Nasa Prashant, Juneja Deven, Jain Ravi, Nasa Ruchi
Department of Critical Care Medicine, NMC Specialty Hospital, Dubai 7832, United Arab Emirates.
Department of Internal Medicine, College of Medicine and Health Sciences, Al Ain 17666, Abu Dhabi, United Arab Emirates.
World J Virol. 2022 Sep 25;11(5):310-320. doi: 10.5501/wjv.v11.i5.310.
Pregnant women are among the high-risk population for severe coronavirus disease 2019 (COVID-19) with unfavorable peripartum outcomes and increased incidence of preterm births. Hemolysis, the elevation of liver enzymes, and low platelet count (HELLP) syndrome and severe preeclampsia are among the leading causes of maternal mortality. Evidence supports a higher odd of pre-eclampsia in women with COVID-19, given overlapping pathophysiology. Involvement of angiotensin-converting enzyme 2 receptors by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) for the entry to the host cells and its downregulation cause dysregulation of the renin-angiotensin-aldosterone system. The overexpression of Angiotensin II mediated p38 Mitogen-Activated Protein Kinase pathways can cause vasoconstriction and uninhibited platelet aggregation, which may be another common link between COVID-19 and HELLP syndrome. On PubMed search from January 1, 2020, to July 30, 2022, we found 18 studies on of SARS-COV-2 infection with HELLP Syndrome. Most of these studies are case reports or series, did not perform histopathology analysis of the placenta, or measured biomarkers linked to pre-eclampsia/HELLP syndrome. Hence, the relationship between SARS-CoV-2 infection and HELLP syndrome is inconclusive in these studies. We intend to perform a mini-review of the published literature on HELLP syndrome and COVID-19 to test the hypothesis on association causation, and gaps in the current evidence and propose an area of future research.
孕妇是2019冠状病毒病(COVID-19)的高危人群,围产期结局不佳,早产发生率增加。溶血、肝酶升高和血小板计数降低(HELLP)综合征以及重度子痫前期是孕产妇死亡的主要原因。鉴于病理生理学重叠,有证据支持COVID-19女性患子痫前期的几率更高。严重急性呼吸综合征冠状病毒2(SARS-CoV-2)通过血管紧张素转换酶2受体进入宿主细胞及其下调导致肾素-血管紧张素-醛固酮系统失调。血管紧张素II介导的p38丝裂原活化蛋白激酶途径的过度表达可导致血管收缩和不受抑制的血小板聚集,这可能是COVID-19与HELLP综合征之间的另一个常见联系。在2020年1月1日至2022年7月30日的PubMed搜索中,我们发现了18项关于SARS-CoV-2感染与HELLP综合征的研究。这些研究大多是病例报告或系列研究,未对胎盘进行组织病理学分析,或测量与子痫前期/HELLP综合征相关的生物标志物。因此,在这些研究中,SARS-CoV-2感染与HELLP综合征之间的关系尚无定论。我们打算对已发表的关于HELLP综合征和COVID-19的文献进行小型综述,以检验关于关联因果关系的假设、当前证据中的差距,并提出未来研究的领域。