Early prediction keys for COVID-19 cases progression: A meta-analysis
- PMID: 33848885
- PMCID: PMC7934660
- DOI: 10.1016/j.jiph.2021.03.001
Early prediction keys for COVID-19 cases progression: A meta-analysis
Abstract
BACKGROUNDː: Coronavirus disease 2019 (COVID-19) is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), within few months of being declared as a global pandemic by WHO, the number of confirmed cases has been over 75 million and over 1.6 million deaths since the start of the Pandemic and still counting, there is no consensus on factors that predict COVID-19 case progression despite the diversity of studies that reported sporadic laboratory predictive values predicting severe progression. We review different biomarkers to systematically analyzed these values to evaluate whether are they are correlated with the severity of COVID-19 disease and so their ability to be a predictor for progression.
Methods: The current meta-analysis was carried out to identify relevant articles using eight different databases regarding the values of biomarkers and risk factors of significance that predict progression of mild or moderate cases into severe and critical cases. We defined the eligibility criteria using a PICO model.
Results: Twenty-two relevant articles were selected for meta-analysis the following biomarkers C-reactive protein, interleukin-6, LDH, neutrophil, %PD-1 expression, D-dimer, creatinine, AST and Cortisol all recorded high cut-off values linked to severe and critical cases while low lymphocyte count, and low Albumin level were recorded. Also, we meta- analyzed age and comorbidities as a risk factors of progression as hypertension, Diabetes and chronic obstructive lung diseases which significantly correlated with cases progression (p < 0.05).
Conclusions: ː The current meta-analysis is the first step for analysing and getting cut-off references values of significance for prediction COVID-19 case progression. More studies are needed on patients infected with SARS-CoV-2 and on a larger scale to establish clearer threshold values that predict progression from mild to severe cases. In addition, more biomarkers testing also help in building a scoring system for the prediction and guiding for proper timely treatment.
Keywords: Biomarkers of risk for COVID-19 case progression; COVID-19; Comorbidity of risk for COVID-19 case progression; Meta-analysis; Prediction of critical cases; Prediction of severe cases; SARS-CoV-2.
Copyright © 2021 The Authors. Published by Elsevier Ltd.. All rights reserved.
Figures



Similar articles
-
A meta-analysis of SARS-CoV-2 patients identifies the combinatorial significance of D-dimer, C-reactive protein, lymphocyte, and neutrophil values as a predictor of disease severity.Int J Lab Hematol. 2021 Apr;43(2):324-328. doi: 10.1111/ijlh.13354. Epub 2020 Oct 3. Int J Lab Hematol. 2021. PMID: 33010111 Free PMC article.
-
Laboratory biomarker predictors for disease progression and outcome among Egyptian COVID-19 patients.Int J Immunopathol Pharmacol. 2022 Jan-Dec;36:3946320221096207. doi: 10.1177/03946320221096207. Int J Immunopathol Pharmacol. 2022. PMID: 35622504 Free PMC article.
-
Predictive role of clinical features in patients with coronavirus disease 2019 for severe disease.Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2020 May 28;45(5):536-541. doi: 10.11817/j.issn.1672-7347.2020.200384. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2020. PMID: 32879103 Chinese, English.
-
Risk factors of critical & mortal COVID-19 cases: A systematic literature review and meta-analysis.J Infect. 2020 Aug;81(2):e16-e25. doi: 10.1016/j.jinf.2020.04.021. Epub 2020 Apr 23. J Infect. 2020. PMID: 32335169 Free PMC article.
-
Hematologic, biochemical and immune biomarker abnormalities associated with severe illness and mortality in coronavirus disease 2019 (COVID-19): a meta-analysis.Clin Chem Lab Med. 2020 Jun 25;58(7):1021-1028. doi: 10.1515/cclm-2020-0369. Clin Chem Lab Med. 2020. PMID: 32286245 Review.
Cited by
-
The relationship between C-reactive protein and levels of various cytokines in patients with COVID-19: A systematic review and correlation analysis.Health Sci Rep. 2022 Oct 7;5(6):e868. doi: 10.1002/hsr2.868. eCollection 2022 Nov. Health Sci Rep. 2022. Retraction in: Health Sci Rep. 2023 Jul 25;6(7):e1459. doi: 10.1002/hsr2.1459. PMID: 36248353 Free PMC article. Retracted.
-
COVID-19 lessons to protect populations against future pandemics by implementing PPPM principles in healthcare.EPMA J. 2023 Jul 14;14(3):329-340. doi: 10.1007/s13167-023-00331-7. eCollection 2023 Sep. EPMA J. 2023. PMID: 37605649 Free PMC article. Review.
-
Haematological and radiological-based prognostic markers of COVID-19.J Infect Public Health. 2021 Nov;14(11):1650-1657. doi: 10.1016/j.jiph.2021.09.021. Epub 2021 Sep 30. J Infect Public Health. 2021. PMID: 34627060 Free PMC article.
-
Characteristics of patients with non-severe infections of different SARS-CoV-2 omicron subvariants in China.Front Med (Lausanne). 2024 Dec 18;11:1511227. doi: 10.3389/fmed.2024.1511227. eCollection 2024. Front Med (Lausanne). 2024. PMID: 39744529 Free PMC article.
-
Predictors of Poor Outcome among Critically Ill COVID-19 Patients: A Nationally Representative Sample of the Saudi Arabian Population.J Clin Med. 2022 May 17;11(10):2818. doi: 10.3390/jcm11102818. J Clin Med. 2022. PMID: 35628942 Free PMC article.
References
-
- Hui D.S., Azhar E.I., Madani T.A., Ntoumi F., Kock R., Dar O., et al. The continuing 2019-nCoV epidemic threat of novel coronaviruses to global health — the latest 2019 novel coronavirus outbreak in Wuhan, China. Int J Infect Dis. 2020;91:264–266. doi: 10.1016/j.ijid.2020.01.009. - DOI - PMC - PubMed
-
- WHO | Novel Coronavirus — China [Internet]. World Health Organization [cited Jul 1, 2020]. Available from: http://www.who.int/csr/don/12-january-2020-novel-coronavirus-china/en/.
-
- Gorbalenya Alexander E., Baker Susan C., Baric Ralph S., de Groot Raoul J., Drosten C., Gulyaeva Anastasia A., et al. The species Severe acute respiratory syndrome-related coronavirus: classifying 2019-nCoV and naming it SARS-CoV-2. Nat Microbiol. 2020;5(April (4)):536–544. doi: 10.1038/s41564-020-0695-z. - DOI - PMC - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials
Miscellaneous