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About:
Gendered effects on inflammation reaction and outcome of COVID‐19 patients in Wuhan
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An Entity of Type :
schema:ScholarlyArticle
, within Data Space :
covidontheweb.inria.fr
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document(s)
Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Gendered effects on inflammation reaction and outcome of COVID‐19 patients in Wuhan
Creator
Wang, Ke
Xu, Shuyun
Zhou, Min
Li, Xiaochen
Shi, Jing
Zhou, Ying
Tao, Yu
Wu, Bo
Qin, Lu
Xie,
Liu, ;
Zhang, ;
Xie, Min
Cheng, Chongsheng
Yu, Muqing
Yue, Junqing
Yang, Zhenyu
Source
Medline; PMC
abstract
BACKGROUND: The rapid outbreak of coronavirus disease 2019 (COVID‐19) has turned into a public health emergency of international concern. Epidemiological research showed that gender was associated with the severity of COVID‐19, but the underlying mechanism of gender predisposition remains poorly understood. We aim to study the gendered differences in inflammation reaction, and the association with severity and mortality of COVID‐19. METHODS: In this retrospective study, we enrolled 548 COVID‐19 inpatients from Tongji Hospital from January 26 to February 5, 2020, and followed up to March 3, 2020. Epidemiological, demographic and clinical features, and inflammatory indexes were collected and compared between males and females. Cox proportional hazard regression model was applied to identify gendered effect on mortality of COVID‐19 after adjusting age, comorbidity and smoking history. Multiple linear regression method was used to explore the influence of sex on inflammation reaction. RESULTS: Males had higher mortality than females did (22.2% vs. 10.4%), with the HR of 1.923 (95% CI, 1.181‐3.130); elder age and comorbidity were significantly associated with decease of COVID‐19 patients. Excess inflammation reaction was related to severity of COVID‐19. Male patients had greater inflammation reaction, with higher levels of IL‐10, TNF‐α, LDH, ferritin and hsCRP, but lower lymphocyte count than females adjusted by age and comorbidity. CONCLUSIONS: Gender, age, and comorbidity are critical risk factors for mortality of COVID‐19. Excess innate immunity and proinflammation activity, and deficiency in adaptive immunity response promote males especially elder males to develop cytokine storm, causing potential ARDS, multiple organ failure and decease. This article is protected by copyright. All rights reserved.
has issue date
2020-06-04
(
xsd:dateTime
)
bibo:doi
10.1002/jmv.26137
bibo:pmid
32497297
has license
no-cc
sha1sum (hex)
99243ed977ec57f29798fee3e4cb5a748a7bb56c
schema:url
https://doi.org/10.1002/jmv.26137
resource representing a document's title
Gendered effects on inflammation reaction and outcome of COVID‐19 patients in Wuhan
has PubMed Central identifier
PMC7300463
has PubMed identifier
32497297
schema:publication
J Med Virol
resource representing a document's body
covid:99243ed977ec57f29798fee3e4cb5a748a7bb56c#body_text
is
schema:about
of
named entity 'public health emergency'
named entity 'study'
named entity 'reaction'
named entity 'Epidemiological'
named entity 'inflammation'
named entity 'survival analysis'
named entity 'pattern recognition receptors'
named entity 'lipopolysaccharide'
named entity 'TNF-α'
named entity 'comorbidity'
named entity 'CFR'
named entity 'COVID-19'
named entity 'chronic obstructive pulmonary disease'
named entity 'COVID-19'
named entity 'HBV'
named entity 'lymphocyte count'
named entity 'medical care'
named entity 'epithelial cell'
named entity 'COPD'
named entity 'edema'
named entity 'Tongji Medical College'
named entity 'macrophages'
named entity 'IL-6'
named entity 'COVID'
named entity 'diabetes'
named entity 'IL-8'
named entity 'hsCRP'
named entity 'organ dysfunction'
named entity 'regression model'
named entity 'cytokines'
named entity 'prognosis'
named entity 'IL-10'
named entity 'comorbidity'
named entity 'MERS'
named entity 'adaptive immunity'
named entity 'hepatitis B virus'
named entity 'Pearson's χ2 test'
named entity 'lymphopenia'
named entity 'COVID'
named entity 'viral infections'
named entity 'immune disorders'
named entity 'March 3, 2020'
named entity 'IL-6'
named entity 'American Thoracic Society'
named entity 'case fatality rate'
named entity 'comorbidity'
named entity 'hypertension'
named entity 'viral replication'
named entity 'case fatality rate'
named entity '95% CI'
named entity 'statistical significance'
named entity 'inflammation'
named entity 'monocyte'
named entity 'SARS-CoV-2'
named entity 'inflammatory cytokines'
named entity 'LPS'
named entity 'IL-6'
named entity 'March 3, 2020'
named entity 'IL-10'
named entity 'C-reactive protein'
named entity 'adaptive immunity'
named entity 'IL-6'
named entity '95% CI'
named entity 'CFR'
named entity 'TNF-α'
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