Better prognosis in females with severe COVID-19 pneumonia: possible role of inflammation as potential mediator. (August 2021)
- Record Type:
- Journal Article
- Title:
- Better prognosis in females with severe COVID-19 pneumonia: possible role of inflammation as potential mediator. (August 2021)
- Main Title:
- Better prognosis in females with severe COVID-19 pneumonia: possible role of inflammation as potential mediator
- Authors:
- Mussini, Cristina
Cozzi-Lepri, Alessandro
Menozzi, Marianna
Meschiari, Marianna
Franceschini, Erica
Rogati, Carlotta
Cuomo, Gianluca
Bedini, Andrea
Iadisernia, Vittorio
Volpi, Sara
Milic, Jovana
Tonelli, Roberto
Brugioni, Lucio
Pietrangelo, Antonello
Girardis, Massimo
Cossarizza, Andrea
Clini, Enrico
Guaraldi, Giovanni
Bacca, Erica
Bedini, Andrea
Borghi, Vanni
Burastero, Giulia
Carli, Federica
Ciusa, Giacomo
Corradi, Luca
Di Gaetano, Margherita
Faltoni, Matteo
Franceschi, Giacomo
Orlando, Gabriella
Pellegrino, Francesco
Puzzolante, Cinzia
Raimondi, Alessandro
Santoro, Antonella
Tutone, Marco
Yaacoub, Dina
Andreotti, Alberto
Biagioni, Emanuela
Bondi, Filippo
Busani, Stefano
Chierego, Giovanni
Scotti, Marzia
Serio, Lucia
Bellinazzi, Caterina
Borella, Rebecca
De Biasi, Sara
De Gaetano, Anna
Fidanza, Lucia
Gibellini, Lara
Iannone, Anna
Lo Tartaro, Domenico
Mattioli, Marco
Paolini, Annamaria
Fogliani, Rossella
Righini, Grazia
Lugli, Mario
… (more) - Abstract:
- Abstract: Objectives: Sex differences in COVID-19 severity and mortality have been described. Key aims of this analysis were to compare the risk of invasive mechanical ventilation (IMV) and mortality by sex and to explore whether variation in specific biomarkers could mediate this difference. Methods: This was a retrospective, observational cohort study among patients with severe COVID-19 pneumonia. A survival analysis was conducted to compare time to the composite endpoint of IMV or death according to sex. Interaction was formally tested to compare the risk difference by sex in sub-populations. Mediation analysis with a binary endpoint IMV or death (yes/no) by day 28 of follow-up for a number of inflammation/coagulation biomarkers in the context of counterfactual prediction was also conducted. Results: Among 415 patients, 134 were females (32%) and 281 males (67%), median age 66 years (IQR 54–77). At admission, females showed a significantly less severe clinical and respiratory profiles with a higher PaO2 /FiO2 (254 mmHg vs. 191 mmHg; p 0.023). By 28 days from admission, 49.2% (95% CI 39.6–58.9%) of males vs. 31.7% (17.9–45.4%) of females underwent IMV or death (log-rank p < 0.0001) and this amounted to a difference in terms of HR of 0.40 (0.26–0.63, p 0.0001). The area under the curve in C-reactive protein (CRP) over the study period appeared to explain 85% of this difference in risk by sex. Discussion: Our analysis confirms a difference in the risk of COVID-19 clinicalAbstract: Objectives: Sex differences in COVID-19 severity and mortality have been described. Key aims of this analysis were to compare the risk of invasive mechanical ventilation (IMV) and mortality by sex and to explore whether variation in specific biomarkers could mediate this difference. Methods: This was a retrospective, observational cohort study among patients with severe COVID-19 pneumonia. A survival analysis was conducted to compare time to the composite endpoint of IMV or death according to sex. Interaction was formally tested to compare the risk difference by sex in sub-populations. Mediation analysis with a binary endpoint IMV or death (yes/no) by day 28 of follow-up for a number of inflammation/coagulation biomarkers in the context of counterfactual prediction was also conducted. Results: Among 415 patients, 134 were females (32%) and 281 males (67%), median age 66 years (IQR 54–77). At admission, females showed a significantly less severe clinical and respiratory profiles with a higher PaO2 /FiO2 (254 mmHg vs. 191 mmHg; p 0.023). By 28 days from admission, 49.2% (95% CI 39.6–58.9%) of males vs. 31.7% (17.9–45.4%) of females underwent IMV or death (log-rank p < 0.0001) and this amounted to a difference in terms of HR of 0.40 (0.26–0.63, p 0.0001). The area under the curve in C-reactive protein (CRP) over the study period appeared to explain 85% of this difference in risk by sex. Discussion: Our analysis confirms a difference in the risk of COVID-19 clinical progression by sex and provides a hypothesis for potential mechanisms leading to this. Specifically, CRP showed a predominant role to mediate the difference in risk by sex. … (more)
- Is Part Of:
- Clinical microbiology and infection. Volume 27:Number 8(2021)
- Journal:
- Clinical microbiology and infection
- Issue:
- Volume 27:Number 8(2021)
- Issue Display:
- Volume 27, Issue 8 (2021)
- Year:
- 2021
- Volume:
- 27
- Issue:
- 8
- Issue Sort Value:
- 2021-0027-0008-0000
- Page Start:
- 1137
- Page End:
- 1144
- Publication Date:
- 2021-08
- Subjects:
- COVID-19 -- COVID-19 pneumonia -- Inflammation -- Mediation -- Prognosis -- Sex differences
Medical microbiology -- Periodicals
Diagnostic microbiology -- Periodicals
Communicable diseases -- Periodicals
Infection -- Periodicals
616.01 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1469-0691 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1016/j.cmi.2020.12.010 ↗
- Languages:
- English
- ISSNs:
- 1198-743X
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.305520
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