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非典型性筛查还是特异性筛查:哪种在检测非唐氏染色体异常方面更具优势?

Atypicality or specific screen: which is better at detecting non-Down's chromosomal anomalies?

作者信息

Reynolds T M

机构信息

Clinical Chemistry Department, Queen's Hospital, Burton-on-Trent, Staffordshire, UK.

出版信息

Ann Clin Biochem. 1997 Nov;34 ( Pt 6):675-80. doi: 10.1177/000456329703400613.

Abstract

I evaluated the value of adding a trisomy 18 screen to routine Down's screening and compared it with the benefits of atypicality screening. I studied 5080 unaffected pregnancies, 144 Down's syndrome and 190 non-Down's syndrome chromosome abnormalities (20 trisomy 13; 79 trisomy 18; 20 Turner's syndrome; 29 other sex chromosome abnormalities; 8 triploidy; and 34 miscellaneous). Using a one in 250 cut off, the Down's screen gave a screen positive rate of 4.07%; addition of atypicality without a trisomy 18 screen gave an extra 0.9% screen positives; trisomy 18 screening without atypicality gave an extra 0.51% screen positives; and atypicality screening after trisomy 18 screening gave 0.52% screen positives. Total screen positive rates were: Down's screening only, 4.07%; Down's screening + atypicality, 4.97%; Down's screening + trisomy 18 screen, 4.58%; Down's screening + trisomy 18 screen + atypicality, 5.09%. The detection rate for Down's syndrome using a one in 250 cut off was 58.9% and with addition of trisomy 18 and atypicality screening this increased to 59.3%, indicating that the extra screens add little to detection of Down's syndrome. For the other chromosomal abnormalities, Down's screening alone detected 22.6% of cases overall and addition of trisomy 18 and atypicality screening increased this to 49%. Examination of the marginal benefits of the extra screening tests revealed that the trisomy 18 screen was better at detecting chromosomal abnormalities than the Down's screen and that it would, therefore, be worthwhile adding this to all screening programs. Atypicality proved to be much less effective and it is suggested that this screen should only be applied in the early days of a screening program until sufficient data is available to design specific screens.

摘要

我评估了在常规唐氏筛查中增加18三体筛查的价值,并将其与非典型性筛查的益处进行了比较。我研究了5080例未受影响的妊娠、144例唐氏综合征和190例非唐氏综合征染色体异常(20例13三体;79例18三体;20例特纳综合征;29例其他性染色体异常;8例三倍体;以及34例其他杂项)。以1/250的截断值,唐氏筛查的筛查阳性率为4.07%;在不进行18三体筛查的情况下增加非典型性筛查,额外增加了0.9%的筛查阳性率;在不进行非典型性筛查的情况下进行18三体筛查,额外增加了0.51%的筛查阳性率;在18三体筛查后进行非典型性筛查,筛查阳性率为0.52%。总筛查阳性率分别为:仅唐氏筛查,4.07%;唐氏筛查+非典型性筛查,4.97%;唐氏筛查+18三体筛查,4.58%;唐氏筛查+18三体筛查+非典型性筛查,5.09%。以1/250的截断值,唐氏综合征的检出率为58.9%,增加18三体和非典型性筛查后,该检出率提高到59.3%,这表明额外的筛查对唐氏综合征的检出增加不多。对于其他染色体异常,仅唐氏筛查总体上能检出22.6%的病例,增加18三体和非典型性筛查后,这一比例提高到49%。对额外筛查试验的边际效益进行检查后发现,18三体筛查在检测染色体异常方面比唐氏筛查更好,因此,将其添加到所有筛查项目中是值得的。事实证明,非典型性筛查的效果要差得多,建议在筛查项目开展初期仅应用该筛查,直到有足够的数据来设计特定的筛查。

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