Moorman A V, Roman E, Willett E V, Dovey G J, Cartwright R A, Morgan G J
Leukaemia Research Fund Centre for Clinical Epidemiology at Leeds University, Leeds, UK. anthonym@ lrf.leeds.ac.uk
Cancer Genet Cytogenet. 2001 Apr 15;126(2):155-61. doi: 10.1016/s0165-4608(00)00414-3.
A novel hierarchical cytogenetic classification for acute myeloid leukemia (AML) has been developed. Patients with successful cytogenetics and a diagnosis of AML were categorized into four mutually exclusive karyotype groups: normal, translocation, deletion and trisomy. Patients with more than one chromosomal abnormality were classified using the hierarchy: established translocation>established deletion>established trisomy>non-established translocation>non-established deletion>non-established trisomy. A total of 593 AML patients from a large population-based case-control study of acute leukemia were classified according to their diagnostic karyotype. The four karyotype groups showed different age distributions. Overall the frequency of patients increased with age as did the frequency of patients with a deletion, trisomy or normal karyotype. Although the increase of patients with age was much sharper for patients with a deletion. In contrast, the distribution of patients with a translocation was roughly constant with age. We concluded that there was a link between karyotype and the age of the patient at diagnosis. Furthermore, two karyotype groups, translocations and deletions, may define disease entities with different etiologies. This novel cytogenetic classification will allow other studies to examine whether AML cases with very different types of chromosomal abnormality have the same etiology.
一种针对急性髓系白血病(AML)的新型分层细胞遗传学分类方法已经开发出来。细胞遗传学检查成功且诊断为AML的患者被分为四个相互排斥的核型组:正常、易位、缺失和三体。存在一种以上染色体异常的患者按照以下分层进行分类:已确定的易位>已确定的缺失>已确定的三体>未确定的易位>未确定的缺失>未确定的三体。在一项基于大量人群的急性白血病病例对照研究中,共有593例AML患者根据其诊断性核型进行了分类。这四个核型组显示出不同的年龄分布。总体而言,患者的频率随年龄增加,缺失、三体或正常核型患者的频率也是如此。尽管对于缺失型患者,年龄增长导致的患者增加更为明显。相比之下,易位型患者的分布随年龄大致保持不变。我们得出结论,核型与患者诊断时的年龄之间存在关联。此外,两个核型组,即易位和缺失,可能定义了具有不同病因的疾病实体。这种新型细胞遗传学分类将使其他研究能够检验具有非常不同类型染色体异常的AML病例是否具有相同的病因。