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Table 7 Associations between miR expression changes and MRD parameters or risk factors

From: Circulating microRNAs as minimal residual disease biomarkers in childhood acute lymphoblastic leukemia

miR

Time points

Fold change

Independent variable

Patient subgroup

Pearson’s r

Adjusted p

miR-128-3p

Day 8 vs day 0

0.107

Flow cytometry MRD in day 15 bone marrow

Whole cohort

0.88

2.71*10−4

miR-222-3p

Day 8 vs day 0

0.267

Flow cytometry MRD in day 15 bone marrow

Whole cohort

0.81

2.99*10−3

miR-128-3p

Day 8 vs day 0

0.149

Flow cytometry MRD in day 15 bone marrow

Normal karyotypea

0.99

7.53*10−4

miR-222-3p

Day 8 vs day 0

0.270

Flow cytometry MRD in day 15 bone marrow

Normal karyotypea

0.97

2.74*10−2

miR-222-3p

Day 8 vs day 0

0.190

Absolute peripheral blast count on day 8

t(12;21)

0.96

4.63*10−2

miR-181b-5p

Day 33 vs day 0

0.061

Absolute lymphocyte count on day 33

Normal karyotypea

0.95

2.98*10−2

miR-222-3p

Day 33 vs day 0

0.156

Absolute lymphocyte count on day 33

Normal karyotypea

0.94

3.87*10−2

  1. In these analyses, the dependent variable is the normalized miR expression change between the time points compared, all measured in PB PFP. Fold change indicates change in the normalized miR expression between the two time points, the median of these values are provided. Pearson’s r indicates the correlation between the dependent and the independent variables. Adjusted p refers to the statistical significance of the Pearson’s correlation
  2. aNormal karyotype: no alteration on FISH, DNA index diploid and cytogenetics normal or unsuccessful