Risk factors contributing to infection with SARS-CoV-2 are modulated by sex

PLoS One. 2024 Feb 28;19(2):e0297901. doi: 10.1371/journal.pone.0297901. eCollection 2024.

Abstract

Throughout the early stages of the COVID-19 pandemic in Mexico (August-December 2020), we closely followed a cohort of n = 100 healthcare workers. These workers were initially seronegative for Immunoglobulin G (IgG) antibodies against SARS-CoV-2, the virus that causes COVID-19, and maintained close contact with patients afflicted by the disease. We explored the database of demographic, physiological and laboratory parameters of the cohort recorded at baseline to identify potential risk factors for infection with SARS-CoV-2 at a follow-up evaluation six months later. Given that susceptibility to infection may be a systemic rather than a local property, we hypothesized that a multivariate statistical analysis, such as MANOVA, may be an appropriate statistical approach. Our results indicate that susceptibility to infection with SARS-CoV-2 is modulated by sex. For men, different physiological states appear to exist that predispose to or protect against infection, whereas for women, we did not find evidence for divergent physiological states. Intriguingly, male participants who remained uninfected throughout the six-month observation period, had values for mean arterial pressure and waist-to-hip ratio that exceeded the normative reference range. We hypothesize that certain risk factors that worsen the outcome of COVID-19 disease, such as being overweight or having high blood pressure, may instead offer some protection against infection with SARS-CoV-2.

MeSH terms

  • Antibodies, Viral
  • COVID-19* / epidemiology
  • Female
  • Health Personnel
  • Humans
  • Immunoglobulin G
  • Male
  • Pandemics / prevention & control
  • Risk Factors
  • SARS-CoV-2*

Substances

  • Immunoglobulin G
  • Antibodies, Viral

Grants and funding

This research was funded by the Consejo Nacional de Humanidades, Ciencia y Tecnología (CONAHCYT México) with grant number 312512 to JDCR, and the CONAHCYT-FORDECYT-PRONACES program with grant number 610285/2020, and grant number 263377/2020 to ALR. Funding was received also from the Dirección General de Asuntos del Personal Académico (DGAPA) from the Universidad Nacional Autónoma de México (UNAM) with grant number PAPIIT IN110321 to RF. OAL is a doctoral student from the Programa de Doctorado en Ciencias Biomédicas from the Universidad Nacional Autónoma de México (UNAM) and has received fellowship 697939 from CONAHCYT México. We are also grateful for financial support from the Research Division of HGMEL with grant number DI/20/501/04/32 to AGAV, NBH, JDCR, EVB, and GE. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.