Identifying a causal link between prolactin signaling pathways and COVID-19 vaccine-induced menstrual changes

Abstract COVID-19 vaccines have been instrumental tools in the fight against SARS-CoV-2 helping to reduce disease severity and mortality. At the same time, just like any other therapeutic, COVID-19 vaccines were associated with adverse events. Women have reported menstrual cycle irregularity after r...

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Main Authors: Rima Hajjo, Ensaf Momani, Dima A. Sabbah, Nancy Baker, Alexander Tropsha
Format: Article
Language:English
Published: Nature Portfolio 2023-09-01
Series:npj Vaccines
Online Access:https://doi.org/10.1038/s41541-023-00719-6
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author Rima Hajjo
Ensaf Momani
Dima A. Sabbah
Nancy Baker
Alexander Tropsha
author_facet Rima Hajjo
Ensaf Momani
Dima A. Sabbah
Nancy Baker
Alexander Tropsha
author_sort Rima Hajjo
collection DOAJ
description Abstract COVID-19 vaccines have been instrumental tools in the fight against SARS-CoV-2 helping to reduce disease severity and mortality. At the same time, just like any other therapeutic, COVID-19 vaccines were associated with adverse events. Women have reported menstrual cycle irregularity after receiving COVID-19 vaccines, and this led to renewed fears concerning COVID-19 vaccines and their effects on fertility. Herein we devised an informatics workflow to explore the causal drivers of menstrual cycle irregularity in response to vaccination with mRNA COVID-19 vaccine BNT162b2. Our methods relied on gene expression analysis in response to vaccination, followed by network biology analysis to derive testable hypotheses regarding the causal links between BNT162b2 and menstrual cycle irregularity. Five high-confidence transcription factors were identified as causal drivers of BNT162b2-induced menstrual irregularity, namely: IRF1, STAT1, RelA (p65 NF-kB subunit), STAT2 and IRF3. Furthermore, some biomarkers of menstrual irregularity, including TNF, IL6R, IL6ST, LIF, BIRC3, FGF2, ARHGDIB, RPS3, RHOU, MIF, were identified as topological genes and predicted as causal drivers of menstrual irregularity. Our network-based mechanism reconstruction results indicated that BNT162b2 exerted biological effects similar to those resulting from prolactin signaling. However, these effects were short-lived and didn’t raise concerns about long-term infertility issues. This approach can be applied to interrogate the functional links between drugs/vaccines and other side effects.
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spelling doaj.art-22fcaec77d4a41caa482049a41f886d02023-11-26T12:16:38ZengNature Portfolionpj Vaccines2059-01052023-09-018111510.1038/s41541-023-00719-6Identifying a causal link between prolactin signaling pathways and COVID-19 vaccine-induced menstrual changesRima Hajjo0Ensaf Momani1Dima A. Sabbah2Nancy Baker3Alexander Tropsha4Department of Pharmacy, Faculty of Pharmacy, Al-Zaytoonah University of JordanDepartment of Basic Medical sciences, Faculty of Medicine, Al Balqa’ Applied UniversityDepartment of Pharmacy, Faculty of Pharmacy, Al-Zaytoonah University of JordanParlezChemLaboratory for Molecular Modeling, Division of Chemical Biology and Medicinal Chemistry, Eshelman School of Pharmacy, The University of North Carolina at Chapel HillAbstract COVID-19 vaccines have been instrumental tools in the fight against SARS-CoV-2 helping to reduce disease severity and mortality. At the same time, just like any other therapeutic, COVID-19 vaccines were associated with adverse events. Women have reported menstrual cycle irregularity after receiving COVID-19 vaccines, and this led to renewed fears concerning COVID-19 vaccines and their effects on fertility. Herein we devised an informatics workflow to explore the causal drivers of menstrual cycle irregularity in response to vaccination with mRNA COVID-19 vaccine BNT162b2. Our methods relied on gene expression analysis in response to vaccination, followed by network biology analysis to derive testable hypotheses regarding the causal links between BNT162b2 and menstrual cycle irregularity. Five high-confidence transcription factors were identified as causal drivers of BNT162b2-induced menstrual irregularity, namely: IRF1, STAT1, RelA (p65 NF-kB subunit), STAT2 and IRF3. Furthermore, some biomarkers of menstrual irregularity, including TNF, IL6R, IL6ST, LIF, BIRC3, FGF2, ARHGDIB, RPS3, RHOU, MIF, were identified as topological genes and predicted as causal drivers of menstrual irregularity. Our network-based mechanism reconstruction results indicated that BNT162b2 exerted biological effects similar to those resulting from prolactin signaling. However, these effects were short-lived and didn’t raise concerns about long-term infertility issues. This approach can be applied to interrogate the functional links between drugs/vaccines and other side effects.https://doi.org/10.1038/s41541-023-00719-6
spellingShingle Rima Hajjo
Ensaf Momani
Dima A. Sabbah
Nancy Baker
Alexander Tropsha
Identifying a causal link between prolactin signaling pathways and COVID-19 vaccine-induced menstrual changes
npj Vaccines
title Identifying a causal link between prolactin signaling pathways and COVID-19 vaccine-induced menstrual changes
title_full Identifying a causal link between prolactin signaling pathways and COVID-19 vaccine-induced menstrual changes
title_fullStr Identifying a causal link between prolactin signaling pathways and COVID-19 vaccine-induced menstrual changes
title_full_unstemmed Identifying a causal link between prolactin signaling pathways and COVID-19 vaccine-induced menstrual changes
title_short Identifying a causal link between prolactin signaling pathways and COVID-19 vaccine-induced menstrual changes
title_sort identifying a causal link between prolactin signaling pathways and covid 19 vaccine induced menstrual changes
url https://doi.org/10.1038/s41541-023-00719-6
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