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自然流产中染色体异常的发生率及谱系:一项12年研究的新见解

Incidence and spectrum of chromosome abnormalities in spontaneous abortions: new insights from a 12-year study.

作者信息

Menasha Joshua, Levy Brynn, Hirschhorn Kurt, Kardon Nataline B

机构信息

Department of Human Genetics, Mount Sinai School of Medicine, New York, New York 10029, USA.

出版信息

Genet Med. 2005 Apr;7(4):251-63. doi: 10.1097/01.gim.0000160075.96707.04.

Abstract

PURPOSE

Despite advances in harvesting and culturing techniques, analysis of the impact of these improvements on the observed frequency of chromosomal abnormalities in spontaneous abortions (SAB) has not been determined. We sought to evaluate the effect of these refinements on the success rate of our cultures and on the resulting frequency of detected chromosomal abnormalities.

METHODS

Between 1990 and 2002, 2301 specimens obtained from the products of conception (POC) of SABs were submitted to our laboratory for cytogenetic analysis. Due to refinements in specimen processing and culture techniques introduced at the end of 1997, our data were analyzed for two periods: Period A from 1990 through 1997 with 907 eligible specimens and Period B from 1998 through 2002 with 1273 eligible specimens.

RESULTS

Modifications in physician communication and sample processing contributed to significant improvements in the culture success rate and in the ratio of male-to-female cases with normal karyotypes. Additionally, increased detection of trisomic, triploid, and multiple aneuploid cases in Period B resulted in a significant increase in the percentage of cases with abnormal karyotypes (42.8% in Period A vs. 65.8% in Period B). Monosomy X accounted for < 10% of all abnormalities in Period B. Eighty five multiple aneuploid karyotypes, including 57 double trisomies, comprised 7.7% of our 1099 abnormal cases. These karyotypes were detected predominantly in POCs from the older women in our study. This collection of multiple aneuploidies is the largest published to date and includes abnormalities not reported in prior studies. We also present a table empirically derived from the data in Period B that indicates the likelihood of a specific abnormal karyotype based on maternal age. The table can be utilized by health care providers, who counsel patients after a spontaneous miscarriage.

CONCLUSION

Improvements in laboratory technique have led to reduced contamination and growth failure of POCs, irrespective of maternal age. This in turn has led to a more balanced male-to-female ratio and to the detection of an increased number of abnormal cases.

摘要

目的

尽管在采集和培养技术方面取得了进展,但这些改进对自然流产(SAB)中观察到的染色体异常频率的影响尚未确定。我们试图评估这些改进对我们培养成功率以及由此产生的检测到的染色体异常频率的影响。

方法

1990年至2002年期间,从2301例自然流产的妊娠产物(POC)中获取的标本被提交到我们实验室进行细胞遗传学分析。由于1997年底引入了标本处理和培养技术的改进,我们的数据按两个时期进行分析:A期为1990年至1997年,有907例符合条件的标本;B期为1998年至2002年,有1273例符合条件的标本。

结果

医生沟通和样本处理方面的改进显著提高了培养成功率以及核型正常的男性与女性病例的比例。此外,B期三体、三倍体和多种非整倍体病例检测的增加导致核型异常病例的百分比显著增加(A期为42.8%,B期为65.8%)。X单体在B期占所有异常的比例不到10%。85种多种非整倍体核型,包括57种双三体,占我们1099例异常病例的7.7%。这些核型主要在我们研究中年龄较大的女性的POC中检测到。这一多种非整倍体的集合是迄今为止发表的最大规模的,并且包括先前研究中未报告的异常情况。我们还给出了一个根据B期数据经验得出的表格,该表格显示了基于母亲年龄的特定异常核型的可能性。该表格可供在自然流产后为患者提供咨询的医疗保健提供者使用。

结论

实验室技术的改进导致POC的污染和生长失败减少,与母亲年龄无关。这反过来又导致了更平衡的男女比例,并检测到更多数量的异常病例。

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