Horwitz M, Goode E L, Jarvik G P
Division of Medical Genetics, School of Medicine, University of Washington, Seattle 98195, USA.
Am J Hum Genet. 1996 Nov;59(5):990-8.
Anticipation refers to worsening severity or earlier age at onset with each generation for an inherited disease and primarily has been described for neurodegenerative illnesses resulting from expansion of trinucleotide repeats. We have tested for evidence of anticipation in familial leukemia. Of 49 affected individuals in nine families transmitting autosomal dominant acute myelogenous leukemia (AML), the mean age at onset is 57 years in the grandparental generation, 32 years in the parental generation, and 13 years in the youngest generation (P < .001). Of 21 parent-child pairs with AML, 19 show younger ages at onset in the child and demonstrate a mean decline in age at onset of 28 years (P < .001). Of 18 affected individuals from seven pedigrees with autosomal dominant chronic lymphocytic leukemia (CLL), the mean age at onset in the parental generation is 66 years versus 51 years in the youngest generation (P = .008). Of nine parent-child pairs with CLL, eight show younger ages at onset in the child and reveal a mean decline in age at onset of 21 years (P = .001). Inspection of rare pedigrees transmitting acute lymphocytic leukemia, chronic myelogenous leukemia, multiple types of leukemia, and lymphoma is also compatible with anticipation. Sampling bias is unlikely to explain these findings. This suggests that dynamic mutation of unstable DNA sequence repeats could be a common mechanism of inherited hematopoietic malignancy with implications for the role of somatic mutation in the more frequent sporadic cases. We speculate on three possible candidate genes for familial leukemia with anticipation: a locus on 21q22.1-22.2, CBL2 on 11q23.3, and CBFB or a nearby gene on 16q22.
遗传早现是指一种遗传性疾病在每一代中病情严重程度加重或发病年龄提前,主要见于因三核苷酸重复序列扩增导致的神经退行性疾病。我们对家族性白血病中的遗传早现证据进行了检测。在9个传递常染色体显性急性髓性白血病(AML)的家族中的49名患者中,祖代的平均发病年龄为57岁,亲代的平均发病年龄为32岁,最年轻一代的平均发病年龄为13岁(P <.001)。在21对患有AML的亲子对中,19对显示子代发病年龄更小,发病年龄平均下降28岁(P <.001)。在7个患有常染色体显性慢性淋巴细胞白血病(CLL)的家系中的18名患者中,亲代的平均发病年龄为66岁,而最年轻一代的平均发病年龄为51岁(P =.008)。在9对患有CLL的亲子对中,8对显示子代发病年龄更小,发病年龄平均下降21岁(P =.001)。对传递急性淋巴细胞白血病、慢性髓性白血病、多种白血病及淋巴瘤的罕见家系进行的检查结果也符合遗传早现。抽样偏倚不太可能解释这些发现。这表明不稳定DNA序列重复的动态突变可能是遗传性造血系统恶性肿瘤的常见机制,这对于体细胞突变在更常见的散发性病例中的作用具有启示意义。我们推测了三个可能与遗传早现相关的家族性白血病候选基因:21q22.1 - 22.2上的一个位点、11q23.3上的CBL2以及16q22上的CBFB或其附近的一个基因。