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. 2014 Oct 3;9(10):e109470. doi: 10.1371/journal.pone.0109470

Table 5. Distribution of mtDNA copy number among subgroups of PCa patients stratified by different levels of clinicopathological characteristics.

Variable mtDNA high, No. (%)a mtDNA low, No. (%)a OR (95% CI)b P value
PSA, ng/ml
<10 16 (13.2) 8 (11.1) 1 (reference)
10∼20 11 (9.1) 7 (9.7) 0.66(0.17–2.58) 0.545
≥20 94 (77.7) 57 (79.2) 0.55(0.20–1.53) 0.253
P trend 0.908
AJCC stagec
II A + II B 11 (9.2) 18 (25.4) 1(reference)
III 23 (19.3) 14 (19.7) 2.93(1.01–8.50) 0.049
IV 85 (71.4) 39 (54.9) 3.38(1.33–8.57) 0.010
P trend 0.009
Gleason scored
5–6 29 (24.6) 29 (40.8) 1(reference)
7 45 (38.1) 21 (29.6) 1.80(0.83–3.92) 0.136
8–10 44 (37.3) 21 (29.6) 1.61(0.73–3.53) 0.237
P trend 0.063

Abbreviations: mtDNA  =  mitochondrial DNA; PCa  =  prostate cancer; OR  =  odds ratio; CI  =  confidence intervals; PSA  =  prostate-specific antigen; AJCC  =  American Joint Committee on Cancer.

a

mtDNA copy number was grouped based on the median mtDNA copy number in controls.

b

Analyses were performed using unconditional models adjusted for age, PSA level, AJCC stage and Gleason score where appropriate.

c

Data of AJCC stage were classified by the 7th AJCC staging system; data were not available for 3 cases.

d

Data of Gleason score were not available for 4 cases.