Association between circulating mononuclear cell mitochondrial DNA copy number and in-hospital mortality in septic patients: A prospective observational study based on the Sepsis-3 definition

PLoS One. 2019 Feb 22;14(2):e0212808. doi: 10.1371/journal.pone.0212808. eCollection 2019.

Abstract

Purpose: To explore the association between circulating mononuclear cell mitochondrial DNA copy number and the prognosis of sepsis patients based on the Third International Consensus Definitions for Sepsis and Septic Shock (Sepsis-3 definition).

Methods: A total of 200 adult patients who had recently devoloped sepsis were prospectively recruited as the study cohort. Demographic and clinical data were recorded along with a 28-day outcome. Mononuclear cell mtDNA copy number was assessed by quantitative PCR.

Results: The 28-day outcome of sepsis patients was significantly associated with circulating mononuclear cell mtDNA copy number. The median mononuclear cell relative mtDNA copy number of survivors was significantly higher than that of nonsurvivors (406.68, range 196.65-625.35 vs. 320.57, range 175.98-437.33, p = 0.001). The Cox proportional hazard survival model analysis indicated that mononuclear cell relative mtDNA copy number was significantly negative associated with the 28-day outcome. For every additional unit of mononuclear cell mtDNA relative copy number, the risk of death falls by 0.1% (HR = 0.999, 95% CI = 0.998 to 1.000, p = 0.017).

Conclusions: Our data indicate first that circulating mononuclear cellular mtDNA copy number might be helpful for outcome predictions in sepsis patients, and second that lower mtDNA copy number implied poor prognosis.

Publication types

  • Clinical Trial
  • Observational Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Cell-Free Nucleic Acids / blood*
  • DNA, Mitochondrial / blood*
  • Hospital Mortality*
  • Humans
  • Leukocytes, Mononuclear*
  • Middle Aged
  • Prospective Studies
  • Sepsis* / blood
  • Sepsis* / mortality

Substances

  • Cell-Free Nucleic Acids
  • DNA, Mitochondrial

Grants and funding

The study design and preparation of the manuscript were supported by the grants from the National Nature Science Foundation of China (No.81670621) and the Nature Science Foundation of Zhejiang Province (No. LY16H050001), which were both received by Dr. Yi Yang.