Low neutrophil alkaline phosphatase score is a new aspect of calreticulin-mutated myeloproliferative neoplasms
Calreticulin ( CALR ) and JAK2 -V617F gene mutations, which are major genetic mutations in patients with primary myelofibrosis (PMF) and essential thrombocythemia (ET), exert different effects on the clinical features and outcomes of these diseases. We analyzed 88 and 9 patients with ET and PMF, res...
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Published in: | SpringerPlus Vol. 5; no. 1; p. 1146 |
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Main Authors: | , , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Cham
Springer International Publishing
22-07-2016
Springer Nature B.V |
Subjects: | |
Online Access: | Get full text |
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Summary: | Calreticulin (
CALR
) and
JAK2
-V617F gene mutations, which are major genetic mutations in patients with primary myelofibrosis (PMF) and essential thrombocythemia (ET), exert different effects on the clinical features and outcomes of these diseases. We analyzed 88 and 9 patients with ET and PMF, respectively, and determined the differences in the clinical characteristics of ET patients with
JAK2
-V617F compared with
CALR
mutations. The frequency of the
JAK2
-V617F and
CALR
mutations were 64 and 22 %, respectively. Patients with
CALR
mutations were younger, had a lower white blood cell count, and had a lower rate of thrombotic events than patients with the
JAK2
mutation. The neutrophil alkaline phosphatase (NAP) score of 16 patients with
CALR
mutations was significantly lower than the normal controls, which was mainly due to the high proportion of NAP-negative neutrophils. This is the first report to show an association between
CALR
mutations in patients with myeloproliferative neoplasms (MPN) and the NAP score. Although the mechanism is unclear, the NAP score could be a useful and reliable biochemical marker to discriminate the mutational status of MPN patients. Further investigation is warranted to determine whether these characteristics contribute to the pathogenesis of MPN and the NAP score. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2193-1801 2193-1801 |
DOI: | 10.1186/s40064-016-2829-6 |