Evidence map›Paper›PMID 40735564›Full record

ArticlePakistan journal of medical sciences2025

Landscape of somatic mutations in myeloproliferative neoplasm in Pakistani population.

Mehreen Ali Khan, Suhaib Ahmed, Muhammad Arif Sadiq, Maryam Khan, Memoona Khan, Zaineb Akram

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Article in Pakistan journal of medical sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Mehreen Ali KhanMehreen Ali Khan, MCPS, FCPS, Armed Forces Bone Marrow Transplant Centre, Rawalpindi, Pakistan.
Suhaib AhmedSuhaib Ahmed, FCPS, PhD Department of Pathology, Riphah International University, Islamabad, Pakistan.
Muhammad Arif SadiqMuhammad Arif Sadiq, FCPS, PhD, Armed Forces Bone Marrow Transplant Centre, Rawalpindi, Pakistan.
Maryam KhanMaryam Khan, MRCP, FCPS, Armed Forces Bone Marrow Transplant Centre, Rawalpindi, Pakistan.
Memoona KhanMemoona Khan, FCPS, Armed Forces Bone Marrow Transplant Centre, Rawalpindi, Pakistan.
Zaineb AkramZaineb Akram, PhD Department of Biological Sciences, National University of Medical Sciences, Islamabad, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: This study aimed to screen myeloproliferative neoplasm (MPN) patients for four known genetic variants to establish a diagnosis before treatment. Methods: This descriptive cross-sectional study was conducted at the Armed Forces Bone Marrow Transplant Center (AFBMTC), Rawalpindi, between January 2018 to January 2021. A total of 159 MPN patients were enrolled. Peripheral blood samples were screened for somatic variants in JAK2 V617F, JAK2 exon 12, CALR, and cMPL genes. The JAK2 V617F and cMPL mutations were analyzed using conventional PCR, while JAK2 Exon 12 and CALR mutations were analyzed using the fragment analysis technique. The gene scan data was interpreted by analyzing the electropherograms and the genotyping data sheet. The data were analyzed using the Statistical Package for Social Sciences (SPSS) version 25.0. Results: Out of a total of 159 MPN patients, 104 (65.4%) were males and 55 (34.6%) females. The median age of patients was 54 years (IQR: 38-64). 69 (43.4%) were diagnosed with primary myelofibrosis (PMF), 60 (37.7%) as polycythemia vera (PV), and 30 (18.9%) as essential thrombocytosis (ET). The frequency of the JAK2 V617F mutation in PV, ET, and PMF patients was 52.6%, 11.1%, and 37.3%, respectively. CALR mutation was observed only in 1 PMF and 5 (16.7%) ET patients. Additionally, cMPL mutation was not found among our patients. Conclusions: The four analyzed mutations are among the diagnostic criteria established by the World Health Organization, which enable a quick and reliable diagnosis of MPN.

Indexed as

CALRJAK2 exon 12JAK2 V617FMyeloproliferative neoplasm

Identifiers

PMID40735564
PMCPMC12302079

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