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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, respec...

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Autores principales: Kondo, Toshinori, Tasaka, Taizo, Tomioka, Nanako, Sano, Fuminori, Tokunaga, Hirotoshi, Suemori, Shin-ichiro, Tsujioka, Takayuki, Matsuhashi, Yoshiko, Nakanishi, Hidekazu, Wada, Hideho, Tohyama, Kaoru, Sugihara, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4956637/
https://www.ncbi.nlm.nih.gov/pubmed/27504244
http://dx.doi.org/10.1186/s40064-016-2829-6
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author Kondo, Toshinori
Tasaka, Taizo
Tomioka, Nanako
Sano, Fuminori
Tokunaga, Hirotoshi
Suemori, Shin-ichiro
Tsujioka, Takayuki
Matsuhashi, Yoshiko
Nakanishi, Hidekazu
Wada, Hideho
Tohyama, Kaoru
Sugihara, Takashi
author_facet Kondo, Toshinori
Tasaka, Taizo
Tomioka, Nanako
Sano, Fuminori
Tokunaga, Hirotoshi
Suemori, Shin-ichiro
Tsujioka, Takayuki
Matsuhashi, Yoshiko
Nakanishi, Hidekazu
Wada, Hideho
Tohyama, Kaoru
Sugihara, Takashi
author_sort Kondo, Toshinori
collection PubMed
description 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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spelling pubmed-49566372016-08-08 Low neutrophil alkaline phosphatase score is a new aspect of calreticulin-mutated myeloproliferative neoplasms Kondo, Toshinori Tasaka, Taizo Tomioka, Nanako Sano, Fuminori Tokunaga, Hirotoshi Suemori, Shin-ichiro Tsujioka, Takayuki Matsuhashi, Yoshiko Nakanishi, Hidekazu Wada, Hideho Tohyama, Kaoru Sugihara, Takashi Springerplus Research 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. Springer International Publishing 2016-07-22 /pmc/articles/PMC4956637/ /pubmed/27504244 http://dx.doi.org/10.1186/s40064-016-2829-6 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Research
Kondo, Toshinori
Tasaka, Taizo
Tomioka, Nanako
Sano, Fuminori
Tokunaga, Hirotoshi
Suemori, Shin-ichiro
Tsujioka, Takayuki
Matsuhashi, Yoshiko
Nakanishi, Hidekazu
Wada, Hideho
Tohyama, Kaoru
Sugihara, Takashi
Low neutrophil alkaline phosphatase score is a new aspect of calreticulin-mutated myeloproliferative neoplasms
title Low neutrophil alkaline phosphatase score is a new aspect of calreticulin-mutated myeloproliferative neoplasms
title_full Low neutrophil alkaline phosphatase score is a new aspect of calreticulin-mutated myeloproliferative neoplasms
title_fullStr Low neutrophil alkaline phosphatase score is a new aspect of calreticulin-mutated myeloproliferative neoplasms
title_full_unstemmed Low neutrophil alkaline phosphatase score is a new aspect of calreticulin-mutated myeloproliferative neoplasms
title_short Low neutrophil alkaline phosphatase score is a new aspect of calreticulin-mutated myeloproliferative neoplasms
title_sort low neutrophil alkaline phosphatase score is a new aspect of calreticulin-mutated myeloproliferative neoplasms
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4956637/
https://www.ncbi.nlm.nih.gov/pubmed/27504244
http://dx.doi.org/10.1186/s40064-016-2829-6
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