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唐氏综合征:人口统计学因素及产前诊断对未来活产患病率的影响

Down syndrome: effects of demographic factors and prenatal diagnosis on the future livebirth prevalence.

作者信息

Cornel M C, Breed A S, Beekhuis J R, te Meerman G J, ten Kate L P

机构信息

Department of Medical Genetics, University of Groningen, The Netherlands.

出版信息

Hum Genet. 1993 Sep;92(2):163-8. doi: 10.1007/BF00219685.

Abstract

In northwest European countries maternal age is increasing. This will lead to an increase of the prevalence of Down syndrome conceptuses. Meanwhile, the increased use of prenatal cytogenetic diagnosis (PCD) will lead to a decrease in the prevalence of Down syndrome among livebirths. We were interested to know what the result of these two opposite developments would be in the near future, and we describe here a model to quantify these processes and the resulting livebirth prevalence of Down syndrome. The model is demonstrated for The Netherlands from 1992 to 2001. The predicted livebirth prevalence for The Netherlands in 1992 is 1.36 per 1000. Demographic factors will cause an increase to 1.76 per 1000 in 2001 with present indications for PCD and a utilization ratio of 50%. An increase of the utilization ratio to 90% in 2001 will lead to a prevalence of 1.22 per 1000, a little less than the present prevalence. Alternative screening programs, including maternal serum screening, could lead to a further decrease of the livebirth prevalence. The model described here can be used for evaluation of the consequences of alternative forms of Down syndrome screening.

摘要

在西北欧国家,产妇年龄在增加。这将导致唐氏综合征胎儿患病率上升。与此同时,产前细胞遗传学诊断(PCD)使用的增加将导致活产儿中唐氏综合征的患病率下降。我们想知道这两种相反趋势在不久的将来会产生什么结果,在此我们描述一个模型来量化这些过程以及由此产生的唐氏综合征活产患病率。该模型以1992年至2001年的荷兰为例进行了演示。1992年荷兰预测的活产患病率为每1000例中有1.36例。在目前PCD的指征和50%的利用率情况下,人口因素将导致2001年患病率增至每1000例中有1.76例。2001年利用率增至90%将导致患病率为每1000例中有1.22例,略低于目前的患病率。包括孕妇血清筛查在内的其他筛查方案可能会导致活产患病率进一步下降。这里描述的模型可用于评估唐氏综合征替代筛查形式的后果。

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