# Enduring insights from sex differences in COVID-19: a retrospective post hoc analysis from a large Italian patient cohort

**Authors:** Carmine Siniscalchi, Angela Guerra, Nicoletta Cerundolo, Pierpaolo Di Micco, Claudio Tana, Beatrice Prati, Alberto Parise, Antonio Nouvenne, Tiziana Meschi

PMC · DOI: 10.3389/fmed.2026.1764966 · Frontiers in Medicine · 2026-02-11

## TL;DR

This study found that female patients with COVID-19 had milder symptoms and lower mortality than males, despite being older and frailer, suggesting biological sex differences in disease response.

## Contribution

The study provides empirical evidence of sex-based differences in clinical and radiological outcomes of early-phase COVID-19.

## Key findings

- Females had lower CT visual scores and less lung involvement compared to males.
- Females showed reduced inflammatory markers and lower in-hospital mortality.
- Female sex was independently protective against mortality in multivariable analysis.

## Abstract

In the early phase of the coronavirus disease 2019 (COVID-19) pandemic, before containment strategies and without vaccines or targeted therapies, clinical outcomes among hospitalized patients were heterogeneous. Preliminary reports suggested possible sex-related differences in susceptibility and disease severity. This study examined sex-based differences in clinical presentation, radiological involvement, laboratory findings, and in-hospital outcomes among patients admitted during the pre-lockdown phase of the outbreak in Italy.

We conducted a retrospective observational study of 689 consecutive adults hospitalized at Parma University Hospital between 28 February and 22 March 2020, with chest CT findings consistent with COVID-19–related interstitial pneumonia, regardless of RT-PCR results. Demographics, comorbidities, symptoms, laboratory parameters, and outcomes were compared between males and females. Lung involvement was quantified using a CT visual score. Multivariable logistic regression identified predictors of in-hospital mortality.

Females accounted for 39% of the cohort and were significantly older and frailer than males, with a higher prevalence of Rockwood ≥7 (15 vs. 5%). Despite this, females demonstrated a lower CT visual score (25 vs. 30%), higher oxygenation parameters, and a less pronounced inflammatory and tissue-damage profile, including lower CRP, LDH, and CPK. Females had shorter hospital stays (5 vs. 6 days) and lower age-adjusted mortality. Multivariable analysis confirmed female sex as independently protective (OR 0.597), an effect largely mediated by reduced radiological lung involvement and attenuated inflammatory response.

Females showed milder radiological and biochemical profiles and reduced mortality despite being older and frailer. These findings highlight intrinsic sex-related biological differences in host response. These early patterns remain relevant today, as sex-specific vulnerability may inform precision medicine and risk stratification.

## Linked entities

- **Diseases:** coronavirus disease 2019 (MONDO:0100096)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, PIK3C2A (phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha) [NCBI Gene 5286] {aka CPK, OCSKD, PI3-K-C2(ALPHA), PI3-K-C2A, PI3K-C2-alpha, PI3K-C2alpha}, ACE2 (angiotensin converting enzyme 2) [NCBI Gene 59272] {aka ACEH}
- **Diseases:** thyroid disorders (MESH:D013959), interstitial pneumonia (MESH:D017563), dementia (MESH:D003704), heart disease (MESH:D006331), asthenia (MESH:D001247), infectious diseases (MESH:D003141), epilepsy (MESH:D004827), death (MESH:D003643), coagulation (MESH:D001778), COVID-19 (MESH:D000086382), hypoxemic respiratory failure (MESH:D012131), COPD (MESH:D029424), pneumonia (MESH:D011014), Fever (MESH:D005334), -damage (MESH:D020263), Frailty (MESH:D000073496), hypoxemia (MESH:D000860), respiratory infections (MESH:D012141), inflammation (MESH:D007249), pulmonary involvement (MESH:C566343), dyslipidemia (MESH:D050171), PD (MESH:D010300), dyspnea (MESH:D004417), Lung (MESH:D008171), endothelial dysfunction (MESH:D014652), lymphopenia (MESH:D008231), diabetes (MESH:D003920), malignancy (MESH:D009369), lung injury (MESH:D055370)
- **Chemicals:** creatinine (MESH:D003404), oxygen (MESH:D010100)
- **Species:** Homo sapiens (human, species) [taxon 9606], Severe acute respiratory syndrome coronavirus 2 (no rank) [taxon 2697049]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12932140/full.md

## References

19 references — full list in the complete paper: https://tomesphere.com/paper/PMC12932140/full.md

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Source: https://tomesphere.com/paper/PMC12932140