Background: Chronic Lymphocytic Leukemia (CLL) has a variable clinical course, of which IgVH mutational status of the malignant B cells is a strong independent predictor for outcome.

Objective: We studied the expression of 5 different genes for their value to predict IgVH mutational status and overall survival (OS).

Methods: mRNA levels were quantified by real time PCR in lymphoprep separated but unsorted blood samples from 110 morphologically and fenotypically characterised CLL patients for the following genes: ZAP70, lipoprotein lipase (LPL), ADAM29, KIAA0610 and nRIP1. Expression levels were compared wih respect to IgVH mutational status (mutation = % germline < 98%), using logistic regression and with respect to OS (= time from day of laboratory tests to death due to any cause), using Cox regression analysis.

Results: The predictive value of the expression of these 5 genes for IgVH mutational status is shown in table 1. Each of these genes showed to be an independent marker for the prediction of IgVH mutational status. LPL as a single marker was the best predictor for mutation. These factors taken together had a high predictive value towards mutational IgVH status (area under ROC curve = 0.93).

table 1

NOdds ratioP value
ZAP70 no 85  
(>5.2) yes 25 0.098 0.002 
LPL no 73  
(>0.04) yes 37 0.029 <0.001 
ADAM29 no 73  
(>30) yes 37 6.61 0.012 
KIAA0610 no 81  
(>0.25) yes 29 0.19 0.045 
NRIP1 no 88  
(>10) yes 22 48.73 0.008 
NOdds ratioP value
ZAP70 no 85  
(>5.2) yes 25 0.098 0.002 
LPL no 73  
(>0.04) yes 37 0.029 <0.001 
ADAM29 no 73  
(>30) yes 37 6.61 0.012 
KIAA0610 no 81  
(>0.25) yes 29 0.19 0.045 
NRIP1 no 88  
(>10) yes 22 48.73 0.008 

The predictive value of IgVH mutation and the expression of these 5 genes for OS is shown in table 2. From the six parameters tested, IgVH mutational status and LPL were predictors for OS at a significant level of 5%, while ZAP70 was of borderline significance.

table 2

Conclusion: measured in unsorted CLL samples, all genes, and especially LPL, had predictive value towards the presence of IgVH mutation. Expression of LPL and absence of mutation were adverse prognostic factors for survival. Thus, the replacement of the assessment of both IgVH mutational status and ZAP70 by assessment of LPL levels for the prediction of prognosis in CLL patients may be considered.

Nsurvival at 24monthsP value
mutation no 36 70%  
 yes 44 93% 0.041 
ZAP70 no 66 87%  
 yes 18 70% 0.078 
LPL no 55 94%  
 yes 29 66% 0.001 
ADAM29 no 57 84%  
 yes 27 84% 0.486 
KIAA0610 no 63 88%  
 yes 21 71% 0.133 
NRIP no 71 81%  
 yes 13 100% 0.167 
Nsurvival at 24monthsP value
mutation no 36 70%  
 yes 44 93% 0.041 
ZAP70 no 66 87%  
 yes 18 70% 0.078 
LPL no 55 94%  
 yes 29 66% 0.001 
ADAM29 no 57 84%  
 yes 27 84% 0.486 
KIAA0610 no 63 88%  
 yes 21 71% 0.133 
NRIP no 71 81%  
 yes 13 100% 0.167 

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