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. 2015 Feb 6;33(4):1639–1649. doi: 10.3892/or.2015.3787

Table V.

Association of miR-24 expression and clinical features with the risk of relapse to ALL.

Without relapse
n (%)
With relapse
n (%)
P-value Univariate analysis Multivariate analysis


OR CI 95% P-valuea OR CI 95% P-valueb
Gender
 Female 16 (41.03) 25 (34.72) 0.542 1.00
 Male 23 (58.97) 47 (65.28) 1.31 0.59–2.91 0.512
Immunophenotype
 B-lineage 36 (92.31) 57 (79.17) 1.00
 T-lineage 2 (5.13) 9 (12.50) 0.198 2.84 0.58–13.90 0.197
 B/T-lineage 1 (2.56) 6 (8.33) 3.78 0.44–32.78 0.226
 B-lineage 36 (92.31) 57 (79.17) 1.00
 T-lineage + B/T-lineage 3 (7.69) 15 (20.83) 0.105 3.15 0.85–11.67 0.085
FAB classification
 ALL
  L1 31 (79.49) 62 (86.11) 1.60 0.57–4.46 0.369
  L2 8 (20.51) 10 (13.89) 0.423 1.00
Risk by age and leukocytes at diagnosis
 Low-risk (1–10 years and <50,000 leukocytes/mm3) 27 (69.23) 21 (29.17) <0.001c 1.00
 High-risk (<1 and >10 years and >50,000 leukocytes/mm3) 12 (30.77) 51 (70.83) 5.46 2.34–12.77 <0.001c 5.20 2.19–12.32 <0.001c
miR-24 levels
 Downregulated 27 (69.23) 34 (47.22) 0.030c 1.00
 Upregulated 12 (30.77) 38 (52.78) 2.51 1.10–5.72 0.028c 2.27 1. 94–5.51 0.020c

OR, odds ratio; CI, confidence interval;

a

p-value was obtained by logistic regression analysis, taking reference to female, B-lineage, L2, 1–10 years, <50,000 leukocytes/mm3 (low-risk) and downregulated levels of miR-24.

b

p-value was obtained by multivariate logistic regression analysis.

c

Significant p<0.05, ALL, acute lymphoblastic leukemia.