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亚特兰大的唐氏综合征产前诊断、妊娠终止及患病率

Prenatal diagnosis, pregnancy terminations and prevalence of Down syndrome in Atlanta.

作者信息

Siffel Csaba, Correa Adolfo, Cragan Janet, Alverson C J

机构信息

Division of Birth Defects and Developmental Disabilities, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, Atlanta, Georgia 30333, USA.

出版信息

Birth Defects Res A Clin Mol Teratol. 2004 Sep;70(9):565-71. doi: 10.1002/bdra.20064.

Abstract

BACKGROUND

The impact of prenatal diagnosis on the live birth prevalence of Down syndrome (trisomy 21) has been described. This study examines the prevalence of Down syndrome before (1990-1993) and after inclusion of prenatally diagnosed cases (1994-1999) in a population-based registry of birth defects in metropolitan Atlanta.

METHODS

We identified infants and spontaneous fetal deaths with Down syndrome (n = 387), and pregnancies electively terminated after a prenatal diagnosis of Down syndrome (n = 139) from 1990 to 1999 among residents of metropolitan Atlanta from a population-based registry of birth defects, the Metropolitan Atlanta Congenital Defects Program (MACDP). Only diagnoses of full trisomy 21 were included. Denominator information on live births was derived from State of Georgia birth certificate data. We compared the prevalence of Down syndrome by calendar period (1990-1993, 1994-1999), maternal age (<35 years, 35+ years), and race/ethnicity (White, Black, other), using chi-square and Fisher's exact tests.

RESULTS

During the period when case ascertainment was based only on hospitals (1990-1993), the prevalence of Down syndrome was 8.4 per 10,000 live births when pregnancy terminations were excluded and 8.8 per 10,000 when terminations were included. When case ascertainment also included perinatal offices (1994-1999), the prevalence of Down syndrome was 10.1 per 10,000 when terminations were excluded and 15.3 when terminations were included. During 1990-1993, the prevalence of Down syndrome was 24.7 per 10,000 among offspring to women 35+ years of age compared to 6.8 per 10,000 among offspring to women <35 years of age (rate ratio [RR] = 3.65, 95% confidence interval [CI] = 2.53-5.28). During 1994-1999, the prevalence of Down syndrome was 55.3 per 10,000 among offspring to women 35+ years compared to 8.5 per 10,000 among offspring to women <35 years (RR = 6.55, 95% CI = 5.36-7.99). There was no statistically significant variation in the prevalence of Down syndrome by race/ethnicity within maternal age and period of birth strata. During 1994-1999, the proportion of cases that were electively terminated was greater for women 35+ years compared to women <35 years (RR = 5.10, 95% CI = 3.14-8.28), and lower for Blacks compared to Whites among women 35+ years of age (RR = 0.33, 95% CI = 0.16-0.66).

CONCLUSIONS

In recent years, perinatal offices have become an important source of cases of Down syndrome for MACDP, contributing at least 34% of cases among pregnancies in women 35+ years of age. Variation in the prevalence of Down syndrome by race/ethnicity, before or after inclusion of cases ascertained from perinatal offices, was not statistically significant. Among Down syndrome pregnancies in mothers 35+ years we found a lower proportion of elective termination among Black women compared to White women. We suggest that future reports on the prevalence of Down syndrome by race/ethnicity take into account possible variations in the frequency of prenatal diagnosis or elective termination by race/ethnicity.

摘要

背景

已描述了产前诊断对唐氏综合征(21三体)活产患病率的影响。本研究调查了在佐治亚州大都市亚特兰大基于人群的出生缺陷登记处纳入产前诊断病例前后(1990 - 1993年和1994 - 1999年)唐氏综合征的患病率。

方法

我们从基于人群的出生缺陷登记处——大都市亚特兰大先天性缺陷项目(MACDP)中,识别出1990年至1999年期间亚特兰大大都市居民中患有唐氏综合征的婴儿和自然流产胎儿(n = 387),以及产前诊断为唐氏综合征后选择性终止妊娠的孕妇(n = 139)。仅纳入完全21三体的诊断。活产的分母信息来自佐治亚州出生证明数据。我们使用卡方检验和费舍尔精确检验,按日历时间段(1990 - 1993年,1994 - 1999年)、母亲年龄(<35岁,35岁及以上)和种族/族裔(白人、黑人、其他)比较唐氏综合征的患病率。

结果

在仅基于医院确定病例的时期(1990 - 1993年),排除妊娠终止情况时,唐氏综合征的患病率为每10000例活产8.4例,纳入终止妊娠情况时为每10000例8.8例。当病例确定也包括围产期诊所时(1994 - 1999年),排除终止妊娠情况时,唐氏综合征的患病率为每10000例10.1例,纳入终止妊娠情况时为15.3例。在1990 - 1993年期间,35岁及以上女性后代中唐氏综合征的患病率为每10000例24.7例,而35岁以下女性后代中为每10000例6.8例(率比[RR] = 3.65,95%置信区间[CI] = 2.53 - 5.28)。在1994 - 1999年期间,35岁及以上女性后代中唐氏综合征的患病率为每10000例55.3例,而35岁以下女性后代中为每10000例8.5例(RR = 6.55,95% CI = 5.36 - 7.99)。在母亲年龄和出生时间段内,按种族/族裔划分的唐氏综合征患病率无统计学显著差异。在1994 - 1999年期间,35岁及以上女性选择性终止妊娠的比例高于35岁以下女性(RR = 5.10,95% CI = 3.14 - 8.28),在35岁及以上女性中,黑人的比例低于白人(RR = 0.33,95% CI = 0.16 - 0.66)。

结论

近年来,围产期诊所已成为MACDP中唐氏综合征病例的重要来源,在35岁及以上女性的妊娠中至少占34%的病例。纳入围产期诊所确定的病例前后,按种族/族裔划分的唐氏综合征患病率差异无统计学意义。在35岁及以上母亲的唐氏综合征妊娠中,我们发现黑人女性选择性终止妊娠的比例低于白人女性。我们建议未来关于按种族/族裔划分的唐氏综合征患病率的报告应考虑到产前诊断或选择性终止妊娠频率可能因种族/族裔而异。

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