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流产史及后续妊娠中胎儿非整倍体发生率增加。

History of miscarriage and increased incidence of fetal aneuploidy in subsequent pregnancy.

作者信息

Bianco Katherine, Caughey Aaron B, Shaffer Brian L, Davis Regina, Norton Mary E

机构信息

Department of Obstetrics, Gynecology, and Reproductive Sciences, University of California, San Francisco, California 94143, USA.

出版信息

Obstet Gynecol. 2006 May;107(5):1098-102. doi: 10.1097/01.AOG.0000215560.86673.22.

Abstract

OBJECTIVE

The purpose of this study was to examine the association between history of spontaneous abortion and aneuploidy in a subsequent pregnancy.

METHODS

This was a retrospective cohort study of women who underwent fetal karyotype analysis with amniocentesis or chorionic villus sampling at a single prenatal diagnosis center. Information on spontaneous abortions, parity, maternal age, ethnicity, type of prenatal diagnosis, and karyotype was assessed. Univariable and multivariable analyses were conducted.

RESULTS

A total of 46,939 women were included in our analysis. Women with no prior spontaneous abortions had a 1.39% risk for any aneuploidy. In women with one prior spontaneous abortion, this risk increased to 1.67%; for women with 2 previous spontaneous abortions, the risk increased to 1.84%; and for those women who had had 3 or more prior spontaneous abortions, the risk increased further to 2.18% (P < .007). When controlling for maternal age, parity, ethnicity, and mode of prenatal diagnosis and compared with women with no prior spontaneous abortions, women with one prior spontaneous abortion (adjusted odds ratio [AOR] 1.21, 95% confidence interval [CI] 1.01-1.47) or 3 or more prior spontaneous abortions (AOR 1.51, 95% CI 1.02-2.25) had a statistically significant increase in aneuploidy in a subsequent pregnancy. Women with 2 prior spontaneous abortions had an AOR of 1.26 for aneuploidy, but the 95% CI contained unity.

CONCLUSION

An increased risk of karyotypic abnormality identified at the time of prenatal diagnosis is demonstrated in patients with an increasing number of spontaneous abortions. This study provides information regarding this risk among women presenting for prenatal diagnosis. According to our data, for a woman with an a priori risk of 1 in 300 for Down syndrome, 3 prior spontaneous abortions would increase that risk by 47% to 1 in 204. These results should be confirmed in low-risk populations.

摘要

目的

本研究旨在探讨自然流产史与后续妊娠中染色体非整倍体之间的关联。

方法

这是一项对在单一产前诊断中心接受羊膜穿刺术或绒毛取样进行胎儿核型分析的女性进行的回顾性队列研究。评估了自然流产、产次、产妇年龄、种族、产前诊断类型和核型等信息。进行了单变量和多变量分析。

结果

我们的分析共纳入了46939名女性。既往无自然流产史的女性发生任何染色体非整倍体的风险为1.39%。有1次既往自然流产史的女性,该风险增至1.67%;有2次既往自然流产史的女性,风险增至1.84%;而有3次或更多次既往自然流产史的女性,风险进一步增至2.18%(P <.007)。在控制产妇年龄、产次、种族和产前诊断方式后,与既往无自然流产史的女性相比,有1次既往自然流产史(调整优势比[AOR] 1.21,95%置信区间[CI] 1.01 - 1.47)或3次或更多次既往自然流产史(AOR 1.5

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