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Chronic lymphocytic leukemia (CLL) is characterized by a variety of different genetic abnormalities, including the failure to express the tumor suppressor p53 due to loss of the remaining allele (p53 mutation). Here, we analyzed the impact of p53 mutation on the expression profile of 859 human microRNAs in lymphocytes of CLL patients compared to healthy controls. We observed marked differential expression for 165 microRNAs in p53 wild-type and 17 in p53 mutant CLL. Moreover, we also performed a meta-analysis for the gene expression of 75 microRNAs in 10 different studies comparing normal controls and CLL patients and observed a consistent down-regulation of miR-152 in CLL patients.An individual’s health status and the clinical care they receive are generally determined by personal attributes such as age, gender, race, income and education. The health status and clinical care received by a group of individuals (for example, a panel of members) depend on similar personal attributes. For example, a panel of diabetics are likely to receive worse care as compared to a panel of non-diabetics because of the disease itself, but also because some insurance policies do not pay for insulin and the diabetic panel members are likely to receive poorer medical care than the non-diabetic panel members due to the generally worse health of diabetics.
The aforementioned risks and differences in access to care are more generally applicable to any group of individuals, and so it is desirable to find a mechanism for systematically capturing and analyzing clinical data across all, or a substantial proportion of
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