peters SAE, Yang L, Guo Y, et al. Pregnancy, pregnancy loss and the risk of diabetes in chinese women: findings from the China kadoorie biobank. Eur J Epidemiol. 2020;35(3):295–303. doi: 10.1007/s10654-019-00582-7.
   PubMed Web of Science ®Google Scholar
• You Q, Jiang Q, Shani I, et al. Miscarriage, stillbirth and the risk of diabetes in women: a systematic review and meta-analysis. Diabetes Res Clin Pract. 2023;195:110224. doi: 10.1016/j.diabres.2022.110224.
   PubMed Web of Science ®Google Scholar
• Horn J, Tanz LJ, Stuart JJ, et al. Early or late pregnancy loss and development of clinical cardiovascular disease risk factors: a prospective cohort study. BJOG. 2019;126(1):33–42. doi: 10.1111/1471-0528.15452.
   PubMed Web of Science ®Google Scholar
• Wang B, Hong W, Sheng Q, et al. Nitrogen dioxide exposure during pregnancy and risk of spontaneous abortion: a case-control study in China. J Matern Fetal Neonatal Med. 2022;35(19):3700–3706. doi: 10.1080/14767058.2020.1837772.
   PubMed Web of Science ®Google Scholar
• Kan HD. [A review of standard value of fine particulate matter (PM(2.5)) ruled by national ambient air quality standards (GB3095-2012) in China]. Zhonghua Yu Fang Yi Xue Za Zhi. 2012;46(5):396–398.
   PubMedGoogle Scholar
• Rai R, Regan L. Recurrent miscarriage. Lancet. 2006;368(9535):601–611. doi: 10.1016/S0140-6736(06)69204-0.
   PubMed Web of Science ®Google Scholar
• Schwerdtfeger KL, Shreffler KM. Trauma of pregnancy loss and infertility for mothers and involuntarily childless women in the contemporary United States. J Loss Trauma. 2009;14(3):211–227. doi: 10.1080/15325020802537468.
   PubMed Web of Science ®Google Scholar
• Eschenbach DA. Treating spontaneous and induced septic abortions. Obstet Gynecol. 2015;125(5):1042–1048. doi: 10.1097/AOG.0000000000000795.
   PubMed Web of Science ®Google Scholar
• Ha S, Sundaram R, Buck Louis GM, et al. Ambient air pollution and the risk of pregnancy loss: a prospective cohort study. Fertil Steril. 2018;109(1):148–153. doi: 10.1016/j.fertnstert.2017.09.037.
   PubMed Web of Science ®Google Scholar
• Wang H, Li J, Liu H, et al. Association of maternal exposure to ambient particulate pollution with incident spontaneous pregnancy loss. Ecotoxicol Environ Saf. 2021;224:112653. doi: 10.1016/j.ecoenv.2021.112653.
   PubMed Web of Science ®Google Scholar
• Di Ciaula A, Bilancia M. Relationships between mild PM10 and ozone urban air levels and spontaneous abortion: clues for primary prevention. Int J Environ Health Res. 2015;25(6):640–655. doi: 10.1080/09603123.2014.1003041.
   PubMed Web of Science ®Google Scholar
• Hou HY, Wang D, Zou XP, et al. Does ambient air pollutants increase the risk of fetal loss? A case-control study. Arch Gynecol Obstet. 2014;289(2):285–291. doi: 10.1007/s00404-013-2962-1.
   PubMed Web of Science ®Google Scholar
• Dastoorpoor M, Khanjani N, Moradgholi A, et al. Prenatal exposure to ambient air pollution and adverse pregnancy outcomes in ahvaz, Iran: a generalized additive model. Int Arch Occup Environ Health. 2021;94(2):309–324. doi: 10.1007/s00420-020-01577-8.
   PubMed Web of Science ®Google Scholar
• Liang Z, Xu C, Liang S, et al. Short-term ambient nitrogen dioxide exposure is associated with increased risk of spontaneous abortion: a hospital-based study. Ecotoxicol Environ Saf. 2021;224:112633. doi: 10.1016/j.ecoenv.2021.112633.
   PubMed Web of Science ®Google Scholar
• Aitken RJ. Impact of oxidative stress on male and female germ cells: implications for fertility. Reproduction. 2020;159(4):R189–R201. doi: 10.1530/REP-19-0452.
   PubMed Web of Science ®Google Scholar
• Colicino E, Cowell W, Foppa Pedretti N, et al. Maternal steroids during pregnancy and their associations with ambient air pollution and temperature during preconception and early gestational periods. Environ Int. 2022;165:107320. doi: 10.1016/j.envint.2022.107320.
   PubMed Web of Science ®Google Scholar
• Familari M, Naav A, Erlandsson L, et al. Exposure of trophoblast cells to fine particulate matter air pollution leads to growth inhibition, inflammation and ER stress. PLoS One. 2019;14(7):e0218799. doi: 10.1371/journal.pone.0218799.
   PubMed Web of Science ®Google Scholar