Analysis of the susceptibility to COVID-19 in pregnancy and recommendations on potential drug screening

Eur J Clin Microbiol Infect Dis. 2020 Jul;39(7):1209-1220. doi: 10.1007/s10096-020-03897-6. Epub 2020 Apr 23.

Abstract

To analyze the susceptibility of SARS-CoV-2 in pregnancy and the drugs that can be used to treat pregnancy with COVID-19, so as to provide evidence for drug selection in clinic. By reviewing the existing literature, this paper analyzes the susceptibility of pregnant women to virus, especially to SARS-CoV-2, from the aspects of anatomical, reproductive endocrine and immune changes during pregnancy and screens effective and fetal-safe treatments from the existing drugs. The anatomical structure of the respiratory system is changed during pregnancy, and the virus transmitted by droplets and aerosols is more easily inhaled by pregnant women and is difficult to remove. Furthermore, the prognosis is worse after infection when compared with non-pregnancy women. And changes in reproductive hormones and immune systems during pregnancy collectively make them more susceptible to certain infections. More importantly, angiotensin-converting enzyme (ACE)-2, the SARS-CoV-2 receptor, has been proven highly increased during pregnancy, which may contribute to the susceptibility to SARS-CoV-2. When it comes to treatment, specific drugs for COVID-19 have not been found at present, and taking old drugs for new use in treating COVID-19 has become an emergency method for the pandemic. Particularly, drugs that show superior maternal and fetal safety are worthy of consideration for pregnant women with COVID-19, such as chloroquine, metformin, statins, lobinavir/ritonavir, glycyrrhizic acid, and nanoparticle-mediated drug delivery (NMDD), etc. Pregnant women are susceptible to COVID-19, and special attention should be paid to the selection of drugs that are both effective for maternal diseases and friendly to the fetus. However, there are still many deficiencies in the study of drug safety during pregnancy, and broad-spectrum, effective and fetal-safe drugs for pregnant women need to be developed so as to cope with more infectious diseases in the future.

Keywords: Antiviral treatment; Fetal safety; New coronavirus disease; Pregnancy; Virus susceptibility.

Publication types

  • Review

MeSH terms

  • Angiotensin-Converting Enzyme 2
  • Anti-Inflammatory Agents / therapeutic use
  • Antimalarials / therapeutic use
  • Antiviral Agents / therapeutic use
  • Basal Metabolism
  • Betacoronavirus / metabolism
  • COVID-19
  • COVID-19 Drug Treatment
  • Cardiovascular Physiological Phenomena*
  • Chloroquine / therapeutic use
  • Congenital Abnormalities / epidemiology
  • Coronavirus Infections / drug therapy
  • Coronavirus Infections / epidemiology
  • Coronavirus Infections / immunology
  • Coronavirus Infections / metabolism*
  • Disease Susceptibility / immunology
  • Disease Susceptibility / metabolism
  • Drug Combinations
  • Drug Delivery Systems
  • Female
  • Functional Residual Capacity
  • Glycyrrhizic Acid / therapeutic use
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / therapeutic use
  • Hypoglycemic Agents / therapeutic use
  • Interferon Type I / therapeutic use
  • Lopinavir / therapeutic use
  • Metformin / therapeutic use
  • Nanoparticles
  • Oxygen Consumption
  • Pandemics
  • Peptidyl-Dipeptidase A / metabolism
  • Pneumonia, Viral / drug therapy
  • Pneumonia, Viral / epidemiology
  • Pneumonia, Viral / immunology
  • Pneumonia, Viral / metabolism*
  • Pregnancy / immunology
  • Pregnancy / metabolism
  • Pregnancy / physiology*
  • Pregnancy Complications, Infectious / drug therapy
  • Pregnancy Complications, Infectious / epidemiology
  • Pregnancy Complications, Infectious / immunology
  • Pregnancy Complications, Infectious / metabolism*
  • Progesterone / metabolism
  • Prognosis
  • Respiratory Physiological Phenomena*
  • Ritonavir / therapeutic use
  • SARS-CoV-2
  • Spike Glycoprotein, Coronavirus / metabolism
  • Stillbirth / epidemiology
  • Ventilation-Perfusion Ratio

Substances

  • Anti-Inflammatory Agents
  • Antimalarials
  • Antiviral Agents
  • Drug Combinations
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Hypoglycemic Agents
  • Interferon Type I
  • Spike Glycoprotein, Coronavirus
  • lopinavir-ritonavir drug combination
  • spike protein, SARS-CoV-2
  • Lopinavir
  • Progesterone
  • Glycyrrhizic Acid
  • Chloroquine
  • Metformin
  • Peptidyl-Dipeptidase A
  • ACE2 protein, human
  • Angiotensin-Converting Enzyme 2
  • Ritonavir