Huether C A, Haroldson K, Ellis P M, Ramsay C N
Department of Biological Sciences, University of Cincinnati, OH 45221-0006, USA.
Genet Epidemiol. 1996;13(4):367-75. doi: 10.1002/(SICI)1098-2272(1996)13:4<367::AID-GEPI5>3.0.CO;2-1.
Ramsay et al. [(1991) Biomed Pharmacother 45:267-272] reported on the livebirth prevalence of Down syndrome in the Lothian region of Scotland during 1978-1989. Their results suggested a temporal association between the events of Chernobyl in April 1986 and a significant-excess of cases in 1987. In the current study the data were extended for 3 years and reanalyzed, a major objective being to correct for the differential loss of fetuses with Down syndrome which occurs between prenatal diagnosis and birth. Other objectives were to estimate the prevalence reduction due to prenatal diagnosis, quinquennial maternal age-specific risk rates, and the level of ascertainment of cases. The reanalysis found a 12-year prevalence rate of 1.29 vs. the previous rate of 1.34, and a shift of the annual prevalence peak to 1988, with a reduced prevalence in 1987 compared to that found in the earlier study. The new results are less consistent in showing an association of Down syndrome clustering with the Chernobyl accident. For the 15-year study period, a 23% overall reduction in prevalence occurred due to prenatal diagnosis and elective abortion of affected fetuses, with a 50% reduction to women > or = 35 years of age. For 1988-1992, these reductions were 33% and 60%, which are among the highest reported in the literature for these time periods. The estimated quinquennial maternal risk rates were very similar to others already reported, and the data are consistent with a high level of case ascertainment. Since these women are approaching the upper limits of fetal detection through advanced maternal age alone, continued reduction in prevalence rates for Down syndrome through prenatal diagnosis and elective abortion will come mostly from increased use of other (chemical) screening techniques now available.
拉姆齐等人[(1991年)《生物医学与药物治疗》45:267 - 272]报告了1978 - 1989年期间苏格兰洛锡安地区唐氏综合征的活产患病率。他们的结果表明,1986年4月切尔诺贝利事件与1987年病例显著增多之间存在时间关联。在当前研究中,数据延长了3年并重新进行分析,一个主要目标是校正产前诊断和出生之间唐氏综合征胎儿的差异丢失情况。其他目标是估计产前诊断导致的患病率降低、每五年的孕产妇年龄特异性风险率以及病例的确诊水平。重新分析发现12年患病率为1.29,而之前的患病率为1.34,年患病率峰值转移到了1988年,与早期研究相比,1987年的患病率有所降低。新结果在显示唐氏综合征聚集与切尔诺贝利事故的关联方面不太一致。在15年的研究期内,由于产前诊断和对受影响胎儿的选择性流产,总体患病率降低了23%,35岁及以上女性的患病率降低了50%。对于1988 - 1992年,这些降低率分别为33%和60%,这是这些时间段文献中报道的最高降幅之一。估计的每五年孕产妇风险率与其他已报道的非常相似,并且数据与高病例确诊水平一致。由于这些女性仅通过高龄产妇已接近胎儿检测的上限,通过产前诊断和选择性流产持续降低唐氏综合征的患病率将主要来自更多使用现有的其他(化学)筛查技术。