慢性淋巴细胞白血病和其他淋巴细胞增生性疾病家庭的预测。

Haneef Awan, Viggo Jønsson, Tom B Johannesen, Bernt Ly, Geir E Tjønnfjord
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引用次数: 8

摘要

在38个家庭中独立确定了51对患有慢性淋巴细胞白血病(CLL)或其他淋巴细胞增生性疾病(非CLL),如恶性淋巴瘤、多发性骨髓瘤或其他类型的淋巴细胞白血病。CLL-CLL亲代对30对,亲代和/或子代非cll对21对。当比较所有51对时,后代的发病年龄中位数比父母低13岁(P < 0.001)。这种差异主要是由于父母非CLL的后代发病年龄明显较低(P < 0.001),父亲的疾病主要转移给儿子,而父母患有CLL的后代发病年龄与父母相同(P = 0.130),儿子和女儿的转移几乎相等。低恶性滤泡小b细胞淋巴瘤是非cll的主要诊断。预期被指出是后代比父母发病年龄低的一个可能的机制,即使这种差异的一部分归因于后代比父母更早地使用现代技术进行诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Anticipation in families with chronic lymphocytic leukemia and other lymphoproliferative disorders.

Anticipation in families with chronic lymphocytic leukemia and other lymphoproliferative disorders.

Fifty-one parent-offspring pairs with chronic lymphocytic leukemia (CLL) or other lymphoproliferative disorders (nonCLL) such as malignant lymphoma, multiple myeloma, or other types of lymphocytic leukemia than CLL were ascertained independently in 38 families. There were 30 CLL-CLL parent-offspring pairs and 21 pairs with nonCLL in parents and/or in offspring. The median age of onset of disease was 13 years lower in the offspring than in the parents when comparing all 51 pairs (P < 0.001). This difference was mainly caused by a significantly lower age at onset in offspring with parental nonCLL (P < 0.001) where paternal disease was transferred especially to sons, while affected offspring to parents with CLL have the same age at debut of disease than their parents (P = 0.130) and a nearly equal transfer to sons and daughters. The low-malignant follicular small B-cell lymphoma was the predominant diagnosis within nonCLL. Anticipation is pointed out as one likely mechanism behind the lower age at onset of disease in offspring than in parents, even if a part of this difference is ascribed to a generally earlier diagnosis with modern technology in offspring than in parents.

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