Changes in circulating cell-free nuclear DNA and mitochondrial DNA of patients with adolescent idiopathic scoliosis

BMC Musculoskelet Disord. 2019 Oct 25;20(1):479. doi: 10.1186/s12891-019-2869-5.

Abstract

Background: Adolescent idiopathic scoliosis (AIS) which characterized by complex three-dimensional deformity of spine has been difficult to cure because of the unknown etiopathology and uncertainty of progression. Nowadays, circulating cell-free (ccf) DNA was found to be a potential biomarker for several benign and malignant diseases. However, whether ccf DNA can be a biomarker for AIS has not been reported yet. In this study, we investigate the circulating cell-free nuclear DNA (ccf n-DNA) and mitochondrial DNA (ccf mt-DNA) concentrations in the plasma of patients with AIS and controls (CT), and the changed plasma ccf n-DNA and ccf mt-DNA levels and their association with clinical parameters were assessed.

Methods: The plasma of peripheral blood from 69 AIS patients and 21 age-matched CT was collected for ccf DNA analysis. Quantitative PCR was used to detect ccf n-DNA and ccf mt-DNA levels, and correlation analyses between the ccf n-DNA and ccf mt-DNA levels and clinical characteristics were conducted. Receiver operator curves (ROC) were used to analyze the sensitivity and specificity of ccf n-DNA and ccf mt-DNA levels to different characteristics.

Results: The plasma ccf n-DNA levels of both GAPDH and ACTB were significantly decreased in AIS patients compared with those in controls, while the plasma ccf mt-DNA levels did not changed. According to sex-related analyses, the ccf n-DNA levels in male CT-M was higher than that in female CT and male AIS, but the ccf n-DNA levels in female AIS was not significantly changed when compared with male AIS or female CT. However, the concentration of ccf mt-DNA in female AIS increased significantly when compared with male AIS. Surprisingly, Lenke type-related analyses suggested that Lenke type 1 patients had lower ccf n-DNA levels, whereas Lenke type 5 patients had higher ccf mt-DNA levels compared with those of controls. However, a lower sensitivity and specificity of AIS predicted by ccf n-DNA or ccf mt-DNA levels was observed, whether in total, by sex, or by Lenke type.

Conclusion: Although with no/little predictive accuracy of AIS/progressed AIS by ccf DNA levels, significantly changed plasma ccf DNA levels were observed in AIS patients compared with those in controls.

Keywords: Adolescent idiopathic scoliosis; Circulating cell-free mitochondrial DNA; Circulating cell-free nuclear DNA; Lenke types; Sex differences.

MeSH terms

  • Actins / genetics
  • Adolescent
  • Biomarkers / blood
  • Cell Nucleus / genetics
  • Cell-Free Nucleic Acids / blood*
  • Cell-Free Nucleic Acids / isolation & purification
  • Child
  • DNA, Mitochondrial / blood*
  • DNA, Mitochondrial / isolation & purification
  • Disease Progression
  • Female
  • Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating) / genetics
  • Humans
  • Male
  • Predictive Value of Tests
  • Real-Time Polymerase Chain Reaction
  • Retrospective Studies
  • Scoliosis / blood
  • Scoliosis / diagnosis*
  • Scoliosis / genetics
  • Sensitivity and Specificity
  • Sex Factors

Substances

  • Actins
  • Biomarkers
  • Cell-Free Nucleic Acids
  • DNA, Mitochondrial
  • Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating)