Study of biomarkers to determine severity and lung damages in COVID-19 patients

Authors

  • Alfian Nur Rosyid Doctoral Program of Medical Science, Faculty of Medicine, Universitas Airlangga, Surabaya, Indonesia https://orcid.org/0000-0001-7042-996X
  • Arina Dery Puspitasari Universitas Airlangga Hospital, Surabaya, Indonesia
  • Wiwin Is Effendy Department of Pulmonary and Respiratory Medicine, Faculty of Medicine, Universitas Airlangga, Surabaya, Indonesia https://orcid.org/0000-0003-3716-2452
  • Herley Windo Setiawan Department of Pulmonary and Respiratory Medicine, Faculty of Medicine, Universitas Airlangga, Surabaya, Indonesia https://orcid.org/0000-0002-6693-7301
  • Arief Bakhtiar Department of Pulmonary and Respiratory Medicine, Faculty of Medicine, Universitas Airlangga, Surabaya, Indonesia
  • Isnin Anang Marhana Department of Pulmonary and Respiratory Medicine, Faculty of Medicine, Universitas Airlangga, Surabaya, Indonesia
  • Anggraini Dwi Sensusiati Universitas Airlangga Hospital, Surabaya, Indonesia
  • Jusak Nugraha Universitas Airlangga Hospital, Surabaya, Indonesia
  • Muhammad Amin Department of Pulmonary and Respiratory Medicine, Faculty of Medicine, Universitas Airlangga, Surabaya, Indonesia https://orcid.org/0000-0002-7801-6294

DOI:

https://doi.org/10.3855/jidc.19635

Keywords:

COVID-19, infection, biomarkers, lung, severity, pathophysiology

Abstract

Introduction: Identifying inflammation and lung damage markers is crucial in reducing morbidity and mortality of coronavirus disease 2019 (COVID-19). This study aimed to examine the validity and reliability of severity and post-infection lung damage and analyse their relationship.

Methodology: This was a prospective analysis study at the Airlangga University Hospital, Surabaya, Indonesia, from March to August 2021. The infection`s severity was measured by examining angiotensin-converting enzyme 2 (ACE2) levels and complete blood count. Lung damage was estimated by reviewing Krebs von de Lungen (KL)-6, matrix metalloproteinase (MMP)-9, tissue inhibitor metalloproteinase (TIMP)-1, and MMP-9/TIMP-1. Two-factor confirmatory factor analysis (CFA) and canonical correlation were calculated using Lisrel and SPSS (version 25).

Results: The research sample included 76 patients. The t count loading factor values were calculated: ACE2 (6.00), neutrophils (-0.80), lymphocytes (-0.63), neutrophil-lymphocyte ratio (NLR, 1.27), eosinophils (-1.52), basophils (1.72), monocytes (0.05), platelets (0.53), leukocytes (-0.51), platelet-lymphocyte ratio (PLR, -1.15), KL-6 (10.47), MMP-9 (11.91), TIMP-1 (11.79), and MMP-9/TIMP-1 (-0.24). The t values were: neutrophil covariance error (6.11), lymphocytes (6.12), NLR (6.10), eosinophils (6.08), basophils (6.07), monocytes (6.12), platelets (6.12), leukocytes (6.12), PLR (6.10), ACE2 (0.97), KL-6 (5.63), MMP-9 (2.08), TIMP-1 (2.77), and MMP-9/TIMP-1 (6.12). t value canonical correlation of 7.04 (t count > 1.96) indicated a correlation between the severity of the patient and post-infection lung damage.

Conclusions: The severity was adequately measured through ACE2, IL-6, IL-10, neutrophils, lymphocytes, leukocytes, and NLR. Lung damage was measured with KL-6, MMP-9, and TIMP-1. There was a correlation between disease severity and lung damage.

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Published

2024-09-30

How to Cite

1.
Rosyid AN, Puspitasari AD, Effendy WI, Setiawan HW, Bakhtiar A, Marhana IA, Sensusiati AD, Nugraha J, Amin M (2024) Study of biomarkers to determine severity and lung damages in COVID-19 patients. J Infect Dev Ctries 18:1320–1328. doi: 10.3855/jidc.19635

Issue

Section

Coronavirus Pandemic

Funding data