4 Discussion
This is the first study carried out on an ethnic group from Mizoram, a northeast state of India, relating placenta pathology with the outcome of pregnancies in a cohort of pregnant Mizo women diagnosed as SARS-CoV-2-positive. Invaluable information for enhancing disease pathogenesis concepts and identifying underlying causes of adverse pregnancy outcomes can be extracted from placental examinations. Of the 72 pregnant women who were referred to ZMCH, nearly 40% were asymptomatic. This is in agreement with two systematic reviews and meta-analyses by Ma et al., 2021 (asymptomatic = 40.5%) and Villar et at, 2021 (asymptomatic = 44%) showed that around 2/5th of the individuals confirmed positive for SARS-CoV-2 were asymptomatic12,13. Asymptomatic infections play a significant role in spreading SARS-CoV-2 within the community with the gradual return of public life. However, the exact reason for an individual to be asymptotic is unknown; a combination of genetic factors, age, the virus' virulence, and the subject's susceptibility may be involved.14
The relationship between SARS-CoV-2 and its afflictions on the developing fetus during pregnancy is yet not fully established. These complications may include stillbirth, pre-term birth, or prolonged complications for the newborn. Adverse pregnancy and neonatal outcomes of a study conducted on 827 pregnant women vaccinated with the SARS-CoV-2 mRNA vaccine were comparable to those reported in similar studies conducted before the pandemic15. Moreover, it is postulated that the SARS-CoV-2 infection triggers a “cytokine storm,” amplifying the mother's immune system through an uninhibited inflammatory cytokine release and causing increased incidences of pre-term labor, fetal growth restriction, placental damage, and abortion16,17. In our study, 18% of women delivered pre-term. Two studies from northern states of India reported pre-term deliveries in 52%18 and 15.5%19 of women diagnosed as SARS-CoV-2-positive. In 2021, Son et al., working on a US-based extensive population data, could not determine any association between adverse pregnancy outcomesand SARS-CoV-2 infection of the mother, including pre-term birth or Cesarean birth, or postpartum hemorrhage20. In contrast, Jering et al.observed a clear link between SARS-COV-2 deliveries and most of the above-mentioned outcomes21. Metz et al. commented that both of these studies have no mention of the risk severity of SARS-CoV-2 in their studies18,22.
In this study, 93.1% of women had Cesarean deliveries either due to SARS-CoV-2-related issues or pre-existing obstetrics complications, or fetal distress. In Indian studies, it ranges from 64.7% to 77% against the national average of 21.5% reported by the National Family Health Survey13,18. Data from a group of 68 infected women who delivered from December 2019 to March 2020 in China also showed a cesarean section rate of 93%, confirming the increased caesarean section rate among infected pregnant women who delivered in the first wave of SARS-CoV-2 pandemic23. Notably, most studies do not present evidence of a SARS-CoV-2 infection in neonatal throat swabs, amniotic fluid, umbilical cord, or breast milk samples. This is linked to the fact that an immunological barrier is present in the human placenta to block the entry of pathogens and maintain fetal cell immune tolerance. The innate immune system has been proposed to be crucial in protecting fetuses and neonates against SARS-CoV-2 infection24. The various immune cells of the innate immune system present in the maternofetal interface, including decidual macrophages, natural killer cells, and CD4 T cells, all act as barriers to transmission25. Also, the outermost chorionic villilayer comprising syncytiotrophoblast cells and in direct contact with the maternal blood, lack intercellular gap junctions and thus effectively prevents pathogen entry from the bloodstream.
Collectively, the structural barrier, innate immune system, and interactions of the invading fetal extravillous trophoblasts and the decidual immune cells play a significant role in the protective mechanisms of the placenta against SARS-CoV-2 viral invasion25. However, a multinational cohort study observed that the cesarean delivery mode/in SARS-CoV-2-positive mothers was associated with increased risk for neonatal test positivity (RR, 2.15; 95% CI, 1.18–3.91)26. Chorionic villi contain fetal blood vessels (BVs) and continuously form branching villi throughout gestation. Exchange between maternal blood and the fetal compartment occurs across the villus surface via syncytiotrophoblasts (STBs) a multinucleate syncytium for exchange of key substances and a physical barrier to the entry of pathogens. Maternal viremia and infection of cells in the basal decidua therefore expose STBs to virions in blood and released locally into the intervillous blood. In addition, infection in the parietal decidua could spread to the chorionic membrane adjacent to the amniotic membrane27.
All deliveries resulted in the birth of singleton live babies. In two studies from India, >97% of cases resulted in the birth of live babies19,26. In this study,80.6% had more than 2.5 kg birth weight, and most of the neonates showed APGAR (at 5 min), with scores ranging between 4 and 6. Based on 246 articles, Chao Met al. concluded that the status of maternal SARS-CoV-2 positivity is related to an APGAR score of less than 7 in neonates25. However, in this study, most neonates did well, and only 10 required resuscitations, of which 8 (11.1%) were later admitted to the NICU, which is comparable to other studies from India19,26,28.
Fever and cough were the most typical symptoms in patients enrolled in our study. This is consistent with other studies8,26,29. Hemoglobin (Hb) level and Total leucocyte count (TLC) were normal in most women in our study. However, in a retrospective cohort study, Hb levels were shown to be significantly lower and TLC significantly higher in pregnant women diagnosed as SARS-CoV-2-positive than in pregnant women who tested negative for SARS-CoV-230.
Pregnancy-specific disorders are the primary cause of abnormal results in liver function tests during pregnancy. The prevalence of liver injury in pregnant women diagnosed as SARS-CoV-2-positive was reported to be high31,32. In contrast, we found liver function tests deranged in only 6.9% (n = 5) of the study population (the placental pathology associated with the deranged liver is given in Supplementary Table 1.)
The coronavirus potentially damages kidney tissues by infecting kidney cells with receptors enabling the virus to attach, invade, and make copies of itself. According to an update released on corona in May 2022 by Dr. Seprati CJ, Director of the Nephrology Fellowship Training Program, John Hopkins Medicine stated that besides the virusinvading kidney cells and causing damage directly, virus-induced hypoxia, cytokine storm, and blood clots might damage the kidney as well33. He further added many studies indicate that >30% of patients hospitalized with SARS-CoV-2 infection develop kidney injury, and >50% of patients in the intensive care unit with kidney injury require dialysis. Thankfully, in the study, only 2.7% of women had deranged kidney function tests (the placental pathology associated with a deranged kidney is given in Supplementary Table 1).
A systematic review of 151 autopsies in SARS-CoV-2-positive cases revealed that 85 (56.3%) cases had the presence of microthrombi in the lungs34. The endotheliotropicbehavior of SARS-CoV-2 via the ACE2 receptor on endothelial cells makes it prone to cause vascular endothelial dysfunction, leading to a complement-induced coagulopathy state in SARS-COV-2 infected patients and henceforth susceptible to microthrombi formation35. In the current study, contrast-enhanced computerized tomography of the chest demonstrated the presence of abnormal pathology in 6 out of 9 (66.7%) cases, with 4 of them havingmoderate to severe pathologies. Compared to controls, anomalous or injured maternal vessels and intervillous thrombi are significantly higher in the placentas of SARS-CoV-2- afflicted women.
Increased microcalcifications and fibrin thrombi were observed in the placentas of SARS-CoV-2-positive pregnant women, reflecting either an underlying hypercoagulable state induced by SARS-CoV-2 infection or major injury to syncytia-trophoblast36. In consistency with these findings, in our study, we observed an increased prevalence of microthrombi (11.1%), microcalcifications (22.2%), and syncytial knotting (6.9%).
We observed focal infarctions in 28% of cases. Infractions in the placenta are, in general, seen in about 25% of all uncomplicated pregnancies and do not affect the pregnancy. However, more serious infarctions due to severe SARS-CoV-2 infection and preeclampsia can directly cause fetal distress and are associated with developmental delays and cerebral palsy37,38. A notably high frequency (38.9%) of Chorangiosiswas observed in our study, as reported previously by Shane et al.39. Chorangiosis is characterized by decreased maternal oxygen saturation and is common in women inhabiting high altitudes like Mizoram. In contrast to findings by Smithgall et al., which described that villous agglutination was statistically more common in SARS-CoV-2 cases, we observed villous agglutination in only a single case40. In normal pregnancy, villous agglutination occurs in about 2% of cases39. Further, we observed placentas of deliveries beyond 37 weeks of gestations showed maximum pathological abnormalities compared to earlier weeks of gestation (Details are given in Supplementary Table 2).
No significant differences between the symptomatic and asymptomatic groups were observed in placenta pathologies. About 17.9%∼33.3% of infected patients were estimated tostay asymptomatic41,42. Similarly, the placental pathology of neonates requiring admission to NICU did not differ from the neonates not requiring NICU admission.