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经产妇年龄调整后的唐氏综合征报告活产患病率的国际差异。

International variation in reported livebirth prevalence rates of Down syndrome, adjusted for maternal age.

作者信息

Carothers A D, Hecht C A, Hook E B

机构信息

MRC Human Genetics Unit, Western General Hospital Edinburgh, UK.

出版信息

J Med Genet. 1999 May;36(5):386-93.

Abstract

Reported livebirth prevalence of Down syndrome (DS) may be affected by the maternal age distribution of the population, completeness of ascertainment, accuracy of diagnosis, extent of selective prenatal termination of affected pregnancies, and as yet unidentified genetic and environmental factors. To search for evidence of the latter, we reviewed all published reports in which it was possible to adjust both for effects of maternal age and for selective termination (where relevant). We constructed indices that allowed direct comparisons of prevalence rates after standardising for maternal age. Reference rates were derived from studies previously identified as having near complete ascertainment. An index value significantly different from 1 may result from random fluctuations, as well as from variations in the factors listed above. We found 49 population groups for which an index could be calculated. Methodological descriptions suggested that low values could often be attributed to under-ascertainment. A possible exception concerned African-American groups, though even among these most acceptable studies were compatible with an index value of 1. As we have reported elsewhere, there was also a suggestive increase in rates among US residents of Mexican or Central American origin. Nevertheless, our results suggest that "real" variation between population groups reported to date probably amounts to no more than +/-25%. However, reliable data in many human populations are lacking including, surprisingly, some jurisdictions with relatively advanced health care systems. We suggest that future reports of DS livebirth prevalence should routinely present data that allow calculation of an index standardised for maternal age and adjusted for elective prenatal terminations.

摘要

报告的唐氏综合征(DS)活产患病率可能受到以下因素影响:人群的母亲年龄分布、确诊的完整性、诊断的准确性、受影响妊娠选择性产前终止的程度,以及尚未明确的遗传和环境因素。为了寻找后者的证据,我们回顾了所有已发表的报告,在这些报告中可以同时调整母亲年龄的影响和选择性终止(如适用)的影响。我们构建了一些指数,以便在对母亲年龄进行标准化后直接比较患病率。参考率来自先前确定为确诊率接近100%的研究。指数值与1有显著差异可能是由于随机波动,也可能是由于上述因素的变化。我们发现有49个人群组可以计算指数。方法学描述表明,低值往往可归因于确诊不足。一个可能的例外是非洲裔美国人组,不过即使在这些组中,大多数可接受的研究的指数值也与1相符。正如我们在其他地方所报告的,墨西哥或中美洲裔美国居民中的患病率也有提示性的增加。然而,我们的结果表明,迄今为止报告的人群组之间的“真实”差异可能不超过±25%。然而,许多人群缺乏可靠数据,令人惊讶的是,包括一些医疗保健系统相对先进的司法管辖区。我们建议,未来关于DS活产患病率的报告应常规提供能够计算针对母亲年龄标准化并针对选择性产前终止进行调整的指数的数据。

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