Severe COVID-19 in pregnancy has a distinct serum profile, including greater complement activation and dysregulation of serum lipids

Background Pregnancies complicated by Coronavirus Disease 2019 (COVID-19) are at an increased risk of severe morbidity due to physiologic changes in immunologic, cardiovascular, and respiratory function. There is little is known about how severity of COVID-19 changes protein and metabolite expression in pregnancy. Objective This study aims to investigate the pathophysiology behind various clinical trajectories in pregnant patients diagnosed with COVID-19 using multi-omics profiling. Study design This is a prospective cohort study of 30 pregnant patients at a single tertiary care center. Participants were categorized by severity of COVID-19 disease (control, asymptomatic, mild/moderate, or severe). Maternal serum samples underwent LC-MS-based multiomics analysis for profiling of proteins, lipids, electrolytes, and metabolites. Linear regression models were used to assess how disease severity related to analyte levels. Reactome pathway enrichment analysis was conducted on differential analytes. Results Of 30 participants, 25 had confirmed diagnosis of COVID-19 (6 asymptomatic (one post-infection), 13 mild/moderate (all post-infection), 6 severe), and 5 participants were controls. Severe COVID-19 was associated with distinct profiles demonstrating significant proteomic and lipidomic signatures which were enriched for annotations related to complement and antibody activity. (FDR < 0.05). Downregulated analytes were not significantly enriched but consisted of annotation terms related to lipoprotein activity (FDR > 0.2). Post-infection mild/moderate COVID-19 did not have significantly altered serum protein, metabolite, or lipid metabolite levels compared to controls. Conclusions Pregnancies with severe COVID-19 demonstrate greater inflammation and complement activation and dysregulation of serum lipids. This altered multiomic expression provides insight into the pathophysiology of severe COVID-19 in pregnancy and may serve as potential indicators for adverse pregnancy outcomes.

[1]  D. Goffman,et al.  The Epidemiology of COVID-19 in Pregnancy , 2021, Clinical obstetrics and gynecology.

[2]  S. Erzurum,et al.  The systemic inflammatory landscape of COVID-19 in pregnancy: Extensive serum proteomic profiling of mother-infant dyads with in utero SARS-CoV-2 , 2021, Cell Reports Medicine.

[3]  C. Nelson-Piercy,et al.  COVID-19 in pregnancy. , 2021, Clinical medicine.

[4]  A. Mangoni,et al.  Serum Complement C3 and C4 and COVID-19 Severity and Mortality: A Systematic Review and Meta-Analysis With Meta-Regression , 2021, Frontiers in Immunology.

[5]  A. Zamora,et al.  Low HDL and high triglycerides predict COVID-19 severity , 2021, Scientific Reports.

[6]  A. Iafrate,et al.  COVID-19-neutralizing antibodies predict disease severity and survival , 2020, Cell.

[7]  Alison Chu,et al.  Perinatal Maternal-Fetal/Neonatal Transmission of COVID-19: A Guide to Safe Maternal and Neonatal Care in the Era of COVID-19 and Physical Distancing. , 2020, NeoReviews.

[8]  E. Holmes,et al.  Blood molecular markers associated with COVID‐19 immunopathology and multi‐organ damage , 2020, The EMBO journal.

[9]  Mark M. Davis,et al.  Multi-Omics Resolves a Sharp Disease-State Shift between Mild and Moderate COVID-19 , 2020, Cell.

[10]  T. Lyngdoh,et al.  Deciphering the COVID‐19 cytokine storm: Systematic review and meta‐analysis , 2020, European journal of clinical investigation.

[11]  Dain R. Brademan,et al.  Large-Scale Multi-omic Analysis of COVID-19 Severity , 2020, Cell Systems.

[12]  Shaoying Huang,et al.  The cytokine storm and COVID‐19 , 2020, Journal of medical virology.

[13]  Huanhuan Gao,et al.  Proteomic and Metabolomic Characterization of COVID-19 Patient Sera , 2020, Cell.

[14]  M. Choolani,et al.  Coronavirus disease 2019 (COVID-19) pandemic and pregnancy , 2020, American Journal of Obstetrics and Gynecology.

[15]  Zunyou Wu,et al.  Characteristics of and Important Lessons From the Coronavirus Disease 2019 (COVID-19) Outbreak in China: Summary of a Report of 72 314 Cases From the Chinese Center for Disease Control and Prevention. , 2020, JAMA.

[16]  M. Daha,et al.  Dysregulation of Complement Activation and Placental Dysfunction: A Potential Target to Treat Preeclampsia? , 2020, Frontiers in Immunology.

[17]  S. Meri,et al.  Regulation of the complement system and immunological tolerance in pregnancy. , 2019, Seminars in immunology.

[18]  Clinical Spectrum of SARS-CoV-2 Infection , 2022 .

[19]  Brad T. Sherman,et al.  Systematic and integrative analysis of large gene lists using DAVID bioinformatics resources , 2008, Nature Protocols.