Leucocyte Subsets Effectively Predict the Clinical Outcome of Patients With Covid-19 Pneumonia
A Retrospective Case-Control Study
Dados Bibliográficos
| ID | 22079171 |
|---|---|
| Autores | Jiahua Gan (Tongji Hospital), Jingjing Li (0009-0006-0033-1522, Union Hospital), Shusheng Li (0000-0002-6052-8355, Tongji Hospital), Chunguang Yang (0000-0002-3882-4940, Huazhong University of Science and Technology, autor correspondente) |
| Ano | 2020 |
| Volume | 8 |
| Páginas | 299-299 |
| Data de publicação | 2020-06-18 |
| Peer Reviewed | Sim |
| Open Access | Sim |
| Tipo | ARTICLE |
| Periódico | Frontiers in Public Health (JOURNAL) |
| Identificadores do periódico | ISSN: 2296-2565 • E-ISSN: 2296-2565 |
| Editora | Frontiers Media SA (PUBLISHER • CH) |
| DOI | 10.3389/fpubh.2020.00299 |
| PMID | 32626680 |
| OpenAlex | W3014786535 |
| Idioma | EN |
| Referências citadas | 17 |
Background: Clinical characteristics of the coronavirus disease 2019 (COVID-19) have been well studied, while effective predictors for clinical outcome and research on underlying mechanism are scare. Methods: Hospitalized COVID-19 pneumonia patients with definitive clinical outcome (cured or died) were retrospectively studied. The diagnostic performance of the leucocyte subsets and other parameters were compared using the area under the receiver operating characteristic curve value (AUC). Further, the correlations between leucocyte subsets and inflammation related factors associated with clinical outcome were subsequently investigated. Results: Among 95 subjects included, 56 patients were cured and 39 cases died. Older age, higher aspartate aminotransferase levels, lower albumin levels, higher total bilirubin levels, higher serum lactate dehydrogenase levels, higher blood urea nitrogen levels, higher prothrombin time, high D-dimer levels, higher procalcitonin levels, higher serum cytokines (IL2R, IL6, IL8, IL10 and TNF-α) levels, higher leucocyte count or neutrophil count, lower lymphocyte count indicated poor outcome in patients with COVID-19 pneumonia. Lymphocyte subset (Lymphocyte, T cells, helper T cells, suppressor T cells, natural killer cells, T cells+ B cells+ NK cells) count was positively associated with clinical outcome (AUC: 0.777; AUC: 0.925; AUC: 0.900; AUC: 0.902; AUC: 0.877; AUC: 0.918, resp.). Neutrophil-to-lymphocyte ratio (NLR), neutrophil to T lymphocyte count ratio (NTR), neutrophil percentage to T lymphocyte ratio (NpTR) effectively predicted the mortality (AUC: 0.900; AUC: 0.905; AUC: 0.932, resp.). Binary logistic regression showed that NpTR was an independent prognostic factor for mortality. Serum IL6 levels were positively correlated with leucocyte count, neutrophil count and eosinophil count, while negatively correlated with lymphocyte count. Conclusion: These results indicate that leucocyte subsets predict the clinical outcome of patients with COVID-19 pneumonia in high efficiency. Non-self-limiting inflammatory response is involved in the development of fatal pneumonia
Absolute neutrophil count · Area under the curve · Biology · Lactate dehydrogenase · Logistic regression · Lymphocyte · Neutropenia · Neutrophil to lymphocyte ratio · Pneumonia · Procalcitonin · Receiver operating characteristic · Sepsis · Toxicity · COVID-19 Clinical Research Studies · Long-Term Effects of COVID-19 · Medicine · SARS-CoV-2 and COVID-19 Research · Gastroenterology · Immunology · Internal Medicine
Clinical Characteristics of 138 Hospitalized Patients With 2019 Novel Coronavirus–Infected Pneumonia in Wuhan, China
Pathological findings of Covid-19 associated with acute respiratory distress syndrome
Risk Factors Associated With Acute Respiratory Distress Syndrome and Death in Patients With Coronavirus Disease 2019 Pneumonia in Wuhan, China
Early Transmission Dynamics in Wuhan, China, of Novel Coronavirus–Infected Pneumonia
Clinical course and risk factors for mortality of adult inpatients with Covid-19 in Wuhan, China
A Novel Coronavirus from Patients with Pneumonia in China, 2019
| Velocidade de citação | historical |
|---|---|
| Altamente citado | Não |