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Cytogenetic Profile of de novo Acute Myeloid Leukemia Patients in Malaysia
Acute myeloid leukemia (AML) is a heterogeneous disease in terms of cytogenetics and molecular genetics. AML is the most common acute leukemia in adults and its incidence increases with age. Diagnostic cytogenetics is an important prognostic indicator for predicting outcome of AML. We examined the k...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Master Publishing Group
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3644412/ https://www.ncbi.nlm.nih.gov/pubmed/23675286 |
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author | Meng, Chin Yuet Noor, Puteri J. Ismail, Azli Ahid, Mohd Fadly Md Zakaria, Zubaidah |
author_facet | Meng, Chin Yuet Noor, Puteri J. Ismail, Azli Ahid, Mohd Fadly Md Zakaria, Zubaidah |
author_sort | Meng, Chin Yuet |
collection | PubMed |
description | Acute myeloid leukemia (AML) is a heterogeneous disease in terms of cytogenetics and molecular genetics. AML is the most common acute leukemia in adults and its incidence increases with age. Diagnostic cytogenetics is an important prognostic indicator for predicting outcome of AML. We examined the karyotypic patterns of 480 patients with de novo AML seen at government hospitals throughout the country and evaluated the association of chromosome aberrations with the age of patient. Chromosome abnormalities were detected in 146 (30.4%) patients. The most common cytogenetic abnormality was balanced translocation t (8; 21), followed by trisomy 8 (as sole abnormality) and t (15; 17). The age of our Malaysian patients at diagnosis ranged from four months to 81 years, with a median age of 39 years. The normal karyotype was found mainly in patients aged 15-30 years. About 75% of patients with t (8; 21) were below 40 years of age, and the complex karyotype was found with the highest frequently (34.3%) in elderly patients (age above 60 years). More than half of the patients with complex karyotype were above 50 years of age. The deletion 5q was detected only in patients aged above 50 years. Different cytogenetic abnormalities in AML show different frequencies with increasing age. Probably different genetic mechanisms are involved in the pathogenesis of AML and these mechanisms might occur at different frequencies over lifetime. |
format | Online Article Text |
id | pubmed-3644412 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Master Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-36444122013-05-07 Cytogenetic Profile of de novo Acute Myeloid Leukemia Patients in Malaysia Meng, Chin Yuet Noor, Puteri J. Ismail, Azli Ahid, Mohd Fadly Md Zakaria, Zubaidah Int J Biomed Sci Original Article Acute myeloid leukemia (AML) is a heterogeneous disease in terms of cytogenetics and molecular genetics. AML is the most common acute leukemia in adults and its incidence increases with age. Diagnostic cytogenetics is an important prognostic indicator for predicting outcome of AML. We examined the karyotypic patterns of 480 patients with de novo AML seen at government hospitals throughout the country and evaluated the association of chromosome aberrations with the age of patient. Chromosome abnormalities were detected in 146 (30.4%) patients. The most common cytogenetic abnormality was balanced translocation t (8; 21), followed by trisomy 8 (as sole abnormality) and t (15; 17). The age of our Malaysian patients at diagnosis ranged from four months to 81 years, with a median age of 39 years. The normal karyotype was found mainly in patients aged 15-30 years. About 75% of patients with t (8; 21) were below 40 years of age, and the complex karyotype was found with the highest frequently (34.3%) in elderly patients (age above 60 years). More than half of the patients with complex karyotype were above 50 years of age. The deletion 5q was detected only in patients aged above 50 years. Different cytogenetic abnormalities in AML show different frequencies with increasing age. Probably different genetic mechanisms are involved in the pathogenesis of AML and these mechanisms might occur at different frequencies over lifetime. Master Publishing Group 2013-03 /pmc/articles/PMC3644412/ /pubmed/23675286 Text en © Chin Yuet Meng et al. Licensee Master Publishing Group http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.5/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Original Article Meng, Chin Yuet Noor, Puteri J. Ismail, Azli Ahid, Mohd Fadly Md Zakaria, Zubaidah Cytogenetic Profile of de novo Acute Myeloid Leukemia Patients in Malaysia |
title | Cytogenetic Profile of de novo Acute Myeloid Leukemia Patients in Malaysia |
title_full | Cytogenetic Profile of de novo Acute Myeloid Leukemia Patients in Malaysia |
title_fullStr | Cytogenetic Profile of de novo Acute Myeloid Leukemia Patients in Malaysia |
title_full_unstemmed | Cytogenetic Profile of de novo Acute Myeloid Leukemia Patients in Malaysia |
title_short | Cytogenetic Profile of de novo Acute Myeloid Leukemia Patients in Malaysia |
title_sort | cytogenetic profile of de novo acute myeloid leukemia patients in malaysia |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3644412/ https://www.ncbi.nlm.nih.gov/pubmed/23675286 |
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