Evidence map›Paper›PMID 40862415›Full record

ArticleRevista do Instituto de Medicina Tropical de Sao Paulo2025

Findings and outcomes of hospitalized unvaccinated patients during the COVID-19 pandemic: impact of comorbidities on clinical, laboratory, and immunological parameters.

Georon Ferreira de Sousa, Jéssica Pires Farias, Bárbara Rafaela da Silva Barros, Danilo Bancalero Mendonça Lucchi, Simone Ravena Maia Alves, Guilherme Antonio da Souza Silva, Leonardo Carvalho de Oliveira Cruz, Rodrigo Cesar Abreu de Aquino, Edson Barbosa de Souza, Evonio de Barros Campelo Junior and 4 more

Abstract read
In one paragraph

Article in Revista do Instituto de Medicina Tropical de Sao Paulo, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Georon Ferreira de SousaUniversidade Federal de Pernambuco, Centro de Biociências, Laboratório de Análises Imunológicas e Antitumorais, Departamento de Antibióticos, Recife, Pernambuco, Brazil.ORCID http://orcid.org/0000-0001-8780-202X
Jéssica Pires FariasUniversidade de São Paulo, Instituto de Ciências Biomédicas, Departamento de Microbiologia, Laboratório de Desenvolvimento de Vacinas, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0001-5479-8175
Bárbara Rafaela da Silva BarrosUniversidade Federal de Pernambuco, Centro de Biociências, Laboratório de Análises Imunológicas e Antitumorais, Departamento de Antibióticos, Recife, Pernambuco, Brazil.ORCID http://orcid.org/0000-0003-4697-0937
Danilo Bancalero Mendonça LucchiUniversidade Federal de São Paulo, Escola Paulista de Medicina, Departamento de Microbiologia, Imunologia e Parasitologia, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-3860-8957
Simone Ravena Maia AlvesUniversidade Federal de São Paulo, Escola Paulista de Medicina, Departamento de Microbiologia, Imunologia e Parasitologia, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0003-2440-9831
Guilherme Antonio da Souza SilvaUniversidade Federal de Pernambuco, Centro de Biociências, Laboratório de Análises Imunológicas e Antitumorais, Departamento de Antibióticos, Recife, Pernambuco, Brazil.ORCID http://orcid.org/0000-0003-4364-6648
Leonardo Carvalho de Oliveira CruzUniversidade Federal de Pernambuco, Centro de Biociências, Laboratório de Análises Imunológicas e Antitumorais, Departamento de Antibióticos, Recife, Pernambuco, Brazil.ORCID http://orcid.org/0000-0003-4388-3643
Rodrigo Cesar Abreu de AquinoUniversidade Federal de Pernambuco, Centro de Biociências, Laboratório de Análises Imunológicas e Antitumorais, Departamento de Antibióticos, Recife, Pernambuco, Brazil.ORCID http://orcid.org/0000-0002-1883-5001
Edson Barbosa de SouzaUniversidade Federal de Pernambuco, Hospital das Clínicas, Recife, Pernambuco, Brazil.ORCID http://orcid.org/0000-0002-3716-6907
Evonio de Barros Campelo JuniorUniversidade Federal de Pernambuco, Hospital das Clínicas, Recife, Pernambuco, Brazil.ORCID http://orcid.org/0000-0002-9825-9656
Antonio Carlos de FreitasUniversidade Federal de Pernambuco, Centro de Biociências, Departamento de Genética, Laboratório de Estudos Moleculares e Terapia Experimental, Recife, Pernambuco, Brazil.ORCID http://orcid.org/0000-0002-4957-9549
Luís Carlos de Souza FerreiraUniversidade de São Paulo, Instituto de Ciências Biomédicas, Departamento de Microbiologia, Laboratório de Desenvolvimento de Vacinas, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-4883-1693
Carla Torres BraconiUniversidade Federal de São Paulo, Escola Paulista de Medicina, Departamento de Microbiologia, Imunologia e Parasitologia, São Paulo, São Paulo, Brazil.ORCID http://orcid.org/0000-0002-5370-8980
Cristiane Moutinho-MeloUniversidade Federal de Pernambuco, Centro de Biociências, Laboratório de Análises Imunológicas e Antitumorais, Departamento de Antibióticos, Recife, Pernambuco, Brazil.ORCID http://orcid.org/0000-0002-8831-0163

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The COVID-19 pandemic continues to highlight the significant impact of pre-existing comorbidities on disease progression and patient outcomes due to the risk factors for severe disease in unvaccinated patients. We evaluated the association between several clinical/laboratory findings and comorbidities in a cohort of unvaccinated patients hospitalized in the intensive care unit in Recife, Pernambuco State, Brazil. We enrolled 36 unvaccinated volunteers, and performed clinical, biochemical, hematological, and microbiological analyses. Cellular immunity, cytokine measurement, and gene expression were also analyzed. Additionally, serum samples were submitted to serological and neutralization assays by using SARS-CoV-2 B.1 Lineage, Gamma (P.1), Delta (B.1.617.2-like), and Omicron (BA.1) variants. Hypertension was the most common comorbidity in patients requiring oxygen supplementation, followed by diabetes and metabolic syndrome. Such conditions were linked to increased disease severity, with elevated levels of inflammatory biomarkers (D-dimer, C-reactive protein), neutrophilia, and lymphopenia. Chronic inflammation, which is often seen in diabetes and metabolic syndrome, worsens the inflammatory response triggered by COVID-19, which exacerbates endothelial injury and leads to a hypercoagulable state. Additionally, patients with comorbidities had impaired humoral immunity, and showed reduced seroconversion and neutralizing activity, which hindered their ability to combat the virus effectively. Furthermore, this study revealed that patients with diabetes and metabolic syndrome had an exaggerated Th17-driven immune response, which contributed to severe outcomes and multi-organ failure. These findings underscore the importance of personalized care and targeted interventions for patients with comorbidities, thus highlighting the need for further research on metabolic disorders, immune dysfunction, and COVID-19.

Indexed as

COVID-19SARS-CoV-2AdultAgedBrazilComorbidityFemaleHospitalizationHumansIntensive Care UnitsMaleMiddle AgedRisk FactorsSeverity of Illness Index

Identifiers

PMID40862415
PMCPMC12377831

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.