Cell-free DNA as prognostic and diagnostic biomarkers for adult sepsis: a systematic review and meta-analysis

Author:

Charoensappakit Awirut1,Sae-khow Kritsanawan2,Rattanaliam Pongpera3,Vutthikraivit Nuntanuj4,Pecheenbuvan Monvasi4,Udomkarnjananun Suwasin5,leelahavanichkul Asada2

Affiliation:

1. Medical Microbiology, Interdisciplinary and International Program, Graduate School, Chulalongkorn University

2. Center of Excellence on Translational Research in Inflammation and Immunology (CETRII), Faculty of Medicines, Chulalongkorn University

3. Department of Clinical Microscopy, Faculty of Allied Health Sciences, Chulalongkorn University

4. Division of Critical Care Medicine, Department of Internal Medicine, Chulalongkorn University

5. Division of Nephrology, Department of Medicine, Faculty of Medicine, Chulalongkorn University

Abstract

Abstract Background: Although cell-free DNA (cfDNA) is an emerging sepsis biomarker, the use of cfDNA, especially as diagnostic and prognostic indicators, has surprisingly not been systemically analyzed. Methods: Data of adult patients with sepsis that conducted cfDNA measurement within 24 h of the admission was collected from PubMed, ScienceDirect, Scopus, and Cochrane Library until October 2022. The Quality in Prognosis Studies (QUIPS) and Quality Assessment in Diagnostic Studies-2 (QUADAS-2) tools were used to reduce the risk of biased assessment. The mean difference (MD) of cfDNA concentration and the standardized mean difference (SMD) between populations was calculated using Review Manager (RevMan) version 5.4.1 package software. Results: Pooled analysis from 18 included studies demonstrated increased serum cfDNA levels in sepsis when compared with healthy control (SMD = 1.02; 95% confidence interval (CI) 0.46-1.57) or non-sepsis patients in the intensive care unit (ICU) (SMD = 1.03; 95% CI 0.65-1.40), respectively. Meanwhile, a slight decrease in the statistical value was observed when compared with non-sepsis ICU patients with SIRS (SMD = 0.74; 95% 0.41-1.06). The lower cfDNA levels were also observed in sepsis survivors compared to the non-survivors (SMD at 1.43; 95%CI 0.69-2.17) with the pooled area under the receiver operating characteristic curve (AUC) of 0.76 (95% CI 0.64-0.87) for the mortality prediction. Levels of cfDNA showed a pooled sensitivity of 0.81 (95% CI 0.75 - 0.86) and specificity of 0.72 (95% CI 0.65 - 0.78) with pooled diagnostic odd ratio (DOR) at 25.03 (95% CI 5.48 – 114.43) for the identification of sepsis in critically ill conditions. Conclusions: The cfDNA levels were significantly higher in patients with sepsis and being a helpful indicator for the critically ill conditions of sepsis. Nevertheless, results of the test must be interpreted carefully with the context of all clinical situations.

Publisher

Research Square Platform LLC

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