Review Article

Quantitative and Qualitative Analysis of Circulating Cell-Free DNA Can Be Used as an Adjuvant Tool for Prostate Cancer Screening: A Meta-Analysis

Table 2

Summary diagnostic performance of miRNAs for prostate cancer.

AnalysisGroupSubgroupSensitivity (95% CI)Specificity (95% CI)

Quantitative analysisOverall0.73 (0.62–0.82)0.80 (0.70–0.87)
EthnicityAsian0.73 (0.63–0.81)0.82 (0.63–0.80)
Other ethnicities0.74 (0.61–0.84)0.83 (0.72–0.90)
Sample typesSerum0.81 (0.75–0.86)0.78 (0.68–0.86)
Plasma0.78 (0.65–0.78)0.80 (0.70–0.87)
Source of controlHealthy control0.79 (0.68–0.86)0.82 (0.71–0.91)
BPH/benign patients0.75 (0.70–0.79)0.77 (0.71–0.82)

Qualitative analysisOverall
EthnicityAsian0.32 (0.28–0.36)0.99 (0.96–0.99)
Other ethnicities0.24 (0.22–0.27)0.98 (0.96–0.99)
Sample typesSerum0.19 (0.16–0.21)0.99 (0.98–0.99)
Plasma0.43 (0.32–0.56)0.95 (0.87–0.99)
Source of controlHealthy control0.21 (0.19–0.27)0.99 (0.97–1.00)
BPH/benign patients0.27 (0.25–0.29)0.97 (0.96–0.99)
Assay methodsN-MSP0.39 (0.33–0.45)0.99 (0.97–1.00)
Other methods0.24 (0.22–0.26)0.97 (0.96–0.98)
Methylation gene locationGSTP10.41 (0.25–0.59)0.98 (0.94–1.00)
Other genes0.22 (0.20–0.25)0.98 (0.96–0.99)

MS-PCR (nonquantitative) and quantitative methylation-sensitive PCR; quantitative methylation-specific PCR; spectrophotometric assay; and bisulphite sequencing.